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Erschienen in: Nutrition & Metabolism 1/2012

Open Access 01.12.2012 | Research

A diet based on multiple functional concepts improves cardiometabolic risk parameters in healthy subjects

verfasst von: Juscelino Tovar, Anne Nilsson, Maria Johansson, Rickard Ekesbo, Ann-Margreth Åberg, Ulla Johansson, Inger Björck

Erschienen in: Nutrition & Metabolism | Ausgabe 1/2012

Abstract

Background

Different foods can modulate cardiometabolic risk factors in persons already affected by metabolic alterations. The objective of this study was to assess, in healthy overweight individuals, the impact of a diet combining multiple functional concepts on risk markers associated with cardiometabolic diseases (CMD).

Methods

Fourty-four healthy women and men (50-73 y.o, BMI 25-33, fasting glycemia ≤ 6.1 mmol/L) participated in a randomized crossover intervention comparing a multifunctional (active) diet (AD) with a control diet (CD) devoid of the "active" components. Each diet was consumed during 4 wk with a 4 wk washout period. AD included the following functional concepts: low glycemic impact meals, antioxidant-rich foods, oily fish as source of long-chain omega-3 fatty acids, viscous dietary fibers, soybean and whole barley kernel products, almonds, stanols and a probiotic strain (Lactobacillus plantarum Heal19/DSM15313).

Results

Although the aim was to improve metabolic markers without promoting body weight loss, minor weight reductions were observed with both diets (0.9-1.8 ± 0.2%; P < 0.05). CD did not modify the metabolic variables measured. AD promoted significant changes in total serum cholesterol (-26 ± 1% vs baseline; P < 0.0001), LDL-cholesterol (-34 ± 1%; P < 0.0001), triglycerides (-19 ± 3%; P = 0.0056), LDL/HDL (-27 ± 2%; P < 0.0001), apoB/apoA1 (-10 ± 2%; P < 0.0001), HbA1c (-2 ± 0.4%; P = 0.0013), hs-CRP (-29 ± 9%; P = 0.0497) and systolic blood pressure (-8 ± 1%¸ P = 0.0123). The differences remained significant after adjustment for weight change. After AD, the Framingham cardiovascular risk estimate was 30 ± 4% (P < 0.0001) lower and the Reynolds cardiovascular risk score, which considers CRP values, decreased by 35 ± 3% (P < 0.0001).

Conclusion

The improved biomarker levels recorded in healthy individuals following the multifunctional regime suggest preventive potential of this dietary approach against CMD.
Hinweise

Electronic supplementary material

The online version of this article (doi:10.​1186/​1743-7075-9-29) contains supplementary material, which is available to authorized users.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

IB, JT and MJ were responsible for the study concept and design; JT, A-MÅ and AN conducted the research; UJ designed the menus; UJ and JT were responsible for the participant's dietetic instruction and coaching; RE was the medical supervisor of the study; JT. and AN analyzed data; JT drafted the manuscript; JT and IB had primary responsibility for final content. All authors revised, discussed and approved the final paper.
Abkürzungen
AD
active diet
apoA
apolipoprotein A
Apo B1
apolipoprotein B1
BP
blood pressure
CD
control diet
CMD
cardiometabolic diseases
CRP
C-reactive protein
FFA
free fatty acids
HBA1c
glycated hemoglobin
HDL
high density lipoprotein
hs-CRP
high sensitivity C-reactive protein
HOMA-IR
homeostatic model assessment of insulin resistance
IL-6
interleukin 6
LDL
low density lipoprotein
MetS
Metabolic syndrome
PAI-1
plasminogen activator inhibitor 1
TNF-α
tumor necrosis factor alpha.

Background

Cardiometabolic diseases (CMD), i.e. cardiovascular disease and diabetes mellitus, are important causes of morbidity and mortality worldwide [1]. Therefore, any person with multiple cardiometabolic risk factors would benefit from lifestyle changes, including improvement of dietary habits, to favorably modify as many as possible risk-associated features [2]. Current recommendations for dietary management of subjects with high metabolic risk involve quantitative and qualitative changes in fat and sugar intakes and high consumption of fruits, vegetables, and whole grains [3]. These guidelines focus on lowering LDL cholesterol, fasting glycemia, body weight and blood pressure as a way to reduce the risk of heart disease [2, 3]. In this context, a portfolio of vegetarian foods has been shown capable of improving LDL cholesterol, HDL cholesterol and CRP values in hypercholesterolemic subjects [47]. Similarly, a Nordic-type diet can modulate the blood lipid profile of hypercholesterolemics [8].
However, a more comprehensive approach to the dietary prevention of CMD also requires attention to other risk factors besides altered blood lipids or glycemia. An increasing number of studies show that different functional foods and ingredients [9, 10] may exert positive effects on particular parameters related to the metabolic syndrome (MetS), a cluster of pathophysiologic conditions increasing cardiometabolic risk [1113]. Such observations may provide the basis for an effective preventive dietary strategy, in which the inclusion of an ample spectrum of active food components or properties may decrease multiple risk factors. The present investigation explores the CMD preventive potential of a diet based on a combination of functional concepts, chosen on the basis of their beneficial effects on single metabolic risk markers.
Since subclinical chronic inflammation is considered an important factor in the etiology of CMD and MetS [2, 12, 13], the components of the multifunctional "active" diet (AD) were selected mainly for their perceived abilities to reduce inflammatory tonus. Within this frame, AD included low glycemic impact foods/meals, foods naturally rich in antioxidant polyphenols and fish products rich in omega-3 fatty acids [1417]. Moreover, the active diet also contained a probiotic Lactobacillus strain capable to decrease the inflammatory response in an animal model [18] and an important supply of soluble dietary fiber from barley and oat, with suggested prebiotic antiinflammatory action in humans [1921]. Another functional concept encompassed in the diet corresponds to foods and ingredients with recognized blood lipid-modulating actions, cholesterol lowering items in particular [2, 4].
We hypothesized that a combination of the above food concepts may target sub-clinical inflammation in a synergistic way and thus allow for the prescription of practically feasible intakes of the active foods. The study was performed in a healthy middle-aged group of overweight volunteers, comparing the AD vs. a control diet (CD) using a cross-over design, with 4-wk study periods. The aim was to improve cardiometabolic risk-associated parameters by changing dietary composition without promoting weight loss.

Participants and methods

Participants

Volunteers without any known medical condition (36 females, 8 men) were recruited through advertisement in local newspapers and were informed orally and in writing of the project disposal, emphasizing the non weight-loss character of the investigation. Inclusion criteria were age between 50 and 73, body mass index in the 25-33 kg/m2 range and fasting plasma glucose value ≤ 6.1 mmol/L. Only medications accepted were hormone replacement for thyroid problems (if constant during the whole trial; 1 female subject) and prescription-free painkillers without antinflammatory action. Baseline data collected at the time of the first clinical visit are shown in Table 1.
Table 1
Characteristics of participants at baselinea
 
Whole group
(n = 44)
Females
(n = 36)b
Males
(n = 8)
Age (y)
63.3 ± 0.8
63.2 ± 0.8
63.6 ± 1.9
Body weight (kg)
79.4 ± 1.4
77.4 ± 1.9
88.6 ± 2.5
BMI (kg/m2)
28.5 ± 0.3
28.5 ± 0.4
28.3 ± 0.3
Cholesterol (mmol/L)
   
Total
5.75 ± 0.16
5.79 ± 0.16
5.55 ± 0.25
LDL
3.65 ± 0.15
3.64 ± 0.80
3.68 ± 0.40
HDL
1.54 ± 0.05
1.62 ± 0.06
1.20 ± 0.01
Triacylglycerols (mmol/L)
1.33 ± 0.11
1.17 ± 0.05
2.09 ± 0.20
Apolipoproteins (g/L)
   
Apo A-1
1.64 ± 0.03
1.68 ± 0.04
1.42 ± 0.07
Apo B
0.96 ± 0.04
0.96 ± 0.02
0.96 ± 0.11
Insulin (mU/L)
6.75 ± 0.66
6.06 ± 0.21
9.87 ± 0.01
Glucose (mmol/L)
5.20 ± 0.06
5.18 ± 0.11
5.32 ± 0.03
HOMA-IR
1.41 ± 0.15
1.25 ± 0.07
2.16 ± 0.01
HbA1c (%)
4.58 ± 0.05
4.59 ± 0.03
4.53 ± 0.05
Free fatty acids (mmol/L)
0.39 ± 0.02
0.41 ± 0.07
0.35 ± 0.05
CRP (mg/L)
2.58 ± 0.34
2.79 ± 0.22
1.61 ± 0.15
IL-6 (ng/L)
0.82 ± 0.07
0.82 ± 0.03
0.81 ± 0.13
TNF-α (ng/L)
10.51 ± 0.36
10.55 ± 0.35
10.38 ± 2.00
PAI-1 (U/mL)
24.56 ± 2.28
22.83 ± 0.31
30.63 ± 2.67
Blood Pressure (mm Hg)
   
Systolic
138.5 ± 2.8
139.1 ± 4.0
136.3 ± 1.2
Diastolic
80.3 ± 1.3
80.5 ± 2.0
79.8 ± 7.5
aValues are means ± SEM
b Thirty-five post-menopausal, 1 peri-menopausal.

