McCutchan J Allen, Wu Julia W, Robertson Kevin, Koletar Susan L, Ellis Ronald J, Cohn Susan, Taylor Michael, Woods Steven, Heaton Robert, Currier Judith, Williams Paige L
University of California-San Diego, 150 West Washington Street, San Diego, CA 92103, USA.
AIDS. 2007 May 31;21(9):1109-17. doi: 10.1097/QAD.0b013e3280ef6acd.
HIV can damage neurons leading to cognitive impairment. Epidemiological observations suggest that neuropsychological impairment might progress despite successful HAART therapy, but available prevalence estimates are based on populations that were selected for impairment.
Of 433 advanced AIDS patients with documented immune reconstitution (CD4 lymphocyte counts < 50 before and > 100 cells/microl after HAART), 286 had brief assessments of cognition (Trailmaking A/B and Digit Symbol Tests) at least once, no confounding neurological conditions, and available neuropsychological norms with comprehensive demographic corrections. At entry, most were immune reconstituted on HAART (median CD4 cell count 230 cells/microl) and HIV was suppressed (65% < 500; only 14% > 20 000 RNA copies/ml).
Over one quarter (27%) of participants exhibited impairment at their initial neuropsychological assessment, a rate nearly twice that expected in a normal (HIV-uninfected) reference population (14%). These impaired participants did not differ from the unimpaired group with respect to age, sex, education, race, CD4 lymphocyte counts, or HIV-RNA levels. Improved performance on neuropsychological tests was documented over a 2-year period 3-5 years after initiating HAART. This improvement was marginally associated with the continued or improving control of plasma HIV-RNA levels, but not with concurrent levels of immune recovery (CD4 lymphocyte counts).
Most advanced AIDS patients responding to HAART for prolonged periods have stable or improving cognition, but remain more likely to be impaired than the general population. During HAART, improving test performance probably reflects both practice effects and continuing neurological recovery after more than 3 years of HAART.
HIV可损害神经元,导致认知障碍。流行病学观察表明,尽管高效抗逆转录病毒治疗(HAART)取得成功,但神经心理障碍仍可能进展,不过现有的患病率估计是基于有损伤的特定人群得出的。
在433例有免疫重建记录的晚期艾滋病患者(HAART治疗前CD4淋巴细胞计数<50,治疗后>100个细胞/微升)中,286例至少接受过一次认知简短评估(连线测验A/B和数字符号测验),无混杂的神经疾病,且有可用于综合人口统计学校正的神经心理常模。入组时,大多数患者通过HAART实现了免疫重建(CD4细胞计数中位数为230个细胞/微升),HIV得到抑制(65%<500;仅14%>20000 RNA拷贝/毫升)。
超过四分之一(27%)的参与者在首次神经心理评估时表现出损伤,这一比例几乎是正常(未感染HIV)参照人群预期比例(14%)的两倍。这些有损伤的参与者在年龄、性别、教育程度、种族、CD4淋巴细胞计数或HIV-RNA水平方面与未受损伤组无差异。在开始HAART治疗3至5年后的两年期间,神经心理测试表现有所改善。这种改善与血浆HIV-RNA水平的持续控制或改善略有相关,但与同时期的免疫恢复水平(CD4淋巴细胞计数)无关。
大多数长期接受HAART治疗的晚期艾滋病患者认知稳定或改善,但仍比一般人群更易出现损伤。在HAART治疗期间,测试表现的改善可能既反映了练习效应,也反映了HAART治疗三年多后持续的神经恢复。