Cardiovascular risk factors associated with lower baseline cognitive performance in HIV-positive persons

被引:150
|
作者
Wright, E. J. [1 ,2 ,3 ]
Grund, B. [4 ]
Robertson, K. [5 ]
Brew, B. J. [6 ,7 ]
Roediger, M. [4 ]
Bain, M. P. [6 ,7 ]
Drummond, F. [8 ]
Vjecha, M. J. [9 ]
Hoy, J. [3 ]
Miller, C. [4 ]
de Oliveira, A. C. Penalva [10 ]
Pumpradit, W. [11 ]
Shlay, J. C. [12 ]
El-Sadr, W. [13 ]
Price, R. W. [14 ]
机构
[1] Alfred Hosp, Infect Dis Unit, Melbourne, Vic 3004, Australia
[2] Burnet Inst, Melbourne, Vic, Australia
[3] Monash Univ, Melbourne, Vic 3004, Australia
[4] Univ Minnesota, Minneapolis, MN USA
[5] Univ N Carolina, Sch Med, Dept Neurol, Chapel Hill, NC 27599 USA
[6] St Vincents Hosp, Dept Neurol, Sydney, NSW 2010, Australia
[7] St Vincents Hosp, Dept HIV Med, Sydney, NSW 2010, Australia
[8] Univ New S Wales, Natl Ctr HIV Epidemiol & Clin Res, Sydney, NSW, Australia
[9] Washington Vet Affairs Med Ctr, Washington, DC USA
[10] Inst Infectol Emilio Ribas, Dept Neurol, Sao Paulo, Brazil
[11] HIV NAT, Bangkok, Thailand
[12] Denver Publ Hlth, Denver, CO USA
[13] Columbia Univ, Mailman Sch Publ Hlth, Int Ctr AIDS Care & Treatment Programs, New York, NY USA
[14] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
基金
英国医学研究理事会;
关键词
INSULIN-RESISTANCE; VASCULAR DEMENTIA; ALZHEIMER-DISEASE; INFECTED PATIENTS; IMPAIRMENT; DISORDERS; DECLINE; MARKERS;
D O I
10.1212/WNL.0b013e3181f11bd8
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To determine factors associated with baseline neurocognitive performance in HIV-infected participants enrolled in the Strategies for Management of Antiretroviral Therapy (SMART) neurology substudy. Methods: Participants from Australia, North America, Brazil, and Thailand were administered a 5-test neurocognitive battery. Z scores and the neurocognitive performance outcome measure, the quantitative neurocognitive performance z score (QNPZ-5), were calculated using US norms. Neurocognitive impairment was defined as z scores <-2 in two or more cognitive domains. Associations of test scores, the QNPZ-5, and impairment with baseline factors including demographics and risk factors for HIV-associated dementia (HAD) and cardiovascular disease (CVD) were determined in multiple regression. Results: The 292 participants had a median CD4 cell count of 536 cells/mm(3), 88% had an HIV viral load <= 400 copies/mL, and 92% were taking antiretrovirals. Demographics, HIV, and clinical factors differed between locations. The mean QNPZ-5 score was -0.72; 14% of participants had neurocognitive impairment. For most tests, scores and z scores differed significantly between locations, with and without adjustment for age, sex, education, and race. Prior CVD was associated with neurocognitive impairment. Prior CVD, hypercholesterolemia, and hypertension were associated with poorer neurocognitive performance but conventional HAD risk factors and the CNS penetration effectiveness rank of antiretroviral regimens were not. Conclusions: In this HIV-positive population with high CD4 cell counts, neurocognitive impairment was associated with prior CVD. Lower neurocognitive performance was associated with prior CVD, hypertension, and hypercholesterolemia, but not conventional HAD risk factors. The contribution of CVD and cardiovascular risk factors to the neurocognition of HIV-positive populations warrants further investigation. Neurology (R) 2010; 75:864-873
引用
收藏
页码:864 / 873
页数:10
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