Study Protocol

The study was designed as a randomized, controlled, crossover trial of the effect of a multifunctional AD on markers related to cardiometabolic risk. Participants were randomly assigned to one of two treatment orders starting with the AD or the CD, respectively. Each diet phase lasted 4 wk with a 4-wk washout period. The whole trial included four clinical visits, one before and one after each intervention period. During the first visit the participants underwent a physical examination, including auscultation of heart and lungs.
On each clinical visit, fasting body weight was recorded and BP was measured twice, while seating, in the non-dominant arm with a mercury sphyngomanometer. Venous blood was then drawn for the assessment of fasting blood glucose, insulin, HbA1c, cholesterol (total, LDL and HDL), triglycerides, high sensitivity CRP (hs-CRP), PAI-1, IL-6, TNF-α, FFA, apo A1, apo B.
Consumption of dietary supplements such as fish oil (9 subjects), probiotic-containing products (11 subjects) and herbal extracts (11 subjects), was stopped 2 weeks before the start of the trial. Before each dietary phase, the participants attended an introductory session with the nutritionist, who explained practical details of the upcoming diet period.
Volunteers were asked to maintain their normal physical activity regime during the study. A pretrial questionnaire indicated that 48% of the subjects had physical activity equivalent to 1 h/day or more, 30% had 30-60 min/day and 22% reported a low activity level (< 30 min/day). Subjects were also instructed to record their fasting body weight weekly. Variations larger than 1 Kg were reported to the nutritionist, who suggested compensatory dietary modifications. The intake of key components in AD was not affected by these modifications.
Except for almonds and fresh, frozen and smoked fish, the active food items required for the 4-wk AD were provided. Some of the foods included in the CD were also provided. In order to assess dietary compliance, participants completed a daily menu checklist covering each 4-wk diet period. They also completed a questionnaire investigating their experience with each diet. Coaching support was provided by the nutritionist, who contacted each participant at least once per diet period. The study was approved by the Regional Ethical Review Board, Lund, Sweden (Dnr 593/2008).

Diets

Participants ate their habitual diet before and between the experimental periods. A dietary habit questionnaire completed before randomization to the starting dietary treatment was used to help the participants to resume their eating habits during the washout period. To ensure good compliance the participants were provided with a detailed 2-wk rotating menu plan for each dietary period (AD and CD) with all foods ingredients expressed in weight and/or volume measures. Electronic self-taring scales were made available whenever needed. The menu plan also included recipes for preparing meals.
The nutritional profiles of CD and AD are shown in Table 2. Both diets were designed in close agreement with the Nordic Nutrition Recommendations [22] and supplied 2,500-2,600 Kcal/d for men and 2,000-2,100 Kcal/d for women, combining foods from plant and animal origin. Both diets incorporated commercial foods available in food stores, but the AD also included prototypes. For a detailed list of products included in AD see additional file 1.
Table 2
Nutritional profile of CD and AD
 
Control Diet
Active Diet
 
Women
Men
Women
Men
Energy (kcal/day)*
2045
2570
2100
2615
Protein (E%)
15
14
19
18
Carbohydrate (E%)
56
55
51
50
Fat (E%)
29
30
31
31
Saturated fat (E%)
12.8
13.2
5.9
5.9
Monounsaturated fat (E%)
10.5
11.1
13.0
13.6
Polyunsaturated fat (E%)
3.6
3.7
8.2
8.4
ω-6 fatty acids (E%)
2.9
3.1
4.2
4.3
ω-3 fatty acids (E%)
0.8
0.8
2.2
2.3
ω-6/ω-3 ratio
3.8
3.8
1.9
1.9
Dietary fiber (g/day)
22
26
49
61
Cholesterol (mg/day)
200
240
140
160
* Increased energy intake was prescribed for subjects that experienced weight loss during the initial weeks (see Study Protocol section)
AD combined several functional concepts with potential to modulate different physiological variables related to the inflammatory tonus and cardiometabolic risk, including:
a)
food items naturally rich in antioxidants which, in addition to the anti-inflammatory action of their antioxidants [16], contain phenolics that may improve BP and blood lipids [2325].
 
b)
omega-3 fatty acids, especially those long-chained present in oily fish, which have antiinflammatory and triglyceride-lowering properties [17, 26]. In addition, the overall fat quality was also a concept included in the diet design. Thus, the unsaturated-to-saturated fat ratio was larger in AD than in CD (3.6 vs 1.2, respectively; Table 2).
 
c)
ingredients with potential to beneficially affect the gut microbiota: a probiotic strain (Lactobacillus plantarum Heal19, DSM 15313) [18], and prebiotics, i.e. beta-glucans and resistant starch [19, 20] in intact barley kernels, whole kernel rye flour and isolated barley fiber, which were used for baking an experimental beta-glucan-rich bread. Additional sources of viscous fermentable dietary fibre were a prototype oat-based fiber drink, a rye/oat breakfast cereal and an oat-based muesli.
 
d)
low glycemic impact foods/meals were included for their association with reduced risk for the MetS [27] and Type-2 diabetes [28], and its perceived ability to ameliorate the inflammatory tonus in healthy individuals [29]. Low GI foods were represented by products with high beta-glucan content which, besides their prebiotic role, may improve glycemic regulation in a 10-h post-ingestion perspective, through mechanisms related to colonic fermentation and lowered inflammatory tonus [20, 21]. AD also included another high-fibre bread, baked from a wheat flour/guar gum blend: This item promotes a low glycemic response, with reduced peak and prolonged duration of net increment above fasting glucose levels (A. Nilsson, K. Radeborg et al., unpublished results). Additionally, AD included ingredients that lower the post-meal glycemic excursion, such as whey protein and vinegar [14, 15].
 
e)
ingredients with acknowledged abilities to normalize blood levels of both total and LDL cholesterol were also provided: different soybean products, a margarine enriched in stanol esters and dry almonds [4, 12, 3032].
 
The mean daily quantities of the different functional ingredients in AD and the main functional properties considered for their selection are summarized in Table 3. None of the active ingredients were included in the CD, except for minor amounts of ω-3 fatty acids.
Table 3
Proposed functional action, previously tested dose and actual average content of active components in the active diet
 
Main functional
role
Previously tested dose (g/day)
References
Content in the AD (g/day)
    
Women
Men
Soybean/soy protein
Cholesterol-lowering, anti-inflammatory
25-47
[4, 30, 3335]
21
25
Viscous fibers
Cholesterol- lowering, prebiotic, GI-reducing
10-25
[12, 19]
  
β-glucans
   
5.8
6.2
Guar gum
   
5.6
6.7
Total
   
11.4
12.9
Long chain ω-3 fatty acids (20:5 + 22:6)
Triglyceride-lowering, anti-inflammatory
2-6
[17, 26]
2.4
3.0
Almonds
Cholesterol-lowering
28-100
[4, 32]
28
28
Plant stanols
Cholesterol-lowering
2-3
[4, 31]
2.0
2.7
Cinnamon
Antioxidant
6
[25]
3.0
3.0
Blueberries
Antioxidant, prebiotic
350
[36]
74.5
94.5
Vinegar
GI -reducing
20
[14]
22.5
22.5
Probiotic
Cholesterol-lowering, anti-inflammatory
1010 CFU
[18, 37, 38]
0.1
(1010 CFU)
0.1
(1010 CFU)
Whey protein*
GI-reducing
10
[15]
4.3
4.3
*Whey protein (10 g) was only consumed simultaneously with high glycemic index meals (potatoes, parsnip), 3 times per week.
Participants were provided with a 14-day rotating menu plan. For representative 1-day menu plans for the CD and AD see additional file 2. A limited amount of alcohol-containing drinks were allowed during both dietary periods (30 and 37 g ethanol/wk for women and men, respectively). These limits, however, did not compel low-drinkers to increase their habitual alcohol consumption. Due to the low overall energy contribution from such contingent alcoholic drinks, they were not included in the estimation of the energy content of diets. The volunteers' coffee and tea drinking habits were not modified during the trial.

Analyses

Routine blood tests were analyzed at the Clinical Chemistry Laboratory/Skåne University Hospital Lund, on fasting plasma (total and HDL cholesterol, triacylglycerols, apo A-1, apo B, high-sensitivity C-reactive protein), serum (insulin) or on total blood samples (HbA1c). LDL cholesterol concentrations were calculated [39]. HOMA-IR was calculated from fasting blood plasma-glucose and serum insulin values [40].
Venous plasma glucose concentrations were measured immediately after bleeding (HemoCue®B-glucose, HemoCueAB, Ängelholm, Sweden). Serum concentrations of TNF-α and IL-6 were measured with a chemiluminescent immunometric assay, Immulite®/Immulite® 1000 TNF-α (Siemens, Deerfield, IL, USA) and a sensitive enzyme-linked immunosorbent assay, Quantikine® HS (RD Systems Inc, Abingdon, UK), respectively. Samples with high IL-6 concentration (> 10 ng/L) in the ELISA were also measured with the Immulite®/Immulite®1000 IL-6 assay (Siemens, Deerfield, IL, USA). Serum FFA were assessed with an enzymatic colorimetric assay kit (Wako Chemicals GmbH, Germany). Plasminogen activator inhibitor (PAI-1) activity in plasma was measured with TriniLize PAI-1 Activity kit (Trinity Biotech, Jamestown NJ, USA).
The diet compositions were analyzed using the 2009 food database from the Swedish National Food Administration and a computerized calculation program (Dietist XP 3.1; Kost och Näringsdata AB, Bromma, Sweden).

Calculations and statistical analysis

The results are expressed as means ± SEM. Data were evaluated by mixed model ANOVA with sequence and interaction between diet and start/end of treatment periods as fixed effects, and participants within sequence and visit as random effects. Least square means were estimated for the start (Active-week 0, Control-week 0) and end values (Active-wk 4, Control-wk 4) for each diet. Least square means and confidence intervals were calculated for the differences between Active/wk 0, Control/wk 0, Active/wk 4 and Control/wk 4, as well as for the net difference between the diets, i.e. (Active/wk 4 - Active/wk 0) - (Control/wk 4 - Control/wk 0). Another set of analyses with body weight included as a continuous covariate was performed. Analyses were carried out using SAS PROC Mixed (v. 8.2, SAS Institute Inc., Cary, NC, USA). Ten-year coronary heart disease risk was calculated both with the Framingham Study equation [41] considering age, gender, total cholesterol, HDL-cholesterol, smoking and systolic BP values, and the Reynolds Risk Score [42, 43], which also incorporates CRP values.

