Adherence to cardiovascular medications and risk of cardiovascular disease in breast cancer patients: A causal inference approach in the Pathways Heart Study.


Journal

PloS one
ISSN: 1932-6203
Titre abrégé: PLoS One
Pays: United States
ID NLM: 101285081

Informations de publication

Date de publication:
2024
Historique:
received: 14 06 2024
accepted: 03 09 2024
medline: 20 9 2024
pubmed: 20 9 2024
entrez: 19 9 2024
Statut: epublish

Résumé

Women with breast cancer (BC) are at high risk of developing cardiovascular disease (CVD). We examined adherence to CVD medications and their association with major CVD events over 14 years of follow-up in the Pathways Heart Study, a prospective study of 4,776 stage I-III BC patients diagnosed from 2005-2013. Eligibility included being alive 6 months post-BC diagnosis, with dyslipidemia, hypertension, or diabetes at diagnosis along with ≥1 prior outpatient order or dispensing for a statin, anti-hypertensive, or diabetes medication, respectively, in the 30 months prior. Medication adherence was measured from pharmacy data to calculate cumulative average adherence (CAA). Incident heart failure (HF), ischemic heart disease (IHD), and stroke were determined via validated diagnosis and procedure codes. Working marginal structural models (MSM) fitted with inverse probability weighting evaluated the effect of adherence regimens on the hazards for each CVD event, while controlling for baseline and time-varying confounders. MSM parameterizations included: 1) CAA<100% versus CAA = 100% (ref), 2) CAA<80% versus CAA≥80% (ref) and 3) CAA<80% versus 80%≤CAA<100% versus CAA = 100%. Poor statin adherence (CAA<80%) was associated with higher risk of composite CVD (HR = 2.54; 95% CI: 1.09, 5.94) versus CAA≥80%. Poor statin adherence was also associated with a higher risk of stroke (HR = 8.13; 95% CI: 2.03, 32.51) but not risk of IHD and HF. Further, compared with perfect adherence (CAA = 100%), good adherence (80%≤CAA<100%) was associated with lower risk (HR = 0.35; 95% CI: 0.13, 0.92) while poor adherence (CAA<80%) was associated with higher risk of composite CVD (HR = 2.45; 95% CI: 1.05, 5.70). Levels of adherence to anti-hypertensives and diabetes medications had mixed or null associations with risk of CVD. Maintaining good adherence (≥80%) to statins after BC treatment is beneficial for cardiovascular health in patients with dyslipidemia. Future studies should determine factors associated with lower adherence to statins and ways to improve adherence.

Identifiants

pubmed: 39298390
doi: 10.1371/journal.pone.0310531
pii: PONE-D-24-22739
doi:

Substances chimiques

Cardiovascular Agents 0
Hydroxymethylglutaryl-CoA Reductase Inhibitors 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e0310531

Informations de copyright

Copyright: © 2024 Kwan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Déclaration de conflit d'intérêts

The authors have declared that no competing interests exist.

Auteurs

Marilyn L Kwan (ML)

Division of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.

Noel Pimentel (N)

Division of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.

Monika Izano (M)

Insights Epidemiology and Analytics, Syapse, San Francisco, California, United States of America.

Carlos Iribarren (C)

Division of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.

Jamal S Rana (JS)

Division of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.
Cardiology, Oakland Medical Center, Kaiser Permanente Northern California, Oakland, California, United States of America.

Mai Nguyen-Huynh (M)

Division of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.
Neurology, Walnut Creek Medical Center, Kaiser Permanente Northern California, Walnut Creek, California, United States of America.

Richard Cheng (R)

Division of Cardiology, University of Washington Medical Center, Seattle, Washington, United States of America.

Cecile A Laurent (CA)

Division of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.

Valerie S Lee (VS)

Division of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.

Janise M Roh (JM)

Division of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.

Eileen Rillamas-Sun (E)

Division of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.

Dawn L Hershman (DL)

Medical Oncology, Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, New York, United States of America.

Lawrence H Kushi (LH)

Division of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.

Heather Greenlee (H)

Division of Public Health Sciences, Fred Hutchinson Cancer Center, Seattle, Washington, United States of America.

Romain Neugebauer (R)

Division of Research, Kaiser Permanente Northern California, Pleasanton, California, United States of America.
Department of Health System Science, Kaiser Permanente Bernard J. Tyson School of Medicine, Pasadena, California, United States of America.

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Classifications MeSH