Peripheral Blood Mononuclear Cells HIV DNA Levels Impact Intermittently on Neurocognition

被引:17
|
作者
Cysique, Lucette A. [1 ,3 ,6 ]
Hey-Cunningham, William J. [2 ,6 ]
Dermody, Nadene [1 ,7 ]
Chan, Phillip [4 ,5 ,8 ]
Brew, Bruce J. [3 ,4 ,5 ,6 ]
Koelsch, Kersten K. [2 ,4 ,5 ,6 ]
机构
[1] Neurosci Res Australia, Sydney, NSW, Australia
[2] UNSW Australia, UNSW Med, Kirby Inst, Sydney, NSW, Australia
[3] St Vincents Ctr Appl Med Res, Peter Duncan Neurosci Unit, Sydney, NSW, Australia
[4] St Vincents Hosp, Dept Neurol, Sydney, NSW 2010, Australia
[5] St Vincents Hosp, Dept HIV, Sydney, NSW 2010, Australia
[6] Univ New S Wales, Sydney, NSW, Australia
[7] Macquarie Univ, Sydney, NSW 2109, Australia
[8] Queen Elizabeth Hosp, Hong Kong, Hong Kong, Peoples R China
来源
PLOS ONE | 2015年 / 10卷 / 04期
基金
英国医学研究理事会;
关键词
CEREBROSPINAL-FLUID; IMPAIRMENT; INFECTION; DYNAMICS; THERAPY; PERSIST; COHORT;
D O I
10.1371/journal.pone.0120488
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Objectives To determine the contribution of peripheral blood mononuclear cells' (PBMCs) HIV DNA levels to HIV-associated dementia (HAD) and non-demented HIV-associated neurocognitive disorders (HAND) in chronically HIV-infected adults with long-term viral suppression on combined antiretroviral treatment (cART). Methods Eighty adults with chronic HIV infection on cART (>97% with plasma and CSF HIV RNA <50 copies/mL) were enrolled into a prospective observational cohort and underwent assessments of neurocognition and pre-morbid cognitive ability at two visits 18 months apart. HIV DNA in PBMCs was measured by real-time PCR at the same time-points. Results At baseline, 46% had non-demented HAND; 7.5% had HAD. Neurocognitive decline occurred in 14% and was more likely in those with HAD (p<.03). Low pre-morbid cognitive ability was uniquely associated with HAD (p<.05). Log(10) HIV DNA copies were stable between study visits (2.26 vs. 2.22 per 10(6) PBMC). Baseline HIV DNA levels were higher in those with lower pre-morbid cognitive ability (p<.04), and higher in those with no ART treatment during HIV infection 1st year (p = .03). Baseline HIV DNA was not associated with overall neurocognition. However, % ln HIV DNA change was associated with decline in semantic fluency in unadjusted and adjusted analyses (p = .01-.03), and motor-coordination (p = .02-.12) to a lesser extent. Conclusions PBMC HIV DNA plays a role in HAD pathogenesis, and this is moderated by pre-morbid cognitive ability in the context of long-term viral suppression. While the HIV DNA levels in PBMC are not associated with current non-demented HAND, increasing HIV DNA levels were associated with a decline in neurocognitive functions associated with HAND progression.
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页数:13
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