Department of Medicine, Division of Infectious Diseases, University of Alabama at Birmingham, Birmingham, AL, USA.
Department of Epidemiology, School of Public Health, University of Alabama at Birmingham, Birmingham, AL, USA.
J Clin Lipidol. 2018 Jul-Aug;12(4):988-998.e5. doi: 10.1016/j.jacl.2018.03.082. Epub 2018 Mar 29.
Meta-analyses of general population studies report mean low-density lipoprotein cholesterol (LDL-C) reductions of 30% to <50% with moderate-intensity and ≥50% with high-intensity statins. Persons living with human immunodeficiency virus (PLWH) are at high risk for atherosclerotic cardiovascular disease (ASCVD), yet many have elevated LDL-C.
To evaluate LDL-C response after statin initiation among PLWH.
We conducted a retrospective cohort study of PLWH initiating statins between 2009 and 2013 (N = 706). Patients were categorized into mutually exclusive groups in the following hierarchy: history of coronary heart disease (CHD), diabetes, prestatin LDL-C ≥190 mg/dL, 10-year predicted ASCVD risk ≥7.5%, and none of the above (ie, unknown statin indication). The primary outcome was a ≥30% reduction in LDL-C after statin initiation.
Among patients initiating statins, 5.8% had a history of CHD, 13.6% had diabetes, 6.2% had LDL-C ≥190 mg/dL, 35.4% had 10-year ASCVD risk ≥7.5%, and 39.0% had an unknown statin indication. Among patients with a history of CHD, 31.7% achieved a ≥30% LDL-C reduction compared with 25.0%, 59.1%, and 33.9% among those with diabetes, LDL-C ≥190 mg/dL, and 10-year ASCVD risk ≥7.5%, respectively. In multivariable adjusted analyses and compared to patients with an unknown statin indication, LDL-C ≥ 190 mg/dL was associated with a prevalence ratio for an LDL-C reduction ≥30% of 1.81 (95% confidence interval, 1.34-2.45), whereas no statistically significant association was present for history of CHD, diabetes, and 10-year ASCVD risk ≥7.5%.
A low percentage of PLWH achieved the expected reductions in LDL-C after statin initiation, highlighting an unmet need for ASCVD risk reduction.
对一般人群进行的荟萃分析报告称,中等强度他汀治疗可使 LDL-C 降低 30%至<50%,高强度他汀治疗可使 LDL-C 降低≥50%。感染人类免疫缺陷病毒(HIV)的患者发生动脉粥样硬化性心血管疾病(ASCVD)的风险较高,但许多患者的 LDL-C 水平升高。
评估 HIV 感染者开始使用他汀类药物后 LDL-C 的反应。
我们进行了一项回顾性队列研究,纳入 2009 年至 2013 年期间开始使用他汀类药物的 HIV 感染者(N=706)。患者按以下层次分为互斥组:冠心病(CHD)史、糖尿病、他汀治疗前 LDL-C≥190mg/dL、10 年 ASCVD 风险预测值≥7.5%,以及无上述任何情况(即他汀类药物使用指征未知)。主要结局为他汀类药物治疗开始后 LDL-C 降低≥30%。
在开始使用他汀类药物的患者中,5.8%有 CHD 史,13.6%有糖尿病,6.2%有 LDL-C≥190mg/dL,35.4%有 10 年 ASCVD 风险预测值≥7.5%,39.0%的他汀类药物使用指征未知。在有 CHD 史的患者中,31.7%的患者 LDL-C 降低≥30%,而在有糖尿病、LDL-C≥190mg/dL 和 10 年 ASCVD 风险预测值≥7.5%的患者中,分别有 25.0%、59.1%和 33.9%的患者 LDL-C 降低≥30%。多变量调整分析显示,与他汀类药物使用指征未知的患者相比,LDL-C≥190mg/dL 患者 LDL-C 降低≥30%的患病率比为 1.81(95%置信区间,1.34-2.45),而 CHD 史、糖尿病和 10 年 ASCVD 风险预测值≥7.5%与 LDL-C 降低≥30%之间无统计学显著关联。
在开始使用他汀类药物后,只有很少比例的 HIV 感染者达到 LDL-C 降低的预期水平,这突出表明需要降低 ASCVD 风险。