Metabolism Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts (K.V.F., M.V.Z., M.R.D., A.K.G., S.K.Gupta).
Division of Infectious Diseases, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts (J.M.-G.).
Ann Intern Med. 2024 Nov;177(11):1449-1461. doi: 10.7326/ANNALS-24-00944. Epub 2024 Oct 8.
REPRIEVE (Randomized Trial to Prevent Vascular Events in HIV) led to new guidelines for statin use among people with HIV (PWH) with low to moderate risk for atherosclerotic cardiovascular disease (ASCVD). Little is known about the natural history of diabetes mellitus (DM) or mechanisms contributing to statin effects on DM among this population.
To determine the contribution of known DM risk factors to excess risk for DM with pitavastatin in REPRIEVE.
Phase 3, primary ASCVD prevention trial over a median of 5.6 years of follow-up. (ClinicalTrials.gov: NCT02344290).
Global, multicenter trial.
7731 PWH aged 40 to 75 years with low to moderate ASCVD risk (by the pooled cohort equations from the American College of Cardiology and American Heart Association) without DM at study entry.
Random 1:1 assignment to pitavastatin, 4 mg daily, or placebo.
New-onset DM was determined at each visit by clinical diagnosis requiring initiation of medication treatment for DM. The incidence of new-onset DM was assessed in relation to predefined demographic and metabolic risk factors, stratified by treatment group. Treatment effects of pitavastatin on progression to new DM in key subgroups were determined.
Participants with at least 3 DM risk factors (vs. no risk factors) had increased risk for DM in each treatment group (incidence rate, 3.24 per 100 person-years [PY] vs. 0.34 per 100 PY [pitavastatin] and 2.66 per 100 PY vs. 0.27 per 100 PY [placebo]). The incidence of DM was highest in South Asia. In adjusted analyses, high body mass index, prediabetes, and metabolic syndrome components were strongly associated with new-onset DM (all < 0.005).
Pitavastatin was the only statin assessed; DM was assessed clinically.
Metabolic risk factors, including prediabetes and obesity, contributed to new-onset DM in statin- and placebo-treated participants. A clinically significant effect of pitavastatin on DM was seen primarily among those with multiple risk factors for DM at entry. Strategies targeting key metabolic risk factors, like obesity and prediabetes, may help protect against DM among PWH.
National Heart, Lung, and Blood Institute of the National Institutes of Health.
REPRIEVE(预防 HIV 人群血管事件的随机试验)制定了新的他汀类药物使用指南,适用于低至中度动脉粥样硬化性心血管疾病(ASCVD)风险的 HIV 感染者(PWH)。对于糖尿病(DM)的自然史或他汀类药物对该人群中 DM 影响的机制知之甚少。
确定 REPRIEVE 中,使用培伐他汀治疗与已知的 DM 危险因素对 DM 风险增加的关系。
中位随访 5.6 年的 3 期 ASCVD 一级预防试验。(ClinicalTrials.gov:NCT02344290)。
全球多中心试验。
7731 名年龄在 40 至 75 岁之间的 PWH,在研究入组时无 ASCVD 低至中度风险(根据美国心脏病学会和美国心脏协会的 pooled cohort equations 计算)且无 DM。
随机 1:1 分配至培伐他汀 4mg 每日组或安慰剂组。
通过需要开始 DM 药物治疗的临床诊断确定新发 DM。评估了新发 DM 的发生率与既定的人口统计学和代谢危险因素之间的关系,并按治疗组分层。还确定了培伐他汀在关键亚组中对新发 DM 进展的治疗效果。
至少有 3 项 DM 危险因素(vs. 无危险因素)的参与者在每个治疗组中都有更高的 DM 风险(发生率,培伐他汀组为 3.24/100 人年,vs. 0.34/100 人年;安慰剂组为 2.66/100 人年,vs. 0.27/100 人年)。南亚的 DM 发生率最高。在调整分析中,高体重指数、糖尿病前期和代谢综合征成分与新发 DM 强烈相关(均<0.005)。
仅评估了培伐他汀;DM 通过临床评估。
代谢危险因素,包括糖尿病前期和肥胖,与他汀类药物和安慰剂治疗的参与者的新发 DM 相关。在主要终点分析中,培伐他汀对 DM 的显著影响主要见于入组时具有多种 DM 危险因素的参与者中。针对肥胖和糖尿病前期等关键代谢危险因素的策略可能有助于预防 PWH 发生 DM。
美国国立卫生研究院国家心肺血液研究所。