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Effect of statins and testosterone replacement therapy on incident cardiovascular disease among male hormone-related cancer survivors

PURPOSE: Statins and testosterone replacement therapy (TTh) have been previously linked with prostate, colorectal and male breast cancer (hereinafter we will refer as hormone related cancers [HRCa]), and cardiovascular disease (CVD). However, there is a poor understanding about the combined associat...

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Detalles Bibliográficos
Autores principales: El Haddad, Danielle, Kim, Hyunkyoung, Polychronopolou, Efstathia, Baillargeon, Jacques, Villasante-Tezanos, Alejandro, Kuo, Yong-Fang, Gilani, Syed, Khalife, Wissam I., Lopez, David S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10635393/
https://www.ncbi.nlm.nih.gov/pubmed/37961677
http://dx.doi.org/10.21203/rs.3.rs-3530181/v1
Descripción
Sumario:PURPOSE: Statins and testosterone replacement therapy (TTh) have been previously linked with prostate, colorectal and male breast cancer (hereinafter we will refer as hormone related cancers [HRCa]), and cardiovascular disease (CVD). However, there is a poor understanding about the combined association of statins and TTh with incident CVD among HRCa survivors and a matched cancer-free cohort. METHODS: We identified 44,330 men of whom 22,165 were previously diagnosed with HRCa, and 22,165 were age-and index-matched cancer-free in SEER-Medicare 2007–2015. Pre-diagnostic prescription of statins and TTh prior to CVD development was ascertained for this analysis in the two matched cohorts. Weighted multivariable-adjusted conditional logistic regression models were used to evaluate the independent and combined associations of statins and TTh with CVD. RESULTS: We found that use of statins (OR = 0.51, 95% CI: 0.46–0.55) and TTh (OR = 0.81, 95% CI: 0.67–0.97) were each independently inversely associated with incident CVD in the overall sample. TTh plus statins was also inversely associated with CVD. Associations were similar in the matched cancer-free cohort. Among HRCa survivors, only statins and combination of TTh plus statins (OR = 0.60, 95% CI: 0.44–0.98) were inversely associated with CVD, but the independent use of TTh was not associated with CVD. CONCLUSION: In general, pre-diagnostic use of statins and TTh, prior to CVD development, independently or in combination, were inversely associated with CVD in the overall, cancer-free population, and among HRCa survivors (mainly combination). Independent effects and combination of statins and TTh remained to be confirmed with specific CVD outcomes among HRCa survivors.