Mortality following myocardial infarction among HIV-infected persons: the Center for AIDS Research Network Of Integrated Clinical Systems (CNICS).


Journal

BMC medicine
ISSN: 1741-7015
Titre abrégé: BMC Med
Pays: England
ID NLM: 101190723

Informations de publication

Date de publication:
31 07 2019
Historique:
received: 16 04 2019
accepted: 09 07 2019
entrez: 1 8 2019
pubmed: 1 8 2019
medline: 15 1 2020
Statut: epublish

Résumé

Persons with human immunodeficiency virus (HIV) have higher risks for myocardial infarction (MI) than the general population. This is driven in part by higher type 2 MI (T2MI, due to coronary supply-demand mismatch) rates among persons with HIV (PWH). In the general population, T2MI has higher mortality than type 1 MI (T1MI, spontaneous and generally due to plaque rupture and thrombosis). PWH have a greater burden of comorbidities and may therefore have an even greater excess risk for complication and death in the setting of T2MI. However, mortality patterns after T1MI and T2MI in HIV are unknown. We analyzed mortality after MI among PWH enrolled in the multicenter, US-based Centers for AIDS Research Network of Integrated Clinical Systems (CNICS) cohort (N = 28,186). Incident MIs occurring between January 1, 1996, and December 31, 2014, were centrally adjudicated and classified as T1MI or T2MI. We first compared mortality following T1MI vs. T2MI among PWH. Cox survival analyses and Bayesian model averaging were then used to evaluate pre-MI covariates associated with mortality following T1MI and T2MI. Among the 596 out of 28,186 PWH who experienced MI (2.1%; 293 T1MI and 303 T2MI), mortality rates were significantly greater after T2MI (22.2/100 person-years; 1-, 3-, and 5-year mortality 39%, 52%, and 62%) than T1MI (8.2/100 person-years; 1-, 3-, and 5-year mortality 15%, 22%, and 30%). Significant mortality predictors after T1MI were higher HIV viral load, renal dysfunction, and older age. Significant predictors of mortality after T2MI were low body-mass index (BMI) and detectable HIV viral load. Mortality is high following MI for PWH and substantially greater after T2MI than T1MI. Predictors of death after MI differed by type of MI, reinforcing the different clinical scenarios associated with each MI type and the importance of considering MI types separately.

Sections du résumé

BACKGROUND
Persons with human immunodeficiency virus (HIV) have higher risks for myocardial infarction (MI) than the general population. This is driven in part by higher type 2 MI (T2MI, due to coronary supply-demand mismatch) rates among persons with HIV (PWH). In the general population, T2MI has higher mortality than type 1 MI (T1MI, spontaneous and generally due to plaque rupture and thrombosis). PWH have a greater burden of comorbidities and may therefore have an even greater excess risk for complication and death in the setting of T2MI. However, mortality patterns after T1MI and T2MI in HIV are unknown.
METHODS
We analyzed mortality after MI among PWH enrolled in the multicenter, US-based Centers for AIDS Research Network of Integrated Clinical Systems (CNICS) cohort (N = 28,186). Incident MIs occurring between January 1, 1996, and December 31, 2014, were centrally adjudicated and classified as T1MI or T2MI. We first compared mortality following T1MI vs. T2MI among PWH. Cox survival analyses and Bayesian model averaging were then used to evaluate pre-MI covariates associated with mortality following T1MI and T2MI.
RESULTS
Among the 596 out of 28,186 PWH who experienced MI (2.1%; 293 T1MI and 303 T2MI), mortality rates were significantly greater after T2MI (22.2/100 person-years; 1-, 3-, and 5-year mortality 39%, 52%, and 62%) than T1MI (8.2/100 person-years; 1-, 3-, and 5-year mortality 15%, 22%, and 30%). Significant mortality predictors after T1MI were higher HIV viral load, renal dysfunction, and older age. Significant predictors of mortality after T2MI were low body-mass index (BMI) and detectable HIV viral load.
CONCLUSIONS
Mortality is high following MI for PWH and substantially greater after T2MI than T1MI. Predictors of death after MI differed by type of MI, reinforcing the different clinical scenarios associated with each MI type and the importance of considering MI types separately.

Identifiants

pubmed: 31362721
doi: 10.1186/s12916-019-1385-7
pii: 10.1186/s12916-019-1385-7
pmc: PMC6668167
doi:

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

149

Subventions

Organisme : NIAID NIH HHS
ID : P30 AI027757
Pays : United States
Organisme : NIAID NIH HHS
ID : K24 AI112393
Pays : United States
Organisme : NHGRI NIH HHS
ID : R01 HG010649
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI027763
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL126538
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL125027
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI117943
Pays : United States
Organisme : NIAID NIH HHS
ID : R24 AI067039
Pays : United States
Organisme : NIAID NIH HHS
ID : P30 AI050410
Pays : United States

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Auteurs

Matthew J Feinstein (MJ)

Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, 680 N. Lake Shore Drive, Suite 1400, Chicago, IL, 60611, USA. matthewjfeinstein@northwestern.edu.

Robin M Nance (RM)

University of Washington School of Medicine, Seattle, USA.

J A Chris Delaney (JAC)

School of Public Health, University of Washington, Seattle, USA.

Susan R Heckbert (SR)

School of Public Health, University of Washington, Seattle, USA.

Matthew J Budoff (MJ)

University of California-Los Angeles School of Medicine, Los Angeles, USA.

Daniel R Drozd (DR)

University of Washington School of Medicine, Seattle, USA.

Greer A Burkholder (GA)

University of Alabama-Birmingham School of Medicine, Birmingham, USA.

James H Willig (JH)

University of Alabama-Birmingham School of Medicine, Birmingham, USA.

Michael J Mugavero (MJ)

University of Alabama-Birmingham School of Medicine, Birmingham, USA.

William C Mathews (WC)

Department of Medicine, University of California-San Diego Medical Center, San Diego, USA.

Richard D Moore (RD)

Johns Hopkins University, Baltimore, USA.

Joseph J Eron (JJ)

University of North Carolina School of Medicine, Chapel Hill, USA.

Sonia Napravnik (S)

University of North Carolina School of Medicine, Chapel Hill, USA.

Peter W Hunt (PW)

University of California-San Francisco School of Medicine, San Francisco, USA.

Elvin Geng (E)

University of California-San Francisco School of Medicine, San Francisco, USA.

Priscilla Hsue (P)

University of California-San Francisco School of Medicine, San Francisco, USA.

Inga Peter (I)

Mount Sinai School of Medicine, New York City, USA.

William B Lober (WB)

School of Public Health, University of Washington, Seattle, USA.

Kristina Crothers (K)

University of Washington School of Medicine, Seattle, USA.

Carl Grunfeld (C)

University of California-San Francisco School of Medicine, San Francisco, USA.

Michael S Saag (MS)

University of Alabama-Birmingham School of Medicine, Birmingham, USA.

Mari M Kitahata (MM)

University of Washington School of Medicine, Seattle, USA.

Donald M Lloyd-Jones (DM)

Division of Cardiology, Department of Medicine, Northwestern University Feinberg School of Medicine, 680 N. Lake Shore Drive, Suite 1400, Chicago, IL, 60611, USA.

Heidi M Crane (HM)

University of Washington School of Medicine, Seattle, USA.

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