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RGS2基因C1114G多态性与高血压患者体重增加的关系

RGS2 C1114G polymorphism and body weight gain in hypertensive patients.

作者信息

Sartori Michelangelo, Ceolotto Giulio, Dorigatti Francesca, Mos Lucio, Santonastaso Massimo, Bratti Paolo, Papparella Italia, Semplicini Andrea, Palatini Paolo

机构信息

Department of Angiology and Blood Coagulation, S. Orsola-Malpighi, University Hospital, 40138 Bologna, Italy.

出版信息

Metabolism. 2008 Mar;57(3):421-7. doi: 10.1016/j.metabol.2007.10.021.

Abstract

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.

摘要

RGS2是Gα蛋白信号传导的负调节因子,并促进脂肪细胞分化。最近,我们在一项横断面研究中描述了C1114G位点的一种多态性,其中G等位基因与高血压相关。本研究的目的是评估RGS2 C1114G是否可预测I级高血压年轻受试者的超重情况。我们对406名(男性,n = 294;女性,n = 112)从未接受过高血压治疗且心血管风险较低的白人高血压受试者(年龄33±9岁)的RGS2 C1114G位点进行了基因分型。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)高于CC基因型患者(26.1±0.3 vs 25.3±0.3 kg/m²,P <.05)。BMI≥25的男性患者在G等位基因患者和CC基因型患者中的频率相似(55.1% vs 47.8%,P =无显著性差异)。两组在体力活动、血压和心率方面未观察到显著差异。随访结束时,携带G等位基因的男性患者的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的男性患者频率更高(69.0% vs 52.2%,P <.01)。根据Cox回归分析,等位基因G是随访期间发生超重或肥胖的显著预测因子。这些流行病学关系在女性患者中不显著。在I级高血压年轻男性患者中,RGS2 1114G等位基因与BMI增加以及发生超重或肥胖的风险增加相关。RGS2 1114G等位基因可被视为预测个体体重增加易感性的遗传标记。

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