Clinical phenogroup diversity and multiplicity: impact on mechanisms of exercise intolerance in heart failure with preserved ejection fraction

被引:3
|
作者
Larson, Kathryn [1 ]
Omar, Massar [1 ,2 ,3 ]
Sorimachi, Hidemi [1 ,4 ]
Omote, Kazunori [1 ]
Alogna, Alessio [1 ,5 ,6 ]
Popovic, Dejana [1 ]
Tada, Atsushi [1 ]
Doi, Shunichi [1 ]
Naser, Jwan [1 ]
Reddy, Yogesh N. V. [1 ]
Redfield, Margaret M. [1 ]
Borlaug, Barry A. [1 ,7 ]
机构
[1] Mayo Clin, Dept Cardiovasc Med, Rochester, MN USA
[2] Odense Univ Hosp, Dept Cardiol, Odense, Denmark
[3] Odense Univ Hosp, Steno Diabet Ctr, Odense, Denmark
[4] Gunma Univ, Dept Cardiovasc Med, Grad Sch Med, Maebashi, Japan
[5] Deutsch Herzzentrum Charite, Dept Cardiol Angiol & Intens Care Med, Campus Virchow Klinikum, Berlin, Germany
[6] German Ctr Cardiovasc Res DZHK, Partner Site Berlin, Berlin, Germany
[7] Mayo Clin & Mayo Fdn, 200 First St SW, Rochester, MN 55905 USA
关键词
Exercise capacity; Heart failure; HFpEF; Outcome; Phenotype; OBESE PHENOTYPE; DETERMINANTS;
D O I
10.1002/ejhf.3105
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aims We aimed to clarify the extent to which cardiac and peripheral impairments to oxygen delivery and utilization contribute to exercise intolerance and risk for adverse events, and how this relates to diversity and multiplicity in pathophysiologic traits. Methods and results Individuals with heart failure with preserved ejection fraction (HFpEF) and non-cardiac dyspnoea (controls) underwent invasive cardiopulmonary exercise testing and clinical follow-up. Haemodynamics and oxygen transport responses were compared. HFpEF patients were then categorized a priori into previously-proposed, non-exclusive descriptive clinical trait phenogroups, including cardiometabolic, pulmonary vascular disease, left atrial myopathy, and vascular stiffening phenogroups based on clinical and haemodynamic profiles to contrast pathophysiology and clinical risk. Overall, patients with HFpEF (n = 643) had impaired cardiac output reserve with exercise (2.3 vs. 2.8 L/min, p = 0.025) and greater reliance on peripheral oxygen extraction augmentation (4.5 vs. 3.8 ml/dl, p < 0.001) compared to dyspnoeic controls (n = 219). Most (94%) patients with HFpEF met criteria for at least one clinical phenogroup, and 67% fulfilled criteria for multiple overlapping phenogroups. There was greater impairment in peripheral limitations in the cardiometabolic group and greater cardiac output limitations and higher pulmonary vascular resistance during exertion in the other phenogroups. Increasing trait multiplicity within a given patient was associated with worse exercise haemodynamics, poorer exercise capacity, lower cardiac output reserve, and greater risk for heart failure hospitalization or death (hazard ratio 1.74, 95% confidence interval 1.08-2.79 for 0-1 vs. >= 2 phenogroup traits present). Conclusions Though cardiac output response to exercise is limited in patients with HFpEF compared to those with non-cardiac dyspnoea, the relative contributions of cardiac and peripheral limitations vary with differing numbers and types of clinical phenotypic traits present. Patients fulfilling criteria for greater multiplicity and diversity of HFpEF phenogroup traits have poorer exercise capacity, worsening haemodynamic perturbations, and greater risk for adverse outcome. [GRAPHICS] .
引用
收藏
页码:564 / 577
页数:14
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