Factors associated with postprandial lipemia and apolipoprotein A-V levels in individuals with familial combined hyperlipidemia
verfasst von:
Paloma Almeda-Valdes, Daniel Cuevas-Ramos, Roopa Mehta, Liliana Muñoz-Hernandez, Ivette Cruz-Bautista, Oscar Perez-Mendez, Maria Teresa Tusie-Luna, Francisco J Gomez-Perez, Päivi Pajukanta, Niina Matikainen, Marja-Riitta Taskinen, Carlos A Aguilar-Salinas
Alterations in postprandial metabolism have been described in familial combined hyperlipidemia (FCH); however, their underlying mechanisms are not well characterized. We aimed to identify factors related to the magnitude of postprandial lipemia and apolipoprotein (apo) A-V levels in subjects with FCH.
Methods
FCH cases (n = 99) were studied using a standardized meal test. Abdominal obesity was assessed using the waist to hip ratio (WHR). A linear regression model was performed to investigate the variables associated with the triglycerides incremental area under the curve (iAUC). Independent associations between metabolic variables and apo A-V iAUC were also investigated in a randomly selected subgroup (n = 44). The study sample was classified according to the presence of fasting hypertriglyceridemia (≥150 mg/dL) and abdominal obesity (WHR ≥0.92 in men and ≥0.85 in women) to explore differences in parameters.
Results
The fasting apo B-48 levels (r = 0.404), and the WHR (r = 0.359) were independent factors contributing to the triglycerides iAUC (r2 = 0.29, P < 0.001). The triglycerides iAUC was independently associated with the apo A-V iAUC (r2 = 0.54, P < 0.01). Patients with both hypertriglyceridemia and abdominal obesity showed the most robust triglycerides and apo A-V postprandial responses.
Conclusions
In patients with FCH the fasting apo B-48 level is the main factor associated with postprandial lipemia. Abdominal obesity also contributes to the magnitude of the postprandial response.
The triglycerides postprandial increment is the principal factor associated with the apo A-V postprandial response.
The online version of this article (doi:10.1186/1472-6823-14-90) contains supplementary material, which is available to authorized users.
Competing interests
The authors declare they have no competing interests.
Authors’ contributions
PA: conducted the study, performed data collection, data analysis, data interpretation, and manuscript writing; DC: performed data collection and reviewed the manuscript; RM: performed data interpretation and reviewed the manuscript; LM: conducted the study and performed data collection; IC: conducted the study; OP, MT, and FG: reviewed the manuscript; PP, NM, and MT: performed analysis and reviewed the manuscript; CA: designed the study, performed data interpretation and reviewed the manuscript. All authors read and approved the final manuscript.
Abkürzungen
FCH
Familial combined hyperlipidemia
iAUC
Incremental area under the curve
WHR
Waist to hip ratio
TRL
Triglycerides rich lipoproteins
CVD
Cardiovascular disease
VLDL
Very low density lipoproteins
HDL
High density lipoprotein
HDL-c
HDL-cholesterol
LPL
Lipoprotein lipase
BMI
Body mass index
AST
Aspartate aminotransferase
ALT
Alanine aminotransferase
GGT
Gamma glutamyltransferase
LDL-c
LDL-cholesterol
MEIA
Micro-particle enzymatic immunoanalysis
ELISA
Enzyme-linked immunosorbent assays
SD
Standard deviation
IQR
Interquartile range
ANOVA
Analysis of variance
HTG
Hypertriglyceridemia
NTG
Normotriglyceridemia.
Background
Postprandial lipemia refers to the increment of triglycerides rich lipoproteins (TRL) in plasma after a meal. This process is associated with an increase in very low density lipoproteins (VLDL) that are transformed to low density lipoproteins (LDL) and delivered to the arterial wall, a decrease of high-density lipoprotein (HDL) particle number and function, and production of small-dense LDL. This unfavorable lipid profile increases cardiovascular disease (CVD) risk [1]. Postprandial lipemia magnitude is affected by the degree of secretion of TRL and their rate of clearance [2].
