Sullivan Shannon D, Jablonski Kathleen A, Florez Jose C, Dabelea Dana, Franks Paul W, Dagogo-Jack Sam, Kim Catherine, Knowler William C, Christophi Costas A, Ratner Robert
Corresponding author: Shannon D. Sullivan,
Diabetes Care. 2014 Apr;37(4):909-11. doi: 10.2337/dc13-0700. Epub 2013 Nov 22.
OBJECTIVE The Diabetes Prevention Program (DPP) trial investigated rates of progression to diabetes among adults with prediabetes randomized to treatment with placebo, metformin, or intensive lifestyle intervention. Among women in the DPP, diabetes risk reduction with metformin was greater in women with prior gestational diabetes mellitus (GDM) compared with women without GDM but with one or more previous live births. RESEARCH DESIGN AND METHODS We asked if genetic variability could account for these differences by comparing β-cell function and genetic risk scores (GRS), calculated from 34 diabetes-associated loci, between women with and without histories of GDM. RESULTS β-Cell function was reduced in women with GDM. The GRS was positively associated with a history of GDM; however, the GRS did not predict progression to diabetes or modulate response to intervention. CONCLUSIONS These data suggest that a diabetes-associated GRS is associated with development of GDM and may characterize women at risk for development of diabetes due to β-cell dysfunction.
目的 糖尿病预防计划(DPP)试验研究了糖尿病前期成年人随机接受安慰剂、二甲双胍治疗或强化生活方式干预后进展为糖尿病的发生率。在DPP研究的女性中,与既往无妊娠糖尿病(GDM)但有一次或多次活产史的女性相比,既往有GDM的女性使用二甲双胍降低糖尿病风险的效果更好。研究设计与方法 通过比较有和无GDM病史的女性的β细胞功能以及根据34个糖尿病相关基因座计算的遗传风险评分(GRS),我们探究了基因变异性是否可以解释这些差异。结果 GDM女性的β细胞功能降低。GRS与GDM病史呈正相关;然而,GRS不能预测糖尿病进展或调节干预反应。结论 这些数据表明,与糖尿病相关的GRS与GDM的发生有关,并且可能是因β细胞功能障碍而有糖尿病发生风险的女性的特征。