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CILP-1 Is a Biomarker for Backward Failure and Right Ventricular Dysfunction in HFrEF
Annika Weidenhammer1, Suriya Prausmüller1, Clemens Partsch1
1Department of Internal Medicine II, Clinical Division of Cardiology, Medical University of Vienna, 1090 Vienna, Austria.
Cartilage intermediate layer protein-1 (CILP-1) correlates with heart failure with reduced ejection fraction severity and backward failure. While CILP-1 may indicate mortality risk, it is not independent of NT-proBNP levels.
Area of Science:
- Cardiovascular Medicine
- Biomarker Discovery
- Heart Failure Research
Background:
- Cartilage intermediate layer protein-1 (CILP-1) is implicated in myocardial fibrosis and remodeling.
- Previous research suggests CILP-1 indicates right ventricular dysfunction (RVD) in pulmonary hypertension (PH) and heart failure (HF).
Purpose of the Study:
- To investigate CILP-1 as a potential biomarker for RVD in patients with heart failure with reduced ejection fraction (HFrEF).
- To assess the prognostic value of CILP-1 for mortality and hospitalization in HFrEF patients on guideline-directed medical therapy.
Main Methods:
- CILP-1 levels were measured in 610 HFrEF patients from a prospective registry (2016-2022).
- Correlations with echocardiographic and hemodynamic data were analyzed.
- Association with RVD, mortality, and cardiovascular hospitalization was evaluated.
Main Results:
- CILP-1 levels increased with HF severity, correlating with NT-proBNP and NYHA class.
- CILP-1 showed associations with backward failure indicators (e.g., elevated left atrial diameter, sPAP, RVF) but not cardiac index or SVR.
- CILP-1 trended as a risk factor for all-cause mortality but lost significance after adjustment for NT-proBNP.
Conclusions:
- CILP-1 correlates with HFrEF severity and backward failure, potentially indicating mortality risk, but is not an independent predictor.
- The association of CILP-1 with RVD warrants further investigation to determine if it stems from pulmonary pressures or is specific to RVD.
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