Power calculation

Primary outcome measure was change in plasma LDL cholesterol. Assuming a 0.5 mmol/L (approximately 10%) post-diet difference and a 0.97 SD [44], with α = 0.05 and 1-β = 0.8, a minimum of 30 participants were required. Among additional measures, changes in hs-CRP were also taken into account. Assuming a 0.44 mg/L (10%) post-diet difference and a SD of 1.0 [45], the required sample size was 42 subjects. Data obtained from hypercholesterolemics with normal CRP levels [7] confirmed that this n value provides sufficient power for assessing CRP changes.

Results

Study population and dietary compliance

Recruitment began February 2009. Trials took place between March 2009 and February 2010. Forty-six volunteers enrolled in the study. The volunteers came from different towns and rural areas in Southwestern Sweden. One participant dropped out during the first week. Forty-five completed the two phases of the intervention. One completer declared to have suffered a minor cerebro-vascular incident some years ago and was therefore excluded from the evaluation. Results from 44 completers (36 women and 8 men) aged 51 - 73 (mean 63.3) were analysed. Only 2 subjects were smokers.
Baseline data confirmed the healthy condition of the cohort studied. This was also evident from the fact that 26 out of the 44 completers (i.e. 59%) showed none of the MetS features assessed (total cholesterol > 150 mg/dL, BP > 130/85 mm Hg and HDL-cholesterol < 50 mg/dL) [46].
Adherence to the dietary plan was good, with similar compliance (P = 0.07) for AD (92 ± 2%) and CD (89 ± 5%). No major problem to consume the prescribed foods was reported. Fifty percent of the participants described AD as more satiating than their habitual diet and 25% expressed that sensation for CD. Ninety percent of the participants experienced increased intestinal gas production with AD as compared to their regular regimes; however, only five participants (11%) qualified this as a burden.

Body weight

Despite the dietary advice provided, weight losses were registered after CD (-0.9%) and AD (-1.8%) (Table 4). Although final body weight was similar with the two treatments, there was a significant difference between diets (P = 0.0113) (Table 4).
Table 4
Effect of CD and AD on plasma lipids, parameters of insulin sensitivity and blood pressurea
 
Control Diet
Active Diet
  
 
Week 0
Week 4
Change (%)
Week 0
Week 4
Change (%)
P (A-C) b
P (A-C; weight corrected) c
Body weight (kg)d
78.9 ± 1.7
78.2 ± 1.34h
-0.9
79.4 ± 1.36i
78.0 ± 1.30f
-1.8
0.0113
 
Cholesterol (mmol/L)
  
Totald
5.73 ± 0.16
5.79 ± 1.39
1
5.81 ± 0.17
4.29 ± 0.10f
-26
< 0.0001
< 0.0001
LDLd
3.66 ± 0.15
3.70 ± 0.16
1
3.65 ± 0.16
2.42 ± 0.10f
-34
< 0.0001
< 0.0001
HDLe
1.53 ± 0.04
1.43 ± 0.04h
-7
1.54 ± 0.05
1.39 ± 0.04g
-10
0.1637
0.1501
Triglycerides (mmol/L)d
1.36 ± 0.11
1.38 ± 0.62
1
1.32 ± 0.09
1.07 ± 0.06g
-19
0.0056
0.0011
Apolipoproteins (g/L)
  
Apo A-1d
1.62 ± 0.03
1.54 ± 0.03f
5
1.62 ± 0.04
1.40 ± 0.02f
-14
< 0.0001
< 0.0001
Apo Bd
0.95 ± 0.04
0.95 ± 0.03
0
0.94 ± 0.04
0.72 ± 0.02f
-23
< 0.0001
< 0.0001
Ratios
        
LDL/HDLd
2.53 ± 0.03
2.73 ± 0.03h
8
2.51 ± 0.02
1.83 ± 0.03f
-27
< 0.0001
< 0.0001
ApoB/ApoA-1d
0.60 ± 0.03
0.63 ± 0.03
5
0.59 ± 0.03
0.53 ± 0.02f
-10
< 0.0001
< 0.0001
Insulin (mU/L)e
6.70 ± 0.42
5.70 ± 0.25
-14
6.08 ± 0.42
5.03 ± 0.36h
-17
0.9410
0.9826
Glucose (mmol/L)d
5.21 ± 0.07
5.13 ± 0.07
-1
5.17 ± 0.07
5.46 ± 0.08g
6
0.0002
0.0002
HOMA-IR
1.39 ± 0.08
1.17 ± 0.08
-16
1.26 ± 0.09
1.09 ± 0.06
-14
0.7376
0.6983
HbA1c (%)d
4.56 ± 0.05
4.58 ± 0.05
1
4.55 ± 0.05
4.47 ± 0.05h
-2
0.0007
0.0013
Free fatty acids (mmol/L)
0.37 ± 0.02
0.37 ± 0.02
0
0.37 ± 0.02
0.37 ± 0.03
0
0.9673
0.9627
Blood pressure (mm Hg)
  
Systolice
135 ± 2
132 ± 2
-2
136 ± 2
128 ± 2f
-8
0.0123
0.0134
Diastolic
79 ± 1
76 ± 1
-4
79 ± 1
76 ± 1
-4
0.9984
0.9265
a Values are means ± SEM. To convert cholesterol and triglyceride values to mg/dL, multiply by 38.67 and 88.57, respectively. To convert apo A-1 and apo B values to mg/dL, multiply by 100.
bP value for the comparison of changes after Active diet and Control diet.
cP value for the comparison of changes after Active diet and Control diet, after correction for weight change
d, e The overall effect of diet was significant: dP < 0.001, eP < 0.05.
f, g, h Significantly different from baseline (Week 0): fP < 0.0001, gP < 0.001, hP < 0.05.
iActive diet baseline (Week 0) significantly different from control diet baseline, P < 0.05.

Blood lipids and lipoproteins

AD reduced total cholesterol (P < 0.0001), LDL cholesterol (P < 0.0001) and triglycerides (P = 0.0004) by 26%, 24% and 19%, respectively, while no change was recorded after the CD period (Table 4). The difference between the two dietary treatments remained after correction for body weight reduction (P < 0.0001, P < 0.0001 and P = 0.0011, respectively; Table 4).
HDL-cholesterol values were similarly reduced by both diets (P = 0.01635) but AD improved both the LDL/HDL ratio (from 2.51 to 1.83, ie. -27%, P < 0.0001) and ApoB to ApoA-1 ratio (from 0.59 to 0.53; -10%; P < 0.0001). The difference between diets was significant (P < 0.0001) after correction for weight changes (Table 4).

Glycemic control variables

No difference in the effect on fasting insulin concentrations was recorded between AD and CD (P = 0.9410), although AD promoted a significant (P = 0.0436) reduction from baseline (Table 4). AD increased fasting blood glucose levels by 6%, with a significant difference between diets after correction for weight changes (P = 0.0002; Table 4). None of the diets affected HOMA-IR values or fasting FFA levels. A 2% decrease in HbA1c was detected after AD, an effect that remained significant after correction for body weight variation (P = 0.0013; Table 4).

Blood pressure

Systolic BP was 8% lower after AD whereas CD had no effect. The difference between diets remained significant after weight correction (P = 0.0134; Table 4). Diastolic pressure values were not affected by any of the diets (Table 4).

Inflammatory and pro-thrombotic status markers

AD reduced hs-CRP value by 29%, with no effect for CD (Table 5). The difference between diets was significant after correction for body weight reduction (P = 0.0497). In spite of a 26% drop in PAI-1 after AD, no net difference was registered between the two diets (P = 0.3854). None of the diets affected fasting IL-6 or TNF-α concentrations.
Table 5
Effect of CD and AD on circulating inflammatory and thrombotic markersa
 
Control Diet
Active Diet
  
 
Week 0
Week 4
Change (%)
Week 0
Week 4
Change (%)
P (A-C) b
P (A-C; weight corrected) c
CRP (mg/L)
2.59 ± 0.34
2.89 ± 0.42
12
2.79 ± 0.39
1.99 ± 0.27e
-29
0.0446
0.0497
IL-6 (ng/L)
0.96 ± 0.09
0.93 ± 0.09
-3
0.71 ± 0.05d
0.81 ± 0.09
14
0.6232
0.3807
TNF-α (ng/L)
9.95 ± 0.36
10.09 ± 0.45
1
11.04 ± 0.46d
10.38 ± 0.42
-6
0.0971
0.1094
PAI-1 (U/mL)
23.34 ± 1.69
19.33 ± 1.68
-19
23.70 ± 2.17
17.65 ± 1.47e
-26
0.3854
0.4104
aValues are expressed as means ± SEM.
bP value for the comparison of changes after Active diet and Control diet.
cP value for the comparison of changes after Active diet and Control diet, after correction for weight change
dActive diet baseline (Week 0) significantly different from control diet baseline, P < 0.05.
eSignificantly different from baseline (Week 0), P < 0.05.

Cardiovascular risk

Significantly lower overall cardiovascular risk scores were calculated after AD (Table 6). The Framingham Study algorithm indicated a 30-percent risk drop (P < 0.0001). The Reynolds risk score predicted a larger risk decline (35%; P < 0.0001). The CD did not reduce risk estimates. The reduction in risk estimates with AD remained significant after weight correction.
Table 6
Effect of CD and AD on 10-y cardiovascular riska
 
Control Diet
Active Diet
P(A-C)b
P(A-C; weight corrected)c
Calculated 10-y CHD risk (%)
Week 0
Week 4
Change (%)
Week 0
Week 4
Change (%)
  
Framingham equationd, f
5.0 ± 0.8
5.2 ± 0.8
4
5.2 ± 0.8
3.6 ± 0.6e
-30
< 0.0001
0.0002
Reynolds scored, g
6.2 ± 0.8
6.2 ± 0.8
1
6.3 ± 0.9
4.1 ± 0.6e
-35
< 0.0001
< 0.0001
a Values are means ± SEM.
bP value for the comparison of changes after Active diet and Control diet.
cP value for the comparison of changes after Active diet and Control diet, after correction for weight change.
d The overall effect of diet was significant: P < 0.0001.
e Significantly different from baseline (Week 0), P < 0.0001.
f CHD risk calculated using the Framingham cardiovascular disease predictive equation [41] considering gender, age, total cholesterol, HDL-cholesterol, and smoking habits.
g CHD risk calculated using the Reynolds risk score [42, 43] considering gender, age, total cholesterol, HDL-cholesterol, CRP and smoking habits.

