Allostatic load and cardiovascular outcomes in males with prostate cancer

Author:

Stabellini Nickolas1234ORCID,Cullen Jennifer45,Bittencourt Marcio S6,Moore Justin X7,Cao Lifen2,Weintraub Neal L89,Harris Ryan A1011,Wang Xiaoling12,Datta Biplab1314ORCID,Coughlin Steven S1314,Garcia Jorge2,Shanahan John15,Hamerschlak Nelson16,Waite Kristin17,Fillmore Nathanael R1819,Terris Martha2021,Montero Alberto J2,Barnholtz-Sloan Jill S1722,Guha Avirup232425ORCID

Affiliation:

1. Graduate Education Office, Case Western Reserve University School of Medicine , Cleveland, OH, USA

2. Department of Hematology-Oncology, University Hospitals Seidman Cancer Center , Cleveland, OH, USA

3. Faculdade Israelita de Ciências da Saúde Albert Einstein, Hospital Israelita Albert Einstein , São Paulo, SP, Brazil

4. Department of Population and Quantitative Health Sciences, Case Western Reserve University School of Medicine , Cleveland, OH, USA

5. Case Western Reserve University Case Comprehensive Cancer Center, , Cleveland, OH, USA

6. Division of Cardiology, Department of Medicine, University of Pittsburgh , Pittsburgh, PA, USA

7. Cancer Prevention, Control, & Population Health Program, Department of Medicine, Medical College of Georgia at Augusta University , GA, USA

8. Department of Medicine, Cardiology Division, Medical College of Georgia at Augusta University , Augusta, GA, USA

9. Vascular Biology Center, Medical College of Georgia at Augusta University , Augusta, GA, USA

10. Department of Medicine, Georgia Prevention Institute, Augusta University , Augusta, GA, USA

11. Sport and Exercise Science Research Institute, Ulster University , Jordanstown, Northern Ireland, UK

12. Department of Medicine, Medical College of Georgia, Augusta University , Augusta, GA, USA

13. Department of Population Health Sciences, Medical College of Georgia, Augusta University , Augusta, GA, USA

14. Institute of Public and Preventive Health, Augusta University , Augusta, GA, USA

15. Cancer Informatics, Seidman Cancer Center at University Hospitals of Cleveland , Cleveland, OH, USA

16. Oncohematology Department, Hospital Israelita Albert Einstein , São Paulo, SP, Brazil

17. Trans-Divisional Research Program (TDRP), Division of Cancer Epidemiology and Genetics (DCEG), National Cancer Institute, National Institutes of Health , Bethesda, MD, USA

18. Cooperative Studies Program (CSP) Informatics Center, Massachusetts Veterans Epidemiology Research and Information Center (MAVERIC), VA Boston Healthcare System , Boston, MA, USA

19. Harvard Medical School , Boston, MA, USA

20. Urology Section, Department of Surgery, Veterans Affairs Medical Centers , Augusta, GA, USA

21. Division of Urologic Surgery, Department of Surgery, Medical College of Georgia , Augusta, GA, USA

22. Center for Biomedical Informatics and Information Technology (CBIIT), National Cancer Institute, National Institutes of Health , Bethesda, MD, USA

23. Department of Medicine, Case Western Reserve University School of Medicine , Cleveland, OH, USA

24. Cardio-Oncology Program, Ohio State University , OH, USA

25. Cardio-Oncology Program, Department of Medicine, Cardiology Division, Medical College of Georgia, Augusta University , Augusta, GA, USA

Abstract

AbstractBackgroundCardiovascular disease (CVD) is the leading cause of death in men with prostate cancer (PC). Accumulated stress plays an important role in CVD development. The cumulative burden of chronic stress and life events can be measured using allostatic load (AL).MethodsThe initial cohort included males aged 18 years and older diagnosed with PC (2005-2019). AL was modeled as an ordinal variable (0-11). Fine-Gray competing risk regressions measured the impact of precancer diagnosis AL and postdiagnosis AL in 2-year major cardiac events (MACE). The effect of AL changes over time on MACE development was calculated via piecewise Cox regression (before, and 2 months, 6 months, and 1 year after PC diagnosis).ResultsWe included 5261 PC patients of which 6.6% had a 2-year MACE. For every 1-point increase in AL before and within 60 days after PC diagnosis, the risk of MACE increased 25% (adjusted hazard ratio [aHR] =1.25, 95% confidence interval [CI] = 1.18 to 1.33) and 27% (aHR = 1.27, 95% CI = 1.20 to 1.35), respectively. Using AL as a time-varying exposure, the risk of MACE increased 19% (aHR = 1.19, 95% CI = 1.11 to 1.27), 22% (aHR = 1.22, 95% CI = 1.14 to 1.33), 28% (aHR = 1.28, 95% CI = 1.23 to 1.33), and 31% (aHR = 1.31, 95% CI = 1.27 to 1.35) for every 1-point increase in AL before, 2 months after, 6 months after, and 1 year after PC diagnosis, respectively.ConclusionAL and its changes over time are associated with MACE in PC patients, suggesting a role of a biological measure of stress as a marker of CVD risk among men with PC.

Funder

American Heart Association-Strategically Focused Research Network

Publisher

Oxford University Press (OUP)

Subject

Cancer Research,Oncology

Reference73 articles.

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