Metabolomic Profile in HFpEF vs HFrEF Patients

医学 内科学 心脏病学 糖尿病 射血分数 射血分数保留的心力衰竭 心力衰竭 纤维化 氧化应激 内分泌学 内皮功能障碍 炎症
作者
Camilla Hage,Lars Löfgren,Filippos Michopoulos,Ralf Nilsson,Pia Davidsson,Chanchal Kumar,Mattias Ekström,Maria Eriksson,Patrik Lyngå,Bengt Persson,Häkan Wallén,Li Gan,Hans Persson,Cecilia Linde
出处
期刊:Journal of Cardiac Failure [Elsevier]
卷期号:26 (12): 1050-1059 被引量:45
标识
DOI:10.1016/j.cardfail.2020.07.010
摘要

Background Heart failure with preserved ejection fraction (HFpEF) and HF with reduced ejection fraction (HFrEF) are associated with metabolic derangements, which may have different pathophysiological implications. Methods and Results In new-onset HFpEF (EF of ≥50%, n = 46) and HFrEF (EF of <40%, n = 75) patients, 109 endogenous plasma metabolites including amino acids, phospholipids and acylcarnitines were assessed using targeted metabolomics. Differentially altered metabolites and associations with clinical characteristics were explored. Patients with HFpEF were older, more often female with hypertension, atrial fibrillation, and diabetes compared with patients with HFrEF. Patients with HFpEF displayed higher levels of hydroxyproline and symmetric dimethyl arginine, alanine, cystine, and kynurenine reflecting fibrosis, inflammation and oxidative stress. Serine, cGMP, cAMP, l-carnitine, lysophophatidylcholine (18:2), lactate, and arginine were lower compared with patients with HFrEF. In patients with HFpEF with diabetes, kynurenine was higher (P = .014) and arginine lower (P = .014) vs patients with no diabetes, but did not differ with diabetes status in HFrEF. Decreasing kynurenine was associated with higher eGFR only in HFpEF (Pinteraction = .020). Conclusions Patients with new-onset HFpEF compared with patients with new-onset HFrEF display a different metabolic profile associated with comorbidities, such as diabetes and kidney dysfunction. HFpEF is associated with indices of increased inflammation and oxidative stress, impaired lipid metabolism, increased collagen synthesis, and downregulated nitric oxide signaling. Together, these findings suggest a more predominant systemic microvascular endothelial dysfunction and inflammation linked to increased fibrosis in HFpEF compared with HFrEF. Clinical Trial Registration: ClinicalTrials.gov NCT03671122 https://clinicaltrials.gov
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