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Published on: June 10, 2025
Phenylacetylglutamine as a risk factor and prognostic indicator of heart failure
Xiao Zong1,2, Qin Fan1, Qian Yang1,2
1Department of Cardiovascular Medicine, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
Insights
Serum phenylacetylglutamine (PAGln) is elevated in chronic heart failure (HF) patients and indicates a higher risk of cardiovascular death and renal dysfunction. PAGln serves as a valuable biomarker for HF.
Area of Science:
- Biochemistry
- Cardiology
- Nephrology
Background:
- Heart failure (HF) is a complex clinical syndrome with significant morbidity and mortality.
- Identifying novel biomarkers for HF risk stratification and management is crucial.
Purpose of the Study:
- To investigate the association between serum phenylacetylglutamine (PAGln) and chronic heart failure (HF).
- To evaluate PAGln as a potential indicator of HF risk, renal dysfunction, and cardiovascular mortality.
Main Methods:
- Serum PAGln levels were measured in 956 subjects using liquid chromatography-tandem mass spectrometry.
- Correlation and regression analyses assessed the association between PAGln, HF, and renal indicators.
- Kaplan-Meier curves and Cox proportional hazards analysis evaluated the prognostic value of PAGln in HF patients.
Main Results:
- Serum PAGln levels were significantly higher in chronic HF patients compared to controls (3.322 ± 8.220 μM vs. 1.249 ± 1.168 μM, P < 0.001).
- Elevated PAGln was independently associated with HF risk (OR, 1.507; P < 0.001) and renal dysfunction (OR, 1.853; P < 0.001).
- High PAGln levels predicted increased risk of cardiovascular death in HF patients (HR, 2.049; P = 0.038).
Conclusions:
- Elevated serum PAGln is an independent risk factor for chronic heart failure.
- High PAGln levels are associated with increased risk of cardiovascular death and may indicate renal dysfunction in HF patients.
- PAGln shows potential as a valuable biomarker for HF assessment and prognosis.
Aims:
To explore the associations between serum phenylacetylglutamine (PAGln) and chronic heart failure (HF).
Methods And Results:
Totally 956 subjects were enrolled consecutively from the Department of Cardiovascular Medicine, Ruijin Hospital. Baseline data were obtained from all participants, and 471 stable chronic HF subjects were followed up. Serum PAGln was analysed by liquid chromatography-tandem mass spectrometry. The association between PAGln and basic renal indicators was assessed by simple correlation analysis. Logistic regression analysis was conducted to measure the association between PAGln and HF risk. Event-free survival was determined by Kaplan-Meier curves, and differences in survival were assessed using log-rank tests. Cox proportional hazards analysis was used to assess the prognostic value of PAGln in HF. Serum PAGln levels were increased in patients with chronic HF (3.322 ± 8.220 μM vs. 1.249 ± 1.168 μM, P < 0.001) and were associated with HF after full adjustment [odds ratio (OR), 1.507; 95% confidence interval (CI): 1.213-1.873; P < 0.001]. PAGln levels were correlated with the levels of basic renal indicators. High PAGln levels indicated a high risk of renal dysfunction in HF (OR: 1.853; 95% CI: 1.344-2.556; P < 0.001), and elevated PAGln levels were associated with a high risk of cardiovascular death in patients with chronic HF (HR: 2.049; 95% CI: 1.042-4.029; P = 0.038).
Conclusions:
Elevated PAGln levels are an independent risk factor for HF and are associated with a higher risk of cardiovascular death. High PAGln levels could indicate renal dysfunction in HF patients. PAGln can be a valuable indicator of HF.
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