Legacy effect on neuropsychological function in HIV-infected men on combination antiretroviral therapy

被引:14
作者
Qu, Yang [1 ]
Weinstein, Andrea [2 ]
Wang, Zheng [3 ]
Cheng, Yu [1 ,3 ]
Kingsley, Lawrence [4 ,5 ]
Levine, Andrew [6 ]
Martin, Eileen [7 ]
Munro, Cynthia [8 ]
Ragin, Ann B. [9 ]
Rubin, Leah H. [8 ,9 ,10 ]
Sacktor, Ned W. [10 ]
Seaberg, Eric C. [11 ]
Becker, James T. [2 ,12 ,13 ]
机构
[1] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Stat, Pittsburgh, PA 15213 USA
[2] Univ Pittsburgh, Dept Psychiat, 3501 Forbes Ave, Pittsburgh, PA 15213 USA
[3] Univ Pittsburgh, Dept Biostat, Pittsburgh, PA 15213 USA
[4] Univ Pittsburgh, Dept Epidemiol, Grad Sch Publ Hlth, Pittsburgh, PA 15213 USA
[5] Univ Pittsburgh, Grad Sch Publ Hlth, Infect Dis & Microbiol, Pittsburgh, PA 15213 USA
[6] Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurol, Los Angeles, CA 90095 USA
[7] Rush Univ, Dept Psychiat, Sch Med, Chicago, IL 60612 USA
[8] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD 21205 USA
[9] Northwestern Univ, Dept Radiol, Evanston, IL USA
[10] Johns Hopkins Univ, Sch Med, Dept Neurol, Baltimore, MD 21205 USA
[11] Johns Hopkins Univ, Bloomberg Sch Publ Hlth, Dept Epidemiol, Baltimore, MD USA
[12] Univ Pittsburgh, Dept Neurol, 3501 Forbes Ave, Pittsburgh, PA 15213 USA
[13] Univ Pittsburgh, Dept Psychol, 3501 Forbes Ave, Pittsburgh, PA 15213 USA
关键词
combination antiretroviral therapy; cognition; HIV; legacy effect; Multicenter AIDS Cohort Study; MULTICENTER AIDS COHORT; NEUROCOGNITIVE IMPAIRMENT; DISEASE; PREVALENCE; DISORDERS; SYMPTOMS; DECLINE; ERA;
D O I
10.1097/QAD.0000000000003071
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objective: To determine whether combination antiretroviral therapy (cART) initiation alters the trajectory of cognitive performance in HIV+ men, and whether cognition prior to cART predicts postcART function. Design: Longitudinal cohort study. Multicenter AIDS Cohort Study. Methods: From an initial set of 3701 men with complete neuropsychological data, men with HIV infection were initially matched with men without infection on cognitive status, race, age, and timeline (T-0 defined as cART initiation). Propensity score matching was then used to match pairs on depressive symptoms at T-0, education, T-0 cognitive scores, and recruitment cohort. There were 506 matched pairs of infected and uninfected men in the final analysis. Mixed effect models were constructed to analyze the trajectories of cognitive functions and to test the effect of cART and HIV on cognitive functions over time. Results: Performance in each cognitive domain did not change following the initiation of cART among HIV-infected men with prior impairment and was comparable to the performance of their matched uninfected men. However, among the infected men who were unimpaired prior to cART, motor function declined significantly faster than it did for uninfected controls. Conclusions: Cognitive dysfunction is persistent in HIV-infected men and cART does not alter the trajectory of cognitive decline in men who were impaired prior to effective therapy. This suggests that current cognitive impairment in HIV+ men results from a legacy effect, and from factors other than the HIV itself. Furthermore, motor skills may be uniquely vulnerable to the virus, cART, or age-related co-morbidities.
引用
收藏
页码:19 / 27
页数:9
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