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Testosterone concentrations andoutcomes in hemodialysis patients of the EVOLVE trial
Örebro University, School of Medical Sciences. Örebro University Hospital. Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Sweden.ORCID iD: 0000-0001-6968-6934
Division of Renal Medicine, Department of Clinical Science, Intervention and Technology, Karolinska Institutet, Stockholm, Sweden.
Division of Nephrology, Department of Medicine, Stanford University School of Medicine, USA.
Division of Nephrology, Department of Medicine, Stanford University School of Medicine, USA.
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2023 (English)In: Nephrology, Dialysis and Transplantation, ISSN 0931-0509, E-ISSN 1460-2385, Vol. 38, no 6, p. 1519-1527Article in journal (Refereed) Published
Abstract [en]

BACKGROUND: Hypogonadism is common in end-stage kidney disease and may contribute to morbidity and mortality.

METHODS: Using data from the randomized controlled EVOLVE trial of cinacalcet, we analyzed the associations of total testosterone, free testosterone, and sex-hormone binding globulin (SHBG) serum concentrations with mortality and major cardiovascular events in 1692 men and 1059 women receiving hemodialysis. We also describe the effect of cinacalcet treatment on serum concentrations of testosterone.

RESULTS: Among men, lower serum free testosterone (OR 0.18 95%, CI 0.04-0.82, p = 0.026) and higher SHBG (OR 1.05 per 10 nmol/L, 95% CI 1.01-1.10, p = 0.012), but not total testosterone, were associated with higher risk of death or cardiovascular event. Only SHBG was associated with all-cause mortality (OR 1.07 per 10 nmol/L, 95% CI 1.02-1.12, p = 0.0073). Among women, neither total- or free testosterone, nor SHBG were associated with outcomes. We found no statistically significant effect of cinacalcet treatment on SHBG, free- or total testosterone.

CONCLUSIONS: Lower free testosterone and higher SHBG in serum are associated with higher risk of death or cardiovascular event in men undergoing chronic hemodialysis.

Place, publisher, year, edition, pages
Oxford University Press, 2023. Vol. 38, no 6, p. 1519-1527
Keywords [en]
Cardiovascular disease, hemodialysis, mortality, testosterone
National Category
Cardiology and Cardiovascular Disease
Identifiers
URN: urn:nbn:se:oru:diva-101599DOI: 10.1093/ndt/gfac278ISI: 000874337600001PubMedID: 36175142Scopus ID: 2-s2.0-85161623930OAI: oai:DiVA.org:oru-101599DiVA, id: diva2:1700397
Note

Funding agencies:

Bayer AG  

Amgen

Available from: 2022-09-30 Created: 2022-09-30 Last updated: 2025-02-10Bibliographically approved

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