Discussion

This investigation looked at the possibility of modulating diverse cardiometabolic risk factors by a diet based on multiple functional food concepts. Although a number of therapy-oriented dietary studies have been reported in dyslipidemic subjects [4, 6, 8, 45, 47], no randomized intervention has examined the potential CMD preventive power of a complex functional food array targeting subclinical inflammation. Present results put forward interesting possibilities for this dietary approach.
One characteristic of this study is the healthy condition of the cohort evaluated. The volunteers had no particular diagnosis, beyond being considered at risk for cardiometabolic alterations due to their age (63.3 ± 0.8 y) and BMI (28.5 ± 0.3 kg/m2). According to mean baseline values for blood lipids, BP and glucose homeostasis parameters (Table 1), the group represents the healthy segment of the Swedish population in the 50-75 year-old range. This judgment is supported by the fact that 59% of the volunteers exhibited none of the MetS features evaluated, which contrasts with data from a recent survey of MetS prevalence among 50-60 year olders living in Gothenburg, showing that only 5% of this population group has no risk factor associated to the syndrome [48].
The AD evaluated here included a cluster of functional concepts selected for their abilities to influence different CMD-associated factors, with emphasis on anti-inflammatory properties. The efficacy of the individual concepts has been documented at various levels including intervention studies with humans. Furthermore, since the concepts influence different aspects of the pathophysiological processes associated with CMD, synergistic interaction between functional agents may occur and facilitate the overall modulation of multiple risk indicators. Thus, the daily dosage of some functional components was set below the amount required for optimal effect when tested separately (Table 3), improving the general palatability of the diet.
CD exhibited a good nutritional profile, which matched the Nordic Nutritional Recommendations. Although its dietary fiber content was lower, the CD contribution approached the current estimated fiber intake for the Swedish population (Swedish Food Administration, Personal Communication). Also, besides being rich in functional ingredients, AD had an improved fat quality (Table 2) and its long-chain ω-3 fatty acid content was 10 times larger than in CD. Both diets were well accepted and tolerated by the participants. The variety of foods encompassed, the inclusion of meat and other animal products and the minor amount of alcoholic drinks allowed favored the high dietary adherence and completion rates recorded.
A somewhat greater weight loss was observed after AD, which agrees with the marked satiating action reported for this diet by most participants, an effect that may be due to its higher dietary fiber and protein contents. In fact, 50% of the participants were prescribed increased dietary energy after the first 2 weeks on the regime when their weight loss tendency became evident, in contrast to only 25% requiring that intervention during the CD period. In spite of that a 1.8% (1.4 ± 0.2 kg) mean decrease was recorded after AD. Nonetheless, the statistical adjustment made for the impact of weight variation showed that most of the metabolic improvement observed after AD was attributable to the dietary modification per se and not to a mere weight loss effect.
Blood lipid and apolipoprotein profiles were practically unaffected by CD but sharp reductions in triglycerides, total cholesterol, LDL cholesterol as well as in LDL/HDL and apoB/apoA1 ratios were recorded after the AD period. The latter observation is noteworthy, given the strong association between this quotient and the MetS [49]. The beneficial impact of a low glycemic index diet on blood cholesterol [50] together with the triglyceride-reducing action of polyunsaturated fatty acids from marine origin [10] and content of other known cholesterol-lowering foods and ingredients (soybeans and soy protein, viscous dietary fibers, plant stanols and almonds) are most probably responsible for the overall effect observed with AD.
None of the diets affected insulin sensitivity as estimated by HOMA-IR, although AD promoted slightly higher fasting glucose values than CD. Such an increased glycemia should not pose a risk for healthy individuals, a presumption supported by the reduction recorded in HbA1c and unchanged values for fasting FFA.
The minor decrease in HbA1-c observed with AD might be the consequence of modulated glycation rate during the AD period. The diet's low glycemic impact and high phenolic content, both with anti-glycative effects [51, 52], may have contributed to this result.
CRP is an indicator of the inflammatory status of recognized importance in relation to cardiometabolic alterations [42, 53], with independent predictive value for incident diabetes and cardiovascular diseases [7, 54]. The biomarker decreased markedly after AD, with significant difference between diets after adjustment for weight change. It is tempting to speculate that the improved CRP levels may be due to the antinflammatory properties of AD. The CRP-lowering effectivity of a diet enriched in oily fish, blueberries and wholegrain products was recently shown in patients with impaired glucose tolerance [55].
In addition to improving metabolic risk indicators, AD promoted a significant drop in systolic BP. Such a change may be related, for instance, to the high supply of long chain ω-3 fatty acids, ingredients with suggested BP-modulating activity [56]. Although the present cohort was normotensive (Table 1), the observed pressure reduction resembles that observed with a composite drug treatment in hypertensive volunteers [57].
Besides modulating individual markers associated to CMD, AD also decreased cardiovascular risk as estimated by two different models. The Reynolds algorithm resulted in larger variation from baseline (-34%) than the Framingham score (-30%), stressing the importance of the CRP reduction promoted by this diet.
The improvement achieved for different biomarkers after AD in this relatively low risk group, compares favorably with other dietary interventions. Most of the investigations on the effect of diet CMD-related parameters have been carried out in patients that have metabolic alterations, such as dyslipidemia. A portfolio of cholesterol-lowering foods reduced LDL cholesterol values by 33% in a 4-week trial with hypercholesterolemics [5], which is alike the variation recorded here with a normocholesterolemic group. Furthermore, the presently reported impact of AD on the apoB/Apo A1 ratio, CRP concentration and Framinghams CVD risk is comparable to those previously attained in hypercholesterolemics following the cholesterol-lowering portfolio regime [5, 6].
Also, the effect of AD on total (-26%) and LDL cholesterol levels (-34%) exceeds those reported for the "Nordic" diet in hypercholesterolemic individuals (-16% and -21%, respectively) a regime that, in contrast to ours, did not affect triglycerides or systolic BP beyond weight-loss effects [8]. The AD also promoted greater LDL-cholesterol, triglyceride and CRP reductions than Mediterranean-style regimes administered to individuals at high cardiovascular risk [58].
Compared to other dietary interventions performed in healthy volunteers, the action of the AD on different CMD-related variables is also remarkable. Its effects on systolic BP are similar to those of reduced sodium/DASH [59] or whole-grain [60] regimes. Moreover, in terms of LDL cholesterol reduction AD appears impressively more effective than vegetarian [61] or low GI [50] regimes. The larger effectiveness of AD reflects the power of its multifunctional character.
It is relevant noting that the AD effects were observed under conditions aiming to prevent weight changes. In view of the perceived high satiating ability of the diet, larger weight reductions could be expected if it was consumed ad libitum. This potential deserves further investigation, since dietary interventions promoting weight losses of 5% or more generally result in additional metabolic improvement [9, 62, 63].
The present study had limitations. An evident constraint is the unbalanced gender participation, since 80% of the participants were women. Nevertheless, the lower responsiveness of women to treatments targeting metabolic alterations, such as hyperlipidemias [64, 65], stresses the relevance of our results. The relative heterogeneity of the cohort regarding metabolic characteristics may also be seen as limiting. However, the group reflects the healthy mature segment of the local population. The study length represents another limitation. Prolonged open interventions often yield inferior results, a pattern influenced by reduced dietary compliance. Nonetheless, the good acceptability recorded for the AD allows expectations for reasonable treatment adherence in longer term trials. An increased availability of active food items and ingredients in the near future may ease the achievement of this goal.
The possible impact of AD on body composition and fat distribution was not evaluated here. Since these factors are importantly associated with cardiometabolic risk [46, 54], it would be interesting to include them in future studies on the role of functional diets in the prevention of cardiometabolic alterations. At last, the experimental design envisaged sufficient statistical power regarding changes in LDL cholesterol and CRP but the greater statistical dispersion associated to other biomarkers, such as insulin, PAI-1 and TNF-α, may have left the study underpowered to confirm their modification. This should be born in mind when interpreting the non-significant changes recorded in these parameters.

Conclusion

Tested in a group of middle-aged healthy overweight individuals, a multifunctional diet could modulate different CMD-related variables. The beneficial metabolic effects, good acceptability and ease of implementation shown for the diet in this cohort, suggest this type of regime as a promising tool for dietary preventive action against CMD.

