Barrett-Connor Elizabeth, Ensrud Kristine E, Harper Kristine, Mason Timothy M, Sashegyi Andreas, Krueger Kathryn A, Anderson Pamela W
Department of Family and Preventive Medicine, School of Medicine, University of California at San Diego, La Jolla, California 92093-0607, USA.
Clin Ther. 2003 Mar;25(3):919-30. doi: 10.1016/s0149-2918(03)80114-5.
The long-term effects of the selective estrogen-receptor modulator raloxifene hydrochloride on glycemic control and markers of cardiovascular disease risk in postmenopausal women with type 2 diabetes mellitus are unknown.
The aim of this analysis was to compare the effects of 3-year treatment with raloxifene 60 mg/d versus placebo on glycemic control and markers of cardiovascular disease risk in osteoporotic postmenopausal women with and without type 2 diabetes.
In this analysis, we included women from the Multiple Outcomes of Raloxifene Evaluation trial (a multicenter, double-masked trial) who were randomized to receive raloxifene 60 mg/d (n = 2557) or placebo (n = 2576). Baseline and 36-month fasting plasma glucose (FPG) and total cholesterol (TC) were measured for all participants. Glycated hemoglobin (HbA1c), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C), triglycerides (TGs), apolipoprotein (apo) A-I, apo B, and fibrinogen were assessed in approximately 1800 participants from selected larger sites.
At baseline, 202 of all 5133 women (3.9%) had type 2 diabetes. Of the approximately 1800 women who were assessed for HbA1c, LDL-C, TGs, apo A-I, apo B, and fibrinogen, 70 (3.9%) had type 2 diabetes at baseline. Compared with placebo, raloxifene did not significantly affect HbA1c, FPG, HDL-C, or TGs in women with or without diabetes. Raloxifene produced statistically significant reductions in TC, LDL-C, and fibrinogen both in women with diabetes (all P < or = 0.004) and without diabetes (all P < 0.001). Raloxifene significantly increased apo A-I (P < 0.001) and reduced apo B (P < 0.001) in women without diabetes. In the raloxifene-treated group, body weight increased by a mean 0.31 kg (P < 0.001) in women without diabetes.
In osteoporotic postmenopausal women with or without type 2 diabetes, raloxifene 60 mg/d did not affect glycemic control and had favorable effects on TC, LDL-C, and fibrinogen levels.
选择性雌激素受体调节剂盐酸雷洛昔芬对绝经后2型糖尿病女性血糖控制及心血管疾病风险标志物的长期影响尚不清楚。
本分析旨在比较60mg/d雷洛昔芬与安慰剂治疗3年对有或无2型糖尿病的骨质疏松绝经后女性血糖控制及心血管疾病风险标志物的影响。
在本分析中,我们纳入了雷洛昔芬评估试验(一项多中心、双盲试验)中的女性,她们被随机分配接受60mg/d雷洛昔芬(n = 2557)或安慰剂(n = 2576)。测量了所有参与者的基线和36个月时的空腹血糖(FPG)及总胆固醇(TC)。对来自选定较大站点的约1800名参与者评估了糖化血红蛋白(HbA1c)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)、甘油三酯(TGs)、载脂蛋白(apo)A-I、apo B和纤维蛋白原。
在基线时,5133名女性中有202名(3.9%)患有2型糖尿病。在约1800名接受HbA1c、LDL-C、TGs、apo A-I、apo B和纤维蛋白原评估的女性中,70名(3.9%)在基线时患有2型糖尿病。与安慰剂相比,雷洛昔芬对有或无糖尿病女性的HbA1c、FPG、HDL-C或TGs均无显著影响。雷洛昔芬使糖尿病女性(所有P≤0.004)和非糖尿病女性(所有P<0.001)的TC、LDL-C和纤维蛋白原均有统计学显著降低。雷洛昔芬使非糖尿病女性的apo A-I显著升高(P<0.001),apo B降低(P<0.001)。在雷洛昔芬治疗组中,非糖尿病女性体重平均增加0.31kg(P<0.001)。
在有或无2型糖尿病的骨质疏松绝经后女性中,60mg/d雷洛昔芬不影响血糖控制,对TC、LDL-C和纤维蛋白原水平有有益影响。