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Circulating Fibroblast Growth Factor 21 is Associated with Diastolic Dysfunction in Heart Failure Patients with
Ruey-Hsing Chou1,2,3, Po-Hsun Huang1,2,3, Chien-Yi Hsu2,3,4,5
1Division of Cardiology, Department of Medicine Taipei Veterans General Hospital, Taipei, 11217, Taiwan.
Insights
Fibroblast growth factor 21 (FGF21) is linked to diastolic heart failure. Higher FGF21 levels predict adverse cardiac events, suggesting its role in the condition's development.
Area of Science:
- Cardiology
- Endocrinology
- Biochemistry
Background:
- Fibroblast growth factor 21 (FGF21) is known to regulate glucose and lipid metabolism.
- Previous research indicated FGF21 can reduce cardiac hypertrophy.
- The role of FGF21 in diastolic heart failure remained unclear.
Purpose of the Study:
- To investigate the association between FGF21 and diastolic heart failure.
- To determine if FGF21 levels can predict adverse cardiac events in patients with diastolic dysfunction.
Main Methods:
- Plasma FGF21 and NT-pro-BNP levels were measured in 95 patients with diastolic dysfunction and 143 controls.
- Echocardiography assessed left ventricular (LV) function and diastolic parameters.
- Patients were followed for 1 year for cardiac readmission or death.
Main Results:
- Circulating FGF21 levels correlated with echocardiographic measures of diastolic function and LV end-diastolic pressure.
- FGF21 was significantly associated with diastolic dysfunction.
- Both FGF21 and NT-pro-BNP levels predicted 1-year adverse cardiac events.
Conclusions:
- FGF21 may play a role in the pathophysiology of diastolic heart failure.
- Plasma FGF21 levels are a potential biomarker for diastolic dysfunction and adverse cardiac outcomes.
Abstract:
Fibroblast growth factor 21 (FGF21), a polypeptide ligand promoted glucose homeostasis and lipids metabolism, was recently reported to attenuate cardiac hypertrophy. The aim of this study was to investigate the impact of FGF21 in diastolic heart failure. Subjects admitted for coronary angiogram were screened for heart failure, and those with left ventricular (LV) ejection fraction < 45% were excluded. Diastolic dysfunction was defined as functional abnormalities that exist during LV relaxation and filling by echocardiographic criteria. Plasma levels of FGF21 and N-terminal Pro-Brain Natriuretic Peptide (NT-pro-BNP) were determined. All patients were followed up for 1 year, or till the occurrence of heart failure readmission or death. Totally 95 patients with diastolic dysfunction and 143 controls were enrolled. Circulating FGF21 level was correlated with echocardiographic parameters of diastolic function and LV end-diastolic pressure (LVEDP). In multivariate logistic analysis, FGF21 was significantly associated with diastolic dysfunction, either identified by echocardiographic criteria (odds ratio: 2.97, p = 0.012) or confirmed with LVEDP level (odds ratio: 3.73, p = 0.030). Both plasma FGF21 (log rank p < 0.0001) and NT-pro-BNP levels (log rank p = 0.0057) showed good predictive power to the 1-year adverse cardiac events. This finding suggested FGF21 could be involved in the pathophysiology of diastolic heart failure.
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