Rosuvastatin Worsens Insulin Resistance in HIV-Infected Adults on Antiretroviral Therapy

被引:31
|
作者
Erlandson, Kristine M. [1 ]
Jiang, Ying [2 ]
Debanne, Sara M. [2 ]
McComsey, Grace A. [3 ]
机构
[1] Univ Colorado, Div Infect Dis & Geriatr Med, Dept Med, Aurora, CO USA
[2] Case Western Reserve Univ, Dept Epidemiol & Biostat, Cleveland, OH 44106 USA
[3] Case Western Reserve Univ, Div Pediat Infect Dis & Rheumatol, Dept Med & Pediat, Cleveland, OH 44106 USA
基金
美国国家卫生研究院;
关键词
HOMA-IR; insulin resistance; glucose metabolism; statin; inflammation; STATIN THERAPY; MONOCYTE ACTIVATION; DIABETES-MELLITUS; RISK; SIMVASTATIN; SECRETION; INFLAMMATION; SENSITIVITY; PRAVASTATIN; INHIBITION;
D O I
10.1093/cid/civ554
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Statins are associated with increased diabetes risk in large, human immunodeficiency virus (HIV)-uninfected cohorts; the impact of statins on insulin resistance or diabetes in HIV-infected persons has not been assessed within a randomized controlled study. Methods. HIV-infected participants on stable antiretroviral therapy with a low-density lipoprotein cholesterol level of <= 130 mg/dL and heightened immune activation or inflammation were randomized to rosuvastatin 10 mg daily or placebo for 96 weeks. Fasting serum glucose, insulin, and hemoglobin A1C (HgbA1C) were measured; insulin resistance was estimated by calculating the homeostatic model assessment of insulin resistance (HOMA-IR); and a 2-hour oral glucose tolerance test was administered. Results. Seventy-two participants were randomized to rosuvastatin therapy and 75 to placebo. Increases in fasting glucose were observed within both groups but were not different between study arms (P = .115); changes in glucose tolerance and HgbA1C did not differ between study arms (P = .920 and P = .650, respectively). Criteria for diabetes were met by 1 participant in the rosuvastatin and 3 in the placebo arm by week 96. Compared with placebo, rosuvastatin therapy was associated with significantly greater increases in insulin and HOMA-IR (P = .008 and P = .004, respectively). Conclusions. We detected a significant worsening in insulin resistance and an increase in the proportion of participants with impaired fasting glucose but not a clinical diagnosis of diabetes in the rosuvastatin arm. Our findings suggest that prescription of statin therapy should be accompanied by a careful consideration of the risks and benefits, particularly in patients with lower cardiovascular disease risk.
引用
收藏
页码:1566 / 1572
页数:7
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