Effects of pioglitazone in patients with type 2 diabetes with or without previous stroke - Results from PROactive (PROspective pioglitAzone Clinical Trial in macroVascular Events 04)

被引:384
作者
Wilcox, Robert [1 ]
Bousser, Marie-Germaine
Betteridge, D. John
Schernthaner, Guntram
Pirags, Valdis
Kupfer, Stuart
Dormandy, John
机构
[1] Univ Nottingham Hosp, Queens Med Ctr, Dept Cardiovasc Med, Nottingham NG7 2UH, England
[2] UCL Hosp, Dept Med, London, England
[3] Rudolfstiftung Hosp, Dept Med 1, Vienna, Austria
[4] Riga Tech Univ, Paula Stradina Klin Slimnica, Riga, Latvia
[5] Univ London St Georges Hosp, Dept Clin Vasc Res, London SW17 0RE, England
[6] Takeda Global Res & Dev, Deerfield, IL USA
关键词
clinical trials; pioglitazone; stroke; type; 2; diabetes;
D O I
10.1161/01.STR.0000257974.06317.49
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose - Diabetes is an important risk factor for stroke. We conducted analyses in patients who had entered the PROspective pioglitAzone Clinical Trial In macroVascular Events ( PROactive) with a history of stroke or without stroke. Methods - The prospective, double-blind PROactive ( mean duration, 34.5 months) randomized 5238 patients with type 2 diabetes and a history of macrovascular disease to pioglitazone ( titrated to 45 mg) or placebo, in addition to current diabetes and cardiovascular medications. Cardiovascular end-point events were independently adjudicated. This analysis evaluated the risk of stroke and other cardiovascular outcomes in patients with ( n = 984) and without ( n = 4254) prior stroke. Results - In patients with previous stroke ( n = 486 in the pioglitazone group and n = 498 in the placebo group), there was a trend of benefit with pioglitazone for the primary end point of all-cause death, nonfatal myocardial infarction, acute coronary syndrome, and cardiac intervention ( including coronary artery bypass graft or percutaneous coronary intervention), stroke, major leg amputation, or bypass surgery or leg revascularization ( hazard ratio[HR] = 0.78, event rate = 20.2% pioglitazone vs 25.3% placebo; 95% CI = 0.60 - 1.02; P = 0.0670) and for the main secondary end point of all-cause death, nonfatal myocardial infarction, or nonfatal stroke ( HR = 0.78, event rate = 15.6% pioglitazone vs 19.7% placebo; 95% CI = 0.58 - 1.06; P = 0.1095). Pioglitazone reduced fatal or nonfatal stroke ( HR = 0.53, event rate = 5.6% pioglitazone vs 10.2% placebo; 95% CI = 0.34 - 0.85; P = 0.0085) and cardiovascular death, nonfatal myocardial infarction, or nonfatal stroke ( HR = 0.72, event rate = 13.0% pioglitazone vs 17.7% placebo; 95% CI = 0.52 - 1.00; P = 0.0467). Higher event rates were observed in patients with prior stroke compared with those without prior stroke. In patients without prior stroke, no treatment effect was observed for a first stroke. Conclusions - In a subgroup analysis from PROactive, pioglitazone reduced the risk of recurrent stroke significantly in high-risk patients with type 2 diabetes.
引用
收藏
页码:865 / 873
页数:9
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