Antiretroviral Drugs Associated With Subclinical Coronary Artery Disease in the Swiss Human Immunodeficiency Virus Cohort Study.


Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
14 02 2020
Historique:
received: 16 11 2018
accepted: 04 04 2019
pubmed: 9 4 2019
medline: 7 1 2021
entrez: 9 4 2019
Statut: ppublish

Résumé

Coronary artery disease (CAD) events have been associated with certain antiretroviral therapy (ART) agents. In contrast, the influence of ART on subclinical atherosclerosis is not clear. The study objective was to assess the association between individual ART agents and the prevalence and extent of subclinical CAD. Coronary artery calcium (CAC) scoring and coronary computed tomography angiography (CCTA) were performed in ≥45-year-old Swiss Human Immunodeficiency Virus Cohort Study participants. The following subclinical CAD endpoints were analyzed separately: CAC score >0, any plaque, calcified plaque, noncalcified/mixed plaque, segment involvement score (SIS), and segment severity score (SSS). Logistic regression models calculated by inverse probability of treatment weights (IPTW) were used to explore associations between subclinical CAD and cumulative exposure to the 10 most frequently used drugs. There were 403 patients who underwent CCTA. A CAC score >0 was recorded in 188 (47%), any plaque in 214 (53%), calcified plaque in 151 (38%), and noncalcified/mixed plaque in 150 (37%) participants. A CAC score >0 was negatively associated with efavirenz (IPTW adjusted odds ratio per 5 years 0.73, 95% confidence interval [CI] 0.56-0.96), tenofovir disoproxil fumarate (0.68, 95% CI 0.49-0.95), and lopinavir (0.64, 95% CI 0.43-0.96). Any plaque was negatively associated with tenofovir disoproxil fumarate (0.71, 95% CI 0.51-0.99). Calcified plaque was negatively associated with efavirenz (0.7, 95% CI 0.57-0.97). Noncalcified/mixed plaque was positively associated with abacavir (1.46, 95% CI 1.08-1.98) and negatively associated with emtricitabine (0.67, 95% CI 0.46-0.99). For SSS and SIS, we found no association with any drug. An increased risk of noncalcified/mixed plaque was only found in patients exposed to abacavir. Emtricitabine was negatively associated with noncalcified/mixed plaque, while tenofovir disoproxil fumarate and efavirenz were negatively associated with any plaque and calcified plaque, respectively.

Sections du résumé

BACKGROUND
Coronary artery disease (CAD) events have been associated with certain antiretroviral therapy (ART) agents. In contrast, the influence of ART on subclinical atherosclerosis is not clear. The study objective was to assess the association between individual ART agents and the prevalence and extent of subclinical CAD.
METHODS
Coronary artery calcium (CAC) scoring and coronary computed tomography angiography (CCTA) were performed in ≥45-year-old Swiss Human Immunodeficiency Virus Cohort Study participants. The following subclinical CAD endpoints were analyzed separately: CAC score >0, any plaque, calcified plaque, noncalcified/mixed plaque, segment involvement score (SIS), and segment severity score (SSS). Logistic regression models calculated by inverse probability of treatment weights (IPTW) were used to explore associations between subclinical CAD and cumulative exposure to the 10 most frequently used drugs.
RESULTS
There were 403 patients who underwent CCTA. A CAC score >0 was recorded in 188 (47%), any plaque in 214 (53%), calcified plaque in 151 (38%), and noncalcified/mixed plaque in 150 (37%) participants. A CAC score >0 was negatively associated with efavirenz (IPTW adjusted odds ratio per 5 years 0.73, 95% confidence interval [CI] 0.56-0.96), tenofovir disoproxil fumarate (0.68, 95% CI 0.49-0.95), and lopinavir (0.64, 95% CI 0.43-0.96). Any plaque was negatively associated with tenofovir disoproxil fumarate (0.71, 95% CI 0.51-0.99). Calcified plaque was negatively associated with efavirenz (0.7, 95% CI 0.57-0.97). Noncalcified/mixed plaque was positively associated with abacavir (1.46, 95% CI 1.08-1.98) and negatively associated with emtricitabine (0.67, 95% CI 0.46-0.99). For SSS and SIS, we found no association with any drug.
CONCLUSIONS
An increased risk of noncalcified/mixed plaque was only found in patients exposed to abacavir. Emtricitabine was negatively associated with noncalcified/mixed plaque, while tenofovir disoproxil fumarate and efavirenz were negatively associated with any plaque and calcified plaque, respectively.

Identifiants

pubmed: 30958888
pii: 5432300
doi: 10.1093/cid/ciz283
doi:

Substances chimiques

Pharmaceutical Preparations 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

884-889

Investigateurs

V Aubert (V)
M Battegay (M)
E Bernasconi (E)
J Böni (J)
D L Braun (DL)
H C Bucher (HC)
C Burton-Jeangros (C)
A Calmy (A)
M Cavassini (M)
G Dollenmaier (G)
M Egger (M)
L Elzi (L)
J Fehr (J)
J Fellay (J)
H Furrer (H)
C A Fux (CA)
M Gorgievski (M)
H Günthard (H)
D Haerry (D)
B Hasse (B)
H H Hirsch (HH)
M Hoffmann (M)
I Hösli (I)
C Kahlert (C)
L Kaiser (L)
O Keiser (O)
T Klimkait (T)
R Kouyos (R)
H Kovari (H)
B Ledergerber (B)
G Martinetti (G)
B Martinez de Tejada (B)
C Marzolini (C)
K Metzner (K)
N Müller (N)
D Nadal (D)
D Nicca (D)
G Pantaleo (G)
A Rauch (A)
C Rudin (C)
F Schöni-Affolter (F)
P Schmid (P)
R Speck (R)
M Stöckle (M)
P Tarr (P)
A Trkola (A)
P Vernazza (P)
R Weber (R)
S Yerly (S)

Informations de copyright

© The Author(s) 2019. Published by Oxford University Press for the Infectious Diseases Society of America. All rights reserved. For permissions, e-mail: journals.permissions@oup.com.

Auteurs

Helen Kovari (H)

Division of Infectious Diseases and Hospital Epidemiology, University Hospital, University of Zurich, Switzerland.

Alexandra Calmy (A)

Division of Infectious Diseases, University of Geneva, Switzerland.

Thanh Doco-Lecompte (T)

Division of Infectious Diseases, University of Geneva, Switzerland.

René Nkoulou (R)

Division of Cardiology, University Hospital Geneva, University of Geneva, Switzerland.

Alex Marzel (A)

Division of Infectious Diseases and Hospital Epidemiology, University Hospital, University of Zurich, Switzerland.

Rainer Weber (R)

Division of Infectious Diseases and Hospital Epidemiology, University Hospital, University of Zurich, Switzerland.

Philipp A Kaufmann (PA)

Department of Nuclear Medicine, Cardiac Imaging, University Hospital Zurich, University of Zurich, Switzerland.

Ronny R Buechel (RR)

Department of Nuclear Medicine, Cardiac Imaging, University Hospital Zurich, University of Zurich, Switzerland.

Bruno Ledergerber (B)

Division of Infectious Diseases and Hospital Epidemiology, University Hospital, University of Zurich, Switzerland.

Philip E Tarr (PE)

Department of Medicine and Division of Infectious Diseases and Hospital Epidemiology, Kantonsspital Baselland, University of Basel, Bruderholz, Switzerland.

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