Skip to main content
Erschienen in: Pediatric Nephrology 10/2012

Open Access 01.10.2012 | Original Article

Oxidative stress in hypertensive children before and after 1 year of antihypertensive therapy

verfasst von: Joanna Śladowska-Kozłowska, Mieczysław Litwin, Anna Niemirska, Paweł Płudowski, Aldona Wierzbicka, Ewa Skorupa, Zbigniew T. Wawer, Roman Janas

Erschienen in: Pediatric Nephrology | Ausgabe 10/2012

Abstract

Background

The relation between primary hypertension (PH), target organ damage (TOD) and oxidative stress (SOX) is not known.

Methods

We assessed SOX in 86 children with PH before and after 12 months of standard non-pharmacological and pharmacological therapy based on renin-angiotensin system blockade.

Results

Patients with left ventricular hypertrophy (LVH) and with carotid intima-media thickness (cIMT) >2SDS had higher thiobarbituric acid reactive substances (TBARS) concentrations in comparison to patients without LVH or with normal cIMT. Patients with metabolic syndrome (MS) had lower activity of gluthatione peroxidase, higher asymmetric dimethyloarginine (ADMA) and oxidized LDL cholesterol (oxyLDL) in comparison to patients without MS. TBARS correlated with left ventricular concentric hypertrophy, cIMT, albuminuria and SBP/24 h. ADMA and oxyLDL correlated with CRP and TG/HDL ratio. After 1 year of antihypertensive treatment blood pressure, TOD and prevalence of MS decreased. TBARS decreased and glutathione concentrations increased. The decrease of TBARS concentration correlated with the decrease of body mass index (BMI). Decrease of oxyLDL and ADMA correlated with increased insulin sensitivity, however markers of SOX did not correlate with BP decrease.

Conclusion

SOX in children with PH correlates with TOD, metabolic abnormalities, changes in fat amount and improvement of insulin sensitivity, but not with BP decrease.
Hinweise
Joanna Śladowska-Kozłowska and Mieczysław Litwin contributed equally to the study and should be cited together.
This work has been presented during European Society of Hypertension Meeting, Milano 2011

Introduction

Primary hypertension (PH) is considered as a state of oxidative stress (SOX) that contributes to the development of arterio- and atherosclerosis and target organ damage (TOD) [14]. Abnormally elevated blood pressure causing hemodynamic insult, and typical intermediate phenotype of PH consisting of metabolic disturbances, excessive caloric intake and physical inactivity, leads to impairment of antioxidant defensive capacity [46]. As a consequence, reactive oxygen species cause oxidation of lipids, proteins and DNA with resultant tissue damage [7]. Furthermore, SOX is thought to be associated with adipocytokine release and renin-angiotensin-aldosterone system (RAAS) activation [810]. Moreover, SOX may lead to insulin resistance and is one of the elements of metabolic syndrome [1113].
On the other hand, increased physical activity as a standard non-pharmacological intervention in hypertensive patients led to decreased reactive oxygen species generation, improved nitric oxide bioavailability and vascular function [14, 15]. Some evidence indicates that angiotensin converting enzyme inhibitors (ACEi) and angiotensin receptor blockers (ARB) may reduce oxidative stress and reactive oxygen species formation in adults with PH [1619]. However, there are only single reports on SOX in hypertensive children [2], and there are no reports describing the relationship between SOX, TOD and antihypertensive treatment in children with PH. It is still unresolved whether increased SOX in PH is related to hemodynamic insult or to metabolic abnormalities which accompany both obesity and PH.
We hypothesized that SOX correlates with severity of PH, metabolic abnormalities and TOD in children with PH. Secondly, standard antihypertensive treatment based on non-pharmacological intervention and blockade of RAAS causes a decrease of SOX, which in turn correlates with normalization of metabolic abnormalities and regression of TOD. To test this hypothesis we assessed changes of SOX markers in relation to TOD in children with PH before and after 12 months of standard non-pharmacological and pharmacological therapy based on ACEi or ARB.

Patients and methods

Patients

The study adhered to the principles of the Declaration of Helsinki and was approved by the local Ethical Committee. All parents and children aged above 12 years of age provided written informed consent.
Detailed characteristics of the study group have been described previously [20, 21]. Specifically, out of 200 white, Caucasian children and adolescents admitted consecutively between 2005–2008 for investigation regarding suspected arterial hypertension, and who were not yet treated with antihypertensive drugs and in whom PH was ultimately diagnosed, 86 children aged 14.1 ± 2.4 (range: 5–17) years (20 girls and 66 boys) with untreated PH, who completed all investigative procedures, were included in the recent study. PH was diagnosed after a thorough clinical and laboratory diagnostic work-up, according to recently published recommendations [22, 23]. The exclusion criteria were: diagnosis of secondary hypertension, previous use of antihypertensive drugs, presence of any significant chronic disease (except for PH), as well as acute disease including infections in 6 weeks preceding enrollment. Patients with incomplete biochemical data were also excluded.
In all patients the diagnosis was confirmed by 24 hour ambulatory blood pressure monitoring (ABPM). ABPM was performed at the initial visit and after 12 months. Recordings lasting at least 20 hours with at least 80 % of records were considered as valid. We used the referential ABPM normative values published recently to classify patients as having normal blood pressure, prehypertension, ambulatory hypertension or severe ambulatory hypertension [24, 25]. Patients who decreased systolic blood pressure (SBP) during sleep by more than 10 % in comparison to day-time SBP values were considered as dipppers. Ambulatory hypertension was defined as mean ambulatory SBP above 95th percentile and SBP load between 25 and 50 %, and severe ambulatory hypertension was defined as mean ambulatory SBP above 95th percentile and SBP load above 50 %. Normotension was defined as mean ambulatory SBP below 95th percentile and SBP load below 25 %. Prehypertension was defined as mean SBP below 95th percentile and SBP load in the range 25 – 50 % [25].

Methods

Anthropometrical measurements

In all patients anthropometrical parameters, including body mass index (BMI), waist circumference (WC), waist-to-hip ratio (WHR) and waist-to-height ratio (WHTR) were measured. Obesity and being overweight were diagnosed according to International Obesity Task Force (IOTF) recommendations [26].

Laboratory investigations

Blood samples were taken after 12 hours of fasting and were immediately sent to the laboratory. Plasma lipid peroxides were determined with the spectrofluorometric method of Yagi, and results expressed as concentration of thiobarbiturate reactive substance (TBARS). Glutathione and glutathione peroxidase activity were used as indicators of antioxidant status and were measured spectrophotometrically in erythrocytes (GSH-420(Oxis) and GPx-340(Oxis)). Concentration of oxyLDL and asymmetric dimethyloarginine (ADMA) were measured by ELISA using a commercially available kit.
Methodology of measurement of other biochemical variables, including plasma insulin, blood lipids, L-homocysteine, hsCRP and albuminuria were described previously [20, 21].

Definition of metabolic syndrome

Because some of our patients were below 10 years of age, metabolic syndrome (MS) was diagnosed when at least 3 criteria were present (BMI ≥ 95th percentile for age and gender, arterial hypertension, serum triglycerides > 110 mg/dl, fasting plasma glucose > 100 mg/dl or > 140 mg/dl at 2 h of oral glucose tolerance test and HDL cholesterol < 40 mg/dl [27]).

