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Multi-Omics-Derived Heart Failure Endotypes Predict Clinical Heart Failure Progression

Proteomics + lipidomics integration via Similarity Network Fusion (SNF) to stratify Stage C/D heart failure patients and validate cluster-based risk in an independent asymptomatic cohort.

Data access: Raw patient data cannot be shared due to privacy restrictions. Aggregated intermediate objects and summary statistics are provided in /data. Contact the corresponding author for data access requests.


Cohort overview

Discovery cohort Stage C/D HF
Validation cohort Stage A/B HF
Omics layers Proteomics (Olink) + lipidomics (4D-LC-TIMS lipidomics)
Primary outcome Worsening heart failure (WHF), time-to-event

Analysis pipeline

  1. Data preprocessing — Imputation, near-zero-variance removal, z-score scaling, and decorrelation (Pearson r > 0.9) applied independently to each omics panel.

  2. Network fusion (SNF) — Per-panel affinity matrices fused via Similarity Network Fusion; spectral clustering tested over K = 3–10.

  3. Cluster quality evaluation — Harrell's C-index, log-rank tests, and NMI used to select the optimal K and compare SNF against single-modality clusterings.

  4. Cluster characterisation — Kruskal-Wallis + BH FDR on all features; cluster-wise z-scores; UpSet plots for exclusive markers; LASSO multinomial regression for clinical predictors.

  5. Stability & comparison — Bootstrap subsampling (B = 100, 80% of samples) reporting ARI and NMI; MOFA2 run as a comparison multi-omics method.

  6. Validation cohort transfer — Per-cluster Random Forest classifiers trained on the discovery cohort project cluster labels onto Stage A/B patients; survival and stage-progression outcomes tested in the transferred clusters.


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