4.5 Article

Diastolic dysfunction in individuals with and without heart failure with preserved ejection fraction

期刊

CLINICAL RESEARCH IN CARDIOLOGY
卷 111, 期 4, 页码 416-427

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00392-021-01907-x

关键词

Diastolic dysfunction; ALVDD; HFpEF; Heart failure; Hamburg city health study; General population

资金

  1. Projekt DEAL
  2. Innovative medicine initiative [116074]
  3. Foundation Leducq [16 CVD 03]
  4. euCanSHare grant [825903-euCanSHare H2020]
  5. Deutsche Forschungsgemeinschaft [TH1106/5-1, AA93/2-1]
  6. University Medical Centre Hamburg-Eppendorf
  7. Bayer
  8. Amgen
  9. Astra Zeneca
  10. BASF
  11. Deutsche Gesetzliche Unfallversicherung (DGUV)
  12. Deutsches Krebsforschungszentrum (DKFZ)
  13. Deutsches Zentrum fur Herz-KreislaufForschung (DZHK)
  14. Deutsche Stiftung fur Herzforschung
  15. Novartis
  16. Seefried Stiftung
  17. Unilever

向作者/读者索取更多资源

The study evaluated the prevalence and correlates of left ventricular diastolic dysfunction (DD) in a middle-aged sample of the general population. The results showed that DD without HFpEF (ALVDD) was associated with hypertension and HbA1c, while DD with HFpEF (DDwHFpEF) was associated with factors like female sex, atrial fibrillation, and coronary artery disease.
Aim Left ventricular diastolic dysfunction (DD), a common finding in the general population, is considered to be associated with heart failure with preserved ejection faction (HFpEF). Here we evaluate the prevalence and correlates of DD in subjects with and without HFpEF in a middle-aged sample of the general population. Methods and results From the first 10,000 participants of the population-based Hamburg City Health Study (HCHS), 5913 subjects (mean age 64.4 +/- 8.3 years, 51.3% females), qualified for the current analysis. Diastolic dysfunction (DD) was identified in 753 (12.7%) participants. Of those, 11.2% showed DD without HFpEF (ALVDD) while 1.3% suffered from DD with HFpEF (DDwHFpEF). In multivariable regression analysis adjusted for major cardiovascular risk factors, ALVDD was associated with arterial hypertension (OR 2.0, p < 0.001) and HbA1c (OR 1.2, p = 0.007). Associations of both ALVDD and DDwHFpEF were: age (OR 1.7, p < 0.001; OR 2.7, p < 0.001), BMI (OR 1.2, p < 0.001; OR 1.6, p = 0.001), and left ventricular mass index (LVMI). In contrast, female sex (OR 2.5, p = 0.006), atrial fibrillation (OR 2.6, p = 0.024), CAD (OR 7.2, p < 0.001) COPD (OR 3.9, p < 0.001), and QRS duration (OR 1.4, p = 0.005) were strongly associated with DDwHFpEF but not with ALVDD. Conclusion The prevalence of DD in a sample from the first 10,000 participants of the population-based HCHS was 12.7% of whom 1.3% suffered from HFpEF. DD with and without HFpEF showed significant associations with different major cardiovascular risk factors and comorbidities warranting further research for their possible role in the formation of both ALVDD and DDwHFpEF.

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