Intima-media thickness measurements

Carotid and femoral superficial artery intima-media thickness (cIMT and fIMT), and wall cross-sectional area in carotid artery (WCSA) were evaluated by ultrasound according to the methodology described previously [28]. The median and standard deviation (SD) of normal values for cIMT, fIMT and WCSA were obtained from a study of 250 healthy children published elsewhere [28].

Echocardiography (ECHO)

All ECHO examinations were performed by one examiner blinded to the severity of PH and effectiveness of treatment. ECHO measurements were performed according to American Society of Echocardiography guidelines [29]. To standardize left ventricular mass to height, left ventricular mass index (LVMi) was calculated according to the deSimone formula [30]. Left ventricular hypertrophy (LVH) was defined as an LVMi value above 95th percentile for age and gender, based on the pediatric LVMi reference data of Khoury et al [31]. Relative wall thickness (RWT) was measured at end diastole as the ratio of posterior wall thickness plus interventricular septum thickness over LV internal dimension. A RWT of 0.41, which represents the 95th percentile for RWT for normal children and adolescents, and the 95th percentile for LVMi were used as cutoff points in evaluation of LV geometry [32].

Antihypertensive treatment

Principles of treatment were already described previously [20, 21]. At enrollment no one patient was treated pharmacologically nor received any advice about non-pharmacological treatment. After diagnosis of PH all patients were informed about principles of non-pharmacological treatment, including lifestyle changes, increased physical activity and dietary modifications including salt avoidance, and were referred to an external consultant. All patients were encouraged to increase general physical activity up to 90 minutes daily including sport, walking, climbing stairs, etc. The character of activity (playing football, jogging, aerobic, walking, biking, etc.) was chosen by patients according to personal preferences. Dietary modifications were based on significant reduction of salt use both by patients and family members, and significant reduction of sweets.
Pharmacological treatment was immediately started in patients who had a significant TOD and/or severe ambulatory hypertension. BP was checked at the 3rd and the 6th month during ambulatory visits. If after 3 or 6 months office BP was still in the hypertensive range ABPM was done. In patients who still had ambulatory or severe ambulatory hypertension, pharmacotherapy was started. Finally, ABPM was performed after 12 months of treatment.
Drug therapy was based on the ACEi enalapril (0.2 – 0.3 mg/kg/day bid). Patients who had asthma or who did not tolerate ACEi were prescribed angiotensin 2 receptor type 1 blocker (ARB) losartan in a dose of 0.7 – 1 mg/kg/day in one or two daily doses.
All patients were evaluated at regular 3 months intervals during routine ambulatory, out-patient visits. Compliance to recommended lifestyle modifications was assessed by interview with patients and parents. When the antihypertensive effect was inadequate, amlodipine as the second drug was introduced and in patients treated only with lifestyle intervention, therapy with ACEi, ARB or amlodipine was started. Patients who were still hypertensive after 6 months and/or fulfilled the criteria of stage 2 hypertension based on home and casual BP measurements were prescribed metoprolol in a dose 0.5 mg/day as the third drug.

Statistics

Because the analyzed groups included subjects of different age and gender, BMI and WC values were expressed both as absolute values and as SDS for age and gender. LVM values in g were standardized to height in meters2.7. The change of measured parameters was expressed as a delta value (Δ), ie the difference between measurement at 12 months and at start of treatment. Homogeneity of variance was checked with the Levene test. Continuous variables with a normal distribution were compared by the Student’s t-test for independent variables. Continuous values with non-normal distribution were compared by the Mann–Whitney U test. Comparison between groups was evaluated with an ANOVA test. Measurements taken at the start and after 12 months of treatment were compared using the Wilcoxon test. Dichotomous variables were compared using the Chi-square test, and change in prevalence during treatment was analyzed with the McNemar test. Correlation analysis was done with the Spearman test. P values less than 0.05 were regarded as statistically significant.

Results

At start of treatment 67.4 % of patients were obese or overweight and their mean (±SD) BMI-SDS was +1.9 ±1.8. Metabolic syndrome was diagnosed in 13 patients (15.1 %) [20, 21] (Table 1).
Table 1
Descriptive demographic, clinical and laboratory data of oxidative stress and inflammatory markers at baseline and after 12 months of treatment
 
Baseline
After 12 months of treatment
P
Patients with MS (%)
13 (15 %)
6 (7 %)
p = 0.07, chi2 = 3.27
Patients with normotension (%)
0
54 (62.8 %)
p = 0.0001, chi2 = 75.80
Patients with prehypertension (%)
0
10 (11.6 %)
p = 0.003, chi2 = 8,60
Patients with ambulatory HT (%)
50 (58.1 %)
21 (24.4 %)
p = 0.00001, chi2 = 27.03
Patients with severe HT (%)
36 (41.9 %)
1 (1.2 %)
p = 0.00001, chi2 = 33.03
Patients with LVH (%)
40 (46.5 % )
24 (27.9 % )
p = 0.003; chi2 =8.65
hsCRP (mg/dl)
0.86 (0.02-4.10)
0.41 (0.10-3.90)
<0.001
GSH (μmol/l)
763.4 (361.5-889.4)
778.1 (638.1-825.6)
<0.01
GPX (U/gHb)
31.6( 25.4-39.9)
31.6 (27.6-37.2)
ns
TBARS (μmol/l)
0.56 (0.14-2.73)
0.25 (0.14-1.28)
<0.001
ADMA (μmol/l)
0.54 (0.17-1.45)
0.56 (0.18-1.4)
ns
oxyLDL (mU/ml)
340.1 (104.3-1364.7)
367.5 (110.8-1409.8)
ns
Abbreviations: MS- metabolic syndrome, hsCRP – high-sensivity C-reactive protein, GSH - reduced glutathione, GPX – glutathione peroxidase activity ,TBARS – thiobarbituric acid reactive substances, ADMA – serum asymmetric dimethyloarginine, oxyLDL- oxidized low density lipoprotein cholesterol

Relationship between SOX markers, BP, TOD and metabolic abnormalities at baseline

36 (41.9 %) patients with severe ambulatory HT had significantly lower concentrations of GSH in comparison to 50 (58.1 %) patients with ambulatory HT (748.7 (365.2-862.5) vs 773.6 (361.5 -889.4) μmol/l, p < 0.01). 40 patients with non-dipping status had lower values of GPX than patients with normal nocturnal fall of BP (31,2 ±1.7 vs 32.5 ±3.3 U/g Hb; p = 0.01).
40 patients with LVH had higher values of TBARS compared to 46 patients without LVH (0.33 (0.14-1.28) vs 0.24 (0.16-1.25) μmol/l, p = 0.02) (Figure 1). Similarly, 20 (24 %) patients with cIMT >2 SDS had greater TBARS concentration than patients showing cIMT < 2 SDS (0.36 (0.20-1.25) vs 0.26 (0.14-1.05) μmol/l, p < 0.01) and not significantly higher ADMA concentration (0.71 (0.25-1.37) vs 0.49 (0.17-1.45) μmol/l, p = 0.1) and GPX activity (32.0 (26.2-39.2) vs 31.4 (25.4-39.9) U/gHb, p = 0.1).
Patients with MS had lower activity of GPX, and higher concentrations of ADMA and oxyLDL when compared to patients without MS (Table 2, Figure 2, 3).
Table 2
Baseline biochemical characteristics of patients with metabolic syndrome (MS[+]) and without metabolic syndrome (MS[−])
 
