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

被引:3
|
作者
Wegermann, Kara [1 ]
Fudim, Marat [2 ]
Henao, Ricardo [3 ]
Howe, Catherine F. [4 ]
McGarrah, Robert [2 ]
Guy, Cynthia [5 ]
Abdelmalek, Manal F. [6 ]
Diehl, Anna Mae [1 ]
Moylan, Cynthia A. [1 ,7 ,8 ,9 ]
机构
[1] Duke Univ Hlth Syst, Dept Med, Div Gastroenterol, Durham, NC USA
[2] Duke Univ Hlth Syst, Dept Med, Div Cardiol, Durham, NC USA
[3] Duke Univ, Dept Biostat & Bioinformat, Durham, NC 27710 USA
[4] Mercy Hosp, Div Gastroenterol, St Louis, MO USA
[5] Duke Univ Hosp, Dept Pathol, Durham, NC USA
[6] Mayo Clin, Dept Med, Div Gastroenterol & Hepatol, Rochester, MN USA
[7] Durham Vet Affairs Med Ctr, Dept Med, Durham, NC USA
[8] Duke Univ, DUMC 3256 Snyderman Bldg GSRB1,905 South LaSalle S, Durham, NC 27710 USA
[9] Durham VA Med Ctr, DUMC 3256 Snyderman Bldg GSRB1,905 South LaSalle S, Durham, NC 27710 USA
来源
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2023年 / 12卷 / 14期
基金
美国国家卫生研究院;
关键词
heart failure; metabolic syndrome; metabolomics; nonalcoholic fatty liver disease; AMINO-ACID RESTRICTION; CARDIOVASCULAR-DISEASE; HEART-FAILURE; SEVERITY; STEATOHEPATITIS; EPIDEMIOLOGY; DYSFUNCTION; CARDIOLOGY; DISCOVERY; OXIDATION;
D O I
10.1161/JAHA.123.029873
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BackgroundNonalcoholic 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 ResultsWe 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. ConclusionsWe 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.
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页数:83
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