START or SMART? Timing of Antiretroviral Therapy Initiation and Cardiovascular Risk for People With Human Immunodeficiency Virus Infection

被引:29
作者
Siedner, Mark J. [1 ,2 ]
机构
[1] Massachusetts Gen Hosp, Dept Med, Div Infect Dis, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
antiretroviral therapy; cardiovascular disease; epidemiology; HIV/AIDS; systematic review; INTIMA-MEDIA THICKNESS; T-CELL COUNT; SUBCLINICAL CORONARY ATHEROSCLEROSIS; POPULATION-BASED COHORT; CHRONIC HIV-INFECTION; HEALTH-CARE-SYSTEM; MYOCARDIAL-INFARCTION; HEART-DISEASE; CAROTID ATHEROSCLEROSIS; IMMUNE ACTIVATION;
D O I
10.1093/ofid/ofw032
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The Initiation of Antiretroviral Therapy in Early Asymptomatic HIV Infection (START) study has reinforced the benefits of early initiation of antiretroviral therapy (ART). However, a notable secondary finding from that study was that immediate initiation of ART did not prevent cardiovascular disease (CVD) events (0.17 vs 0.20 events/1000 person-years, P = .65). This result appears to contradict a body of evidence, most notably from the Strategies for Management of Antiretroviral Therapy (SMART) study, which reported a 70% increased hazard of cardiovascular events for those deferring or interrupting treatment. Thus, an important unresolved question is whether the timing of ART impacts CVD risk. In this review, published data on relationships between timing of ART and CVD risk are reviewed. The data support a role for ART in mitigating CVD risk at lower CD4 counts, but data also suggests that, among those initiating therapy early, ART alone appears to suboptimally mitigate CVD risk. Additional interventions to address CVD risk among human immunodeficiency virus-infected populations are likely to be needed.
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