MS[−] N = 73 (86.9 %)
MS[+] N = 13 (15.1 %)
p
HbA1C (%)
5.3 (4.2-6.8)
5.3 (4.1-6.4)
ns
TG/HDL
1.76 (0.67-4.96)
2.74 (1.65-12.9)
0.001
HOMA-IR
2.67 (0.94-9.74)
2.73 (2.04-8.77)
0.11
hsCRP (mg/dl)
0.83 (0.02-4.15)
1.2 (0.14-3.94)
ns
homocysteine(μmol/l)
9.84 ±2.52
10.7 ±1.34
ns
Uric acid (mg/dl)
5.3 ±1.2
6.8 ±1.2
<0.001
GSH (μmol/l)
761.7 (361.5-862.5)
765.1 (658.1-889.4)
ns
GPX (U/g Hb)
31.8 (25.4-39.9)
30.5 (26.2-38.7)
<0.01
TBARS (μmol/l)
0.31 (0.14-1.25)
0.26 (0.18-1.28)
ns
ADMA (μmol/l)
0.49 (0.17-1.37)
0.88 (0.21-1.45)
<0.01
oxyLDL (mU/ml)
309.0 (104.3-1255.2)
489.9 (195.7-1364.7)
0.03
Abbreviations: MS – metabolic syndrome, n – number of patients, HbA1C – glycated hemoglobin concentration, TG/HDL – triglicerydes to high density lipoprotein cholesterol ratio, HOMA-IR – homeostasis model assessment for insulin resistance, hsCRP – high-sensivity C-reactive protein, GSH - reduced glutathione, GPX – glutathione peroxidase activity ,TBARS – thiobarbituric acid reactive substances, ADMA – serum asymmetric dimethyloarginine, oxyLDL- oxidized low density lipoprotein cholesterol
TBARS concentrations correlated with LVMi, RWT, cIMT, cIMT-SDS, WCSA, urinary albumin excretion and SBP/24 h (Table 3). ADMA and oxyLDL concentrations correlated with hsCRP and TG/HDL ratio. GPX activity correlated with TG/HDL ratio and nocturnal fall of blood pressure.
Table 3
Correlations between parameters of oxidative stress and dependent variables at baseline (Spearman correlation analysis)
SOX parameters
Dependent variables
 
TBARS
SBP/24 h
p < 0.05, r = 0.21
LVMi
p = 0.003, r = 0.31
RWT
p = 0.001, r = 0.35
cIMT
p = 0.008, r = 0.29
cIMT-SDS
p = 0.005, r = 0.30
WCSA
p = 0.03, r = 0.26
Urinary albumin excretion/24 h
p < 0.05, r = 0.21
fIMT
p = 0.02, r = −0.28
fIMT-SDS
p = 0.01 r = −0.30
GPX
nocturnal fall of SBP
P = 0.03, r = −0.235
TG/HDL
p = 0.003, r = −0.31
WHR
P = 0.1, r = −0.311
ADMA
WHR
P = 0.05, r = 0.24
hsCRP
P = 0.01, r = 0.34
GPX
p < 0.05, r = −0.24
oxyLDL
p < 0.001, r = 0.66
TG/HDL
p < 0.0001, r = 0.431
oxyLDL
hsCRP
P < 0.001, r = 0.662
TG/HDL
P < 0.0001, r = 0.382
GPX
P < 0.05, r = −0.25
nocturnal fall of SBP
P = 0.016. r = 0.261
Abbreviations: ADMA – serum asymmetric dimethyloarginine; cIMT –carotid intima media thickness; fIMT- femoral intima media thickness; hsCRP – high-sensivity C- reactive protein; GSH - reduced glutathione; GPX – glutathione peroxidase activity; LVMi – left ventricular mass index; oxyLDL- oxidized low density lipoprotein cholesterol; RWT – relative wall thickness; SBP/24 h – mean systolic blood pressure in 24 hour-ambulatory blood pressure monitoring; TBARS – thiobarbituric acid reactive substances;TG/HDL – triglicerydes to high density lipoprotein cholesterol ratio; WCSA – wall cross sectional area; WHR – waist-hip ratio
SOX markers did not differ between overweight/obese vs normal weight patients, between patients with visceral obesity and without, and between patients with positive vs negative family history of cardiovascular disease (data not shown).

Follow- up characteristics

As described previously, after 1 year of antihypertensive treatment, there was a significant decrease of blood pressure, prevalence of TOD and of MS, and improvement of some metabolic abnormalities, such as a decrease of hsCRP, uric acid, total – and LDL cholesterol concentration and a decrease of visceral fat amount [20]. Compared to baseline, TBARS concentrations decreased and GSH increased (Table 1, Figure 4).
SOX markers did not correlate with blood pressure changes. 64 (73.8 %) patients who had lowered blood pressure, did not have significantly different concentrations of ADMA and oxyLDL.
Patients with regression of TOD in comparison to patients with progression/no change of TOD did not differ significantly regarding changes of SOX parameters, however patients who had decreased fIMT-SDS also had decreased oxyLDL concentrations in comparison with patients in whom fIMT-SDS increased or did not change (ΔoxyLDL: - 56.0 (−242.2-460.3) vs 82.3 (−59.1-809.5) mU/ml, p = 0.01). Patients in whom LVMi decreased had no significant change in oxyLDL (ΔoxyLDL: -26.5 (−626.1-810.1) vs 42.2 (−253.1-804.2) mU/ml) and ADMA (ΔADMA: -0.10 (−0.91-0.91) vs 0.18 (−0.25-0.53) μmol/l, both p = 0.07) compared to patients who did not have decreased LVMi.
Changes in SOX markers correlated with changes in insulin resistance and lipids. ADMA and oxyLDL concentrations decreased and GPX activity showed no significant change in patients who lowered TG/HDL ratio in comparison to patients with stabilization/increase of TG/HDL ratio (∆ ADMA: -0.16 (−0.58-0.91) vs 0.12 (−0.91-0.57) μmol/l, p = 0.05, ∆oxyLDL: -59.1 (−626.6-460.3) vs 100 (−295.6-810.1) mU/ml, p = 0.008, ∆GPX: 0.2 (−7.2-10.3) vs −0.1 (−9.1-5.3) U/gHb, p = 0.1). Patients in whom ADMA concentrations decreased at follow-up, had lower insulin and HbA1C concentrations, HOMA-IR, TG/HDL and LDL/HDL ratios when compared to patients with increase/stabilization of ADMA (Table 4).
Table 4
Comparison between patients who decreased ADMA concentrations and patients with stable/increased ADMA concentrations after 12 months of treatment
 
