Scientific ReportsBioinformaticsPeer-reviewed journal article
Stratification of amyotrophic lateral sclerosis patients: a crowdsourcing approach
Robert Kueffner, Neta ZachiD, Maya BronfeldiD, Raquel NoreliD, Nazem AtassiiD, Venkatachalapathy S. K. BalagurusamyiD, Barbara Di CamilloiD, Adriano ChiòiD, Merit CudkowicziD, Donna Eng Dillenberger, Javier Garcı́a-Garcı́aiD, Orla M. HardimaniD, Bruce HoffiD, Joshua Knight, Melanie L. LeitneriD, Guang LiiD, Lara M. MangraviteiD, Thea NormaniD, Liuxia Wang, Rached AlkallasiD, Catalina V. AngheliD, Jeanne Avril, Jaume BacarditiD, Barbara Balser, John P. Balser, , Shihua ZhangiD
Abstract
Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease with substantial heterogeneity in clinical presentation with an urgent need for better stratification tools for clinical development and care. In this study we used a crowdsourcing approach to address the problem of ALS patient stratification. The DREAM Prize4Life ALS Stratification Challenge was a crowdsourcing initiative using data from >10,000 patients from completed ALS clinical trials and 1479 patients from community-based patient registers. Challenge participants used machine learning and clustering techniques to predict ALS progression and survival. By developing new approaches, the best performing teams were able to predict disease outcomes better than currently available methods. At the same time, the integration of clustering components across methods led to the emergence of distinct consensus clusters, separating patients into four consistent groups, each with its unique predictors for classification. This analysis reveals for the first time the potential of a crowdsourcing approach to uncover covert patient sub-populations, and to accelerate disease understanding and therapeutic development.
- Citations
- 55
- FWCI
- 5.91
- Field percentile
- top 3%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Machine learning evaluation of gene expression-based ALS subtypes across brain and blood tissues
Esteban A. Gómez, Ahmad Al Khleifat, … Alfredo Iacoangeli·bioRxiv·Jun 21, 2026
- Detection of Amyotrophic Lateral Sclerosis (ALS) via Acoustic Analysis
Raquel Norel, Mary Pietrowicz, … Guillermo Cecchi·Interspeech (USB)Peer-reviewed·Aug 28, 2018
- Individualized Phenotyping of Functional ALS Pathology in Sensorimotor Cortex
Avinash Kalyani, Alicia Northall, … Esther Kuehn·bioRxiv·Jan 13, 2025
- A scalable screening platform for phenotypic subtyping of ALS patient-derived fibroblasts
Karl Kumbier, Maike A. Roth, … Steven J. Altschuler·bioRxiv·Sep 27, 2022
- ALS molecular subtypes are a combination of cellular, genetic, and pathological features learned by deep multiomics classifiers
Kathryn O’Neill, Regina Shaw, … Molly Hammell·Cell ReportsPeer-reviewed·Mar 1, 2025
- Peripheral immune patterns enable robust cross-platform prediction of ALS onset and progression
Luvna Dhawka, Baggio Evangelista, … Natalie Stanley·bioRxiv·Aug 26, 2025