Kore Idil, Ananworanich Jintanat, Valcour Victor, Fletcher James L K, Chalermchai Thep, Paul Robert, Reynolds Jesse, Tipsuk Somporn, Ubolyam Sasiwimol, Rattanamanee Somprartthana, Jagodzinski Linda, Kim Jerome, Spudich Serena
*Yale University School of Medicine, New Haven, CT; †SEARCH, The Thai Red Cross AIDS Research Center, Bangkok, Thailand; ‡US Military HIV Research Program, Walter Reed Army Institute of Research, Silver Spring, MD; §Henry M. Jackson Foundation for the Advancement of Military Medicine, Bethesda, MD; ‖University of California, San Francisco, CA; ¶Missouri Institute of Mental Health, University of Missouri, St. Louis, MO; #Yale Center for Analytical Sciences, New Haven, CT; and **HIV-NAT, The Thai Red Cross AIDS Research Center, Bangkok, Thailand.
J Acquir Immune Defic Syndr. 2015 Dec 1;70(4):393-9. doi: 10.1097/QAI.0000000000000746.
To investigate neuropsychological performance (NP) during acute HIV infection (AHI) before and after combination antiretroviral therapy (cART).
Prospective study of Thai AHI participants examined at 3 and 6 months after initiation of cART.
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.
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.
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.
研究急性HIV感染(AHI)患者在联合抗逆转录病毒治疗(cART)前后的神经心理学表现(NP)。
对泰国AHI参与者进行前瞻性研究,在开始cART后3个月和6个月进行检查。
36名AHI参与者在cART前(自HIV暴露后中位19天)以及cART后3个月和6个月接受了凹槽钉板测试、色线试验1和2(CT1、CT2)以及连线测验A的评估。原始分数根据年龄和教育程度匹配的251名未感染HIV的泰国人进行标准化。为了考虑学习效应,将NP表现的变化与6个月时的对照组进行比较。分析包括多变量回归、非参数重复测量方差分析和曼-惠特尼U检验。
AHI组的基线NP分数在正常范围内(z分数范围:-0.26至-0.13)。在最初3个月中,CT1、CT2和连线测验A的NP表现有所改善(P<0.01),在最后3个月中无显著变化。只有CT1的改善在6个月时大于对照组(P = 0.018)。在≥2项测试中表现低于正常均值>1个标准差的参与者(n = 8)脑脊液HIV RNA基线水平较高(P = 0.047),cART后无改善。
大多数AHI个体具有正常的NP表现,早期cART可轻微改善其精神运动功能。然而,约25%的个体NP表现受损,这与较高的脑脊液HIV RNA相关,且这些异常未被早期cART逆转,这可能表明一部分AHI个体的认知障碍可逆性有限。