HIV Viremia and Risk of Stroke Among People Living with HIV Who Are Using Antiretroviral Therapy.


Journal

Epidemiology (Cambridge, Mass.)
ISSN: 1531-5487
Titre abrégé: Epidemiology
Pays: United States
ID NLM: 9009644

Informations de publication

Date de publication:
01 05 2021
Historique:
pubmed: 17 2 2021
medline: 1 6 2021
entrez: 16 2 2021
Statut: ppublish

Résumé

Rates of stroke are higher in people living with HIV compared with age-matched uninfected individuals. Causes of elevated stroke risk, including the role of viremia, are poorly defined. Between 1 January 2006 and 31 December 2014, we identified incident strokes among people living with HIV on antiretroviral therapy at five sites across the United States. We considered three parameterizations of viral load (VL) including (1) baseline (most recent VL before study entry), (2) time-updated, and (3) cumulative VL (copy-days/mL of virus). We used Cox proportional hazards models to estimate hazard ratios (HRs) for stroke risk comparing the 75th percentile ("high VL") to the 25th percentile ("low VL") of baseline and time-updated VL. We used marginal structural Cox models, with most models adjusted for traditional stroke risk factors, to estimate HRs for stroke associated with cumulative VL. Among 15,974 people living with HIV, 139 experienced a stroke (113 ischemic; 18 hemorrhagic; eight were unknown type) over a median follow-up of 4.2 years. Median baseline VL was 38 copies/mL (interquartile interval: 24, 3,420). High baseline VL was associated with increased risk of both ischemic (HR: 1.3; 95% CI = 0.96-1.7) and hemorrhagic stroke (HR: 3.1; 95% CI = 1.6-5.9). In time-updated models, high VL was also associated with an increased risk of any stroke (HR: 1.8; 95% CI = 1.4-2.3). We observed no association between cumulative VL and stroke risk. Our findings are consistent with the hypothesis that elevated HIV VL may increase stroke risk, regardless of previous VL levels.

Sections du résumé

BACKGROUND
Rates of stroke are higher in people living with HIV compared with age-matched uninfected individuals. Causes of elevated stroke risk, including the role of viremia, are poorly defined.
METHODS
Between 1 January 2006 and 31 December 2014, we identified incident strokes among people living with HIV on antiretroviral therapy at five sites across the United States. We considered three parameterizations of viral load (VL) including (1) baseline (most recent VL before study entry), (2) time-updated, and (3) cumulative VL (copy-days/mL of virus). We used Cox proportional hazards models to estimate hazard ratios (HRs) for stroke risk comparing the 75th percentile ("high VL") to the 25th percentile ("low VL") of baseline and time-updated VL. We used marginal structural Cox models, with most models adjusted for traditional stroke risk factors, to estimate HRs for stroke associated with cumulative VL.
RESULTS
Among 15,974 people living with HIV, 139 experienced a stroke (113 ischemic; 18 hemorrhagic; eight were unknown type) over a median follow-up of 4.2 years. Median baseline VL was 38 copies/mL (interquartile interval: 24, 3,420). High baseline VL was associated with increased risk of both ischemic (HR: 1.3; 95% CI = 0.96-1.7) and hemorrhagic stroke (HR: 3.1; 95% CI = 1.6-5.9). In time-updated models, high VL was also associated with an increased risk of any stroke (HR: 1.8; 95% CI = 1.4-2.3). We observed no association between cumulative VL and stroke risk.
CONCLUSIONS
Our findings are consistent with the hypothesis that elevated HIV VL may increase stroke risk, regardless of previous VL levels.

Identifiants

pubmed: 33591056
doi: 10.1097/EDE.0000000000001331
pii: 00001648-202105000-00021
pmc: PMC8012252
mid: NIHMS1666969
doi:

Substances chimiques

Anti-HIV Agents 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

457-464

Subventions

Organisme : NIAID NIH HHS
ID : P30 AI027767
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI094189
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL007828
Pays : United States
Organisme : NIAID NIH HHS
ID : R24 AI067039
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI050410
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL126538
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI027757
Pays : United States
Organisme : NIDA NIH HHS
ID : R01 DA047045
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL125027
Pays : United States

Informations de copyright

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

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Auteurs

Barbara N Harding (BN)

Department of Medicine, University of Washington, Seattle, WA.

Tigran Avoundjian (T)

Department of Epidemiology, University of Washington, Seattle, WA.

Susan R Heckbert (SR)

Department of Epidemiology, University of Washington, Seattle, WA.

Bridget M Whitney (BM)

Department of Medicine, University of Washington, Seattle, WA.

Robin M Nance (RM)

Department of Medicine, University of Washington, Seattle, WA.

Stephanie A Ruderman (SA)

Department of Epidemiology, University of Washington, Seattle, WA.

Rizwan Kalani (R)

Department of Medicine, University of Washington, Seattle, WA.

David L Tirschwell (DL)

Department of Medicine, University of Washington, Seattle, WA.

Emily L Ho (EL)

Department of Medicine, University of Washington, Seattle, WA.

Kyra J Becker (KJ)

Department of Medicine, University of Washington, Seattle, WA.

Joseph Zunt (J)

Department of Medicine, University of Washington, Seattle, WA.

Felicia Chow (F)

Department of Medicine, University of California, San Francisco, San Francisco, CA.

Andrew Huffer (A)

Department of Medicine, University of Washington, Seattle, WA.

W Christopher Mathews (WC)

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

Joseph Eron (J)

Department of Medicine, University of North Carolina, Chapel Hill, NC.

Richard D Moore (RD)

Department of Medicine, Johns Hopkins, Baltimore, MD.

Christina M Marra (CM)

Department of Medicine, University of Washington, Seattle, WA.

Greer Burkholder (G)

Department of Medicine, University of Alabama at Birmingham, Birmingham, AL.

Michael S Saag (MS)

Department of Medicine, University of Alabama at Birmingham, Birmingham, AL.

Mari M Kitahata (MM)

Department of Medicine, University of Washington, Seattle, WA.

Heidi M Crane (HM)

Department of Medicine, University of Washington, Seattle, WA.

Joseph C Delaney (JC)

College of Pharmacy, University of Manitoba, Winnipeg, Manitoba, Canada.

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