4.5 Article

Aetiological classification and prognosis in patients with heart failure with preserved ejection fraction

Journal

ESC HEART FAILURE
Volume 9, Issue 1, Pages 519-530

Publisher

WILEY PERIODICALS, INC
DOI: 10.1002/ehf2.13717

Keywords

Heart failure with preserved ejection faction; Prognosis; Classification; Aetiologies

Funding

  1. Assistance Publique - Hopitaux de Paris (AP-HP)
  2. French Investments for the Future Programme (PIA) Project (PACIFIC-PRESERVED, BPIfrance) [2018-PSPC-07]
  3. University Research Federation against Heart Failure (FHU2019, PREVENT_Heart Failure)

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This study classified HFpEF patients into secondary and idiopathic groups based on etiology, revealing differences in prognosis and mortality rates between the two groups. Unsupervised clustering analysis identified three phenogroups, with the one having the highest proportion of idiopathic HFpEF showing a better prognosis and higher prevalence of non-cardiac co-morbidities such as chronic obstructive pulmonary disease and obesity compared to the groups enriched with secondary HFpEF.
Aims Heart failure with preserved ejection fraction (HFpEF) is a heterogeneous syndrome with various causes that may influence prognosis. Methods and results We extracted the electronic medical records for 2180 consecutive patients hospitalized between 2016 and 2019 for decompensated heart failure. Using a text mining algorithm looking for a left ventricular ejection fraction >= 50% and plasma brain natriuretic peptide level >100 pg/mL, we identified 928 HFpEF patients. We screened for a prevailing cause of HFpEF according to European guidelines and found that 418 (45.0%) patients had secondary HFpEF due to either myocardial (n = 125, 13.5%) or loading condition abnormalities (n = 293, 31.5%), while the remaining 510 (55.0%) patients had idiopathic HFpEF. We assessed the association between the causes of HFpEF and survival collected up to 31 December 2020 using Cox proportional hazards analysis. Even though patients with idiopathic HFpEF were older, frequently female, and had frequent co-morbidities and a higher crude mortality rate compared with secondary HFpEF patients, their prognosis was similar after adjustment for age and sex. Unsupervised clustering analysis revealed three main phenogroups with different distribution of idiopathic vs. secondary HFpEF. The phenogroup with the highest proportion of idiopathic HFpEF (69%) had (i) an excess rate of non-cardiac co-morbidities including chronic obstructive pulmonary disease (31%) or obesity (41%) and (ii) a better prognosis compared with the two other phenogroups enriched with secondary HFpEF. Conclusions Aetiological classification provides clinical and prognostic information and may be useful to better decipher the clinical heterogeneity of HFpEF.

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