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RGS2 C1114G polymorphism and body weight gain in hypertensive patients.

机译:高血压患者的RGS2 C1114G基因多态性和体重增加。

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RGS2 is a negative regulator of Galpha protein signaling and promotes adipocyte differentiation. Recently, we described a polymorphism at the C1114G locus with the G allele associated with hypertension in a cross-sectional study. The aim of the present study was to assess whether the RGS2 C1114G is predictive of overweight in young subjects with grade I hypertension. We genotyped at the RGS2 C1114G locus 406 (male, n = 294; female, n = 112) white hypertensive subjects (age, 33 +/- 9 years) never treated for hypertension and at low cardiovascular risk. Median follow-up was 7.85 years. At baseline, male patients carrying the RGS2 1114G allele had higher body mass index (BMI) than patients with CC genotype (26.1 +/- 0.3 vs 25.3 +/- 0.3 kg/m2, P < .05). The frequency of male patients with BMI > or = 25 was similar between the patients with G allele and those with CC genotype (55.1% vs 47.8%, P = not significant). No significant difference between the 2 groups was observed with regard to physical activity, blood pressure, and heart rate. At the end of follow-up, BMI was higher in male patients with G allele compared with patients with CC genotype (26.8 +/- 0.3 vs 25.8 +/- 0.2 kg/m2, P < .01); and the frequency of male patients with BMI >25 kg/m2 was greater in the former (69.0% vs 52.2%, P < .01). According to Cox regression, allele G was a significant predictor of developing overweight or obesity during follow-up. These epidemiologic relations were not significant in female patients. In young male patients with grade I hypertension, RGS2 1114G allele is associated with increased BMI and with greater risk of developing overweight or obesity. The RGS2 1114G allele may be considered a genetic marker that predicts an individual's predisposition to gaining weight.
机译:RGS2是Galpha蛋白信号传导的负调节剂,可促进脂肪细胞分化。最近,我们在一项横断面研究中描述了C1114G基因座的多态性与与高血压相关的G等位基因。本研究的目的是评估RGS2 C1114G是否可预测患有I级高血压的年轻受试者的超重。我们在RGS2 C1114G基因座406(男性,n = 294;女性,n = 112)位白人高血压受试者(33 +/- 9岁)进行基因分型,从未治疗过高血压且心血管风险低。中位随访时间为7。85年。基线时,携带RGS2 1114G等位基因的男性患者的体重指数(BMI)比CC基因型患者高(26.1 +/- 0.3 vs 25.3 +/- 0.3 kg / m2,P <.05)。 G等位基因患者与CC基因型患者之间BMI>或= 25的男性患者的发生频率相似(55.1%vs 47.8%,P =无关)。在体力活动,血压和心率方面,两组之间未观察到显着差异。随访结束时,G等位基因男性患者的BMI高于CC基因型患者(26.8 +/- 0.3 vs 25.8 +/- 0.2 kg / m2,P <.01);前者中BMI> 25 kg / m2的男性患者发生率更高(69.0%比52.2%,P <.01)。根据Cox回归,等位基因G是随访期间发生超重或肥胖的重要预测指标。这些流行病学关系在女性患者中不显着。在患有I级高血压的年轻男性患者中,RGS2 1114G等位基因与BMI升高以及发生超重或肥胖的风险更大有关。 RGS2 1114G等位基因可以被认为是预测个体体重增加倾向的遗传标记。

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