Key result
Anabolic-androgenic steroid exposure is linked to ~2.6-fold higher all-cause mortality.
Why the study?
The magnitude of excess all-cause mortality and the cardiac phenotype of former anabolic-androgenic steroid users remain incompletely defined.
Does non-medical anabolic-androgenic steroid use increase the risk of all-cause mortality and major cardiovascular outcomes compared to non-use?
Meta-Analysis
Does non-medical anabolic-androgenic steroid use increase the risk of all-cause mortality and major cardiovascular outcomes compared to non-use?
Relative Risk: 2.57 (95% CI 1.98–3.33)
Non-medical use of anabolic-androgenic steroids is associated with an increased risk of all-cause mortality and potentially major cardiovascular outcomes, though the current evidence base is limited by observational design and confounding.
Background/Objectives: Non-medical anabolic-androgenic steroid (AAS) use has been associated with adverse cardiac remodelling, but the magnitude of excess all-cause mortality and the cardiac phenotype of former users remain incompletely defined. Methods: We systematically reviewed studies reporting mortality, major cardiovascular outcomes, or cardiac function after cessation in AAS-exposed individuals. All-cause mortality was pooled from comparative cohorts with individually ascertained exposure using random-effects models; global longitudinal strain (GLS) and left ventricular ejection fraction in former users were pooled as mean differences. Risk of bias was assessed with ROBINS-E and certainty with GRADE. Results: Fifteen primary reports were included. Across three cohorts, AAS exposure was associated with higher all-cause mortality (risk ratio 2.57, 95% CI 1.98–3.33; I2 = 0%; 95% prediction interval 0.47–13.87), with consistent sensitivity analyses. In a single large matched cohort, adjusted hazard ratios for cardiovascular outcomes ranged from 2.26 to 8.90, highest for cardiomyopathy. Former users had worse GLS than AAS-naïve controls (3 studies; mean difference +0.90 percentage points, 95% CI +0.13 to +1.66), whereas the pooled ejection-fraction estimate was exploratory and highly heterogeneous. Conclusions: AAS exposure was associated with higher all-cause mortality in three observational cohorts, but residual confounding, differing follow-up, and the small evidence base preclude causal inference. Cardiovascular associations from a single cohort require independent replication, and evidence on residual myocardial dysfunction in former users is of very low certainty.
No takes yet. Share an insight, caveat, or question.
Solá et al. (2026) conducted a meta-analysis in Non-medical anabolic-androgenic steroid (AAS) use. Anabolic-androgenic steroid (AAS) exposure vs. AAS-naïve controls was evaluated on All-cause mortality (RR 2.57, 95% CI 1.98-3.33). Anabolic-androgenic steroid exposure was associated with a higher risk of all-cause mortality (RR 2.57; 95% CI 1.98-3.33) across three observational cohorts.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: