Department of Child and Adolescent Psychiatry, University of Duisburg-Essen, Essen, Germany.
Obes Facts. 2011;4(1):67-75. doi: 10.1159/000324557. Epub 2011 Feb 22.
Association with obesity and increased insulin levels have been reported for two variants (rs17782313 and rs12970134) located downstream of the melanocortin-4 receptor gene (MC4R).
We investigated whether these variants have sex-specific effects on overweight, obesity and 14 related phenotypes in 889 overweight and obese children and adolescents. We also explored the impact of the variants on weight change in 367 of the 889 cases who participated in an intervention program. Prior to these analyses we showed that both variants were associated with overweight/obesity in the analyzed 889 cases versus 442 normal-weight and lean controls (case-control study).
In explorative analyses we observed higher diastolic blood pressure levels in males (rs17782313: β = 2.52 mm Hg per risk allele; p = 0.003) but reduced blood pressure level in females for the same risk allele (β = -1.72 mm Hg; p = 0.039). We also detected a greater BMI standard deviation score (BMI-SDS) reduction in females with the risk allele at rs17782313 (β = 0.086 per risk allele; p = 0.021). Additionally, we observed evidence for an association of the same risk allele with insulin levels (β = 0.029 log (μU/ml); p = 0.044) with no sex-specific effect. For the remaining 11 phenotypes, we observed no evidence for a (sex-specific) association.
In sum, our data support the associations of variants rs17782313 and rs12970134 near MC4R with early onset obesity and increased insulin levels. Exploratory evidence for sex-specific effects of the risk alleles were observed for diastolic blood pressure and BMI-SDS reduction.
据报道,位于黑素皮质素 4 受体基因(MC4R)下游的两个变体(rs17782313 和 rs12970134)与肥胖和胰岛素水平升高有关。
我们调查了这两个变体是否在 889 名超重和肥胖的儿童和青少年中对超重、肥胖以及 14 种相关表型具有性别特异性影响。我们还探讨了这些变体对 889 例病例中 367 例参加干预计划的病例体重变化的影响。在进行这些分析之前,我们已经证明,在分析的 889 例病例中,这两个变体都与超重/肥胖有关,而在 442 例正常体重和瘦对照者中则没有(病例对照研究)。
在探索性分析中,我们观察到男性的舒张压水平升高(rs17782313:每个风险等位基因增加 2.52 毫米汞柱;p = 0.003),但同一风险等位基因使女性的血压水平降低(β = -1.72 毫米汞柱;p = 0.039)。我们还发现,rs17782313 的风险等位基因使女性的 BMI 标准差评分(BMI-SDS)降低更大(每个风险等位基因增加 0.086;p = 0.021)。此外,我们还观察到同一风险等位基因与胰岛素水平的关联(β = 0.029 log(μU/ml);p = 0.044),但没有性别特异性效应。对于其余 11 种表型,我们没有发现(性别特异性)关联的证据。
总的来说,我们的数据支持 rs17782313 和 rs12970134 附近的 MC4R 变体与早期肥胖和胰岛素水平升高有关。对于风险等位基因,我们观察到舒张压和 BMI-SDS 降低的性别特异性效应的探索性证据。