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Updated: Jul 4, 2025

Optimized Protocol for the Extraction of Proteins from the Human Mitral Valve
Published on: June 14, 2017
Proteomics for heart failure risk stratification: a systematic review.
Kayode O Kuku1, Rebecca Oyetoro1, Maryam Hashemian1
1Heart Disease Phenomics Laboratory, Epidemiology and Community Health Branch, National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD, USA.
High-throughput proteomics shows promise for heart failure (HF) risk stratification, but limited common protein signatures were found across studies. Standardized reporting is crucial for future research in HF mortality prediction.
Area of Science:
- Cardiovascular Medicine
- Proteomics
- Biomarker Discovery
Background:
- Heart failure (HF) is a major cause of mortality with high clinical impact.
- High-throughput proteomics offers potential for improved HF risk stratification.
- The contribution of proteomic signatures to HF mortality prediction requires systematic evaluation.
Approach:
- Systematic review of prognostic studies using high-throughput proteomics (2012-2023).
- Included HF proteomics studies on human plasma/serum measuring numerous proteins via aptamer or antibody platforms.
- Assessed risk of bias using ROBINS-I tool.
Key Points:
- Nine observational studies were included, utilizing aptamer (3) and antibody (6) platforms.
- Considerable heterogeneity in study design, HF definitions, and outcome measures was observed.
- Twenty-one proteins were common in aptamer studies for all-cause death in HF with reduced ejection fraction (HFrEF); one protein also linked to cardiovascular death in antibody studies.
Conclusions:
- A limited number of common protein signatures were identified across studies evaluating HF mortality.
- Heterogeneity across studies hinders broad inferences and highlights the need for standardized reporting.
- Standardized reporting criteria are proposed to enhance future proteomic research in heart failure.
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