Testosterone therapy and the risk of cardiovascular disease in older, hypogonadal men.

Aging, obesity, and testosterone Atherosclerosis and testosterone Cardiovascular disease Coronary artery calcium Coronary artery disease Hypogonadism Non-calcified plaque TRAVERSE trial Testosterone therapy

Journal

Progress in cardiovascular diseases
ISSN: 1873-1740
Titre abrégé: Prog Cardiovasc Dis
Pays: United States
ID NLM: 0376442

Informations de publication

Date de publication:
27 Feb 2024
Historique:
received: 25 02 2024
accepted: 25 02 2024
medline: 1 3 2024
pubmed: 1 3 2024
entrez: 29 2 2024
Statut: aheadofprint

Résumé

The debate over the cardiovascular (CV) implications of testosterone therapy (TT) have resulted in diverging safety recommendations and clinical guidelines worldwide. This narrative review synthesizes and critically evaluates long-term studies examining the effects of TT within the context of aging, obesity, and endogenous sex hormones on CV disease (CVD) risk to support informed clinical decision-making. Observational studies have variably linked low endogenous testosterone with increased CVD risk, while randomized controlled trials (RCTs) demonstrate that TT yields cardiometabolic benefits without increasing short-term CV risk. The TRAVERSE trial, as the first RCT powered to assess CVD events, did not show increased major adverse cardiac events (MACE) incidence; however, its limitations - specifically the maintenance of testosterone at low-normal levels, a high participant discontinuation rate, and short follow-up - warrant a careful interpretation of its results. Furthermore, findings from the TTrials cardiovascular sub-study, which showed an increase in non-calcified plaque, indicate the need for ongoing research into the long-term CV impact of TT. The decision to initiate TT should consider the current evidence gaps, particularly for older men with known CVD. The CV effects of maintaining physiological testosterone levels through exogenous means remain to be fully explored. Until more definitive evidence is available, clinical practice should prioritize individualized care and informed discussions on the potential CV implications of TT.

Identifiants

pubmed: 38423237
pii: S0033-0620(24)00036-7
doi: 10.1016/j.pcad.2024.02.015
pii:
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024. Published by Elsevier Inc.

Déclaration de conflit d'intérêts

Declaration of competing interest Matthew J. Budoff: received grants from the following companies: Novo Nordisk, Novartis, Astrazeneca, Heartflow, GE Healthcare, Amgen, and Boehringer Ingleheim, Department of Defense, Centers for Disease Control and the National Institutes of Health. Dr. Budoff received honoraria from Novo Nordisk, Esperion, Astrazeneca, Merck, Janssen, and Eli Lilly. All other authors declare they have no conflict of interest.

Auteurs

Srikanth Krishnan (S)

The Lundquist Institute at Harbor-UCLA. Electronic address: Srikanth.krishnan@lundquist.org.

Jairo Aldana-Bitar (J)

The Lundquist Institute at Harbor-UCLA.

Ilana Golub (I)

The Lundquist Institute at Harbor-UCLA; David Geffen School of Medicine at University of California Los Angeles.

Keishi Ichikawa (K)

The Lundquist Institute at Harbor-UCLA.

Ayesha Shabir (A)

The Lundquist Institute at Harbor-UCLA.

Marziyeh Bagheri (M)

The Lundquist Institute at Harbor-UCLA.

Hossein Hamidi (H)

The Lundquist Institute at Harbor-UCLA.

Travis Benzing (T)

The Lundquist Institute at Harbor-UCLA.

Sina Kianoush (S)

The Lundquist Institute at Harbor-UCLA.

Matthew J Budoff (MJ)

The Lundquist Institute at Harbor-UCLA. Electronic address: mbudoff@lundquist.org.

Classifications MeSH