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Downregulation of serum Foxc2 in dilated cardiomyopathy: association with disease severity and cardiac function
Yufu Cai1,2, Qionghui Huang2,3, Shaobin Zhi2,3
1The Fourth Department of Cardiovasular Diseases, Meizhou People's Hospital, Meizhou, Guangdong, P. R. China.
Insights
Serum Foxc2 levels are significantly lower in patients with dilated cardiomyopathy (DCM). Lower Foxc2 indicates poorer cardiac function and predicts a reduced risk of major adverse cardiovascular events (MACE).
Area of Science:
- Cardiology
- Biomarker Discovery
- Molecular Biology
Background:
- Dilated cardiomyopathy (DCM) is a leading cause of heart failure.
- The role of Foxc2 in DCM pathogenesis is not well understood.
- This study investigates Foxc2 as a potential biomarker in DCM.
Purpose of the Study:
- To compare serum Foxc2 levels between DCM and non-DCM patients.
- To assess the correlation of Foxc2 with cardiac function and biomarkers.
- To evaluate the diagnostic and prognostic value of Foxc2 in DCM.
Main Methods:
- Retrospective study of 92 patients (53 DCM, 39 non-DCM).
- Serum Foxc2 measured by ELISA.
- Correlations with echocardiographic parameters, BNP, cTnI; ROC and Kaplan-Meier analyses performed.
Main Results:
- Serum Foxc2 levels were significantly lower in DCM patients (35.33 vs. 77.51 μg/mL).
- Foxc2 correlated positively with LVEF/LVFS and negatively with LVEDd/BNP/cTnI.
- High diagnostic accuracy (AUC 0.862); lower Foxc2 predicted increased 2-year MACE risk.
Conclusions:
- Foxc2 shows potential as a diagnostic biomarker for DCM.
- Foxc2 may serve as a prognostic indicator for adverse cardiovascular events.
- Further research into Foxc2's mechanistic role in DCM is warranted.
Background:
Dilated cardiomyopathy (DCM) is one of the most frequent non-ischemic causes of heart failure. Foxc2 has been implicated in cardiovascular disease and angiogenesis, but its role in DCM remains undefined. This study aimed to compare serum Foxc2 levels in DCM and non-DCM patients and to assess its clinical relevance.
Methods:
In this retrospective study, 92 patients (53 DCM, 39 non-DCM) were enrolled. Based on echocardiographic and clinical evaluations, patients were classified into non-DCM group (n = 39) and DCM group (n = 53). Serum Foxc2 concentrations were measured via ELISA, and correlations were analyzed with echocardiographic parameters and biomarkers (BNP, cTnI). ROC analysis assessed Foxc2's diagnostic performance, and Kaplan-Meier analysis evaluated 2-year MACE risk.
Results:
Serum Foxc2 levels were significantly lower in the DCM group (35.33 ± 27.99 μg/mL vs. 77.51 ± 28.94 μg/mL), and correlated with cardiac function (positive: LVEF, LVFS; negative: LVEDd, BNP, cTnI). ROC analysis demonstrated high diagnostic accuracy for Foxc2 (AUC 0.862). Patients with Foxc2 levels≥ 33.945 μg/mL showed a reduction in 2-year MACE risk (HR 0.187) compared to those with levels below the threshold.
Conclusion:
Foxc2 may serve as a promising biomarker for DCM diagnosis and prognosis, supporting for further mechanistic investigations.
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