학술논문

Neuropsychological Impairment in Acute HIV and the Effect of Immediate Antiretroviral Therapy
Document Type
article
Source
JAIDS Journal of Acquired Immune Deficiency Syndromes. 70(4)
Subject
Neurosciences
Mental Health
HIV/AIDS
Infectious Diseases
Clinical Research
Acquired Cognitive Impairment
Brain Disorders
Adult
Anti-Retroviral Agents
Antiretroviral Therapy
Highly Active
Female
HIV Infections
Humans
Longitudinal Studies
Male
Nervous System Diseases
Neuropsychological Tests
Prospective Studies
Psychomotor Disorders
Thailand
Treatment Outcome
Young Adult
HIV infection
HIV-associated neurocognitive disorder
neuropsychological tests
mild cognitive impairment
antiretroviral therapy
RV254/SEARCH 010 Study Group
Clinical Sciences
Public Health and Health Services
Virology
Language
Abstract
OBJECTIVE:To investigate neuropsychological performance (NP) during acute HIV infection (AHI) before and after combination antiretroviral therapy (cART). DESIGN:Prospective study of Thai AHI participants examined at 3 and 6 months after initiation of cART. METHODS:Thirty-six AHI participants were evaluated pre-cART at median 19 days since HIV exposure and 3 and 6 months after cART with the Grooved Pegboard test, Color Trails 1 & 2 (CT1, CT2), and Trail Making Test A. Raw scores were standardized to 251 age- and education-matched HIV-uninfected Thais. To account for learning effects, change in NP performance was compared with that of controls at 6 months. Analyses included multivariable regression, nonparametric repeated measures analysis of variance, and Mann-Whitney U test. RESULTS:Baseline NP scores for the AHI group were within normal range (z-scores range: -0.26 to -0.13). NP performance improved on CT1, CT2, and Trail Making Test A in the initial 3 months (P < 0.01) with no significant change during the last 3 months. Only improvement in CT1 was greater than that seen in controls at 6 months (P = 0.018). Participants who performed >1 SD below normative means on ≥2 tests (n = 8) exhibited higher baseline cerebrospinal fluid HIV RNA (P = 0.047) and had no improvement after cART. CONCLUSIONS:Most AHI individuals had normal NP performance, and early cART slightly improved their psychomotor function. However, approximately 25% had impaired NP performance, which correlated with higher cerebrospinal fluid HIV RNA, and these abnormalities were not reversed by early cART possibly indicating limited reversibility of cognitive impairment in a subset of AHI individuals.