Fasting triglycerides concentration represents the main determinant of postprandial lipemia, explaining around 30% of the variance [3, 4]. In selected populations, anthropometric characteristics, insulin, HDL-cholesterol (HDL-c), and apolipoprotein (apo) A-IV, have also been identified as determinants of postprandial lipemia [5, 6].
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Recent studies have suggested a role for apo A-V in modulating triglycerides metabolism [7]. Firstly, it promotes a greater interaction between TRL and lipoprotein lipase (LPL), increasing their hydrolysis. Secondly, apo A-V promotes liver triglyceride synthesis [8].
Familial combined hyperlipidemia (FCH) is the most common genetic form of dyslipidemia [9]. It is associated with a 1.7- to 10-fold increased risk for CVD [10]. Disturbances of lipid metabolism in FCH are complex. Dyslipidemia in patients with FCH is characterized by an overproduction and a delayed catabolism of VLDL [11]. Patients with FCH exhibit a high VLDL level and an exaggerated postprandial lipemia. The specific mechanisms contributing to postprandial lipemia in FCH are not well established.
In this study we explored the factors associated with postprandial lipemia in patients with FCH and whether the metabolic phenotype alters the magnitude of this phenomenon. We first analyzed the determinants of postprandial triglycerides incremental area under the curve (iAUC). Subsequently, in a randomly selected subgroup, we investigated factors associated with fasting and postprandial Apo A-V. Finally, we classified participants according to the presence of fasting hypertriglyceridemia (HTG) and increased waist to hip ratio (WHR) in order to evaluate if the metabolic phenotype modulated the magnitude and time-sequence of the triglycerides iAUC.
Methods
Study subjects
The study population was selected from an out-patient cohort of families with FCH identified at the Instituto Nacional de Ciencias Medicas y Nutricion in Mexico City. None of the subjects were taking lipid-lowering therapy mainly because they were newly diagnosed. FCH was diagnosed using the following criteria: 1) LDL-cholesterol and/or triglycerides concentrations >160 mg/dL and >150 mg/dL, respectively; 2) at least one first-degree relative with hyperlipidemia with a different lipid phenotype, and 3) a concentration of apo B > the 90th percentile for the Mexican population (>108 mg/dL and >99 mg/dL in men and women, respectively) [12‐14]. All study subjects had apo B levels over the 90th percentile for the Mexican population and HTG and/or hypercholesterolemia at diagnosis; however, some of them showed inferior levels at the time of the study due to the already known variability in the lipid profile associated with FCH. None of the subjects had evidence of chronic illnesses or significant organ dysfunction. Subjects were weight-stable (<2 kg change) for at least 6 months before entering the study. We excluded subjects with diabetes mellitus, fasting triglycerides ≥1000 mg/dL, body mass index (BMI) ≥40 kg/m2, alcohol consumption >10 g/day in women and >20 g/day in men, or currently taking medications known to affect lipid metabolism. Individuals with other primary or secondary dyslipidemias were also excluded.
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The Comite de Etica en Investigacion del Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran approved the protocol and informed consent was obtained from all subjects.
Experimental procedures
Subjects completed a comprehensive medical evaluation, including a history and physical examination. Anthropometric measurements including height, weight, waist, and hip circumference, systolic and diastolic blood pressures were measured following standardized procedures.
Meal test
Subjects were asked to attend after a 12-hour fasting period, and a standardized meal was provided. Blood samples were then obtained at 0 (fasting), 3, 4, 6, and 8 hours after meal ingestion [15]. The meal consisted of one quarter pounder with cheese hamburger with 5 grams of mayonnaise, 71 grams of fries, and 250 ml of milk. The energy content of the meal is 919 kcal and the composition 50% (51 g) fat, 32.7% (75 g) carbohydrates, and 17.3% (40 g) protein. After ingestion of the meal subjects were allowed to drink only water.
