Snitker Soren, Watanabe Richard M, Ani Ifeanyi, Xiang Anny H, Marroquin Aura, Ochoa Cesar, Goico Jose, Shuldiner Alan R, Buchanan Thomas A
Department of Medicine, Division of Endocrinology, Diabetes, and Nutrition, University of Maryland, Baltimore School of Medicine, 660 W. Redwood St., Howard Hall Rm. 598-B, Baltimore, MD 21201-1596, USA.
Diabetes Care. 2004 Jun;27(6):1365-8. doi: 10.2337/diacare.27.6.1365.
We have tested whether the Pro12Ala variant of the peroxisome proliferator-activated receptor (PPAR)-gamma nuclear receptor involved in thiazolidinedione (TZD) action accounted for the failure of troglitazone to increase insulin sensitivity in nondiabetic Hispanic women with previous gestational diabetes treated in the Troglitazone in Prevention of Diabetes (TRIPOD) study.
Ninety-three women assigned to troglitazone had intravenous glucose tolerance tests at randomization and after 3 months of treatment with troglitazone, 400 mg/day, and were genotyped for the Pro12Ala variant of the PPAR-gamma gene. Subjects were divided into tertiles based on their change in minimal model insulin sensitivity (S(i)) during the first 3 months of troglitazone treatment.
The mean changes in S(i) in the bottom, middle, and top tertiles of S(i) response were -0.21 +/- 0.57, 0.91 +/- 0.26, and 2.58 +/- 1.32 min(-1) per microU/ml. 10(-4), respectively. Frequencies of the Ala/- genotype were 30, 22, and 26% in the same three tertiles (P = 0.77). Analysis of phenotypes by genotype revealed only small differences between the Pro/Pro and Ala/- groups, respectively, in baseline S(i) (2.76 +/- 0.19 vs. 2.33 +/- 0.33 x 10(-4) min(-1) per microU/ml; P = 0.27), the change in S(i) after 3 months of troglitazone treatment (1.19 +/- 0.17 vs. 0.93 +/- 0.30; P = 0.46), and the cumulative incidence of diabetes during a median follow-up of 30 months (13 vs. 17%; P = 0.66).
Among young Hispanic women at high risk for type 2 diabetes, the Pro12Ala variant of the PPAR-gamma receptor gene did not explain the failure of approximately 1/3 of subjects to increase their insulin sensitivity when placed on troglitazone at a dose of 400 mg/day.
我们检验了参与噻唑烷二酮(TZD)作用的过氧化物酶体增殖物激活受体(PPAR)-γ核受体的Pro12Ala变体,是否可以解释在预防糖尿病的曲格列酮研究(TRIPOD)中,曲格列酮未能增加既往有妊娠糖尿病的非糖尿病西班牙裔女性的胰岛素敏感性。
93名被分配接受曲格列酮治疗的女性在随机分组时以及接受400毫克/天曲格列酮治疗3个月后进行了静脉葡萄糖耐量试验,并对PPAR-γ基因的Pro12Ala变体进行基因分型。根据曲格列酮治疗前3个月最小模型胰岛素敏感性(S(i))的变化将受试者分为三分位数组。
S(i)反应的底部、中间和顶部三分位数组中S(i)的平均变化分别为-0.21±0.57、0.91±0.26和2.58±1.32分钟-1/微单位/毫升。10-4。Ala/-基因型在相同的三个三分位数组中的频率分别为30%、22%和26%(P = 0.77)。按基因型分析表型发现,Pro/Pro组和Ala/-组在基线S(i)(2.76±0.19对2.33±0.33×10-4分钟-1/微单位/毫升;P = 0.27)、曲格列酮治疗3个月后S(i)的变化(1.19±0.17对0.93±0.30;P = 0.46)以及中位随访30个月期间糖尿病的累积发病率(13%对17%;P = 0.66)方面仅存在微小差异。
在2型糖尿病高危的年轻西班牙裔女性中,PPAR-γ受体基因的Pro12Ala变体无法解释约1/3的受试者在接受400毫克/天曲格列酮治疗时未能增加胰岛素敏感性的原因。