Acknowledgements

The authors thank Dr Peter Höglund (Region Skåne Competence Centre for Clinical Research, Lund) for assistance with statistical analyses. This study was funded by the Lund University Antidiabetic Food Center, a VINNOVA VINN Excellence Center (I. Björck).
This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

IB, JT and MJ were responsible for the study concept and design; JT, A-MÅ and AN conducted the research; UJ designed the menus; UJ and JT were responsible for the participant's dietetic instruction and coaching; RE was the medical supervisor of the study; JT. and AN analyzed data; JT drafted the manuscript; JT and IB had primary responsibility for final content. All authors revised, discussed and approved the final paper.
Literatur
1.
Zurück zum Zitat WHO: The Global Burden of Disease: 2004 Update. 2008, Gèneve, Switzerland: World Health Organization WHO: The Global Burden of Disease: 2004 Update. 2008, Gèneve, Switzerland: World Health Organization
2.
Zurück zum Zitat Feldeisen SE, Tucker KL: Nutritional strategies in the prevention and treatment of metabolic syndrome. Appl Physiol Nutr Metab. 2007, 32: 42-60.CrossRef Feldeisen SE, Tucker KL: Nutritional strategies in the prevention and treatment of metabolic syndrome. Appl Physiol Nutr Metab. 2007, 32: 42-60.CrossRef
3.
Zurück zum Zitat Lloyd-Jones DM, Hong Y, Labarthe D, Mozaffarian D, Appel LJ, Van Horn L, Greenlund K, Daniels S, Nichol G, Tomaselli GF, Arnett DK, Fonarow C, Ho M, Lauer MS, Masoudi FA, Robertson RM, Roger V, Schwamm LH, Sorlie P, Yancy CW, Rosamond WD: Defining and setting national goals for cardiovascular health promotion and disease reduction: The American Heart Association's strategic impact goal through 2020 and beyond. Circulation. 2010, 121: 586-613. 10.1161/CIRCULATIONAHA.109.192703.CrossRef Lloyd-Jones DM, Hong Y, Labarthe D, Mozaffarian D, Appel LJ, Van Horn L, Greenlund K, Daniels S, Nichol G, Tomaselli GF, Arnett DK, Fonarow C, Ho M, Lauer MS, Masoudi FA, Robertson RM, Roger V, Schwamm LH, Sorlie P, Yancy CW, Rosamond WD: Defining and setting national goals for cardiovascular health promotion and disease reduction: The American Heart Association's strategic impact goal through 2020 and beyond. Circulation. 2010, 121: 586-613. 10.1161/CIRCULATIONAHA.109.192703.CrossRef
4.
Zurück zum Zitat Jenkins DJA, Kendall CWC, Faulkner D, Vidgen E, Trautwein EA, Parker TL, Marchie A, Koumbridis G, Lapsley KG, Josse R, Leiter LA, Connelly PW: A dietary portfolio approach to cholesterol reduction: Combined effects of plant sterols, vegetable proteins, and viscous fibers in hypercholesterolemia. Metabolism. 2002, 51: 1596-1604. 10.1053/meta.2002.35578.CrossRef Jenkins DJA, Kendall CWC, Faulkner D, Vidgen E, Trautwein EA, Parker TL, Marchie A, Koumbridis G, Lapsley KG, Josse R, Leiter LA, Connelly PW: A dietary portfolio approach to cholesterol reduction: Combined effects of plant sterols, vegetable proteins, and viscous fibers in hypercholesterolemia. Metabolism. 2002, 51: 1596-1604. 10.1053/meta.2002.35578.CrossRef
5.
Zurück zum Zitat Jenkins DJA, Kendall CWC, Marchie A, Faulkner DA, Josse AR, Wong JM, de Souza R, Emam A, Parker TL, Vidgen E, Trautwein EA, Lapsley KG, Josse RG, Leiter LA, Singer W, Connelly PW: Direct comparison of a dietary portfolio of cholesterol-lowering foods with a statin in hypercholesterolemic participants. Am J Clin Nutr. 2005, 81: 380-387. Jenkins DJA, Kendall CWC, Marchie A, Faulkner DA, Josse AR, Wong JM, de Souza R, Emam A, Parker TL, Vidgen E, Trautwein EA, Lapsley KG, Josse RG, Leiter LA, Singer W, Connelly PW: Direct comparison of a dietary portfolio of cholesterol-lowering foods with a statin in hypercholesterolemic participants. Am J Clin Nutr. 2005, 81: 380-387.
6.
Zurück zum Zitat Jenkins DJ, Chiavaroli L, Wong JM, Kendall C, Lewis GF, Vidgen E, Connelly PW, Leiter LA, Josse RG, Lamarche B: Adding monounsaturated fatty acids to a dietary portfolio of cholesterol-lowering foods in hypercholesterolemia. Can Med Assoc J. 2010, 182: 1961-1967. 10.1503/cmaj.092128.CrossRef Jenkins DJ, Chiavaroli L, Wong JM, Kendall C, Lewis GF, Vidgen E, Connelly PW, Leiter LA, Josse RG, Lamarche B: Adding monounsaturated fatty acids to a dietary portfolio of cholesterol-lowering foods in hypercholesterolemia. Can Med Assoc J. 2010, 182: 1961-1967. 10.1503/cmaj.092128.CrossRef
7.
Zurück zum Zitat Jenkins DJ, Kendall CW, Marchie A, Faulkner DA, Josse AR, Wong JM, de Souza R, Emam A, Parker TL: Direct comparison of dietary portfolio vs statin on C-reactive protein. Eur J Clin Nutr. 2005, 59: 851-860. 10.1038/sj.ejcn.1602152.CrossRef Jenkins DJ, Kendall CW, Marchie A, Faulkner DA, Josse AR, Wong JM, de Souza R, Emam A, Parker TL: Direct comparison of dietary portfolio vs statin on C-reactive protein. Eur J Clin Nutr. 2005, 59: 851-860. 10.1038/sj.ejcn.1602152.CrossRef
8.
Zurück zum Zitat Adamsson V, Reumark A, Fredriksson IB, Hammarström E, Vessby B, Johansson G, Risérus U: Effects of a healthy Nordic diet on cardiovascular risk factors in hypercholesterolaemic subjects: a randomized controlled trial (NORDIET). J Intern Med. 2011, 269: 150-159. 10.1111/j.1365-2796.2010.02290.x.CrossRef Adamsson V, Reumark A, Fredriksson IB, Hammarström E, Vessby B, Johansson G, Risérus U: Effects of a healthy Nordic diet on cardiovascular risk factors in hypercholesterolaemic subjects: a randomized controlled trial (NORDIET). J Intern Med. 2011, 269: 150-159. 10.1111/j.1365-2796.2010.02290.x.CrossRef
9.
Zurück zum Zitat O'Keefe JH, Gheewala NM, O'Keefe JO: Dietary strategies for improving post-prandial glucose, lipids, inflammation and cardiovascular health. J Am Coll Cardiol. 2008, 51: 249-255. 10.1016/j.jacc.2007.10.016.CrossRef O'Keefe JH, Gheewala NM, O'Keefe JO: Dietary strategies for improving post-prandial glucose, lipids, inflammation and cardiovascular health. J Am Coll Cardiol. 2008, 51: 249-255. 10.1016/j.jacc.2007.10.016.CrossRef
10.
Zurück zum Zitat Lopez-Alvarenga JC, Ebbesson SOE, Ebbesson LO, Tejero M, Vorugantia S, Comuzzie AG: Polyunsaturated fatty acids effect on serum triglycerides concentration in the presence of metabolic syndrome components. The Alaska-Siberia Project. Metabolism. 2010, 59: 86-92. 10.1016/j.metabol.2009.07.010.CrossRef Lopez-Alvarenga JC, Ebbesson SOE, Ebbesson LO, Tejero M, Vorugantia S, Comuzzie AG: Polyunsaturated fatty acids effect on serum triglycerides concentration in the presence of metabolic syndrome components. The Alaska-Siberia Project. Metabolism. 2010, 59: 86-92. 10.1016/j.metabol.2009.07.010.CrossRef
11.
Zurück zum Zitat Bruce KD, Hanson MA: The developmental origins, mechanisms and implications of metabolic syndrome. J Nutr. 2010, 140: 648-652. 10.3945/jn.109.111179.CrossRef Bruce KD, Hanson MA: The developmental origins, mechanisms and implications of metabolic syndrome. J Nutr. 2010, 140: 648-652. 10.3945/jn.109.111179.CrossRef
12.
Zurück zum Zitat Expert Panel on Detection, and Treatment of High Blood Cholesterol in Adults: Third report of the national cholesterol education program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (adult treatment panel III) final report. Circulation. 2002, 106: 3143-3421. Expert Panel on Detection, and Treatment of High Blood Cholesterol in Adults: Third report of the national cholesterol education program (NCEP) expert panel on detection, evaluation, and treatment of high blood cholesterol in adults (adult treatment panel III) final report. Circulation. 2002, 106: 3143-3421.
13.
Zurück zum Zitat Giugliano D, Ceriello A, Esposito K: The effects of diet on inflammation - Emphasis on the metabolic syndrome. J Am Coll Cardiol. 2006, 48: 677-685. 10.1016/j.jacc.2006.03.052.CrossRef Giugliano D, Ceriello A, Esposito K: The effects of diet on inflammation - Emphasis on the metabolic syndrome. J Am Coll Cardiol. 2006, 48: 677-685. 10.1016/j.jacc.2006.03.052.CrossRef
14.
Zurück zum Zitat Leeman M, Ostman E, Bjorck I: Vinegar dressing and cold storage of potatoes lowers postprandial glycaemic and insulinaemic responses in healthy subjects. Eur J Clin Nutr. 2005, 59: 1266-1271. 10.1038/sj.ejcn.1602238.CrossRef Leeman M, Ostman E, Bjorck I: Vinegar dressing and cold storage of potatoes lowers postprandial glycaemic and insulinaemic responses in healthy subjects. Eur J Clin Nutr. 2005, 59: 1266-1271. 10.1038/sj.ejcn.1602238.CrossRef
15.
