Childs E A, Lyles R H, Selnes O A, Chen B, Miller E N, Cohen B A, Becker J T, Mellors J, McArthur J C
School of Hygiene and Public Health, The Johns Hopkins University, Baltimore, MD, USA.
Neurology. 1999 Feb;52(3):607-13. doi: 10.1212/wnl.52.3.607.
To determine the predictive value of plasma HIV RNA and CD4 lymphocytes for HIV-associated dementia and sensory neuropathy.
A total of 1,604 AIDS-free HIV seropositive men from the Multicenter AIDS Cohort Study were followed over a 10-year period (1985 to 1995). HIV-associated dementia and sensory neuropathy were diagnosed according to standard definitions. Baseline samples were used to measure plasma HIV RNA levels with a branched DNA assay and levels of beta2-microglobulin, CD4 lymphocyte counts, and hemoglobin levels.
Seventy-seven patients with HIV-associated dementia and 213 patients with sensory neuropathy were identified. Baseline HIV RNA levels above 3,000 copies/mL and CD4 counts below 500 cells/mm3 were predictive of both neurologic outcomes, but neither hemoglobin, body mass index, nor beta2-microglobulin were independently predictive. After adjusting for age and level of education, individuals with baseline plasma HIV RNA >30,000 copies/mL had a relative hazard for dementia 8.5 times (p < 0.001) that of those with <3,000 copies/mL, and those with CD4 counts <200 cells/mm3 had a 3.5-fold (p = 0.003) greater hazard relative to those with CD4 counts >500 cells/mm3. Individuals with HIV RNA >10,000 copies/mL had a 2.3-fold (p = 0.008) greater hazard of sensory neuropathy than those with <500 copies/mL, and men with <750 CD4 cells/mm3 had a 1.4-fold (p = 0.03) greater hazard than those with >750 CD4 cells/mm3.
High levels of systemic HIV replication may "drive" the initiation of neurologic disease; effective suppression of HIV may reduce the incidence of dementia and neuropathy. Levels of plasma HIV RNA and CD4 counts, determined before the initiation of antiretroviral therapy, were predictive of HIV-associated dementia and sensory neuropathy.
确定血浆HIV RNA和CD4淋巴细胞对HIV相关痴呆和感觉神经病变的预测价值。
对多中心艾滋病队列研究中1604名未患艾滋病的HIV血清阳性男性进行了为期10年(1985年至1995年)的随访。根据标准定义诊断HIV相关痴呆和感觉神经病变。使用基线样本通过分支DNA检测法测量血浆HIV RNA水平以及β2-微球蛋白水平、CD4淋巴细胞计数和血红蛋白水平。
共识别出77例HIV相关痴呆患者和213例感觉神经病变患者。基线HIV RNA水平高于3000拷贝/mL以及CD4计数低于500个细胞/mm3可预测这两种神经学结局,但血红蛋白、体重指数和β2-微球蛋白均无独立预测作用。在调整年龄和教育水平后,基线血浆HIV RNA>30000拷贝/mL的个体患痴呆的相对风险是血浆HIV RNA<3000拷贝/mL个体的8.5倍(p<0.001),而CD4计数<200个细胞/mm3的个体相对于CD4计数>500个细胞/mm3的个体患痴呆的风险高3.5倍(p = 0.003)。HIV RNA>10000拷贝/mL的个体发生感觉神经病变的风险是HIV RNA<500拷贝/mL个体的2.3倍(p = 0.008),而CD4细胞/mm3<750的男性发生感觉神经病变的风险是CD4细胞/mm3>750男性的1.4倍(p = 0.03)。
高水平的全身性HIV复制可能“驱动”神经疾病的发生;有效抑制HIV可能降低痴呆和神经病变的发生率。在开始抗逆转录病毒治疗之前测定的血浆HIV RNA水平和CD4计数可预测HIV相关痴呆和感觉神经病变。