Decrease of ADMA n = 24
Increase/stabilization of ADMA n = 20
p
∆ HOMA-IR
−0.41(−3.71-1.58)
0.31 (−2.38-1.82)
0.17
∆ HbA1C (%)
−0.1 (−1.1-4.5)
0.05 (−1.4-2)
0.03
∆TG/HDL
−0.28 ( −5.77-1.76)
0.14 (−0.90-4.41)
0.02
∆ homocysteine
−1.02 ± 3.21
1.13 ±2.29
0.02
∆ uric acid (mg/dl)
−0.38 ± 1.14
0.04 ±0.82
0.11
∆LDL/HDL
−0.61 (−1.51-1.18)
0.21 (−0.70-1.48)
0.0002
∆oxyLDL(mU/ml)
−98.95 (−626.14 – 154)
139 (−253.1-818.1)
0.0001
∆ RWT (mm)
−0.03 (−0.35-0.04)
0.007 (−0.15-0.15)
0.04
HOMA-IR at follow-up
2.12 (1.60-6.45)
3.32 (1.93-5.43)
0.008
Glu[0] (mg/dl) at follow-up
86 (71–95)
87 (75–91)
0.02
Ins[0] (mU/ml) at follow-up
10.7 ( 7,3-29)
15.7 (9–159)
0.003
LDL/HDL at follow-up
2.25 (1.50-4.11)
2.83 (1.85-3.70)
0.02
ADMA at follow-up (μmol/l)
0.505 (0.30-1.19)
0.79 (0.47 -1.37)
0.02
oxyLDL at follow-up (mU/ml)
356.12 (131–935.6)
388.7 (129.3-1409.8)
ns
Abbreviations: n - number of patients, Glu[0] – fasting plasma glucose; HOMA-IR – homeostasis model assessment for insulin resistance, HbA1C – glycated hemoglobin concentration, Ins[0] – plasma fasting insulin concentration; TG/HDL – triglicerydes to high density lipoprotein cholesterol ratio, oxyLDL- oxidized low density lipoprotein cholesterol, ADMA – serum asymmetric dimethyloarginine, RWT – relative wall thickness, glucose[0] – fasting glucose concentration, insulin [0] –fasting insulin concentration, insulin[120] – insulin concentration after 120 min. of oral glucose ingestion
The decrease of TBARS concentrations correlated with a decrease of BMI (p = 0.04, r = 0.22) but there was no statistically significant correlation with a decrease of WC (p = 0.1, r = 0.20).
The step-wise regression analysis did not reveal any significant predictors of decrease of TBARS concentrations and of increase of GSH.

Discussion

The main finding of the study is that in newly-diagnosed hypertensive children, the severity of hypertension, TOD, metabolic abnormalities and immune activity were all associated with the magnitude of oxidative stress. The second finding is that standard antihypertensive treatment based on lifestyle modifications and/or blockade of the renin-angiotensin system caused a decrease of SOX and improved antioxidative defense. Further, the changes of SOX after 1 year of treatment correlated with regression of TOD and increased insulin sensitivity, but not directly with decrease of blood pressure.
Several reports have evaluated antioxidative defense and SOX in patients with PH and cardiovascular disease [16, 10, 11, 1619]. However, in studies where classification of blood pressure status was based on clinical measurements it was found that SOX does not correlate with severity of hypertension, and even is not increased in adults with mild to moderate PH [33]. In contrast, we used ABPM to classify severity of hypertension and we found that children with severe ambulatory hypertension, ie those who are at higher risk of LVH, had significantly lower GSH concentrations and non-dippers had lower GPX activity. This may explain why, in contrast to other reports, we found significant differences regarding SOX in relation to stage of hypertension.
The corresponding finding is a strict relationship between SOX and LVH and arterial injury. Finding that SOX markers were associated with blood pressure status and TOD expressed as LVH and/or cIMT and fIMT thickening does not indicate any causation. The common pathway may be metabolic abnormalities. Baykal et al found that, despite a similar decrease of blood pressure, only ACEi and ARBs caused a significant decrease of SOX accompanied by decrease of total cholesterol, triglycerides and LDL-cholesterol concentrations [19]. It is in line with the finding that normalization of metabolic abnormalities and immune activity was the main determinant of regression of TOD in hypertensive children [20, 21]. We found that children with MS had lower GPX activity and higher ADMA and oxyLDL values in comparison to children without MS. The relationship between MS and SOX has already been described by Kelly et al, who found higher SOX in overweight children with MS compared to normal and overweight counterparts without metabolic abnormalities [34]. Siemianowicz et al revealed an association between ADMA and hsCRP levels and insulin resistance [35]. In our study we found a correlation between ADMA and markers of insulin resistance, and the decrease of ADMA concentrations correlated with a decrease of both TG/HDL ratio and direct markers of insulin resistance such as insulin, HbA1c and HOMA-IR. These relationships, observed also in adult patients, suggest that ADMA is the element that links insulin resistance and the arterio-/atherosclerotic process [11, 36, 37]. Increased ADMA concentrations in hypertensive children were found by Goonasekara et al [38]. ADMA is only an indirect marker of SOX, because dimethylarginine dimethylaminohydrolases metabolizing ADMA are inactivated by reactive oxygen species [39]. However, concentrations of ADMA are parallel to direct SOX markers as was also found in our study. Independent of vascular action, impaired nitric acid (NO) bioavailability can be related to a cellular defect in skeletal muscles, where NO regulates metabolic and contractile processes including among others, basal glucose transport [40].
It has been shown that there is relationship between genetic polymorphisms of NADPH oxidase and extent of atherosclerosis [41]. Decrease of GSH in rats caused significant increase of blood pressure, and increased antioxidative capacity diminished the hypertensive effect induced by GSH decrease [42]. However, there is only weak evidence that antioxidants may lower blood pressure [43]. One possible explanation is that SOX is secondary to hemodynamic and metabolic injury to the arterial wall and left ventricle. This is strengthened by strict relationships between changes of metabolic parameters and BMI with SOX markers. Although we found correlation between changes in BMI and changes in TBARS concentrations at follow-up, at baseline obese patients did not differ from normal-weight patients regarding SOX markers. This may be due to the narrow range of BMI in our patients. On the other hand, studies including subjects with wide BMI ranges from 18 to 45, have found that obese subjects had greater lipid peroxides concentrations in comparison with lean subjects [44]. Despite many correlations we did not find any predictors of SOX or predictors of change in SOX during treatment, which suggests that there are other modifying factors linking hypertension, metabolic abnormalities and TOD.
The main limitation of our study is the relatively low number of patients. Moreover, due to ethical reasons, we could not separate the effects of antihypertensive drugs and non-pharmacological treatment, because healthy nutrition and regular physical activity were recommended for all patients. The other limitation of our study is its observational design and lack of normotensive and BMI-matched control group. Therefore, although we found significantly increased oxidative stress in hypertensive children, and especially among children with LVH and arterial injury, we did not find a causative mechanism or explain the influence of obesity and hypertension, separately. On the other hand, the link between increased insulin sensitivity and SOX reduction underlines the importance of non-pharmacological treatment, first of all based on an increase of physical activity.

Conclusions

We have shown the relation between oxidative stress and the severity of hypertension, TOD and metabolic disorders typical for PH. Decrease of SOX correlated with regression of TOD and normalizations of metabolic abnormalities and immune activity, but not with hypotensive effect of treatment. This finding underlines the importance of immuno-metabolic factors in the pathogenesis of hypertensive TOD and indicates that antihypertensive treatment should be focused both on hypotensive effects and metabolic abnormalities.

