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Sex Differences in the Development of Anthracycline-Associated Heart Failure.
Diaz, Andrea Nathalie Rosas; Hurtado, Gabriel Pajares; Manzano, Abul Andres Ariza; Keyes, Michelle J; Turissini, Cole; Choudhary, Arrush; Curtin, Casie; Dommaraju, Sujithraj; Warack, Sarah; Strom, Jordan B; Asnani, Aarti.
Affiliation
  • Diaz ANR; Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA.
  • Hurtado GP; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA.
  • Manzano AAA; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA.
  • Keyes MJ; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA.
  • Turissini C; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA.
  • Choudhary A; Department of Medicine, Beth Israel Deaconess Medical Center, Boston, MA.
  • Curtin C; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA.
  • Dommaraju S; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA.
  • Warack S; Department of Pharmacy, Beth Israel Deaconess Medical Center, Brookline, MA.
  • Strom JB; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA; Richard A. and Susan F. Smith Center for Outcomes Research in Cardiology, Boston, MA.
  • Asnani A; Division of Cardiovascular Medicine, Beth Israel Deaconess Medical Center, Boston, MA. Electronic address: aasnani@bidmc.harvard.edu.
J Card Fail ; 2023 Nov 10.
Article in En | MEDLINE | ID: mdl-37951494
BACKGROUND: Female sex is frequently cited as a risk factor for anthracycline cardiotoxicity based on pediatric data, but the role of sex in the development of cardiotoxicity has not been clearly established in adults. OBJECTIVES: To assess the effect of female sex on the development of incident heart failure (HF) in adult patients treated with anthracyclines. METHODS: This was a retrospective cohort study of 1525 adult patients with no prior history of HF or cardiomyopathy who were treated with anthracyclines between 1992 and 2019. The primary outcome was new HF within 5 years of the first dose of anthracyclines. The effect of sex was assessed using Cox proportional hazards and competing risk models. RESULTS: Over a median (IQR) follow-up of 1.02 (0.30-3.01) years, 4.78% of patients developed HF (44 men and 29 women). Female sex was not associated with the primary outcome in a multivariable Cox proportional hazards model (HR 0.87; 95% CI 0.53-1.43; P = 0.58). Similar results were observed in a multivariable model accounting for the competing risk of death (HR 0.94; 95% CI 0.39-2.25; P = 0.88). Age, coronary artery disease and hematopoietic stem cell transplant were associated with the primary outcome in a multivariable Cox proportional hazards model. Age and body mass index were associated with the primary outcome in a multivariable competing risk model. CONCLUSIONS: In this large, single-center, retrospective cohort study, female sex was not associated with incident HF in adult patients treated with anthracyclines. CONDENSED ABSTRACT: Female sex is frequently cited as a risk factor for anthracycline cardiotoxicity based on pediatric data, but the role of sex in the development of cardiotoxicity has not been clearly established in adults. In this retrospective cohort study, we assessed the effect of female sex on the development of incident heart failure in adult patients treated with anthracyclines. Using Cox proportional hazards and competing risk regression models, we found that there was no association between female sex and heart failure after treatment with anthracyclines.
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Full text: 1 Database: MEDLINE Language: En Journal: J Card Fail Journal subject: CARDIOLOGIA Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Language: En Journal: J Card Fail Journal subject: CARDIOLOGIA Year: 2023 Type: Article