Schuster D, Gaillard T, Rhinesmith S, Habash D, Osei K
Department of Internal Medicine, The Ohio State University College of Medicine and Public Health, Columbus, USA.
Metabolism. 2003 Sep;52(9):1211-7. doi: 10.1016/s0026-0495(03)00160-4.
African Americans (AA) have greater prevalence of type 2 diabetes mellitus (DM), and nondiabetic AA have demonstrated increased insulin resistance when compared with Caucasian Americans (CA). The objective of this study was to examine the impact of chronic use of an insulin sensitizer on glucose metabolism in normal glucose tolerant AA at risk for DM (previous gestational diabetes mellitus [GDM] or first-degree relative with DM). Forty-nine high-risk AA received 200 mg/d troglitazone (TRO) versus 81 age-, weight-, and body mass index (BMI)-matched high-risk AA who received placebo (PLA) for 24 months. Yearly anthropometric measurements, oral glucose tolerance test (OGTT) and frequently sampled intravenous glucose tolerance test (FSIVGTT) were performed. Biochemical parameters were monitored quarterly. There was no significant change in anthropometric measurements over 24 months in TRO versus PLA. There were no significant differences in serum glucose, insulin, or C-peptide incremental area under the curve (AUC) in TRO versus PLA at baseline or 24 months for OGTT and FSIVGTT. The insulin sensitivity (S(I)) for TRO and PLA increased from baseline to 24 months by 17% and 16%, respectively. The TRO demonstrated a 26% increase in insulin/glucose ratio versus 1% increase in the PLA at 24 months. The disposition index (DI) increased 33% from baseline in TRO versus 21% increase in PLA. Modest improvement in glucose metabolism was seen in TRO when compared with PLA. TRO was well tolerated without significant reported adverse events. Based on our current data, the treatment of normal glucose tolerant high-risk AA with thiazolidinedione (TZD) may be beneficial to "reset" and protect glucose metabolism by improving insulin responses. Because of the potential drug-related risks associated with use of TZD and the proven positive impact of diet and exercise in prevention of DM, studies of longer duration with examination of other potentially beneficial parameters, such as cardiovascular indices and inflammatory markers will be necessary to justify the cost in the nondiabetic population.
非裔美国人(AA)2型糖尿病(DM)的患病率更高,与美国白人(CA)相比,非糖尿病非裔美国人已表现出胰岛素抵抗增加。本研究的目的是检验长期使用胰岛素增敏剂对有患糖尿病风险(既往妊娠糖尿病[GDM]或糖尿病一级亲属)的糖耐量正常非裔美国人葡萄糖代谢的影响。49名高危非裔美国人接受200mg/d曲格列酮(TRO),而81名年龄、体重和体重指数(BMI)匹配的高危非裔美国人接受安慰剂(PLA),为期24个月。每年进行人体测量、口服葡萄糖耐量试验(OGTT)和频繁采样静脉葡萄糖耐量试验(FSIVGTT)。每季度监测生化参数。在24个月期间,TRO组与PLA组的人体测量指标无显著变化。在基线或24个月时,OGTT和FSIVGTT的血清葡萄糖、胰岛素或C肽曲线下增量面积(AUC)在TRO组与PLA组之间无显著差异。TRO组和PLA组的胰岛素敏感性(S(I))从基线到24个月分别增加了17%和16%。在24个月时,TRO组的胰岛素/葡萄糖比值增加了26%,而PLA组增加了1%。处置指数(DI)在TRO组较基线增加了33%,而PLA组增加了21%。与PLA组相比,TRO组的葡萄糖代谢有适度改善。TRO耐受性良好,未报告重大不良事件。根据我们目前的数据,用噻唑烷二酮(TZD)治疗糖耐量正常的高危非裔美国人可能有利于通过改善胰岛素反应来“重置”和保护葡萄糖代谢。由于使用TZD存在潜在的药物相关风险,且饮食和运动在预防糖尿病方面已被证实有积极作用,因此有必要进行更长时间的研究,检查其他潜在有益参数,如心血管指标和炎症标志物,以证明在非糖尿病人群中使用该药物的成本是合理的。