Sample analysis
Blood samples were collected in EDTA-containing tubes. Levels of triglycerides, total cholesterol, HDL-cholesterol (HDL-c), glucose, aspartate aminotransferase (AST), alanine aminotransferase (ALT), and gamma glutamyltransferase (GGT) were measured by automated enzymatic assays (Beckman Synchron CX, Brea, CA). LDL-cholesterol (LDL-c) was calculated by the Friedewald formula [16] when the fasting triglycerides levels were <300 mg/dL. Insulin levels were determined utilizing micro-particle enzymatic immunoanalysis (MEIA) (Axym System Abbot, Green Oaks, IL) and apo B levels by kinetic nephelometry (Beckman Immage, Brea, CA). In a randomly selected subgroup, apo A-V and apo B-48 concentrations were measured at the University of Helsinki using ELISA assays (Millipore, MA, USA and Shibayagi Co., Shibukawa, Gunma, Japan, respectively).
Calculations
The iAUC over the 8-hour period was calculated using the trapezoidal method by subtracting the fasting concentration from the total AUC. To evaluate insulin sensitivity the homeostasis model assessment (HOMA-IR) index and the Matsuda index were calculated [17‐19].
Statistical analysis
Data were examined for normality with the Shapiro-Wilk test. Continuous variables are reported as mean ± SD (standard deviation) or median and [interquartile range (IQR)] as appropriate. Categorical variables are reported as frequencies and percentages. Friedman tests were performed to examine the triglycerides, apo B-48, and apo A-V postprandial responses. Following logarithmic transformation of non-normal distributed variables, Pearson correlations were calculated and stepwise multiple linear regression models were constructed to investigate the independent predictors of the iAUC of triglycerides and apo A-V. In the first model, the dependent variable was the triglycerides iAUC and the independent variables were the fasting apo B-48, fasting triglycerides, time of triglycerides peak, WHR, HOMA-IR, and the apo B. In the second model, the dependent variable was the apo A-V iAUC. This model included the triglycerides iAUC, apo B-48 iAUC, fasting triglycerides, apo B, and HDL-c as independent variables.
The population was then classified into four groups according to the presence or absence of HTG (fasting triglycerides level ≥150 mg/dL and <150 mg/dL, respectively) and abdominal obesity (defined using the median WHR of the population, ≥0.92 in men and ≥0.85 and women). One way ANOVA or Kruskal Wallis tests were performed to examine differences between these groups as appropriate. If significance was achieved (P value <0.05) comparisons between individual groups were performed with independent T test or Mann–Whitney U test as appropriate. Statistical analyses were performed using SPSS software version 19.0 (Armonk, NY). A P value <0.05 (two tailed) was considered statistically significant.
Results
Baseline characteristics
Of the 106 subjects recruited, seven were excluded; this was due to an unconfirmed diagnosis of FCH (n = 5), presence of undiagnosed diabetes (n = 1), and an elevated fasting triglycerides concentration (n = 1). The characteristics of the 99 individuals participating in the study are summarized in Table 1. They were 45.4 ± 13.5 years old, with overweight (median BMI of 27.1 [25–29.9] kg/m2), and had a mean waist circumference of 89.1 ± 10.6 cm. The baseline characteristics of the randomly selected subgroup (n = 44) used for apo A-V and apo B-48 analysis were similar in comparison with the whole cohort (Table 1).
