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Updated: Jan 22, 2026

Author Spotlight: Advancing the Analysis of Plasma Extracellular Vesicle Proteome for Cardiovascular Biomarker Studies
Published on: January 31, 2025
Application of Proteomics Profiling for Biomarker Discovery in Hypertrophic Cardiomyopathy
Yuichi J Shimada1,2, Kohei Hasegawa3, Stephanie M Kochav4
1Cardiology Division, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, USA. ys3053@cumc.columbia.edu.
Insights
High-throughput proteomics identified novel plasma biomarkers for hypertrophic cardiomyopathy (HCM). This study accurately distinguishes HCM patients from controls using proteomic profiles.
Area of Science:
- Cardiovascular Research
- Proteomics
- Biomarker Discovery
Background:
- Hypertrophic cardiomyopathy (HCM) lacks established plasma protein biomarkers for diagnosis.
- High-throughput proteomics has not been previously applied to identify HCM biomarkers.
Purpose of the Study:
- To discover plasma protein biomarkers differentiating HCM patients from healthy controls.
- To evaluate the diagnostic accuracy of identified protein signatures.
Main Methods:
- Case-control study involving 15 HCM patients and 22 controls.
- Plasma proteomics profiling of 1129 proteins using the SOMAscan assay.
- Sparse partial least squares discriminant analysis and receiver operating characteristic curve analysis for biomarker identification and validation.
Main Results:
- Identified 50 discriminant proteins with high accuracy (89%) and an average AUC of 0.94.
- 13 identified proteins correlated with troponin I levels.
- 12 proteins correlated with New York Heart Association functional class.
Conclusions:
- High-throughput proteomics is a viable method for discovering protein biomarkers in HCM.
- The identified protein signature shows potential for distinguishing HCM from controls.
- Proteomic profiling offers new avenues for understanding HCM pathophysiology.
Abstract:
High-throughput proteomics profiling has never been applied to discover biomarkers in patients with hypertrophic cardiomyopathy (HCM). The objective was to identify plasma protein biomarkers that can distinguish HCM from controls. We performed a case-control study of patients with HCM (n = 15) and controls (n = 22). We carried out plasma proteomics profiling of 1129 proteins using the SOMAscan assay. We used the sparse partial least squares discriminant analysis to identify 50 most discriminant proteins. We also determined the area under the curve (AUC) of the receiver operating characteristic curve using the Monte Carlo cross validation with balanced subsampling. The average AUC was 0.94 (95% confidence interval, 0.82-1.00) and the discriminative accuracy was 89%. In HCM, 13 out of the 50 proteins correlated with troponin I and 12 with New York Heart Association class. Proteomics profiling can be used to elucidate protein biomarkers that distinguish HCM from controls.
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