Mollan Katie R, Smurzynski Marlene, Eron Joseph J, Daar Eric S, Campbell Thomas B, Sax Paul E, Gulick Roy M, Na Lumine, O'Keefe Lauren, Robertson Kevin R, Tierney Camlin
Ann Intern Med. 2014 Jul 1;161(1):1-10. doi: 10.7326/M14-0293.
The relationship between efavirenz use and suicidality is not well-defined.
To compare time to suicidality with efavirenz-containing versus efavirenz-free antiretroviral regimens for initial treatment of HIV.
Participant-level data were analyzed from 4 AIDS Clinical Trials Group, antiretroviral-naive studies conducted from 2001 to 2010. Within each study, participants were randomly assigned to an efavirenz-containing (n = 3241) or efavirenz-free (n = 2091) regimen. (ClinicalTrials.gov: NCT00013520 [A5095], NCT00050895 [A5142], NCT00084136 [A5175], and NCT00118898 [A5202]).
AIDS Clinical Trials Group sites; 74% of participants enrolled in the United States.
Antiretroviral-naive participants.
Efavirenz versus efavirenz-free regimens.
Suicidality was defined as suicidal ideation or attempted or completed suicide. Groups were compared with a hazard ratio and 95% CI estimated from a Cox model, stratified by study.
Seventy-three percent of participants were men, the median age was 37 years, and 32% had documented psychiatric history or received psychoactive medication within 30 days before entering the study. Median follow-up was 96 weeks. Suicidality incidence per 1000 person-years was 8.08 (47 events) in the efavirenz group and 3.66 (15 events) in the efavirenz-free group (hazard ratio, 2.28 [95% CI, 1.27 to 4.10]; P = 0.006). Incidence of attempted or completed suicide was 2.90 (17 events) and 1.22 (5 events) in the efavirenz and efavirenz-free groups, respectively (hazard ratio, 2.58 [CI, 0.94 to 7.06]; P = 0.065). Eight suicides in the efavirenz group and 1 in the efavirenz-free group were reported.
There was not a standardized questionnaire about suicidal ideation or attempt. Efavirenz was open-label in 3 of 4 studies.
Initial treatment with an efavirenz-containing antiretroviral regimen was associated with a 2-fold increased hazard of suicidality compared with a regimen without efavirenz.
National Institutes of Health.
依法韦仑的使用与自杀倾向之间的关系尚不明确。
比较含依法韦仑与不含依法韦仑的抗逆转录病毒方案用于初始治疗HIV时出现自杀倾向的时间。
分析了2001年至2010年进行的4项艾滋病临床试验组的未接受过抗逆转录病毒治疗的研究中的参与者水平数据。在每项研究中,参与者被随机分配至含依法韦仑方案(n = 3241)或不含依法韦仑方案(n = 2091)。(ClinicalTrials.gov:NCT00013520 [A5095]、NCT00050895 [A5142]、NCT00084136 [A5175]和NCT00118898 [A5202])。
艾滋病临床试验组各研究点;74%的参与者在美国入组。
未接受过抗逆转录病毒治疗的参与者。
依法韦仑方案与不含依法韦仑方案。
自杀倾向定义为自杀意念、自杀未遂或自杀身亡。通过Cox模型估计的风险比和95%可信区间对两组进行比较,并按研究分层。
73%的参与者为男性,中位年龄为37岁,32%的参与者有精神病史记录或在入组研究前30天内接受过精神活性药物治疗。中位随访时间为96周。依法韦仑组每1000人年的自杀倾向发生率为8.08(47例事件),不含依法韦仑组为3.66(15例事件)(风险比,2.28 [95%可信区间,1.27至4.10];P = 0.006)。依法韦仑组和不含依法韦仑组的自杀未遂或自杀身亡发生率分别为2.90(17例事件)和1.22(5例事件)(风险比,2.58 [可信区间,0.94至7.06];P = 0.065)。依法韦仑组报告了8例自杀事件,不含依法韦仑组报告了1例。
没有关于自杀意念或自杀未遂的标准化问卷。4项研究中有3项对依法韦仑采用开放标签。
与不含依法韦仑的方案相比,含依法韦仑的抗逆转录病毒方案进行初始治疗时自杀倾向风险增加2倍。
美国国立卫生研究院。