Table 1
Subjects characteristics
Parameters
All cohort (n = 99)
Subgroup (n = 44)
P
Gender (male/female)
33/66
13/31
0.471
Age (years)
45.4 ± 13.5
46.0 ± 11.6
0.710
BMI (kg/m2)a
27.1 [25–29.9]
27.0 [25.2–30.5]
0.742
Waist circumference (cm)
89.1 ± 10.6
88.0 ± 11.0
0.358
WHR
0.88 ± 0.07
0.86 ± 0.07
0.070
Systolic blood pressure (mmHg)
120 [110–125]
120 [110–125]
0.742
Diastolic blood pressure (mmHg)
80 [70–80]
77.5 [70–83]
0.462
Triglycerides (mg/dL)
201.5 [135.5–309]
197.0 [131.0–318.0]
0.555
CholedL)/dL)
219.6 ± 37
212.6 ± 32
0.118
HDL-c (mg/dL)
42 [36–51]
39 [34–45]
0.052
LDL-c (mg/dL)b
131.4 ± 30.9
133.4 ± 24.5
0.863
Non HDL-c (mg/dl)
175.7 ± 35.9
174.4 ± 32.1
0.757
Apo B (mg/dL)
115.1 ± 25.6
116.9 ± 27.2
0.556
Apo B-48 (μg/mL)
-
5.3 [3–7.4]
-
Apo A-V (ng/mL)
-
303.3 [268.4–390.3]
-
Glucose (mg/dL)
97 [92–107]
94.0 [88–100]
0.054
Insulin (μU/mL)
9.5 [6.8–12.3]
9.5 [7.0–12.6]
0.932
HOMA-IR
2.3 [1.5–3.2]
2.1 [1.4–3.2]
0.390
Matsuda index
30.5 [20.3–39.7]
32.7 [22.1–49.1]
0.259
AST (IU/L)
26 [23–32]
26 [23–32]
0.914
ALT (IU/L)
24.5 [17–34]
22 [17–34]
0.291
GGT (IU/L)
22 [15–37]
20 [14–34]
0.322
Data expressed as means ± SD or medians [IQR].
a The weight in kilograms divided by the square of the height in meters.
b Estimated in 75 subjects with triglycerides levels <300 mg/dl.
Baseline characteristics of study subjects and of the apo A-V and apo B-48 subgroup.
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Postprandial parameters
After the meal challenge, plasma triglycerides, apo B-48, and apo A-V concentrations increased significantly (P < 0.001) (Figure 1). Median peak level of triglycerides was 367 mg/dL [241.5–510.5]; this was observed at 4 hours in 30.3%, and at 3 hours in 25.3% of the population. At the end of the sampling period, triglycerides concentrations returned to baseline only in 25% of the study subjects. On the other hand, the median apo B-48 peak concentration was 11.7 μg/mL [5.5- 16.3] and the time to peak was at 4 hours in 33%, and at 6 hours in 26% of the population. In the majority of patients (83%) levels remained above baseline after eight hours. In addition, the median apo A-V peak concentration was 478.4 ng/dL [378.6–611.7]. This was observed at 4 hours in 42%, and at 6 hours in 28% of cases. In 67%, concentrations did not reach baseline levels after 8 hours. These results are summarized in Figure 1.
Figure 1
Triglycerides, apo B-48, and apo A-V levels during the meal test. Box plots showing median levels of triglycerides, apo B-48, and apo A-V concentrations after the meal test. Boxes show interquartile ranges, and bars represent highest and lowest values (P < 0.001 for all with Friedman test).
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We calculated the apo B48/apo B index, at baseline and at eight hours following the test meal, as a measure of the contribution of chylomicron particles to postprandial lipemia. This index showed a significant change (0.04 [0.03–0.06] vs. 0.06 [0.03–0.11], P < 0.001), representing the chylomicrons increase in response to the meal ingestion.
The fasting and 8-hour apo A-V/triglycerides ratio was estimated to evaluate the change in this index associated with the chylomicrons response after ingestion of the meal. We did not find a significant change in this index comparing the fasting state and 8 hours after ingestion of the meal (1.6 [1.0–2.2] and 1.5 [1.1–2.1], respectively, P = 0.080).
Factors associated with postprandial lipemia
The triglycerides iAUC showed a significant correlation with the fasting apo B-48 and the fasting triglycerides concentrations (r = 0.43, P = 0.004 and r = 0.39, P < 0.001, respectively). In addition, significant positive correlations were found between the triglycerides iAUC and the time of triglycerides peak (r = 0.35, P < 0.001), WHR (r = 0.30, P = 0.003), apo B (r = 0.24, P = 0.017), BMI (r = 0.24, P = 0.017), and HOMA-IR (r = 0.23, P = 0.022). A significant negative correlation was identified between Matsuda index and the triglycerides iAUC (r = -0.20, P = 0.045).
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Despite a positive correlation between the triglycerides iAUC and the apo B-48 iAUC (r = 0.44, P = 0.004), we did not find significant correlations between the apo B-48 iAUC and the studied variables.
Independent factors associated with post-prandial triglycerides response
The linear regression analysis identified the fasting apo B-48 levels (r = 0.40), and the WHR (r = 0.35) as independent parameters determining the triglycerides iAUC, explaining 29% of the variability. The model also included the fasting triglycerides concentration, time of triglycerides peak, HOMA-IR, and the apo B levels, none of these parameters demonstrated an independent association with the triglycerides iAUC (Table 2).
Table 2
Linear regression model
Independent variables
β
Standardized β
t
P
Partial correlations
Fasting apo B-48
0.512
0.377
2.45
0.009
0.404
WHR
4.885
0.328
2.4
0.021
0.359
r2 = 0.29, F = 7.97, P < 0.001.
Dependent variable: triglycerides iAUC; variables included in the model: fasting apo B-48, fasting triglycerides, time of triglycerides peak, apolipoprotein B, HOMA-IR, and waist to hip ratio (WHR).
Stepwise linear regression analysis showing independent variables associated with postprandial triglycerides levels in FCH.
Factors associated with fasting and postprandial apo A-V levels
We explored associations between the fasting apo A-V concentration, apo A-V iAUC, and anthropometric and metabolic parameters. The fasting apo A-V concentration showed significant correlations with the fasting triglycerides levels (r = 0.39, P = 0.010) and apo B levels (r = 0.32, P = 0.032).
The apo A-V iAUC showed significant associations with the triglycerides iAUC (r = 0.72, P < 0.001), apo B levels (r = 0.52, P = 0.001), apo B-48 iAUC (r = 0.47, P = 0.004), and fasting triglycerides levels (r = 0.46, P = 0.004). A negative correlation between the apo A-V iAUC and HDL-c was also found (r = -0.36, P = 0.028).
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Independent factors associated with postprandial apo A-V response
In the linear regression model, the only variable independently associated with the apo A-V iAUC was the triglycerides iAUC, explaining 54.4% of the variability in this variable (P < 0.001). This model also included the apo B-48 iAUC, fasting triglycerides, apo B, and HDL-c levels as independent variables. When the triglycerides iAUC was removed from this model, the apo B-48 iAUC, apo B, and HDL-c were associated with the postprandial apo A-V response, explaining 51.1% of the variability in this parameter.
Parameters according to the presence or absence of fasting hypertriglyceridemia and abdominal obesity
Individuals were classified in four groups according to the level of fasting triglycerides and the median WHR as follows: 1) HTG (≥150 mg/dL) with abdominal obesity (WHR ≥0.92 in men and ≥0.85 in women), 2) HTG without abdominal obesity, 3) normotriglyceridemia (NTG) (<150 mg/dl) with abdominal obesity, and 4) NTG without abdominal obesity. The characteristics of these groups are shown in Table 3.
