Apolipoprotein Proteomic Profiling for the Prediction of Cardiovascular Death in Patients with Heart Failure
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Gilles Lemesle1,2,3, Vincent Chouraki1, Pascal de Groote1,2
1CHU Lille, Institut Pasteur de Lille, U1167 - RID-AGE - Facteurs de risque et déterminants moléculaires des maladies liées au vieillissement, Univ. Lille, Inserm, Lille, F-59000, France.
Insights
Identifying novel biomarkers for heart failure (HF) risk stratification is crucial. Proteomic profiling of apolipoproteins (Apo) revealed Apo-C1, Apo-J, and Apo-M as key predictors of cardiovascular death in HF patients.
Area of Science:
- Cardiology
- Proteomics
- Biomarker Discovery
Background:
- Risk stratification is essential for managing chronic systolic heart failure (HF).
- Identifying new biomarkers can improve prognosis evaluation and understanding of HF.
- Current methods may not fully capture HF patient risk profiles.
Purpose of the Study:
- To identify novel apolipoprotein (Apo) biomarkers for risk stratification in chronic systolic heart failure (HF).
- To improve prognostic evaluation and understand HF physiopathology through proteomic analysis.
Main Methods:
- Proteomic profiling of 15 apolipoproteins (Apo) was performed using LC-MRM-MS.
- 198 patients with chronic systolic HF were studied, matched for age, sex, and HF etiology.
- Patients were divided into two groups: those who died from cardiovascular causes within three years and those who survived.
Main Results:
- Univariate analysis showed lower levels of Apo-B100 and -L1, and higher levels of Apo-C1, -J, and -M in patients who died.
- Apo-C1, Apo-J, and Apo-M individually improved the prediction of cardiovascular death in the final statistical model.
- Pathway analysis linked these three apolipoproteins to lipid metabolism, atherosclerosis signaling, and retinoid X receptor activation.
Conclusions:
- Proteomic profiling of apolipoproteins using LC-MRM-MS shows promise for clinical risk stratification in HF patients.
- Apo-C1, Apo-J, and Apo-M are identified as potential biomarkers for predicting cardiovascular mortality in HF.
- These findings contribute to a better understanding of HF physiopathology and advanced therapy selection.
Purpose:
Risk stratification in chronic systolic heart failure (HF) is critical to identify the patients who may benefit from advanced therapies. It is aimed at identifying new biomarkers to improve prognosis evaluation and help to better understand HF physiopathology.
Experimental Design:
Prognostic evaluation is performed in 198 patients with chronic systolic HF: 99 patients who died from cardiovascular cause within three years are individually matched for age, sex, and HF etiology (ischemic vs not) with 99 patients who are alive after three years of HF evaluation. A proteomic profiling of 15 apolipoproteins (Apo) is performed: Apo-A1, -A2, -A4, -B100, -C1, -C2, -C3, -C4, -D, -E, -F, -H, -J, -L1, and -M using LC-MRM-MS.
Results:
In univariate analysis, the levels of Apo-B100 and -L1 are significantly lower and the levels of Apo-C1, -J, and -M are significantly higher in patients who died from cardiovascular cause as compared with patients alive. In the final statistical model, Apo-C1, Apo-J, and Apo-M improve individually the prediction of cardiovascular death. Ingenuity pathway analysis indicates these three Apo in a network associated with lipid metabolism, atherosclerosis signaling, and retinoid X receptor activation.
Conclusions:
Proteomic profiling of apolipoproteins using LC-MRM-MS might be useful in clinical practice for risk stratification of HF patients.
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