Cited by 138Hormonal and reproductive studiesMenopause: Health Impacts and TreatmentsLipoproteins and Cardiovascular Health

Testosterone and Cardiovascular Risk: Meta-Analysis of Interventional Studies

Corona, Giovanni, Rastrelli, Giulia, Di Pasquale, Giuseppe, Sforza, Alessandra, Mannucci, Edoardo, Maggi, Mario·2018·The Journal of Sexual Medicine

Abstract

Background: The relationship between testosterone (T) and cardiovascular (CV) risk in men is conflicting. Aim: To verify whether T therapy (TTh) represents a possible risk factor for CV morbidity and mortality. Methods: We conducted a random effect meta-analysis considering all available data from pharmaco-epidemiological studies as well as randomized placebo-controlled trials (RCTs). Outcomes: CV mortality and morbidity were investigated. Results: After screening, 15 pharmaco-epidemiological and 93 RCT studies were considered. The analysis of pharmaco-epidemiological studies documented that TTh reduces overall mortality and CV morbidity. Conversely, in RCTs, TTh had no clear effect, either beneficial or detrimental, on the incidence of CV events. However, a protective role of TTh on CV morbidity was observed when studies enrolling obese (body mass index >30 kg/m2) patients were scrutinized (Mantel-Haenszel odds ratio 0.51 [95% CI 0.27–0.96]; P = .04), although this association disappeared when only high-quality RCTs were considered (Mantel-Haenszel odds ratio 0.64 [95% CI 0.22–1.88]; P = .42). Finally, an increased risk of CV diseases was observed in RCTs when T preparations were prescribed at dosages above those normally recommended, or when frail men were considered. Clinical Implications: Pharmaco-epidemiological studies showed that TTh might reduce CV risk, but this effect was not confirmed when RCTs were considered. Strengths & Limitations: Meta-analysis of pharmaco-epidemiological studies indicates that TTh reduces overall mortality and CV morbidity. In addition, even in RCTs, a protective role of TTh on CV morbidity was envisaged when studies enrolling obese (body mass index >30 kg/m2) patients were considered. Pharmaco-epidemiological studies should be considered with caution due to the lack of completeness of follow-up and of the management of missing data. In addition, properly powered placebo-controlled RCTs with a primary CV end point, in men with late-onset hypo-gonadism, are not yet available. Finally, the duration of all studies evaluated in the present meta-analysis is relatively short, reaching a maximum of 3 years. Conclusions: Data from RCTs suggest that treatment with T is not effective in reducing CV risk, however, when TTh is correctly applied, it is not associated with an increase in CV risk and it may have a beneficial effect in some sub-populations.

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Crossref · 10.1016/j.jsxm.2018.04.641

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  • Controversy remains around whether testosterone therapy affects the risk of cardiovascular events.

    “Though testosterone therapy improves bone mineral density, lean body mass, erectile function, and anemia, there is inconclusive evidence on the benefits of testosterone therapy on cognitive function, energy levels, blood glucose or lipid levels, and controversy remains around whether testosterone therapy affects the risk of cardiovascular events (6-13).”
  • Evidence is inconclusive on the benefits of testosterone therapy on cognitive function, energy levels, blood glucose or lipid levels.

    “Though testosterone therapy improves bone mineral density, lean body mass, erectile function, and anemia, there is inconclusive evidence on the benefits of testosterone therapy on cognitive function, energy levels, blood glucose or lipid levels, and controversy remains around whether testosterone therapy affects the risk of cardiovascular events (6-13).”
  • Testosterone therapy improves bone mineral density, lean body mass, erectile function, and anemia.

    “Though testosterone therapy improves bone mineral density, lean body mass, erectile function, and anemia, there is inconclusive evidence on the benefits of testosterone therapy on cognitive function, energy levels, blood glucose or lipid levels, and controversy remains around whether testosterone therapy affects the risk of cardiovascular events (6-13).”

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Authors
Corona, G., Rastrelli, G., Di Pasquale, G., Sforza, A., Mannucci, E., & Maggi, M.
Affiliations
  • Azienda USL di Bologna (IT)
  • University of Florence (IT)
  • Cardiology Unit , Bologna,   Italy
  • Azienda Ospedaliero-Universitaria Careggi (IT)
Corresponding author
Maggi, Mario
Venue
The Journal of Sexual Medicine
Published
2018-06-01
Volume
15
Issue
6
Pages
820-838
ISSN
  • 1743-6095 (ISSN-L)
  • 1743-6109
OpenAlex
W2803859106
Cited by
138
References
158
Citations by year
2026: 8 · 2025: 13 · 2024: 22 · 2023: 19 · 2022: 21 · 2021: 15 · 2020: 22 · 2019: 13 · 2018: 5
FWCI
2.12
Type
journal article
Language
en
Open access
closed
Locations
  • The Journal of Sexual Medicine (publishedVersion)
  • PubMed (publishedVersion)
  • Florence Research (University of Florence) (submittedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Hormonal and reproductive studies
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Menopause: Health Impacts and Treatments
  • Health Sciences › Medicine › Surgery › Lipoproteins and Cardiovascular Health
Keywords
testosterone replacement therapy, cardiovascular risk, cardiovascular mortality, cardiovascular morbidity, andropause, obesity, randomized controlled trials, men's health, study quality bias, publication bias
MeSH terms
Androgens, Cardiovascular Diseases, Humans, Hypogonadism, Male, Risk Factors, Testosterone, Body Mass Index, Randomized Controlled Trials as Topic, Hormone Replacement Therapy

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