Table 3
Subjects subgroups characteristics
Variable
HTG with obesity (n = 48)
HTG without obesity (n = 21)
NTG with obesity (n = 13)
NTG without obesity (n = 17)
P
WHR
0.92 ± 0.05c, e
0.82 ± 0.04d
0.91 ± 0.04e
0.80 ± 0.03
<0.001
Fasting parametersa
Triglycerides (mg/dL)
275 [201–345]d, e
271 [185–346]d, e
126 [103–136]
105 [79–131]
<0.001
Cholesterol (mg/dL)
226.9 ± 37.2d, e
228.8 ± 38.9
206.3 ± 18.9
197.5 ± 34.9
0.010
LDL-c (mg/dL)
129.4 ± 26.4
141.9 ± 44.7
133.7 ± 16.7
129.3 ± 24.9
0.604
Non HDL-c (mg/dL)
173.3 ± 27.2
181.6 ± 41.7d, e
157.7 ± 16.1
150 ± 29.4
0.014
Apo B (mg/dL)
123.2 ± 24.9d, e
122.3 ± 23.1
109.1 ± 11.8
107.3 ± 24.2
<0.001
Apo B-48 (μg/mL)b
6.5 [5.4–8.9]d, e
6.7 [3–7.4]d
1.5 [0.9–2.9]
3.1 [1.3–4.6]
<0.001
Apo A-V (ng/mL)b
365.5
303.3
215.5
287.9
0.096
[301.7–408.3]
[268.4–374.3]
[187.5–326.2]
[267.5–329.8]
Glucose (mg/dL)
103 [95–110]d, e
97 [92–107]
96 [91–101]
91 [87–94]
0.001
Insulin (μU/mL)
11.15 [7.7–13.4]d, e
8.6 [5.6–12.6]
7.6 [6.1–9.5]
8.9 [5.1–9.8]
0.029
HOMA-IR
2.73 [1.91–3.61]d, e
2.03 [1.45–3.21]
1.89 [1.41–2.5]
2.04 [1.28–2.29]
0.010
AST (IU/L)
30 [25–33]d
26 [24–33]
25 [21.5–28]
25 [22–27]
0.073
ALT (IU/L)
30 [21–37]d, e
22 [18–34]
19.5 [15–25]
20 [16–30]
0.015
GGT (IU/L)
28 [18–38]
19 [15–47]
23.5 [10–34.5]
15 [13–29]
0.085
Apo B-48/apo Bb
0.056 ± 0.0d
0.046 ± 0.02
0.015 ± 0.00
0.041 ± 0.02
0.035
Apo A-V/triglyceridesb
1.29 [1.02–1.73]e
1.10 [0.87–1.54]e
1.84 [1.60–2.48]
3.06 [2.24–4.27]
0.001
Postprandial parameters
Triglycerides iAUC
777.2
576.5
433
439.5
<0.001
(mg/dL/h)
[548.5–1092.7]d, e
[213–1028]
[280–595.5]
[243.5–568.5]
Triglycerides peak (mg/dL)
444.5 [353–562]d, e
444 [268–570]d, e
228 [188–291]
211 [180–231]
<0.001
Triglycerides time to peak (h)
5 [4–6]
4 [4–5]
4 [4–5]
3 [3–4]
0.075
Apo B-48 iAUC (μg/mL/h)b
27.1 [15.3–49.3]
23.6 [11.6–29.3]
15 [10.8–23.4]
18.7 [8.7–24.6]
0.373
Apo B-48 peak (μg/mL)b
15.8 [11.6–22.2]d, e
14 [7–16.7]
4.2 [3.1–7.4]
7.4 [3.9–10]
0.002
Apo B-48 time to peak (h)b
6 [4–8]e
6 [4–8]e
5 [3.5–6]
4 [3–4]
0.024
Apo A-V iAUC
1132.9
707.8
363.8
145.1
0.002
(ng/mL/h)b
[826.4–1474.7]d, e
[72.6–1533.8]
[145.0–480.5]
[–5.8–453.0]
Apo A-V peak
603.4
459
323.2
358.6
<0.001
(ng/mL)b
[534–673.7]d, e
[382.9–613.9]
[226.7–439.3]
[299.2–423.9]
Apo A-V time to peak (h)b
6 [4–6]e
4 [4–6]
5 [3.5–6]
3 [3–4]
0.006
Data are expressed as means ± SD or medians [IQR]. HTG: hypertriglyceridemia defined as fasting triglycerides ≥150 mg/dL. Obesity defined as waist to hip ratio (WHR) ≥0.92 in males and ≥0.85 in females. NTG: normotriglyceridemia defined as fasting triglycerides <150 mg/dL. aAll study subjects had apo B levels over the 90th percentile for the Mexican population and HTG and/or hypercholesterolemia at diagnosis; however, some of them showed inferior levels at the time of the study due to the already known variability in the lipid profile associated with FCH.