Funding sources

The study was in part financially supported by Ministry of Science and Higher Education grant: 5412/B/P01/2010/39.

Open Access

This article is distributed under the terms of the Creative Commons Attribution License which permits any use, distribution, and reproduction in any medium, provided the original author(s) and the source are credited.
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 2.0 International License (https://​creativecommons.​org/​licenses/​by/​2.​0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Unsere Produktempfehlungen

e.Med Interdisziplinär

Kombi-Abonnement

Für Ihren Erfolg in Klinik und Praxis - Die beste Hilfe in Ihrem Arbeitsalltag

Mit e.Med Interdisziplinär erhalten Sie Zugang zu allen CME-Fortbildungen und Fachzeitschriften auf SpringerMedizin.de.

e.Med Pädiatrie

Kombi-Abonnement

Mit e.Med Pädiatrie erhalten Sie Zugang zu CME-Fortbildungen des Fachgebietes Pädiatrie, den Premium-Inhalten der pädiatrischen Fachzeitschriften, inklusive einer gedruckten Pädiatrie-Zeitschrift Ihrer Wahl.

e.Med Urologie

Kombi-Abonnement

Mit e.Med Urologie erhalten Sie Zugang zu den urologischen CME-Fortbildungen und Premium-Inhalten der urologischen Fachzeitschriften.

