Serum Metabolites Are Associated With HFpEF in Biopsy‐Proven Nonalcoholic Fatty Liver Disease

Author:

Wegermann Kara1ORCID,Fudim Marat2ORCID,Henao Ricardo3ORCID,Howe Catherine F.4ORCID,McGarrah Robert2ORCID,Guy Cynthia5,Abdelmalek Manal F.6ORCID,Diehl Anna Mae1,Moylan Cynthia A.17ORCID

Affiliation:

1. Division of Gastroenterology, Department of Medicine Duke University Health System Durham NC

2. Division of Cardiology, Department of Medicine Duke University Health System Durham NC

3. Department of Biostatistics and Bioinformatics Duke University Durham NC

4. Division of Gastroenterology Mercy Hospital St. Louis MO

5. Department of Pathology Duke University Hospital Durham NC

6. Division of Gastroenterology and Hepatology, Department of Medicine, Mayo Clinic Rochester MN

7. Department of Medicine, Durham Veterans Affairs Medical Center Durham NC

Abstract

Background Nonalcoholic fatty liver disease (NAFLD) and heart failure with preserved ejection fraction (HFpEF) share common risk factors, including obesity and diabetes. They are also thought to be mechanistically linked. The aim of this study was to define serum metabolites associated with HFpEF in a cohort of patients with biopsy‐proven NAFLD to identify common mechanisms. Methods and Results We performed a retrospective, single‐center study of 89 adult patients with biopsy‐proven NAFLD who had transthoracic echocardiography performed for any indication. Metabolomic analysis was performed on serum using ultrahigh performance liquid and gas chromatography/tandem mass spectrometry. HFpEF was defined as ejection fraction >50% plus at least 1 echocardiographic feature of HFpEF (diastolic dysfunction, abnormal left atrial size) and at least 1 heart failure sign or symptom. We performed generalized linear models to evaluate associations between individual metabolites, NAFLD, and HFpEF. Thirty‐seven out of 89 (41.6%) patients met criteria for HFpEF. A total of 1151 metabolites were detected; 656 were analyzed after exclusion of unnamed metabolites and those with >30% missing values. Fifty‐three metabolites were associated with the presence of HFpEF with unadjusted P value <0.05; none met statistical significance after adjustment for multiple comparisons. The majority (39/53, 73.6%) were lipid metabolites, and levels were generally increased. Two cysteine metabolites (cysteine s‐sulfate and s‐methylcysteine) were present at significantly lower levels in patients with HFpEF. Conclusions We identified serum metabolites associated with HFpEF in patients with biopsy‐proven NAFLD, with increased levels of multiple lipid metabolites. Lipid metabolism could be an important pathway linking HFpEF to NAFLD.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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