bN = 44. cSignificantly different from individuals with HTG without obesity. dSignificantly different from individuals with NTG with obesity. eSignificantly different from individuals with NTG without abdominal obesity.
Subjects characteristics according to the presence of hypertriglyceridemia and abdominal obesity.
Individuals with fasting HTG and abdominal obesity, showed the highest triglycerides iAUC, and the time to triglycerides peak concentration was later (median 5 hours) than in the other groups. In this group apo B-48 peak concentrations were also higher. Triglycerides peak level was higher in the groups with fasting HTG in comparison with the groups with normal fasting triglycerides concentration. The apo B-48 iAUC showed a tendency to be higher in groups with fasting hypertriglyceridemia.
The highest apo A-V iAUC and peak concentrations were observed in the HTG with abdominal obesity group, followed by the group with HTG without abdominal obesity. The group without any of the abnormalities showed the shortest time to peak apo A-V levels. In contrast, the group with both HTG and abdominal obesity showed a later peak. These results are summarized in Figure 2 and Table 3.
Figure 2
Triglycerides iAUC, apo B-48 iAUC, and apo A-V iAUC in subgroups according hypertriglyceridemia and abdominal obesity. Box plots showing median levels of triglycerides iAUC, apo B-48 iAUC, and apo A-V iAUC after the meal test. Boxes show interquartile ranges, and bars represent highest and lowest values P < 0.001 for triglycerides iAUC, P = 0.373 for apo B-48 iAUC, and P = 0.002 for apo A-V iAUC with Kruskal Wallis test.
×
Discussion
The lipoproteins and mechanisms that modulate postprandial lipemia in patients with FCH are not well understood. We studied a cohort of patients with FCH to determine factors related to postprandial lipemia. Our results show that the magnitude of the triglycerides iAUC is determined by the fasting apo B-48 concentration and the WHR. In our second linear regression model the postprandial apo A-V levels were only associated with the triglycerides iAUC. When the study population was classified according to the fasting triglycerides level and the WHR, the most robust postprandial triglycerides response was observed in the group with fasting HTG and abdominal obesity.
These results indicate that the magnitude of the postprandial lipemia in patients with FCH is determined by the fasting apo B-48 concentration and potentiated by the presence of abdominal obesity. However, the linear regression model explained only a modest proportion of the variability in postprandial lipemia; therefore, additional variables related to this phenomenon may be involved.
Interestingly, the apo B-48 postprandial response, reflecting the chylomicrons rise after the meal, was not independently associated with abdominal obesity or fasting hypertriglyceridemia. This result indicates that in patients with FCH the chylomicron response is not determined by the same parameters that influence the postprandial triglycerides iAUC (fasting apo B-48 levels and abdominal obesity).
In contrast to our results, other studies including individuals with diverse cardiovascular risk have reported that fasting triglycerides levels is the major determinant of postprandial lipemia [3, 5, 6, 20]. The novel finding of an independent association between fasting apo B-48 levels and postprandial lipemia in FCH indicate a potential role for intestinal-derived lipoproteins in postprandial metabolism in individuals with FCH.
