Molecular subgroups of ALS patients with distinct survival outcomes identified through plasma proteomics
Year: 2026
Type: preprint
Abstract: Amyotrophic Lateral Sclerosis (ALS) is a phenotypically diverse neurodegenerative disorder characterized by the degeneration of motor neurons, ultimately resulting in loss of motor function. Currently, patients are classified based on clinical factors which does not fully capture the heterogeneity. Using the Olink Explore HT, we profiled ∼5400 plasma proteins in ALS patients (n = 235) from the ALSrisc Study at Karolinska Institutet, Sweden, and applied consensus clustering, which revealed three patient subgroups significantly differing in survival outcome. Weighted gene correlation network analysis (WGCNA) and gene ontology (GO) analysis identified protein modules related to biological functions including cellular stress response and Rho-GTPase activity for the shorter surviving patient group. Cell-type enrichment analysis indicating a broad cellular origin of the circulating proteome, with contributions from nervous system cells, vascular cells, immune cells, and muscle cells. Our work highlights the potential of plasma proteomics for clinically meaningful patient stratification in ALS.
Source: medRxiv
Authors: Inci S. Aksoylu, Louisa Azizi, Linn Öijerstedt, Sofia Lilja, María Bueno Álvez, Solmaz Yazdani, Lovisa Skoglund, Juliette Foucher, Alexander Juto, Christina Seitz, Rayomand Press, Kristin Samuelsson, Ulf Kläppe, Fang Fang, Mathias Uhlén, Fredrik Edfors, Peter Nilsson, Caroline Ingre, Anna Månberg
Language: English
Subfield: Clinical Neurology
Field: Medicine
Domain: Health Sciences
Open Access status: green
Award: G2260567423
OpenAlex ID: W7213534776
