Department of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
J Neurovirol. 2010 Oct;16(5):335-41. doi: 10.3109/13550284.2010.504249.
Older human immunodeficiency virus-seropositive (HIV+) individuals (greater than age 50 years) are twice as likely to develop HIV dementia compared to younger HIV+ individuals. The objective of this study was to examine the impact of both age and serostatus on longitudinal changes in psychomotor speed/executive functioning performance among HIV+ and HIV− individuals. Four hundred and seventy-seven HIV+ and 799 HIV− individuals from the Multicenter AIDS Cohort Study (MACS) were subdivided into three age groups: (1) <40 years, (2) 40-50 years, and (3) >50 years. Psychomotor speed/executive functioning test performance was measured by the Symbol Digit Modalities Test (SDMT) and the Trail Making (TM) Test Parts A and B. Changes in performance were compared among the three age groups for both HIV+ and HIV− individuals. Among HIV+ individuals, on the TM Test Part B the younger group demonstrated improvement in performance over time (P = .007). The older and middle age groups demonstrated decline in performance over time (P = .041 and .030). The older group had a significantly different trajectory relative to the younger group (P = .046). Among the HIV− individuals, there was no effect of age on longitudinal performance. In conclusion, older HIV+ individuals show greater decline over time than younger HIV+ individuals on the TM Test Part B. Our results suggest that both HIV serostatus and age together may impact longitudinal performance on this test. Mild neurocognitive changes over time among older HIV+ individuals are likely to reflect age associated pathophysiological mechanisms including cerebrovascular risk factors.
老年人类免疫缺陷病毒阳性(HIV+)个体(年龄大于 50 岁)比年轻的 HIV+个体更容易发展为 HIV 痴呆症。本研究的目的是检查年龄和血清状态对 HIV+和 HIV−个体的精神运动速度/执行功能表现的纵向变化的影响。来自多中心艾滋病队列研究(MACS)的 477 名 HIV+和 799 名 HIV−个体被分为三组年龄组:(1)<40 岁,(2)40-50 岁,和(3)>50 岁。精神运动速度/执行功能测试表现通过符号数字模态测试(SDMT)和轨迹测试(TM)测试 A 和 B 来测量。在 HIV+和 HIV−个体中,在 TM 测试 B 部分中,年轻组表现出随时间的改善(P =.007)。老年和中年组表现出随时间的下降(P =.041 和.030)。老年组与年轻组相比具有显著不同的轨迹(P =.046)。在 HIV−个体中,年龄对纵向表现没有影响。总之,在 TM 测试 B 部分,老年 HIV+个体随着时间的推移显示出更大的下降。我们的结果表明,HIV 血清状态和年龄共同可能影响该测试的纵向表现。老年 HIV+个体随时间出现的轻度认知变化可能反映了与年龄相关的病理生理机制,包括脑血管危险因素。