Low-Level HIV RNA in Cerebrospinal Fluid and Neurocognitive Performance: A Longitudinal Cohort Study.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
15 08 2021
Historique:
received: 09 12 2020
accepted: 29 03 2021
pubmed: 27 4 2021
medline: 9 11 2021
entrez: 26 4 2021
Statut: ppublish

Résumé

Cognitive complications persist in persons with HIV during suppressive antiretroviral therapy (ART). Low levels of HIV during ART could contribute to these complications. In this study, we measured cerebrospinal fluid (CSF) HIV using a single-copy assay (SCA) to investigate a possible relationship between low-level HIV and cognition. SCA data were analyzed from 3 consecutively paired CSF-plasma specimens collected over a mean of 456 days from 96 participants on suppressive ART. Using mixed models, the presence of CSF HIV by SCA as a risk factor for worse neurocognitive performance was examined. At baseline on the SCA, 45.8% of participants had detectable plasma HIV RNA (median 8 copies/mL and interquartile range = 3-17 among detectable values) and 17.7% had detectable CSF HIV RNA (median CSF concentration= 3 copies/mL and interquartile range= 2-13 among detectable values). The frequency of CSF HIV RNA detection declined over time in CSF (P = 0.018) with a trend toward decline in plasma (P = 0.064). Detectable CSF HIV RNA during the study was associated with worse performance in the domains of recall (P = 0.014) and motor (P = 0.040) and a trend with worse overall global performance (P = 0.078). Integrase inhibitor use, although very infrequent in this cohort, was associated with better performance in 2 domains. Low-level CSF HIV RNA declines with time but is associated with worse cognitive performance in 2 domains. Additional research is needed to better understand the relationship between HIV RNA persistence during long-term ART and central nervous system complications in persons with HIV.

Sections du résumé

BACKGROUND
Cognitive complications persist in persons with HIV during suppressive antiretroviral therapy (ART). Low levels of HIV during ART could contribute to these complications. In this study, we measured cerebrospinal fluid (CSF) HIV using a single-copy assay (SCA) to investigate a possible relationship between low-level HIV and cognition.
DESIGN/METHODS
SCA data were analyzed from 3 consecutively paired CSF-plasma specimens collected over a mean of 456 days from 96 participants on suppressive ART. Using mixed models, the presence of CSF HIV by SCA as a risk factor for worse neurocognitive performance was examined.
RESULTS
At baseline on the SCA, 45.8% of participants had detectable plasma HIV RNA (median 8 copies/mL and interquartile range = 3-17 among detectable values) and 17.7% had detectable CSF HIV RNA (median CSF concentration= 3 copies/mL and interquartile range= 2-13 among detectable values). The frequency of CSF HIV RNA detection declined over time in CSF (P = 0.018) with a trend toward decline in plasma (P = 0.064). Detectable CSF HIV RNA during the study was associated with worse performance in the domains of recall (P = 0.014) and motor (P = 0.040) and a trend with worse overall global performance (P = 0.078). Integrase inhibitor use, although very infrequent in this cohort, was associated with better performance in 2 domains.
CONCLUSIONS
Low-level CSF HIV RNA declines with time but is associated with worse cognitive performance in 2 domains. Additional research is needed to better understand the relationship between HIV RNA persistence during long-term ART and central nervous system complications in persons with HIV.

Identifiants

pubmed: 33901102
doi: 10.1097/QAI.0000000000002714
pii: 00126334-202108150-00012
pmc: PMC8596378
mid: NIHMS1751010
doi:

Substances chimiques

Anti-HIV Agents 0
RNA, Viral 0

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1196-1204

Subventions

Organisme : NIMH NIH HHS
ID : R21 MH085610
Pays : United States
Organisme : NIMH NIH HHS
ID : K24 MH097673
Pays : United States
Organisme : NIDA NIH HHS
ID : K24 DA040550
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH058076
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH128872
Pays : United States
Organisme : NIMH NIH HHS
ID : R21 MH118092
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG062387
Pays : United States
Organisme : NIMH NIH HHS
ID : P30 MH062512
Pays : United States
Organisme : NIMH NIH HHS
ID : R01 MH107345
Pays : United States
Organisme : NIMH NIH HHS
ID : K23 MH095679
Pays : United States

Informations de copyright

Copyright © 2021 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to disclose.

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Auteurs

Albert M Anderson (AM)

Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, GA.

Bin Tang (B)

Department of Psychiatry, University of California, San Diego, CA.

Florin Vaida (F)

Department of Psychiatry, University of California, San Diego, CA.

Daniel Mcclernon (D)

BioMONTR Labs, Research Triangle Park, NC; and.

Reena Deutsch (R)

Department of Psychiatry, University of California, San Diego, CA.

Mariana Cherner (M)

Department of Psychiatry, University of California, San Diego, CA.

Debra Cookson (D)

Department of Psychiatry, University of California, San Diego, CA.

Melanie Crescini (M)

Department of Psychiatry, University of California, San Diego, CA.

Igor Grant (I)

Department of Psychiatry, University of California, San Diego, CA.

Ronald J Ellis (RJ)

Department of Psychiatry, University of California, San Diego, CA.
Departments of Neurosciences; and.

Scott L Letendre (SL)

Department of Psychiatry, University of California, San Diego, CA.
Medicine, University of California, San Diego, CA.

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