Sartori Michelangelo, Ceolotto Giulio, Dorigatti Francesca, Mos Lucio, Santonastaso Massimo, Bratti Paolo, Papparella Italia, Semplicini Andrea, Palatini Paolo
Department of Angiology and Blood Coagulation, S. Orsola-Malpighi, University Hospital, 40138 Bologna, Italy.
Metabolism. 2008 Mar;57(3):421-7. doi: 10.1016/j.metabol.2007.10.021.
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.
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。