Diabetes Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Diabetes Care. 2012 Feb;35(2):363-6. doi: 10.2337/dc11-1328. Epub 2011 Dec 16.
We tested genetic associations with weight loss and weight regain in the Diabetes Prevention Program, a randomized controlled trial of weight loss-inducing interventions (lifestyle and metformin) versus placebo.
Sixteen obesity-predisposing single nucleotide polymorphisms (SNPs) were tested for association with short-term (baseline to 6 months) and long-term (baseline to 2 years) weight loss and weight regain (6 months to study end).
Irrespective of treatment, the Ala12 allele at PPARG associated with short- and long-term weight loss (-0.63 and -0.93 kg/allele, P ≤ 0.005, respectively). Gene-treatment interactions were observed for short-term (LYPLAL1 rs2605100, P(lifestyleSNP) = 0.032; GNPDA2 rs10938397, P(lifestyleSNP) = 0.016; MTCH2 rs10838738, P(lifestyleSNP) = 0.022) and long-term (NEGR1 rs2815752, P(metforminSNP) = 0.028; FTO rs9939609, P(lifestyleSNP) = 0.044) weight loss. Three of 16 SNPs were associated with weight regain (NEGR1 rs2815752, BDNF rs6265, PPARG rs1801282), irrespective of treatment. TMEM18 rs6548238 and KTCD15 rs29941 showed treatment-specific effects (P(lifestyleSNP) < 0.05).
Genetic information may help identify people who require additional support to maintain reduced weight after clinical intervention.
我们在糖尿病预防计划(一项减肥诱导干预(生活方式和二甲双胍)与安慰剂对照的随机临床试验)中测试了与体重减轻和体重反弹相关的遗传关联。
对 16 个肥胖易感单核苷酸多态性(SNP)进行了短期(基线至 6 个月)和长期(基线至 2 年)体重减轻和体重反弹(6 个月至研究结束)的关联测试。
无论治疗如何,PPARG 上的 Ala12 等位基因与短期和长期体重减轻相关(-0.63 和-0.93kg/等位基因,P≤0.005,分别)。在短期(LYPLAL1 rs2605100,P(生活方式SNP)=0.032;GNPDA2 rs10938397,P(生活方式SNP)=0.016;MTCH2 rs10838738,P(生活方式SNP)=0.022)和长期(NEGR1 rs2815752,P(二甲双胍SNP)=0.028;FTO rs9939609,P(生活方式SNP)=0.044)体重减轻中观察到基因-治疗相互作用。16 个 SNP 中有 3 个与体重反弹相关(NEGR1 rs2815752、BDNF rs6265、PPARG rs1801282),无论治疗如何。TMEM18 rs6548238 和 KTCD15 rs29941 显示出治疗特异性效应(P(生活方式SNP)<0.05)。
遗传信息可能有助于识别需要额外支持以维持临床干预后体重减轻的人群。