Effects of pioglitazone hydrochloride on Japanese patients with type 2 diabetes mellitus

被引:11
|
作者
Teramoto, Tamio
Yamada, Nobuhiro
Shirai, Kohji
Saito, Yasushi
机构
[1] Teikyo Univ, Sch Med, Dept Internal Med, Itabashi Ku, Tokyo 1738605, Japan
[2] Univ Tsukuba, Dept Internal Med Metab Endocrinol & Atherosclero, Tsukuba, Ibaraki 305, Japan
[3] Toho Univ, Sch Med, Sakura Med Ctr, Dept Internal Med, Chiba 2748510, Japan
[4] Chiba Univ, Grad Sch Med, Dept Clin Cell Biol, Chiba, Japan
关键词
lipid and glycemic control; HDL-C level; LDL particle size; TG level;
D O I
10.5551/jat.14.86
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Aim: The effects of pioglitazone hydrochloride monotherapy on abnormal lipid control were evaluated in Japanese patients with type 2 diabetes mellitus, comparing with glibenclamide monotherapy. Methods: Patients were randomly assigned to receive, once daily, pioglitazone hydrochloride, at 15 mg or 30 mg (n=46), or glibendamide, at 1.25 mg or 2.5 mg (n=46). The 24-week study included patients with type 2 diabetes having high levels of triglyceride (TG). Results: Pioglitazone hydrochloride produced beneficial effects on dyslipidemia in patients with type 2 diabetes, compared with the baseline and the glibenclamide group, as demonstrated by increases in high-density lipoprotein cholesterol (HDL-C) levels and low-density lipoprotein cholesterol (LDL) particle size, a fall in TG levels, and an increased ratio of visceral to subcutaneous fat volumes (V/S). Pioglitazone hydrochloride reduced fasting serum insulin levels, with low fasting plasma glucose (FPG) and glycohemoglobin levels, compared to the baseline, suggesting an improvement of insulin resistance. Conclusion: As expected, glibenclamide reduced FPG levels through increased insulin secretion. Pioglitazone hydrochloride and glibenclamide were well tolerated. Pioglitazone hydrochloride improved dyslipidemia related to insulin resistance, whereas glibenclamide enhanced insulin secretion, with only a minor effect on lipid control, in Japanese patients with type 2 diabetes.
引用
收藏
页码:86 / 93
页数:8
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