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Cardiovascular Drugs and Therapy

, Volume 29, Issue 4, pp 377–390 | Cite as

Heart Failure in Women – Insights from the Framingham Heart Study

  • Satish KenchaiahEmail author
  • Ramachandran S. Vasan
REVIEW ARTICLE

Abstract

In the latter half of the 20th century, among participants of the Framingham Heart Study, incidence of heart failure (HF) has declined by about a third in women but not in men and survival after the onset of HF has improved in both sexes; however, HF remains highly lethal with over 50 % dying within 5 years after onset of HF. Overall, the 8-year relative risk of HF is 24 % lower in women compared with men. The 8-year incidence rates of HF with preserved ejection fraction (HFPEF; EF >45 %) and HF with reduced EF (HFREF; EF ≤45 %) in women and HFPEF in men are similar; however, men have a 2-fold higher cumulative incidence of HFREF than HFPEF. The lifetime risk of HF is about 20 % in both women and men at 40, 50, 60, 70, and 80 years of age. Contribution of hypertension and diabetes mellitus to the risk of HF was more prominent in women than in men. Serum levels of several biomarkers were distinctly different in women compared with men and had differential effects on left ventricular structure and function; however, the strength and direction of the association between biomarkers levels and HF risk were generally similar in women and men. In individuals with HF, about two-thirds of the underlying cause of death and about one-half of the immediate cause of death were due to cardiovascular causes. Non-cardiovascular underlying and immediate causes of death were more evident in HFPEF.

Keywords

Biomarkers Epidemiology Framingham heart study Gender Heart failure Incidence Men Mortality Risk factors Sex-differences Survival Women 

Notes

Acknowledgments

Dr. Kenchaiah was partly supported by the Translational Research Institute (TRI), grants UL1TR000039 and KL2TR000063 through the National Institutes of Health (NIH) National Center for Research Resources and the National Center for Advancing Translational Sciences. This work was also partly supported by grant No. N01-HC-25195 (Dr. Vasan) from the National Heart, Lung, and Blood Institute, Bethesda, Maryland. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH.

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Copyright information

© Springer Science+Business Media New York 2015

Authors and Affiliations

  1. 1.Division of Cardiovascular Medicine, Department of Internal MedicineUniversity of Arkansas for Medical SciencesLittle RockUSA
  2. 2.Framingham Heart StudyFraminghamUSA
  3. 3.National Heart, Lung, and Blood InstituteBethesdaUSA
  4. 4.Sections of Preventive Medicine and Epidemiology, and Cardiology, Department of MedicineBoston University School of MedicineBostonUSA

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