Zurück zum Zitat Nilsson M, Holst JJ, Bjorck IME: Metabolic effects of amino acid mixtures and whey protein in healthy subjects: studies using glucose-equivalent drinks. Am J Clin Nutr. 2007, 85: 996-1004. Nilsson M, Holst JJ, Bjorck IME: Metabolic effects of amino acid mixtures and whey protein in healthy subjects: studies using glucose-equivalent drinks. Am J Clin Nutr. 2007, 85: 996-1004.
16.
Zurück zum Zitat Valtuena S, Pellegrini N, Franzini L, Bianchi MA, Ardigò D, Del Rio D, Piatti P, Scazzina F, Zavaroni I, Brighenti F: Food selection based on total antioxidant capacity can modify antioxidant intake, systemic inflammation, and liver function without altering markers of oxidative stress. Am J Clin Nutr. 2008, 87: 1290-1297. Valtuena S, Pellegrini N, Franzini L, Bianchi MA, Ardigò D, Del Rio D, Piatti P, Scazzina F, Zavaroni I, Brighenti F: Food selection based on total antioxidant capacity can modify antioxidant intake, systemic inflammation, and liver function without altering markers of oxidative stress. Am J Clin Nutr. 2008, 87: 1290-1297.
17.
Zurück zum Zitat Calder PC: n-3 polyunsaturated fatty acids, inflammation, and inflammatory diseases. Am J Clin Nutr. 2006, 83 (Suppl 6): 1505S-1519S. Calder PC: n-3 polyunsaturated fatty acids, inflammation, and inflammatory diseases. Am J Clin Nutr. 2006, 83 (Suppl 6): 1505S-1519S.
18.
Zurück zum Zitat Osman N, Adawi D, Ahrne S, Jeppsson B, Molin G: Endotoxin- and D-galactosamine-induced liver injury improved by the administration of Lactobacillus, Bifidobacterium and blueberry. Dig Liver Dis. 2007, 39: 849-856. 10.1016/j.dld.2007.06.001.CrossRef Osman N, Adawi D, Ahrne S, Jeppsson B, Molin G: Endotoxin- and D-galactosamine-induced liver injury improved by the administration of Lactobacillus, Bifidobacterium and blueberry. Dig Liver Dis. 2007, 39: 849-856. 10.1016/j.dld.2007.06.001.CrossRef
19.
Zurück zum Zitat Mitsou EK, Panopoulou N, Turunen K, Spiliotis V, Kyriacou A: Prebiotic potential of barley derived beta-glucan at low intake levels: A randomised, double-blinded, placebo-controlled clinical study. Food Res Int. 2010, 43: 1086-1092. 10.1016/j.foodres.2010.01.020.CrossRef Mitsou EK, Panopoulou N, Turunen K, Spiliotis V, Kyriacou A: Prebiotic potential of barley derived beta-glucan at low intake levels: A randomised, double-blinded, placebo-controlled clinical study. Food Res Int. 2010, 43: 1086-1092. 10.1016/j.foodres.2010.01.020.CrossRef
20.
Zurück zum Zitat Nilsson A, Ostman E, Preston T, Björck I: Effects of GI vs content of cereal fibre of the evening meal on glucose tolerance at a subsequent standardized breakfast. Eur J Clin Nutr Nutr. 2008, 62: 712-720. 10.1038/sj.ejcn.1602784.CrossRef Nilsson A, Ostman E, Preston T, Björck I: Effects of GI vs content of cereal fibre of the evening meal on glucose tolerance at a subsequent standardized breakfast. Eur J Clin Nutr Nutr. 2008, 62: 712-720. 10.1038/sj.ejcn.1602784.CrossRef
21.
Zurück zum Zitat Nilsson AC, Ostman EM, Holst JJ, Björck IM: Including indigestible carbohydrates in the evening meal of healthy subjects improves glucose tolerance, lowers inflammatory markers, and increases satiety after a subsequent standardized breakfast. J Nutr. 2008, 138: 732-739. Nilsson AC, Ostman EM, Holst JJ, Björck IM: Including indigestible carbohydrates in the evening meal of healthy subjects improves glucose tolerance, lowers inflammatory markers, and increases satiety after a subsequent standardized breakfast. J Nutr. 2008, 138: 732-739.
22.
Zurück zum Zitat Nordic Council of Ministers: Nutrition Recommendations 2004: integrating nutrition and physical activity. 2004, Copenhagen: Nordic Council of Ministers, 4 Nordic Council of Ministers: Nutrition Recommendations 2004: integrating nutrition and physical activity. 2004, Copenhagen: Nordic Council of Ministers, 4
23.
Zurück zum Zitat Kaliora AC, Dedoussis GVZ: Natural antioxidant compounds in risk factors for CVD. Pharmacol Res. 2007, 56: 99-109. 10.1016/j.phrs.2007.04.018.CrossRef Kaliora AC, Dedoussis GVZ: Natural antioxidant compounds in risk factors for CVD. Pharmacol Res. 2007, 56: 99-109. 10.1016/j.phrs.2007.04.018.CrossRef
24.
Zurück zum Zitat Erlund I, Koli R, Alfthan G, Marniemi J, Puukka P, Mustonen P, Mattila P, Jula A: Favorable effects of berry consumption on platelet function, blood pressure, and HDL cholesterol. Am J Clin Nutr. 2008, 87: 323-331. Erlund I, Koli R, Alfthan G, Marniemi J, Puukka P, Mustonen P, Mattila P, Jula A: Favorable effects of berry consumption on platelet function, blood pressure, and HDL cholesterol. Am J Clin Nutr. 2008, 87: 323-331.
25.
Zurück zum Zitat Dugoua JJ, Seely D, Perri D, Cooley K, Forelli T, Mills E, Koren G: From type 2 diabetes to antioxidant activity: a systematic review of the safety and efficacy of common and cassia cinnamon bark. Can J Physiol Pharmacol. 2007, 85: 837-847. 10.1139/Y07-080.CrossRef Dugoua JJ, Seely D, Perri D, Cooley K, Forelli T, Mills E, Koren G: From type 2 diabetes to antioxidant activity: a systematic review of the safety and efficacy of common and cassia cinnamon bark. Can J Physiol Pharmacol. 2007, 85: 837-847. 10.1139/Y07-080.CrossRef
26.
Zurück zum Zitat Musa-Veloso K, Binns MA, Kocenas AC, Poon T, Elliot JA, Rice H, Oppedal-Olsen H, Lloyd H, Lemke S: Long-chain omega-3 fatty acids eicosapentaenoic acid and docosahexaenoic acid dose-dependently reduce fasting serum triglycerides. Nutr Rev. 2010, 68: 155-167. 10.1111/j.1753-4887.2010.00272.x.CrossRef Musa-Veloso K, Binns MA, Kocenas AC, Poon T, Elliot JA, Rice H, Oppedal-Olsen H, Lloyd H, Lemke S: Long-chain omega-3 fatty acids eicosapentaenoic acid and docosahexaenoic acid dose-dependently reduce fasting serum triglycerides. Nutr Rev. 2010, 68: 155-167. 10.1111/j.1753-4887.2010.00272.x.CrossRef
27.
Zurück zum Zitat McKeown NM, Meigs JB, Liu S, Saltzman E, Wilson PW, Jacques PF: Carbohydrate nutrition, insulin resistance, and the prevalence of the metabolic syndrome in the Framingham Offspring Cohort. Diabetes Care. 2004, 27: 538-546. 10.2337/diacare.27.2.538.CrossRef McKeown NM, Meigs JB, Liu S, Saltzman E, Wilson PW, Jacques PF: Carbohydrate nutrition, insulin resistance, and the prevalence of the metabolic syndrome in the Framingham Offspring Cohort. Diabetes Care. 2004, 27: 538-546. 10.2337/diacare.27.2.538.CrossRef
28.
Zurück zum Zitat Barclay A, Petocz P, McMillan-Price J, Flood V, Prvan T, Mitchell P, Brand-Miller J: Glycemic index, glycemic load and diabetes risk: a meta-analysis. Diabetes Res Clin Pract. 2008, 79 (Suppl 1): S30-S31.CrossRef Barclay A, Petocz P, McMillan-Price J, Flood V, Prvan T, Mitchell P, Brand-Miller J: Glycemic index, glycemic load and diabetes risk: a meta-analysis. Diabetes Res Clin Pract. 2008, 79 (Suppl 1): S30-S31.CrossRef
29.
Zurück zum Zitat Ceriello A, Davidson J, Hanefeld M, Leiter L, Monnier L, Owens D, Tajima N, Tuomilehto J: Postprandial hyperglycaemia and cardiovascular complications of diabetes: an update. Nutr Metab Cardiovasc Dis. 2006, 16: 453-456. 10.1016/j.numecd.2006.05.006.CrossRef Ceriello A, Davidson J, Hanefeld M, Leiter L, Monnier L, Owens D, Tajima N, Tuomilehto J: Postprandial hyperglycaemia and cardiovascular complications of diabetes: an update. Nutr Metab Cardiovasc Dis. 2006, 16: 453-456. 10.1016/j.numecd.2006.05.006.CrossRef
30.
Zurück zum Zitat Azadbakht L, Kimiagar M, Mehrabi Y, Esmaillzadeh A, Padyab M, Hu FB, Willett WC: Soy inclusion in the diet improves features of the metabolic syndrome: a randomized crossover study in postmenopausal women. Am J Clin Nutr. 2007, 85: 735-741. Azadbakht L, Kimiagar M, Mehrabi Y, Esmaillzadeh A, Padyab M, Hu FB, Willett WC: Soy inclusion in the diet improves features of the metabolic syndrome: a randomized crossover study in postmenopausal women. Am J Clin Nutr. 2007, 85: 735-741.
31.
Zurück zum Zitat Derdemezis CS, Filippatos TD, Mikhailidis DP: Effects of plant sterols and stanols beyond low-density lipoprotein cholesterol lowering. J Cardiovasc Pharmacol Ther. 2010, 15: 120-314. 10.1177/1074248409357921.CrossRef Derdemezis CS, Filippatos TD, Mikhailidis DP: Effects of plant sterols and stanols beyond low-density lipoprotein cholesterol lowering. J Cardiovasc Pharmacol Ther. 2010, 15: 120-314. 10.1177/1074248409357921.CrossRef
32.