The relationship between abdominal obesity and postprandial lipemic response is less clear. Abdominal adiposity may be associated with liver fat deposition, a driving force for the overproduction of VLDL [11]. We found a strong and independent association between the WHR, a validated marker of abdominal obesity, and postprandial lipemia. This result is consistent with the finding that patients with fasting HTG and abdominal obesity showed the greatest postprandial triglycerides levels. Studies have confirmed that abdominal obesity, a marker of visceral fat accumulation, is independently associated with the magnitude of postprandial lipemia [5, 6, 21, 22]. These conclusions are in agreement with our findings.
In patients with FCH the postprandial lipid response was aggravated by abdominal obesity. A feasible mechanism for explaining our results is the oversaturation and competition of chylomicrons and VLDL particles for the same removal pathways [23]. This condition added to other known cardiovascular risk factors may play a key role in the increased risk for cardiovascular disease seen in these individuals [1].
A novel finding of our report is the analysis of the fasting and postprandial apo A-V response. Apo A-V postprandial levels were mainly associated with the postprandial triglycerides iAUC. Apo A-V is produced by the liver and is a component of VLDL and HDL lipoprotein fractions [24]. It is presumed to be a factor in the activation of LPL resulting in increased triglycerides hydrolysis [8]. In individuals with type 2 diabetes following a fat load, the apo A-V postprandial response paralleled the increase in VLDL-triglycerides and apo C-III levels. However, an association between the apo A-V postprandial levels and LPL activity was not found [25]. In FCH, polymorphisms on the APOAV have been associated with increased fasting triglycerides concentrations [26]. In this study, following the fat meal, apo A-V levels increased and did not return to the baseline at the end of the test. Interestingly, we found a significant correlation between the apo B-48 and apo A-V postprandial responses. We consider that this finding could reflect an association of apo A-V not only with the VLDL particles, but also with chylomicrons [27]. In the linear regression analysis the only variable independently associated with the postprandial apo A-V response was the triglycerides iAUC. Moreover, after analyzing the subgroups according to their fasting triglyceride levels, the groups with fasting HTG showed a significantly higher postprandial apo A-V response in comparison to the normal fasting triglycerides levels groups. These results confirm that apo A-V is associated with the TRL in the postprandial period, and is in line with the known regulation of VLDL metabolism by apo A-V [8, 26].
Our study has limitations. The cross-sectional design only suggests associations and not causality. In addition, we did not use DEXA or imaging studies to measure fat mass and visceral adipose tissue volume. This would have allowed more precise quantification of abdominal obesity; however, the WHR is a validated marker of visceral tissue accumulation [28]. Also, the WHR is an informative and simple measure to perform in everyday clinical setting. Apo A-V polymorphisms were not investigated in this study. Apo A-V was analyzed in a randomly selected subgroup of the population; nevertheless, this subgroup was representative of the complete sample studied. Finally, we did not include a control group without FCH to compare our results because our focus was to identify the variables related with postprandial lipemia in FCH patients.
Conclusions
In conclusion, in individuals with FCH fasting apo B-48 concentration is the main factor associated with the magnitude of postprandial lipemia. This response is potentiated by abdominal obesity. Finally, the Apo A-V postprandial levels are associated with the postprandial triglycerides increment.
Acknowledgments
The authors thank Luz Elizabeth Guillen-Pineda and Carmen Moreno for technical assistance; Maria Luisa Velasco for her help in performing the studies; and the study subjects for their participation.
Funding
This study was funded by the NIH grants HL-095056 and HL-28481.
This publication received editorial support by Sanofi Mexico.
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made.
The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder.
The authors declare they have no competing interests.
Authors’ contributions
PA: conducted the study, performed data collection, data analysis, data interpretation, and manuscript writing; DC: performed data collection and reviewed the manuscript; RM: performed data interpretation and reviewed the manuscript; LM: conducted the study and performed data collection; IC: conducted the study; OP, MT, and FG: reviewed the manuscript; PP, NM, and MT: performed analysis and reviewed the manuscript; CA: designed the study, performed data interpretation and reviewed the manuscript. All authors read and approved the final manuscript.
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