Erlandson Kristine M, Jiang Ying, Debanne Sara M, McComsey Grace A
Department of Medicine, Divisions of Infectious Diseases and Geriatric Medicine, University of Colorado, Aurora.
Department of Epidemiology and Biostatistics.
Clin Infect Dis. 2015 Nov 15;61(10):1566-72. doi: 10.1093/cid/civ554. Epub 2015 Jul 8.
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.
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.
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).
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.
NCT01218802.
在大型未感染人类免疫缺陷病毒(HIV)的队列研究中,他汀类药物与糖尿病风险增加相关;在随机对照研究中,尚未评估他汀类药物对HIV感染者胰岛素抵抗或糖尿病的影响。
接受稳定抗逆转录病毒治疗、低密度脂蛋白胆固醇水平≤130mg/dL且免疫激活或炎症增强的HIV感染者被随机分为两组,一组每天服用10mg瑞舒伐他汀,另一组服用安慰剂,为期96周。测量空腹血清葡萄糖、胰岛素和糖化血红蛋白(HgbA1C);通过计算胰岛素抵抗稳态模型评估(HOMA-IR)来估计胰岛素抵抗;并进行2小时口服葡萄糖耐量试验。
72名参与者被随机分配接受瑞舒伐他汀治疗,75名接受安慰剂治疗。两组空腹血糖均有升高,但研究组间无差异(P = 0.115);研究组间葡萄糖耐量和HgbA1C的变化无差异(分别为P = 0.920和P = 0.650)。到第96周时,瑞舒伐他汀组有1名参与者、安慰剂组有3名参与者达到糖尿病标准。与安慰剂相比,瑞舒伐他汀治疗与胰岛素和HOMA-IR的显著更大增加相关(分别为P = 0.008和P = 0.004)。
我们发现瑞舒伐他汀组胰岛素抵抗显著恶化,空腹血糖受损参与者比例增加,但未出现糖尿病临床诊断病例。我们的研究结果表明,他汀类药物治疗的处方应仔细权衡风险和益处,尤其是在心血管疾病风险较低的患者中。
NCT01218802。