Zurück zum Zitat Griel AE, Kris-Etherton PM: Tree nuts and the lipid profile: a review of clinical studies. Br J Nutr. 2006, 96 (Suppl 2): S68-S78.CrossRef Griel AE, Kris-Etherton PM: Tree nuts and the lipid profile: a review of clinical studies. Br J Nutr. 2006, 96 (Suppl 2): S68-S78.CrossRef
33.
Zurück zum Zitat Azadbakht L, Kimiagar M, Mehrabi Y, Esmaillzadeh A, Hu FB, Willett WC: Soy consumption, markers of inflammation, and endothelial function: a cross-over study in postmenopausal women with the metabolic syndrome. Diabetes Care. 2007, 30: 967-973. 10.2337/dc06-2126.CrossRef Azadbakht L, Kimiagar M, Mehrabi Y, Esmaillzadeh A, Hu FB, Willett WC: Soy consumption, markers of inflammation, and endothelial function: a cross-over study in postmenopausal women with the metabolic syndrome. Diabetes Care. 2007, 30: 967-973. 10.2337/dc06-2126.CrossRef
34.
Zurück zum Zitat Azadbakht L, Esmaillzadeh A: Soy and cardio-metabolic abnormalities: an update. J Res Med Sci. 2008, 13: 88-96. Azadbakht L, Esmaillzadeh A: Soy and cardio-metabolic abnormalities: an update. J Res Med Sci. 2008, 13: 88-96.
35.
Zurück zum Zitat Nagarajan S: Mechanisms of anti-atherosclerotic functions of soy-based diets. J Nutr Biochem. 2010, 21: 255-260. 10.1016/j.jnutbio.2009.09.002.CrossRef Nagarajan S: Mechanisms of anti-atherosclerotic functions of soy-based diets. J Nutr Biochem. 2010, 21: 255-260. 10.1016/j.jnutbio.2009.09.002.CrossRef
36.
Zurück zum Zitat Basu A, Du M, Leyva MJ, Sanchez K, Betts NM, Wu M, Aston CE, Lyons TJ: Blueberries decrease cardiovascular risk factors in obese men and women with metabolic syndrome. J Nutr. 2010, 140: 1582-1587. 10.3945/jn.110.124701.CrossRef Basu A, Du M, Leyva MJ, Sanchez K, Betts NM, Wu M, Aston CE, Lyons TJ: Blueberries decrease cardiovascular risk factors in obese men and women with metabolic syndrome. J Nutr. 2010, 140: 1582-1587. 10.3945/jn.110.124701.CrossRef
37.
Zurück zum Zitat Lomax AR, Calder PC: Probiotics, immune function, infection and inflammation: A review of the evidence from studies conducted in humans. Curr Pharm Des. 2009, 15: 1428-1518. 10.2174/138161209788168155.CrossRef Lomax AR, Calder PC: Probiotics, immune function, infection and inflammation: A review of the evidence from studies conducted in humans. Curr Pharm Des. 2009, 15: 1428-1518. 10.2174/138161209788168155.CrossRef
38.
Zurück zum Zitat Ooi LG, Liong MT: Cholesterol-lowering effects of probiotics and prebiotics: a review of in vivo and in vitro findings. Int J Mol Sci. 2010, 11: 2499-2522. 10.3390/ijms11062499.CrossRef Ooi LG, Liong MT: Cholesterol-lowering effects of probiotics and prebiotics: a review of in vivo and in vitro findings. Int J Mol Sci. 2010, 11: 2499-2522. 10.3390/ijms11062499.CrossRef
39.
Zurück zum Zitat Friedewald WT, Levy RI, Fredriksson DS: Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972, 18: 499-502. Friedewald WT, Levy RI, Fredriksson DS: Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin Chem. 1972, 18: 499-502.
40.
Zurück zum Zitat Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC: Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985, 28: 412-419. 10.1007/BF00280883.CrossRef Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Treacher DF, Turner RC: Homeostasis model assessment: insulin resistance and beta-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985, 28: 412-419. 10.1007/BF00280883.CrossRef
41.
Zurück zum Zitat Anderson KM, Wilson PWF, Odell PM, Kannel WB: An updated coronary risk profile -a statement for health-professionals. Circulation. 1991, 83: 356-362.CrossRef Anderson KM, Wilson PWF, Odell PM, Kannel WB: An updated coronary risk profile -a statement for health-professionals. Circulation. 1991, 83: 356-362.CrossRef
42.
Zurück zum Zitat Ridker PM, Buring JE, Rifai N, Cook NR: Development and validation of improved algorithms for the assessment of global cardiovascular risk in women - The Reynolds Risk Score. JAMA. 2007, 297: 611-619. 10.1001/jama.297.6.611.CrossRef Ridker PM, Buring JE, Rifai N, Cook NR: Development and validation of improved algorithms for the assessment of global cardiovascular risk in women - The Reynolds Risk Score. JAMA. 2007, 297: 611-619. 10.1001/jama.297.6.611.CrossRef
43.
Zurück zum Zitat Ridker PM, Paynter NP, Rifai N, Gaziano JM, Cook NR: C-Reactive Protein and parental history improve global cardiovascular risk prediction: The Reynolds Risk Score for men. Circulation. 2008, 118: 2243-2251. 10.1161/CIRCULATIONAHA.108.814251.CrossRef Ridker PM, Paynter NP, Rifai N, Gaziano JM, Cook NR: C-Reactive Protein and parental history improve global cardiovascular risk prediction: The Reynolds Risk Score for men. Circulation. 2008, 118: 2243-2251. 10.1161/CIRCULATIONAHA.108.814251.CrossRef
44.
Zurück zum Zitat Hulthe J, Fagerberg B: Circulating oxidized LDL is associated with subclinical atherosclerosis development and inflammatory cytokines (AIR Study). Arterioscler Thromb Vasc Biol. 2002, 22: 1162-1167. 10.1161/01.ATV.0000021150.63480.CD.CrossRef Hulthe J, Fagerberg B: Circulating oxidized LDL is associated with subclinical atherosclerosis development and inflammatory cytokines (AIR Study). Arterioscler Thromb Vasc Biol. 2002, 22: 1162-1167. 10.1161/01.ATV.0000021150.63480.CD.CrossRef
45.
Zurück zum Zitat King DE, Egan BM, Woolson RF, Mainous A, Al-Solaiman Y, Jesri A: Effect of a high-fiber diet vs a fiber-supplemented diet on C-reactive protein level. Arch Intern Med. 2007, 167: 502-506. 10.1001/archinte.167.5.502.CrossRef King DE, Egan BM, Woolson RF, Mainous A, Al-Solaiman Y, Jesri A: Effect of a high-fiber diet vs a fiber-supplemented diet on C-reactive protein level. Arch Intern Med. 2007, 167: 502-506. 10.1001/archinte.167.5.502.CrossRef
46.
Zurück zum Zitat Alberti KG, Eckel RH, Grundy SM, Zimmet PZ, Cleeman JI, Donato KA, Fruchart JC, James WP, Loria CM, Smith SC: Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity. Circulation. 2009, 120: 1640-1645. 10.1161/CIRCULATIONAHA.109.192644.CrossRef Alberti KG, Eckel RH, Grundy SM, Zimmet PZ, Cleeman JI, Donato KA, Fruchart JC, James WP, Loria CM, Smith SC: Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity. Circulation. 2009, 120: 1640-1645. 10.1161/CIRCULATIONAHA.109.192644.CrossRef
47.
Zurück zum Zitat Esposito K, Ciotola M, Giugliano D: Mediterranean diet and the metabolic syndrome. Mol Nutr Food Res. 2007, 51: 1268-1274. Esposito K, Ciotola M, Giugliano D: Mediterranean diet and the metabolic syndrome. Mol Nutr Food Res. 2007, 51: 1268-1274.
48.
Zurück zum Zitat Welin L, Adlerberth A, Caidahl K, Eriksson H, Hansson PO, Johansson S, Rosengren A, Svärdsudd K, Welin C, Wilhelmsen L: Prevalence of cardiovascular risk factors and the metabolic syndrome in middle-aged men and women in Gothenburg, Sweden. BMC Public Health. 2008, 8: 403-10.1186/1471-2458-8-403.CrossRef Welin L, Adlerberth A, Caidahl K, Eriksson H, Hansson PO, Johansson S, Rosengren A, Svärdsudd K, Welin C, Wilhelmsen L: Prevalence of cardiovascular risk factors and the metabolic syndrome in middle-aged men and women in Gothenburg, Sweden. BMC Public Health. 2008, 8: 403-10.1186/1471-2458-8-403.CrossRef
49.
Zurück zum Zitat Sierra-Johnson J, Somers VK, Kuniyoshi FHS, Garza CA, Isley WL, Gami AS, Lopez-Jimenez F: Comparison of apolipoprotein-B/apolipoprotein-A1 in subjects with versus without the metabolic syndrome. Am J Cardiol. 2006, 98: 1369-1373. 10.1016/j.amjcard.2006.06.029.CrossRef Sierra-Johnson J, Somers VK, Kuniyoshi FHS, Garza CA, Isley WL, Gami AS, Lopez-Jimenez F: Comparison of apolipoprotein-B/apolipoprotein-A1 in subjects with versus without the metabolic syndrome. Am J Cardiol. 2006, 98: 1369-1373. 10.1016/j.amjcard.2006.06.029.CrossRef
50.
Zurück zum Zitat de Rougemont A, Normand S, Nazare JA, Skilton MR, Sothier M, Vinoy S, Laville M: Beneficial effects of a 5-week low-glycaemic index regimen on weight control and cardiovascular risk factors in overweight non-diabetic subjects. Br J Nutr. 2007, 98: 1288-1298.CrossRef de Rougemont A, Normand S, Nazare JA, Skilton MR, Sothier M, Vinoy S, Laville M: Beneficial effects of a 5-week low-glycaemic index regimen on weight control and cardiovascular risk factors in overweight non-diabetic subjects. Br J Nutr. 2007, 98: 1288-1298.CrossRef
51.
Zurück zum Zitat Jenkins DJ, Wolever TM, Buckley G, Lam KY, Giudici S, Kalmusky J, Jenkins AL, Patten RL, Bird J: Low-glycemic-index starchy foods in the diabetic diet. Am J Clin Nutr. 1988, 48: 248-254. Jenkins DJ, Wolever TM, Buckley G, Lam KY, Giudici S, Kalmusky J, Jenkins AL, Patten RL, Bird J: Low-glycemic-index starchy foods in the diabetic diet. Am J Clin Nutr. 1988, 48: 248-254.