Literatur
1.
Zurück zum Zitat Watanabe T, Yasunari K, Nakamura M, Maeda K (2006) Carotid artery intima-media thickness and reactive oxygen species formation by monocytes in hypertensive patients. J Human Hypertens 20:336–340CrossRef Watanabe T, Yasunari K, Nakamura M, Maeda K (2006) Carotid artery intima-media thickness and reactive oxygen species formation by monocytes in hypertensive patients. J Human Hypertens 20:336–340CrossRef
2.
Zurück zum Zitat Turi S, Friedman A, Bereczki C, Papp F, Kovàcs J, Karg E, Németh I (2003) Oxidative stress in juvenile essential hypertension. J Hypertens 21:145–152PubMedCrossRef Turi S, Friedman A, Bereczki C, Papp F, Kovàcs J, Karg E, Németh I (2003) Oxidative stress in juvenile essential hypertension. J Hypertens 21:145–152PubMedCrossRef
3.
Zurück zum Zitat Jarvisalo MJ, Putto-Laurila A, Jartti L, Lehtimäki T, Solakivi T, Rönnemaa T, Raitakari OT (2005) Carotid artery intima-media thickness in children with type 1 diabetes. Diabetes 51:493–498CrossRef Jarvisalo MJ, Putto-Laurila A, Jartti L, Lehtimäki T, Solakivi T, Rönnemaa T, Raitakari OT (2005) Carotid artery intima-media thickness in children with type 1 diabetes. Diabetes 51:493–498CrossRef
4.
Zurück zum Zitat Russo C, Olivieri O, Girelli D, Faccini G, Zenari ML, Lombardi S, Corrocher R (1998) Anti-oxidant status and lipid peroxidation in patients with essential hypertension. J Hypertens 16:1267–1271PubMedCrossRef Russo C, Olivieri O, Girelli D, Faccini G, Zenari ML, Lombardi S, Corrocher R (1998) Anti-oxidant status and lipid peroxidation in patients with essential hypertension. J Hypertens 16:1267–1271PubMedCrossRef
5.
Zurück zum Zitat Blankenberg S, Rupprecht HJ, Bickel C, Torzewski M, Hafner G, Tiret L, Smieja M, Cambien F, Meyer J, Lackner KJ, Investigators AtheroGene (2003) Glutathione peroxidase 1 activity and cardiovascular events in patients with coronary artery disease. N Eng J Med 349:1605–1613CrossRef Blankenberg S, Rupprecht HJ, Bickel C, Torzewski M, Hafner G, Tiret L, Smieja M, Cambien F, Meyer J, Lackner KJ, Investigators AtheroGene (2003) Glutathione peroxidase 1 activity and cardiovascular events in patients with coronary artery disease. N Eng J Med 349:1605–1613CrossRef
6.
Zurück zum Zitat Pedro-Botet J, Covas MI, Martin S, Rubies-Prat J (2000) Decreased endogenous antioxidant enzymatic status in essential hypertension. J Hum Hypertens 14:343–345PubMedCrossRef Pedro-Botet J, Covas MI, Martin S, Rubies-Prat J (2000) Decreased endogenous antioxidant enzymatic status in essential hypertension. J Hum Hypertens 14:343–345PubMedCrossRef
7.
Zurück zum Zitat Valko M, Leibfritz D, Moncol J, Cronin MT, Mazur M, Telser J (2007) Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol 39:44–84PubMedCrossRef Valko M, Leibfritz D, Moncol J, Cronin MT, Mazur M, Telser J (2007) Free radicals and antioxidants in normal physiological functions and human disease. Int J Biochem Cell Biol 39:44–84PubMedCrossRef
8.
Zurück zum Zitat Evans JL, Goldfine ID, Maddux BA, Grodsky GM (2003) Are oxidative stress activated signaling pathways mediations of insulin resistance and beta cell dysfunction? Diabetes 52:1–28PubMedCrossRef Evans JL, Goldfine ID, Maddux BA, Grodsky GM (2003) Are oxidative stress activated signaling pathways mediations of insulin resistance and beta cell dysfunction? Diabetes 52:1–28PubMedCrossRef
9.
Zurück zum Zitat Sinaiko AR, Steinberger J, Moran A, Prineas RJ, Vessby B, Basu S, Tracy R, Jacobs DR (2005) Relation of body mass index and insulin resistance to cardiovascular risk factors, inflamatory factors, and oxidative stress during adolescence. Circulation 111:1985–1991PubMedCrossRef Sinaiko AR, Steinberger J, Moran A, Prineas RJ, Vessby B, Basu S, Tracy R, Jacobs DR (2005) Relation of body mass index and insulin resistance to cardiovascular risk factors, inflamatory factors, and oxidative stress during adolescence. Circulation 111:1985–1991PubMedCrossRef
10.
Zurück zum Zitat Kristal B, Shutz-Swirski R, Chezar J, Manaster J, Levy R, Shapiro G, Weissman I, Shasha SM, Sela S (1998) Participation of peripheral polymorphonuclear leukocytes in patients with essentials hypertension. Am J Hypertens 11:921–928PubMedCrossRef Kristal B, Shutz-Swirski R, Chezar J, Manaster J, Levy R, Shapiro G, Weissman I, Shasha SM, Sela S (1998) Participation of peripheral polymorphonuclear leukocytes in patients with essentials hypertension. Am J Hypertens 11:921–928PubMedCrossRef
11.
Zurück zum Zitat Perticone F, Sciacqua A, Maio R, Perticone M, Galiano Leone G, Bruni R, Di Cello S, Pascale A, Talarico G, Greco L, Andreozzi F, Sesti G (2010) Endothelial dysfunction, ADMA and insulin resistance in essentials hypertension. Int J Cardiol 142:236–241PubMedCrossRef Perticone F, Sciacqua A, Maio R, Perticone M, Galiano Leone G, Bruni R, Di Cello S, Pascale A, Talarico G, Greco L, Andreozzi F, Sesti G (2010) Endothelial dysfunction, ADMA and insulin resistance in essentials hypertension. Int J Cardiol 142:236–241PubMedCrossRef
12.
Zurück zum Zitat Rudich A, Tirosh A, Potashnik R, Hemi R, Kanety H, Bashan N (1998) Prolonged oxidative stress impairs insulin-induced GLUT-4 translocation in 3 T3-L1 adipocytes. Diabetes 47:1562–1569PubMedCrossRef Rudich A, Tirosh A, Potashnik R, Hemi R, Kanety H, Bashan N (1998) Prolonged oxidative stress impairs insulin-induced GLUT-4 translocation in 3 T3-L1 adipocytes. Diabetes 47:1562–1569PubMedCrossRef
13.
Zurück zum Zitat Park K, Gross M, Lee DH, Holvoet P, Himes JH, Shikany JM, Jacobs DR (2009) Oxidative stress and insulin resistance. The coronary artery risk development in young adults study. Diabetes 32:1302–1307 Park K, Gross M, Lee DH, Holvoet P, Himes JH, Shikany JM, Jacobs DR (2009) Oxidative stress and insulin resistance. The coronary artery risk development in young adults study. Diabetes 32:1302–1307
14.
Zurück zum Zitat Melikoglu MA, Kaldirimci M, Katkat D, Sen I, Kaplan I, Senel K (2008) The effect of regular long term training on antioxidant enzymatic activities. J Sports Med Phys Fitness 48:388–390PubMed Melikoglu MA, Kaldirimci M, Katkat D, Sen I, Kaplan I, Senel K (2008) The effect of regular long term training on antioxidant enzymatic activities. J Sports Med Phys Fitness 48:388–390PubMed
15.
Zurück zum Zitat Whyte JJ, Laughlin MH (2010) The effects of acute and chronic exercise on the vasculature. Acta Physiol 199:441–450CrossRef Whyte JJ, Laughlin MH (2010) The effects of acute and chronic exercise on the vasculature. Acta Physiol 199:441–450CrossRef
16.
Zurück zum Zitat Yagi S, Morita T, Katayama S (2004) Combined treatment with an AT1 receptor blocker and angiotensin converting enzyme inhibitor has an additive effect on inhibiting neointima formation via improvement of nitric oxide production and suppression of oxidative stress. Hypertens Res 27:129–135PubMedCrossRef Yagi S, Morita T, Katayama S (2004) Combined treatment with an AT1 receptor blocker and angiotensin converting enzyme inhibitor has an additive effect on inhibiting neointima formation via improvement of nitric oxide production and suppression of oxidative stress. Hypertens Res 27:129–135PubMedCrossRef
17.
Zurück zum Zitat Ono H, Minatoguchi S, Watanabe K, Yamada Y, Mizukusa T, Kawasaki H, Takahashi H, Uno T, Tsukamoto T, Hiei K, Fujiwara H (2008) Candesartan decreases carotid intima-media thickness by enhancing nitric oxide and decreasing oxidative stress in patients with hypertension. Hypertens Res 31:271–279PubMedCrossRef Ono H, Minatoguchi S, Watanabe K, Yamada Y, Mizukusa T, Kawasaki H, Takahashi H, Uno T, Tsukamoto T, Hiei K, Fujiwara H (2008) Candesartan decreases carotid intima-media thickness by enhancing nitric oxide and decreasing oxidative stress in patients with hypertension. Hypertens Res 31:271–279PubMedCrossRef
18.
Zurück zum Zitat Yasunari K, Maeda K, Watanabe T, Nakamura M, Yoshikawa J, Asada A (2004) Comparative effects of valsartan versus amlodipine on left ventricular mass and reactive oxygen species formation by monocytes in hypertensive patients with left ventricular hypertrophy. J Am Coll Cardiol 43:2116–2123PubMedCrossRef Yasunari K, Maeda K, Watanabe T, Nakamura M, Yoshikawa J, Asada A (2004) Comparative effects of valsartan versus amlodipine on left ventricular mass and reactive oxygen species formation by monocytes in hypertensive patients with left ventricular hypertrophy. J Am Coll Cardiol 43:2116–2123PubMedCrossRef
19.
Zurück zum Zitat Baykal Y, Yilmaz MI, Celik T, Gok F, Rehber H, Akay C, Kocar IH (2003) Effects of antihypertensive agents, alpha receptor blockers, beta blockers, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers and calcium channel blockers, on oxidative stress. J Hypertens 21:1207–1211PubMedCrossRef Baykal Y, Yilmaz MI, Celik T, Gok F, Rehber H, Akay C, Kocar IH (2003) Effects of antihypertensive agents, alpha receptor blockers, beta blockers, angiotensin-converting enzyme inhibitors, angiotensin receptor blockers and calcium channel blockers, on oxidative stress. J Hypertens 21:1207–1211PubMedCrossRef
20.
Zurück zum Zitat Litwin M, Niemirska A, Śladowska-Kozłowska J, Wierzbicka A, Janas R, Wawer ZT, Wiśniewski A, Feber J (2010) Regression of target organ damage in children and adolescents with primary hypertension. Pediatr Nephrol 25:2489–2499PubMedCrossRef Litwin M, Niemirska A, Śladowska-Kozłowska J, Wierzbicka A, Janas R, Wawer ZT, Wiśniewski A, Feber J (2010) Regression of target organ damage in children and adolescents with primary hypertension. Pediatr Nephrol 25:2489–2499PubMedCrossRef
21.
Zurück zum Zitat Śladowska-Kozłowska J, Litwin M, Niemirska A, Wierzbicka A, Wawer ZT, Janas R (2011) Change in left ventricular geometry during antihypertensive treatment in children with primary hypertension. Pediatr Nephrol 26:2201–2209PubMedCrossRef Śladowska-Kozłowska J, Litwin M, Niemirska A, Wierzbicka A, Wawer ZT, Janas R (2011) Change in left ventricular geometry during antihypertensive treatment in children with primary hypertension. Pediatr Nephrol 26:2201–2209PubMedCrossRef
22.
Zurück zum Zitat National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents (2004) The Fourth Report on Diagnosis, Evaluation and Treatment of High Blood Pressure in Children and Adolescents Pediatrics 114:555–576 National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents (2004) The Fourth Report on Diagnosis, Evaluation and Treatment of High Blood Pressure in Children and Adolescents Pediatrics 114:555–576
23.
