BackgroundObesity has been identified as an important risk factor in the development of
cardiovascular diseases; however, other factors, combined or not with obesity, can
influence cardiovascular risk and should be considered in cardiovascular risk
stratification in pediatrics. ObjectiveTo analyze the association between anthropometry measures and cardiovascular risk
factors, to investigate the determinants to changes in blood pressure (BP), and to
propose a prediction equation to waist circumference (WC) in children and
adolescents. MethodsWe evaluated 1,950 children and adolescents, aged 7 to 18 years. Visceral fat was
assessed by WC and waist hip relationship, BP and body mass index (BMI). In a
randomly selected subsample of these volunteers (n = 578), total cholesterol,
glucose and triglycerides levels were evaluated. ResultsWC was positively correlated with BMI (r = 0.85; p < 0.001) and BP (SBP r =
0.45 and DBP = 0.37; p < 0.001). Glycaemia and triglycerides showed a weak
correlation with WC (r = 0.110; p = 0.008 e r = 0.201; p < 0.001,
respectively). Total cholesterol did not correlate with any of the variables. Age,
BMI and WC were significant predictors on the regression models for BP (p <
0.001). We propose a WC prediction equation for children and adolescents: boys: y
= 17.243 + 0.316 (height in cm); girls: y = 25.197 + 0.256 (height in cm). ConclusionWC is associated with cardiovascular risk factors and presents itself as a risk
factor predictor of hypertension in children and adolescents. The WC prediction
equation proposed by us should be tested in future studies.
Overweight and obesity are associated with chronic and subclinical inflammation due to an imbalance of inflammatory mediators. However, the association with gene polymorphism has been rarely studied in children. The aim of this study was to determine if serum concentrations of C-reactive protein (CRP) and interleukin-6 (IL-6) are related to the IL6 rs1800795, IL6 rs2069845 and CRP rs1205 polymorphisms (SNPs) according to body mass index (BMI) in a sample of children and adolescents. A cross-sectional study in 470 students between 7 and 17yearsof age of anthropometric characteristics, high sensitivity-CRP (Hs-CRP) and IL-6 levels and three SNPs genotyped. The prevalence ratio of hs-CRP>3mg/L in obese individuals was 4.15 (CI 2.43-7.06; p=0.01), and it was 1.91 (CI 1.03-3.55; p=0.03) in overweight individuals and 1.74 (CI 1.05-2.88 p=0.03) in females. Individuals with waist circumference (WC) and body fat percentage (BF%) alterations showed elevated levels of hs-CRP (p=4.3×10 and p=5.3×10). The combination of any two anthropometric measurement increases CRP levels, especially combinations with obesity body mass index (BMI): BMI+WC and BMI+BF%. Among the overweight/obesity group, T allele carriers of CRP rs1205 showed lower levels of hs-CRP (0.5, IQR=0.3-1.8mg/L) than CC homozygotes (1.5, IQR=0.4-3.4mg/L, p=0.018). Additionally, considering subjects with two or three anthropometric alterations for CRP rs1205: rs1205 T allele carriers had lower levels of hs-CRP (0.7, IQR=0.3-2.7mg/L) than CC homozygotes (1.2, IQR=0.5-3.5mg/L, p=0.02). In conclusion, carriers of the rs1205/T allele with higher BMIs had lower levels of hs-CRP. Schoolchildren who were overweight/obese had higher levels of CRP and IL-6, whereas individuals with WC and BF% alterations had higher levels of CRP.
Anti-tuberculosis drug-induced hepatitis (ATD-induced hepatitis) has been linked to polymorphisms in genes encoding drug metabolizing enzymes. N-acetyltransferase 2 (NAT2), cytochrome P450 2E1 (CYP2E1) and glutathione S-transferase (loci GSTM1 and GSTT1) are involved in the metabolism of isoniazid, the most toxic drug for the treatment of tuberculosis (TB). This study was designed to determine the frequency and to evaluate whether polymorphisms at CYP2E1, GSTM1 and GSTT1 genes are associated with drug response, as well as to identify clinical risk factors for ATD-induced hepatitis. A total of 245 Brazilian patients undergoing treatment for TB were genotyped using polymerase chain reaction and restriction fragment length polymorphism and sequencing methods. The frequencies of the CYP2E1 polymorphic alleles RsaI, PstI and DraI are 8%, 8.5% and 12%, respectively. GSTM1 and GSTT1 genes are deleted in 42.9% and 12.4% of the population, respectively. Fifteen patients (6.1%) developed hepatotoxicity. Clinical (HIV, female sex and extrapulmonary TB) and genetic characteristics (CYP2E1 without any mutations, having NAT2 slow acetylator profile) are at higher risk of developing ATD-induced hepatitis in this population. Genotyping for GSTM1 and GSTT1 showed no influence on drug response.
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