Brief Report: Impact of ART Classes on the Increasing Risk of Cerebral Small-Vessel Disease in Middle-Aged, Well-Controlled, cART-Treated, HIV-Infected Individuals.


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 2019
Historique:
pubmed: 21 5 2019
medline: 15 4 2020
entrez: 21 5 2019
Statut: ppublish

Résumé

Cerebral small-vessel disease (CSVD) is a chronic disease accounting for one-third of strokes and the second etiology of dementia. Despite sustained immunovirological control, CSVD prevalence is doubled in middle-aged persons living with HIV (PLHIVs), even after adjustment for traditional cardiovascular risk factors. We aimed to investigate whether exposure to any antiretroviral drug class could be associated with an increasing risk of CSVD. The MicroBREAK-2 case-control study (NCT02210130) enrolled PLHIVs aged 50 years and older, treated with combined antiretroviral therapy for ≥5 years, with plasma HIV load controlled for ≥12 months. Cases were PLHIVs with radiologically defined CSVD, and controls were CSVD-free PLHIVs matched for age (±5 years), sex, and year of HIV diagnosis (±5 years). Multivariable conditional logistic regression analyses focused on cumulative exposure to nucleoside reverse transcriptase inhibitors, non-nucleoside reverse transcriptase inhibitors, protease inhibitors and/or exposure to integrase inhibitors (yes or no), adjusted for hypertension, CD4 nadir, current CD4/CD8 ratio, and HIV transmission group. Between May 2014 and April 2017, 77 cases and 77 controls (85.7% males) were recruited. PLHIVs' median age was 57.6 years, and median HIV diagnosis year was 1992. The increasing risk of CSVD was not associated with exposure to any ART class. No deleterious effect of ART class exposure on the risk of CSVD was found for middle-aged treated PLHIVs.

Sections du résumé

BACKGROUND
Cerebral small-vessel disease (CSVD) is a chronic disease accounting for one-third of strokes and the second etiology of dementia. Despite sustained immunovirological control, CSVD prevalence is doubled in middle-aged persons living with HIV (PLHIVs), even after adjustment for traditional cardiovascular risk factors. We aimed to investigate whether exposure to any antiretroviral drug class could be associated with an increasing risk of CSVD.
METHODS
The MicroBREAK-2 case-control study (NCT02210130) enrolled PLHIVs aged 50 years and older, treated with combined antiretroviral therapy for ≥5 years, with plasma HIV load controlled for ≥12 months. Cases were PLHIVs with radiologically defined CSVD, and controls were CSVD-free PLHIVs matched for age (±5 years), sex, and year of HIV diagnosis (±5 years). Multivariable conditional logistic regression analyses focused on cumulative exposure to nucleoside reverse transcriptase inhibitors, non-nucleoside reverse transcriptase inhibitors, protease inhibitors and/or exposure to integrase inhibitors (yes or no), adjusted for hypertension, CD4 nadir, current CD4/CD8 ratio, and HIV transmission group.
RESULTS
Between May 2014 and April 2017, 77 cases and 77 controls (85.7% males) were recruited. PLHIVs' median age was 57.6 years, and median HIV diagnosis year was 1992. The increasing risk of CSVD was not associated with exposure to any ART class.
CONCLUSION
No deleterious effect of ART class exposure on the risk of CSVD was found for middle-aged treated PLHIVs.

Identifiants

pubmed: 31107300
doi: 10.1097/QAI.0000000000002084
doi:

Substances chimiques

Anti-Retroviral Agents 0

Banques de données

ClinicalTrials.gov
['NCT02210130']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

547-551

Auteurs

Edouard Januel (E)

INSERM, Sorbonne Université, Institut Pierre-Louis d'Epidémiologie et de Santé Publique (IPLESP), Paris, France.

Ophelia Godin (O)

INSERM, Sorbonne Université, Institut Pierre-Louis d'Epidémiologie et de Santé Publique (IPLESP), Paris, France.

Antoine Moulignier (A)

Fondation Adolphe de Rothschild, Service de Neurologie, Paris, France.

François-Xavier Lescure (FX)

Sorbonne Paris Cité, INSERM, Infection, Antimicrobials, Modelling, Evolution, UMR 1137, APHP, Service de Maladies Infectieuses et Tropicales, Hôpital Bichat-Claude-Bernard, Université Paris-Diderot, Paris, France.

Julien Savatovsky (J)

Service de Radiologie, Fondation Adolphe de Rothschild, Paris, France.

Cédric Lamirel (C)

Service d'Ophtalmologie, Fondation Adolphe de Rothschild, Paris, France.

Nadia Valin (N)

APHP, Hôpital Saint-Antoine, Service de Maladies Infectieuses et Tropicales, Paris, France.

Roland Tubiana (R)

INSERM, Sorbonne Université, Institut Pierre-Louis d'Epidémiologie et de Santé Publique (IPLESP), Paris, France.
APHP, Hôpital Pitié-Salpêtrière, Service de Maladies Infectieuses et Tropicales, Paris, France.

Ana Canestri (A)

APHP, Hôpital Tenon, Service de Maladies Infectieuses et Tropicales, Paris, France.

Pascal Roux (P)

Service de Radiologie, Fondation Adolphe de Rothschild, Paris, France.

Jean-Claude Sadik (JC)

Service de Radiologie, Fondation Adolphe de Rothschild, Paris, France.

Laurence Salomon (L)

Fondation Adolphe de Rothschild, Unité de Recherche Clinique, Paris, France.

Christine Katlama (C)

INSERM, Sorbonne Université, Institut Pierre-Louis d'Epidémiologie et de Santé Publique (IPLESP), Paris, France.
APHP, Hôpital Pitié-Salpêtrière, Service de Maladies Infectieuses et Tropicales, Paris, France.

Yazdan Yazdanpanah (Y)

Sorbonne Paris Cité, INSERM, Infection, Antimicrobials, Modelling, Evolution, UMR 1137, APHP, Service de Maladies Infectieuses et Tropicales, Hôpital Bichat-Claude-Bernard, Université Paris-Diderot, Paris, France.

Gilles Pialoux (G)

APHP, Hôpital Tenon, Service de Maladies Infectieuses et Tropicales, Paris, France.

Pierre-Marie Girard (PM)

INSERM, Sorbonne Université, Institut Pierre-Louis d'Epidémiologie et de Santé Publique (IPLESP), Paris, France.
APHP, Hôpital Saint-Antoine, Service de Maladies Infectieuses et Tropicales, Paris, France.

Dominique Costagliola (D)

INSERM, Sorbonne Université, Institut Pierre-Louis d'Epidémiologie et de Santé Publique (IPLESP), Paris, France.

Lambert Assoumou (L)

INSERM, Sorbonne Université, Institut Pierre-Louis d'Epidémiologie et de Santé Publique (IPLESP), Paris, France.

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