Zurück zum Zitat Lurbe E, Cifkova R, Cruickshank JK, Dillon MJ, Ferreira I, Invitti C, Kuznetsova T, Laurent S, Mancia G, Morales-Olivas F, Rascher W, Redon J, Schaefer F, Seeman T, Stergiou G, Wühl E, Zanchetti A, European Society of Hypertension (2009) Management of high blood pressure in children and adolescents: recommendations of the European society of hypertension. J Hypertens 27:1719–1742PubMedCrossRef Lurbe E, Cifkova R, Cruickshank JK, Dillon MJ, Ferreira I, Invitti C, Kuznetsova T, Laurent S, Mancia G, Morales-Olivas F, Rascher W, Redon J, Schaefer F, Seeman T, Stergiou G, Wühl E, Zanchetti A, European Society of Hypertension (2009) Management of high blood pressure in children and adolescents: recommendations of the European society of hypertension. J Hypertens 27:1719–1742PubMedCrossRef
24.
Zurück zum Zitat Wühl E, Witte K, Soergel M, Mehls O, Shaefer F, German Working Group on Pediatric Hypertension (2002) Distribution of 24-h ambulatory blood pressure in children: normalized reference values and role of body dimensions. J Hypertens 20:1995–2007PubMedCrossRef Wühl E, Witte K, Soergel M, Mehls O, Shaefer F, German Working Group on Pediatric Hypertension (2002) Distribution of 24-h ambulatory blood pressure in children: normalized reference values and role of body dimensions. J Hypertens 20:1995–2007PubMedCrossRef
25.
Zurück zum Zitat Urbina E, Alpert B, Flynn J, Hayman L, Harshfield GA, Jacobson M, Mahoney L, McCrindle B, Mietus-Snyder M, Steinberger J, Daniels S, American Heart Association Atherosclerosis, Hypertension, and Obesity in Youth Committee (2008) Ambulatory blood pressure monitoring in children and adolescents recomendations for standard assessment. A scientific statement from the American heart association atherosclerosis, hypertension, and obesity in youth committee of the council on cardiovascular disease in the young and the council for high blood pressure research. Hypertension 52:433–451PubMedCrossRef Urbina E, Alpert B, Flynn J, Hayman L, Harshfield GA, Jacobson M, Mahoney L, McCrindle B, Mietus-Snyder M, Steinberger J, Daniels S, American Heart Association Atherosclerosis, Hypertension, and Obesity in Youth Committee (2008) Ambulatory blood pressure monitoring in children and adolescents recomendations for standard assessment. A scientific statement from the American heart association atherosclerosis, hypertension, and obesity in youth committee of the council on cardiovascular disease in the young and the council for high blood pressure research. Hypertension 52:433–451PubMedCrossRef
26.
Zurück zum Zitat Cole TJ, Bellizzi MC, Flegal KM, Dietz WH (2000) Establishing a standard definition for child overweight and obesity worldwide: international study. BMJ 320:1240–1243PubMedCrossRef Cole TJ, Bellizzi MC, Flegal KM, Dietz WH (2000) Establishing a standard definition for child overweight and obesity worldwide: international study. BMJ 320:1240–1243PubMedCrossRef
27.
Zurück zum Zitat Litwin M, Śladowska J, Antoniewicz J, Niemirska A, Wierzbicka A, Daszkowska J, Wawer ZT, Janas R, Grenda R (2007) Metabolic abnormalities, insulin resistance and metabolic syndrome in children with primary hypertension. Am J Hypertens 20:875–882PubMedCrossRef Litwin M, Śladowska J, Antoniewicz J, Niemirska A, Wierzbicka A, Daszkowska J, Wawer ZT, Janas R, Grenda R (2007) Metabolic abnormalities, insulin resistance and metabolic syndrome in children with primary hypertension. Am J Hypertens 20:875–882PubMedCrossRef
28.
Zurück zum Zitat Jourdan C, Wühl E, Litwin M, Fahr K, Trelewicz J, Jobs K, Schenk JP, Grenda R, Mehls O, Tröger J, Schaefer F (2005) Normative values of intima-media thickness and distensibility of large arteries in healthy adolescents. J Hypertens 23:1707–1715PubMedCrossRef Jourdan C, Wühl E, Litwin M, Fahr K, Trelewicz J, Jobs K, Schenk JP, Grenda R, Mehls O, Tröger J, Schaefer F (2005) Normative values of intima-media thickness and distensibility of large arteries in healthy adolescents. J Hypertens 23:1707–1715PubMedCrossRef
29.
Zurück zum Zitat Devereux RB, Alonso DR, Lutas EM, Gottlieb GJ, Campo E, Sachs I, Reichek N (1986) Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings. Am J Cardiol 57:450–458PubMedCrossRef Devereux RB, Alonso DR, Lutas EM, Gottlieb GJ, Campo E, Sachs I, Reichek N (1986) Echocardiographic assessment of left ventricular hypertrophy: comparison to necropsy findings. Am J Cardiol 57:450–458PubMedCrossRef
30.
Zurück zum Zitat de Simone G, Daniels SR, Devereux RB, Meyer RA, Roman MJ, de Divitiis O, Alderman MH (1992) Left ventricular mass and body size in normotensive children and adults: assessment of allometric relations and impact of overweight. J Am Coll Cardiol 20:1251–1260PubMedCrossRef de Simone G, Daniels SR, Devereux RB, Meyer RA, Roman MJ, de Divitiis O, Alderman MH (1992) Left ventricular mass and body size in normotensive children and adults: assessment of allometric relations and impact of overweight. J Am Coll Cardiol 20:1251–1260PubMedCrossRef
31.
Zurück zum Zitat Khoury PR, Mitsnefes M, Daniels SR, Kimball TR (2009) Age-specific reference intervals for indexed left ventricular mass in children. J Am Soc Echo 22:709–714CrossRef Khoury PR, Mitsnefes M, Daniels SR, Kimball TR (2009) Age-specific reference intervals for indexed left ventricular mass in children. J Am Soc Echo 22:709–714CrossRef
32.
Zurück zum Zitat Daniels SR, Meyer RA, Liang Y, Bove KE (1998) Echocardiographically determined left ventricular mass index in normal children, adolescents and young adults. J Am Coll Cardiol 12:703–708 Daniels SR, Meyer RA, Liang Y, Bove KE (1998) Echocardiographically determined left ventricular mass index in normal children, adolescents and young adults. J Am Coll Cardiol 12:703–708
33.
Zurück zum Zitat Redón J, Oliva MR, Tormos C, Giner V, Chaves J, Iraki A, Sáez GT (2003) Antioxidant activities and oxidative stress byproducts in human hypertension. Hypertension 41:1096–1101PubMedCrossRef Redón J, Oliva MR, Tormos C, Giner V, Chaves J, Iraki A, Sáez GT (2003) Antioxidant activities and oxidative stress byproducts in human hypertension. Hypertension 41:1096–1101PubMedCrossRef
34.
Zurück zum Zitat Kelly AS, Steinberger J, Kaiser DR, Olson TP, Bank AJ, Dengel DR (2006) Oxidative stress and adverse adipokine profile characterize the metabolic syndrome in children. J Cardiometab Syndr 1:248–252PubMedCrossRef Kelly AS, Steinberger J, Kaiser DR, Olson TP, Bank AJ, Dengel DR (2006) Oxidative stress and adverse adipokine profile characterize the metabolic syndrome in children. J Cardiometab Syndr 1:248–252PubMedCrossRef
35.
Zurück zum Zitat Siemianowicz K, Gmiński J, Francuz T, Wójcik A, Posielezna B (2006) Activity of antioxidant enzymes in children from families at high risk of premature coronary heart disease. Scand J Clin Lab Invest 63:151–158 Siemianowicz K, Gmiński J, Francuz T, Wójcik A, Posielezna B (2006) Activity of antioxidant enzymes in children from families at high risk of premature coronary heart disease. Scand J Clin Lab Invest 63:151–158
36.
Zurück zum Zitat Sydov K, Mondon CE, Cooke JP (2005) Insulin resistance: potential role of the endogenous nitric oxide synthase inhibitor ADMA. Vasc Med 10:35–43CrossRef Sydov K, Mondon CE, Cooke JP (2005) Insulin resistance: potential role of the endogenous nitric oxide synthase inhibitor ADMA. Vasc Med 10:35–43CrossRef
37.
Zurück zum Zitat Stühlinger M, Abbasi F, Chu JW, Lamendola C, McLaughlin TL, Cooke JP, Reaven GM, Tsao PS (2002) Relationship between insulin resistance and an endogenous nitric oxide synthase inhibitor. J Am Med Assoc 287:1420–1426CrossRef Stühlinger M, Abbasi F, Chu JW, Lamendola C, McLaughlin TL, Cooke JP, Reaven GM, Tsao PS (2002) Relationship between insulin resistance and an endogenous nitric oxide synthase inhibitor. J Am Med Assoc 287:1420–1426CrossRef
38.
Zurück zum Zitat Goonasekera CD, Rees DD, Woolard P, Frend A, Shah V, Dillon MJ (1997) Nitric oxide synthase inhibitors and hypertension in children and adolescents. J Hypertens 15:901–909PubMedCrossRef Goonasekera CD, Rees DD, Woolard P, Frend A, Shah V, Dillon MJ (1997) Nitric oxide synthase inhibitors and hypertension in children and adolescents. J Hypertens 15:901–909PubMedCrossRef
39.
Zurück zum Zitat Palm AJP, Onozato ML, Luo Z, Wilcox CS (2007) Dimethylarginine dimethylaminohydrolase (DDAH): expression, regulation, and function in the cardiovascular and renal systems. Am J Physiol Heart Circ Physiol 293:H3227–H3245PubMedCrossRef Palm AJP, Onozato ML, Luo Z, Wilcox CS (2007) Dimethylarginine dimethylaminohydrolase (DDAH): expression, regulation, and function in the cardiovascular and renal systems. Am J Physiol Heart Circ Physiol 293:H3227–H3245PubMedCrossRef
40.
Zurück zum Zitat Kapur S, Bedard S, Marcotte B, Cote CH, Marette A (1997) Expression of nitric oxide synthase in skeletal muscle: a novel role for nitric oxide as a modulator of insulin action. Diabetes 46:1691–1700PubMedCrossRef Kapur S, Bedard S, Marcotte B, Cote CH, Marette A (1997) Expression of nitric oxide synthase in skeletal muscle: a novel role for nitric oxide as a modulator of insulin action. Diabetes 46:1691–1700PubMedCrossRef
41.
Zurück zum Zitat Moreno MU, San José G, Fortuño A, Beloqui O, Díez J, Zalba G (2006) The C242T CYBA polymorphism of NADPH oxidase is associated with essential hypertension. J Hypertens 24:1299–306PubMedCrossRef Moreno MU, San José G, Fortuño A, Beloqui O, Díez J, Zalba G (2006) The C242T CYBA polymorphism of NADPH oxidase is associated with essential hypertension. J Hypertens 24:1299–306PubMedCrossRef
42.
Zurück zum Zitat Vaziri ND, Wang XQ, Oveisi F, Rad B (2000) Induction of oxidative stress by glutathione depletion causes severe hypertension in normal rats. Hypertension 36:142–146PubMedCrossRef Vaziri ND, Wang XQ, Oveisi F, Rad B (2000) Induction of oxidative stress by glutathione depletion causes severe hypertension in normal rats. Hypertension 36:142–146PubMedCrossRef
43.
Zurück zum Zitat Touyz RM (2004) Reactive oxygen species, vascular oxidative stress, and redox signaling in hypertension: what is the clinical significance? Hypertension 44:248–252PubMedCrossRef Touyz RM (2004) Reactive oxygen species, vascular oxidative stress, and redox signaling in hypertension: what is the clinical significance? Hypertension 44:248–252PubMedCrossRef
44.
Zurück zum Zitat Brown LA, Kerr CJ, Whiting P, Finer R, McEneny J, Ashton T (2009) Oxidant stress in healthy normal-weight, overweight and obese individuals. Obesity 17:460–466PubMedCrossRef Brown LA, Kerr CJ, Whiting P, Finer R, McEneny J, Ashton T (2009) Oxidant stress in healthy normal-weight, overweight and obese individuals. Obesity 17:460–466PubMedCrossRef
Metadaten
Titel
Oxidative stress in hypertensive children before and after 1 year of antihypertensive therapy
verfasst von
Joanna Śladowska-Kozłowska
Mieczysław Litwin
Anna Niemirska
Paweł Płudowski
Aldona Wierzbicka
Ewa Skorupa
Zbigniew T. Wawer
Roman Janas
Publikationsdatum
01.10.2012
Verlag
Springer-Verlag
Erschienen in
Pediatric Nephrology / Ausgabe 10/2012
Print ISSN: 0931-041X
Elektronische ISSN: 1432-198X
DOI
https://doi.org/10.1007/s00467-012-2193-x

