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Correlation Between Blood Transforming Growth Factor-Beta 1 (TGF-β1) Levels and Cardiac Function Parameters Following
Mukhlis Yazid1, Muhadi Lnu1, Sukamtoe Koesnoe2
1Cardiology, Cipto Mangunkusumo National General Hospital, Jakarta, IDN.
Transforming growth factor-beta 1 (TGF-β1) did not correlate with cardiac function in most cancer patients post-doxorubicin. However, higher TGF-β1 levels were linked to diastolic dysfunction in patients receiving higher cumulative doxorubicin doses.
Area of Science:
- Cardiology
- Oncology
- Biochemistry
Background:
- Doxorubicin chemotherapy can cause significant cardiotoxicity, affecting heart function.
- Transforming growth factor-beta 1 (TGF-β1) is implicated in cardiac fibrosis and doxorubicin-induced cardiotoxicity.
- Limited human studies explore the TGF-β1 link to doxorubicin cardiotoxicity.
Purpose of the Study:
- To assess the correlation between serum TGF-β1 levels and cardiac function parameters.
- Evaluate ejection fraction (EF), E/A, E/E', TAPSE, and GLS post-doxorubicin chemotherapy.
- Investigate TGF-β1 as a potential biomarker for doxorubicin cardiotoxicity.
Main Methods:
- Cross-sectional study of 56 cancer patients 3-12 months post-doxorubicin.
- Measured serum TGF-β1 levels and cardiac function via echocardiography.
- Used correlation analysis (Pearson/Spearman) with significance set at p < 0.05.
Main Results:
- No significant correlation between TGF-β1 and EF, E/A, E/E', TAPSE, or GLS in the overall cohort.
- A significant correlation was found between TGF-β1 and E/E' in patients with cumulative doxorubicin dose ≥600 mg/m² (n=30).
Conclusions:
- TGF-β1 did not correlate with most cardiac function indices in the general cohort.
- TGF-β1 significantly correlated with E/E' (diastolic dysfunction) in patients receiving higher doxorubicin doses.
- TGF-β1 may be a biomarker for anthracycline-induced cardiac fibrosis, especially with higher cumulative doses.
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