Risk factors for cardiac death in women with coronary artery disease

Ida S King1, M Anette Eskuri1, Lauri T Holmström1

  • 1Research Unit of Biomedicine and Internal Medicine, Medical Research Center Oulu, University of Oulu and Oulu University Hospital, PO Box 5000, Oulu 90014, Finland.

Insights

Cardiac death risk in women with coronary artery disease is linked to age, blood pressure, and post-procedure scores. Biomarkers like high-sensitivity troponin T and hemoglobin A1c, along with atrial fibrillation, also indicate higher risk.

Area of Science:

  • Cardiology
  • Women's Health
  • Biomarkers

Background:

  • Coronary artery disease (CAD) affects many women, often with different outcomes than men.
  • Identifying specific risk factors for cardiac death in women with CAD is crucial for targeted interventions.

Purpose of the Study:

  • To investigate potential markers associated with cardiac death in women diagnosed with coronary artery disease.
  • To enhance risk stratification strategies for female CAD patients.

Main Methods:

  • Analysis of the ARTEMIS cohort data (1946 patients, 619 women) with angiographically confirmed CAD.
  • 10-year follow-up to assess cardiac death as the primary endpoint.
  • Multivariate analysis examining traditional risk factors, echocardiographic, electrocardiographic, biomarker, and angiographical parameters.

Main Results:

  • Cardiac death occurred in 7.6% of women during follow-up.
  • Significant predictors of cardiac death included age, post-revascularization SYNTAX Score, systolic blood pressure, high-sensitivity troponin T, hemoglobin A1c, and permanent atrial fibrillation.

Conclusions:

  • Higher post-revascularization SYNTAX Score, age, systolic blood pressure, high-sensitivity troponin T, and hemoglobin A1c are associated with cardiac mortality in women with CAD.
  • Permanent atrial fibrillation may hold prognostic significance and warrants further research.
  • These identified markers can help refine risk stratification for women with coronary artery disease.
Abstract

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