Allostatic Load/Chronic Stress and Cardiovascular Outcomes in Patients Diagnosed With Breast, Lung, or Colorectal Cancer.

allostatic load breast cancer cardiovascular disease colorectal cancer lung cancer stress

Journal

Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524

Informations de publication

Date de publication:
09 Jul 2024
Historique:
medline: 9 7 2024
pubmed: 9 7 2024
entrez: 9 7 2024
Statut: aheadofprint

Résumé

Cardiovascular disease and cancer share a common risk factor: chronic stress/allostatic load (AL). A 1-point increase in AL is linked to up to a 30% higher risk of major cardiac events (MACE) in patients with prostate cancer. However, AL's role in MACE in breast cancer, lung cancer, or colorectal cancer remains unknown. Patients ≥18 years of age diagnosed with the mentioned 3 cancers of interest (2010-2019) and followed up at a large, hybrid academic-community practice were included in this retrospective cohort study. AL was modeled as an ordinal measure (0-11). Adjusted Fine-Gray competing risks regressions estimated the impact of AL precancer diagnosis on 2-year MACE (a composite of heart failure, ischemic stroke, acute coronary syndrome, and atrial fibrillation). The effect of AL changes over time on MACE was calculated via piecewise Cox regression (before, and 2 months, 6 months, and 1 year after cancer diagnosis). Among 16 467 patients, 50.5% had breast cancer, 27.9% had lung cancer, and 21.4% had colorectal cancer. A 1-point elevation in AL before breast cancer diagnosis corresponded to a 10% heightened associated risk of MACE (adjusted hazard ratio, 1.10 [95% CI, 1.06-1.13]). Similar findings were noted in lung cancer (adjusted hazard ratio, 1.16 [95% CI, 1.12-1.20]) and colorectal cancer (adjusted hazard ratio, 1.13 [95% CI, 1.08-1.19]). When considering AL as a time-varying exposure, the peak associated MACE risk occurred with a 1-point AL rise between 6 and 12 months post- breast cancer, lung cancer, and colorectal cancer diagnosis. AL warrants investigation as a potential marker in these patients to identify those at elevated cardiovascular risk and intervene accordingly.

Sections du résumé

BACKGROUND BACKGROUND
Cardiovascular disease and cancer share a common risk factor: chronic stress/allostatic load (AL). A 1-point increase in AL is linked to up to a 30% higher risk of major cardiac events (MACE) in patients with prostate cancer. However, AL's role in MACE in breast cancer, lung cancer, or colorectal cancer remains unknown.
METHODS AND RESULTS RESULTS
Patients ≥18 years of age diagnosed with the mentioned 3 cancers of interest (2010-2019) and followed up at a large, hybrid academic-community practice were included in this retrospective cohort study. AL was modeled as an ordinal measure (0-11). Adjusted Fine-Gray competing risks regressions estimated the impact of AL precancer diagnosis on 2-year MACE (a composite of heart failure, ischemic stroke, acute coronary syndrome, and atrial fibrillation). The effect of AL changes over time on MACE was calculated via piecewise Cox regression (before, and 2 months, 6 months, and 1 year after cancer diagnosis). Among 16 467 patients, 50.5% had breast cancer, 27.9% had lung cancer, and 21.4% had colorectal cancer. A 1-point elevation in AL before breast cancer diagnosis corresponded to a 10% heightened associated risk of MACE (adjusted hazard ratio, 1.10 [95% CI, 1.06-1.13]). Similar findings were noted in lung cancer (adjusted hazard ratio, 1.16 [95% CI, 1.12-1.20]) and colorectal cancer (adjusted hazard ratio, 1.13 [95% CI, 1.08-1.19]). When considering AL as a time-varying exposure, the peak associated MACE risk occurred with a 1-point AL rise between 6 and 12 months post- breast cancer, lung cancer, and colorectal cancer diagnosis.
CONCLUSIONS CONCLUSIONS
AL warrants investigation as a potential marker in these patients to identify those at elevated cardiovascular risk and intervene accordingly.

Identifiants

pubmed: 38979791
doi: 10.1161/JAHA.123.033295
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e033295

Auteurs

Nickolas Stabellini (N)

Case Western Reserve University School of Medicine, Case Western Reserve University Cleveland OH USA.
Department of Hematology-Oncology University Hospitals Seidman Cancer Center Cleveland OH USA.
Faculdade Israelita de Ciências da Saúde Albert Einstein Hospital Israelita Albert Einstein São Paulo SP Brazil.
Department of Medicine Medical College of Georgia at Augusta University Augusta GA USA.

Jennifer Cullen (J)

Case Western Reserve University School of Medicine, Case Western Reserve University Cleveland OH USA.
Case Comprehensive Cancer Center Case Western Reserve University Cleveland OH USA.

Marcio S Bittencourt (MS)

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

Justin X Moore (JX)

Center for Health Equity Transformation, Department of Behavioral Science, Department of Internal Medicine, Markey Cancer Center University of Kentucky College of Medicine Lexington KY USA.

Arnethea Sutton (A)

Department of Kinesiology and Health Sciences College of Humanities and Sciences, Virginia Commonwealth University Richmond VA USA.

Priyanshu Nain (P)

Department of Medicine Medical College of Georgia at Augusta University Augusta GA USA.

Nelson Hamerschlak (N)

Oncohematology Department Hospital Israelita Albert Einstein São Paulo SP Brazil.

Neal L Weintraub (NL)

Department of Medicine Medical College of Georgia at Augusta University Augusta GA USA.
Vascular Biology Center Medical College of Georgia at Augusta University Augusta GA USA.

Susan Dent (S)

Duke Cancer Institute, Department of Medicine Duke University Durham NC USA.

Meng-Han Tsai (MH)

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

Amitava Banerjee (A)

Institute of Health Informatics, University College London London UK.

Arjun K Ghosh (AK)

Cardio-Oncology Service Hatter Cardiovascular Institute, University College London Hospital London UK.

Diego Sadler (D)

Department of Cardiovascular Medicine Cleveland Clinic Florida Weston FL USA.

Steven S Coughlin (SS)

Department of Medicine Medical College of Georgia at Augusta University Augusta GA USA.
Department of Population Health Sciences Medical College of Georgia at Augusta University Augusta GA USA.

Ana Barac (A)

Cardio-Oncology Program Inova Schar Cancer Institute, Inova Heart and Vascular Institute Fairfax VA USA.

John Shanahan (J)

Cancer Informatics Seidman Cancer Center at University Hospitals Cleveland OH USA.

Alberto J Montero (AJ)

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

Avirup Guha (A)

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

Classifications MeSH