52.
Zurück zum Zitat Verzelloni E, Pellacani C, Tagliazucchi D, Tagliaferri S, Calani L, Costa LG, Brighenti F, Borges G, Crozier A, Conte A, Del Rio D: Antiglycative and neuroprotective activity of colon-derived polyphenol catabolites. Mol Nutr Food Res. 2011, 55 (Suppl 1): S35-S43.CrossRef Verzelloni E, Pellacani C, Tagliazucchi D, Tagliaferri S, Calani L, Costa LG, Brighenti F, Borges G, Crozier A, Conte A, Del Rio D: Antiglycative and neuroprotective activity of colon-derived polyphenol catabolites. Mol Nutr Food Res. 2011, 55 (Suppl 1): S35-S43.CrossRef
53.
Zurück zum Zitat Eckel RH, Grundy SM, Zimmet PZ: The metabolic syndrome. Lancet. 2005, 365: 1415-1428. 10.1016/S0140-6736(05)66378-7.CrossRef Eckel RH, Grundy SM, Zimmet PZ: The metabolic syndrome. Lancet. 2005, 365: 1415-1428. 10.1016/S0140-6736(05)66378-7.CrossRef
54.
Zurück zum Zitat Ridker PM, Hennekens CH, Buring JE, Rifai N: C reactive protein and other markers of inflammation in the prediction of cardiovascular disease in women. N Engl J Med. 2000, 342: 836-843. 10.1056/NEJM200003233421202.CrossRef Ridker PM, Hennekens CH, Buring JE, Rifai N: C reactive protein and other markers of inflammation in the prediction of cardiovascular disease in women. N Engl J Med. 2000, 342: 836-843. 10.1056/NEJM200003233421202.CrossRef
55.
Zurück zum Zitat de Mello VDF, Schwab U, Kolemainen M, Koenig W, Siloaho M, Poutanen K, Mykkänen H, Uusitupa M: A diet high in fatty fish, bilberries and wholegrain products improves markers of endothelial function and inflammation in individuals with impaired glucose metabolism in a randomized controlled trial: The Sysdimet study. Diabetologia. 2011, 54: 2755-2767. 10.1007/s00125-011-2285-3.CrossRef de Mello VDF, Schwab U, Kolemainen M, Koenig W, Siloaho M, Poutanen K, Mykkänen H, Uusitupa M: A diet high in fatty fish, bilberries and wholegrain products improves markers of endothelial function and inflammation in individuals with impaired glucose metabolism in a randomized controlled trial: The Sysdimet study. Diabetologia. 2011, 54: 2755-2767. 10.1007/s00125-011-2285-3.CrossRef
56.
Zurück zum Zitat Morris MC, Sacks F, Rosner B: Does fish-oil lower blood pressure? A metanalysis of controlled trials. Circulation. 1993, 88: 523-533.CrossRef Morris MC, Sacks F, Rosner B: Does fish-oil lower blood pressure? A metanalysis of controlled trials. Circulation. 1993, 88: 523-533.CrossRef
57.
Zurück zum Zitat Jamerson K, Weber MA, Bakris GL, Dahlöf B, Pitt B, Shi V, Hester A, Gupte J, Gatlin M, Velazquez EJ: Benazepril plus Amlodipine or Hydrochlorothiazide for hypertension in high-risk patients. N Engl J Med. 2008, 359: 2417-2428. 10.1056/NEJMoa0806182.CrossRef Jamerson K, Weber MA, Bakris GL, Dahlöf B, Pitt B, Shi V, Hester A, Gupte J, Gatlin M, Velazquez EJ: Benazepril plus Amlodipine or Hydrochlorothiazide for hypertension in high-risk patients. N Engl J Med. 2008, 359: 2417-2428. 10.1056/NEJMoa0806182.CrossRef
58.
Zurück zum Zitat Estruch R, Martínez-González MA, Corella D, Salas-Salvadó J, Ruiz-Gutiérrez V, Covas MI, Fiol M, Gómez-Gracia E, López-Sabater MC, Vinyoles E, Arós F, Conde M, Lahoz C, Lapetra J, Sáez G, Ros E, the PREDIMED Study investigators: Effects of a Mediterranean-style diet on cardiovascular risk factors: a randomized trial. Ann Intern Med. 2006, 145: 1-11.CrossRef Estruch R, Martínez-González MA, Corella D, Salas-Salvadó J, Ruiz-Gutiérrez V, Covas MI, Fiol M, Gómez-Gracia E, López-Sabater MC, Vinyoles E, Arós F, Conde M, Lahoz C, Lapetra J, Sáez G, Ros E, the PREDIMED Study investigators: Effects of a Mediterranean-style diet on cardiovascular risk factors: a randomized trial. Ann Intern Med. 2006, 145: 1-11.CrossRef
59.
Zurück zum Zitat Sacks FM, Svetkey LP, Vollmer WM, Appel LJ, Bray GA, Harsha D, Obarzanek E, Conlin PR, Miller ER, Simons-Morton DG, Karanja N, Lin PH, DASH-Sodium Collaborative Research Group: Effects on blood pressure of reduced dietary sodium and the Dietary Approaches to Stop Hypertension (DASH) diet. N Engl J Med. 2001, 344: 3-10. 10.1056/NEJM200101043440101.CrossRef Sacks FM, Svetkey LP, Vollmer WM, Appel LJ, Bray GA, Harsha D, Obarzanek E, Conlin PR, Miller ER, Simons-Morton DG, Karanja N, Lin PH, DASH-Sodium Collaborative Research Group: Effects on blood pressure of reduced dietary sodium and the Dietary Approaches to Stop Hypertension (DASH) diet. N Engl J Med. 2001, 344: 3-10. 10.1056/NEJM200101043440101.CrossRef
60.
Zurück zum Zitat Tighe P, Duthie G, Vaughan N, Brittenden J, Simpson WG, Duthie S, Mutch W, Wahle K, Horgan G, Thies F: Effect of increased consumption of whole-grain foods on blood pressure and other cardiovascular risk markers in healthy middle-aged persons: a randomized controlled trial. Am J Clin Nutr. 2010, 92: 733-740. 10.3945/ajcn.2010.29417.CrossRef Tighe P, Duthie G, Vaughan N, Brittenden J, Simpson WG, Duthie S, Mutch W, Wahle K, Horgan G, Thies F: Effect of increased consumption of whole-grain foods on blood pressure and other cardiovascular risk markers in healthy middle-aged persons: a randomized controlled trial. Am J Clin Nutr. 2010, 92: 733-740. 10.3945/ajcn.2010.29417.CrossRef
61.
Zurück zum Zitat Barnard ND, Scialli AR, Bertron P, Hurlock D, Edmonds K, Talev L: Effectiveness of a low-fat vegetarian diet in altering serum lipids in healthy premenopausal women. Am J Cardiol. 2000, 85: 969-972. 10.1016/S0002-9149(99)00911-X.CrossRef Barnard ND, Scialli AR, Bertron P, Hurlock D, Edmonds K, Talev L: Effectiveness of a low-fat vegetarian diet in altering serum lipids in healthy premenopausal women. Am J Cardiol. 2000, 85: 969-972. 10.1016/S0002-9149(99)00911-X.CrossRef
62.
Zurück zum Zitat Azadbakht L, Mirmiran P, Esmaillzadeh A, Azizi T, Azizi F: Beneficial effects of a Dietary Approaches to Stop Hypertension eating plan on features of the metabolic syndrome. Diabetes Care. 2005, 28: 2823-2831. 10.2337/diacare.28.12.2823.CrossRef Azadbakht L, Mirmiran P, Esmaillzadeh A, Azizi T, Azizi F: Beneficial effects of a Dietary Approaches to Stop Hypertension eating plan on features of the metabolic syndrome. Diabetes Care. 2005, 28: 2823-2831. 10.2337/diacare.28.12.2823.CrossRef
63.
Zurück zum Zitat Dagogo-Jack S, Egbuonu N, Edeoga C: Principles and practice of nonpharmacological interventions to reduce cardiometabolic risk. Med Princ Pract. 2010, 19: 167-175. 10.1159/000285280.CrossRef Dagogo-Jack S, Egbuonu N, Edeoga C: Principles and practice of nonpharmacological interventions to reduce cardiometabolic risk. Med Princ Pract. 2010, 19: 167-175. 10.1159/000285280.CrossRef
64.
Zurück zum Zitat Mehner A, Lindblad U, Råstam L, Boström KB: Cholesterol in women at high cardiovascular risk is less successfully treated than in corresponding men. The Skaraborg Hypertension and Diabetes Project. Eur J Clin Pharmacol. 2008, 64: 815-820. 10.1007/s00228-008-0482-x.CrossRef Mehner A, Lindblad U, Råstam L, Boström KB: Cholesterol in women at high cardiovascular risk is less successfully treated than in corresponding men. The Skaraborg Hypertension and Diabetes Project. Eur J Clin Pharmacol. 2008, 64: 815-820. 10.1007/s00228-008-0482-x.CrossRef
65.
Zurück zum Zitat Santos RD, Waters DD, Tarasenko L, Messig M, Jukema JW, Ferrières J, Verdejo J, Chiang CW, L-TAP 2 Investigators: Low- and high-density lipoprotein cholesterol goal attainment in dyslipidemic women: The Lipid Treatment Assessment Project (L-TAP) 2. Am Heart J. 2009, 158: 860-866. 10.1016/j.ahj.2009.08.009.CrossRef Santos RD, Waters DD, Tarasenko L, Messig M, Jukema JW, Ferrières J, Verdejo J, Chiang CW, L-TAP 2 Investigators: Low- and high-density lipoprotein cholesterol goal attainment in dyslipidemic women: The Lipid Treatment Assessment Project (L-TAP) 2. Am Heart J. 2009, 158: 860-866. 10.1016/j.ahj.2009.08.009.CrossRef
Metadaten
Titel
A diet based on multiple functional concepts improves cardiometabolic risk parameters in healthy subjects
verfasst von
Juscelino Tovar
Anne Nilsson
Maria Johansson
Rickard Ekesbo
Ann-Margreth Åberg
Ulla Johansson
Inger Björck
Publikationsdatum
01.12.2012
Verlag
BioMed Central
Erschienen in
Nutrition & Metabolism / Ausgabe 1/2012
Elektronische ISSN: 1743-7075
DOI
https://doi.org/10.1186/1743-7075-9-29

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