Weitere Artikel der Ausgabe 10/2012

Pediatric Nephrology 10/2012 Zur Ausgabe

Klimaschutz beginnt bei der Wahl des Inhalators

14.05.2024 Klimawandel Podcast

Auch kleine Entscheidungen im Alltag einer Praxis können einen großen Beitrag zum Klimaschutz leisten. Die neue Leitlinie zur "klimabewussten Verordnung von Inhalativa" geht mit gutem Beispiel voran, denn der Wechsel vom klimaschädlichen Dosieraerosol zum Pulverinhalator spart viele Tonnen CO2. Leitlinienautor PD Dr. Guido Schmiemann erklärt, warum nicht nur die Umwelt, sondern auch Patientinnen und Patienten davon profitieren.

Zeitschrift für Allgemeinmedizin, DEGAM

Embryotransfer erhöht womöglich Leukämierisiko der Kinder

13.05.2024 Assistierte Reproduktion Nachrichten

Reproduktionsmedizinische Techniken haben theoretisch das Potenzial, den epigenetischen Code zu verändern und somit das Krebsrisiko der Kinder zu erhöhen. Zwischen Embryotransfer und Leukämie scheint sich ein solcher Zusammenhang bestätigt zu haben.

Darf man die Behandlung eines Neonazis ablehnen?

08.05.2024 Gesellschaft Nachrichten

In einer Leseranfrage in der Zeitschrift Journal of the American Academy of Dermatology möchte ein anonymer Dermatologe bzw. eine anonyme Dermatologin wissen, ob er oder sie einen Patienten behandeln muss, der eine rassistische Tätowierung trägt.

Ein Drittel der jungen Ärztinnen und Ärzte erwägt abzuwandern

07.05.2024 Klinik aktuell Nachrichten

Extreme Arbeitsverdichtung und kaum Supervision: Dr. Andrea Martini, Sprecherin des Bündnisses Junge Ärztinnen und Ärzte (BJÄ) über den Frust des ärztlichen Nachwuchses und die Vorteile des Rucksack-Modells.

Update Pädiatrie

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.