Pioglitazone Prevents Diabetes in Patients With Insulin Resistance and Cerebrovascular Disease

被引:67
作者
Inzucchi, Silvio E. [1 ]
Viscoli, Catherine M. [1 ]
Young, Lawrence H. [1 ]
Furie, Karen L. [2 ]
Gorman, Mark [3 ]
Lovejoy, Anne M. [1 ]
Dagogo-Jack, Samuel [4 ]
Ismail-Beigi, Faramarz [5 ,6 ]
Korytkowski, Mary T. [7 ]
Pratley, Richard E. [8 ]
Schwartz, Gregory G. [9 ,10 ]
Kernan, Walter N. [1 ]
机构
[1] Yale Sch Med, New Haven, CT 06510 USA
[2] Brown Univ, Alpert Med Sch, Providence, RI 02912 USA
[3] Vermont Coll Med, Burlington, VT USA
[4] Univ Tennessee, Ctr Hlth Sci, Memphis, TN 38163 USA
[5] Case Western Reserve Univ, Cleveland, OH 44106 USA
[6] VA Med Ctr, Cleveland, OH USA
[7] Univ Pittsburgh, Sch Med, Pittsburgh, PA USA
[8] Florida Hosp, Orlando, FL USA
[9] VA Med Ctr, Denver, CO USA
[10] Univ Colorado, Sch Med, Denver, CO USA
关键词
BETA-CELL FUNCTION; GLUCOSE-TOLERANCE; BLADDER-CANCER; HEART-FAILURE; RISK; ATHEROSCLEROSIS; INTERVENTION; MEDICATIONS; PROGRESSION;
D O I
10.2337/dc16-0798
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
OBJECTIVE The Insulin Resistance Intervention after Stroke (IRIS) trial recently found that pioglitazone reduced risk for stroke and myocardial infarction in patients with insulin resistance but without diabetes who had had a recent ischemic stroke or transient ischemic attack (TIA). This report provides detailed results on the metabolic effects of pioglitazone and the trial's prespecified secondary aim of diabetes prevention. RESEARCH DESIGN AND METHODS A total of 3,876 patients with recent ischemic stroke or TIA, no history of diabetes, fasting plasma glucose (FPG) <126 mg/dL, and insulin resistance by homeostasis model assessment of insulin resistance (HOMA-IR) score >3.0 were randomly assigned to pioglitazone or placebo. Surveillance for diabetes onset during the trial was accomplished by periodic interviews and annual FPG testing. RESULTS At baseline, the mean FPG, HbA(1c), insulin, and HOMA-IR were 98.2 mg/dL (5.46 mmol/L), 5.8% (40 mmol/mol), 22.4 mu IU/mL, and 5.4, respectively. After 1 year, mean HOMA-IR and FPG decreased to 4.1 and 95.1 mg/dL (5.28 mmol/L) in the pioglitazone group and rose to 5.7 and 99.7 mg/dL (5.54 mmol/L), in the placebo group (all P < 0.0001). Over a median follow-up of 4.8 years, diabetes developed in 73 (3.8%) participants assigned to pioglitazone compared with 149 (7.7%) assigned to placebo (hazard ratio [HR] 0.48 [95% CI 0.33-0.69]; P < 0.0001). This effect was predominately driven by those with initial impaired fasting glucose (FPG >100 mg/dL [5.6 mmol/L]; HR 0.41 [95% CI 0.30-0.57]) or elevated HbA1c (>5.7% [39 mmol/mol]; HR 0.46 [0.34-0.62]). CONCLUSIONS Among patients with insulin resistance but without diabetes who had had a recent ischemic stroke or TIA, pioglitazone decreased the risk of diabetes while also reducing the risk of subsequent ischemic events. Pioglitazone is the first medication shown to prevent both progression to diabetes and major cardiovascular events as prespecified outcomes in a single trial.
引用
收藏
页码:1684 / 1692
页数:9
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