Clinical Phenotypes of Heart Failure across the spectrum of Ejection Fraction: A Cluster Analysis

被引:2
|
作者
Gouda, Pishoy [1 ,2 ]
Alemayehu, Wendimagegn [1 ]
Rathwell, Sarah [1 ]
Paterson, D. Ian [2 ]
Anderson, Todd [3 ]
Dyck, Jason R. B. [4 ]
Howlett, Jonathan G. [3 ]
Oudit, Gavin Y. [2 ]
McAlister, Finlay A. [1 ]
Thompson, Richard B. [5 ]
Ezekowitz, Justin [1 ,2 ]
Alberta HEART Study Investigators
机构
[1] Univ Alberta, Canadian VIGOUR Ctr, Edmonton, AB, Canada
[2] Univ Alberta, Div Cardiol, Edmonton, AB, Canada
[3] Univ Calgary, Libin Cardiovasc Inst, Cumming Sch Med, Calgary, AB, Canada
[4] Univ Alberta, Fac Med, Cardiovasc Res Ctr, Dept Pediat, Edmonton, AB, Canada
[5] Univ Alberta, Dept Biomed Engn, Edmonton, AB, Canada
关键词
D O I
10.1016/j.cpcardiol.2022.101337
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Heart failure (HF), and especially HF with preserved ejection fraction (HFpEF), remains a challenging condition to define. The heterogenous nature of this population may be related to a variety of underlying etiologies interacting myocardial dysfunction. Method: Alberta HEART study was a prospective, observational cohort that enrolled participants along the spectrum of heart failure including: healthy controls, people at risk of HF, and patients with HF and preserved (HFpEF) or reduced ejection fraction (HFrEF). We aimed to explore phenotypes of patients with HF and at-risk of developing HF. Utilising 27 detailed clinical, echocardiographic and bio-marker variables, latent class analysis with and without multiple imputation was undertaken to identify distinct clinical phenotypes. Results: Of 621 participants, 191 (30.8%) and 169 (27.2%) were adjudicated by cardiologists to have HFpEF and HFrEF respectively. In the overall cohort, latent class analysis identified four distinct phenotypes. Phenotype A (n=152, 24.5%) was a healthy and low risk group. Phenotype B (n=129, 20.8%) demonstrated increased left ventricular mass and end-diastolic volumes, with elevated natriuretic peptides and clinical features of congestion. Phenotype C (n=128, 20.6%) was primarily characterised by obesity (80%) and normal indexed cardiac chamber sizes, low natriuretic peptide levels and mini-mal features of congestion. Phenotype D (n=212, 34.1%) consisted of elderly patients with clinical features of congestions. Phenotypes B and D demonstrated the highest risk of mortality and hospitalization over a median follow-up of 3.7 years. Conclusion: Phenotypes with congestive features demonstrated increased risk profiles. Heart failure is a heterogenous classification which requires further work to appropriately categorise patients based on the underlying etiology or mechanism of impairment.
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页数:20
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