Large-scale serum protein biomarkers discovery associated with function and clinical milestones in Duchenne muscular dystrophy

Duchenne muscular dystrophy (DMD) is characterized by progressive muscle wasting and weakness. Serum proteins may offer insight into disease processes and clinical decline. This observational study uses the 7 K SomaScan® assay to discover serum proteins associated with muscle function and disease milestones. In total 702 serum samples from 153 male patients, collected across two centers (2009-2022), are analyzed. Using linear mixed effects modelling, we evaluate age and corticosteroid use as covariates affecting protein levels and assess protein correlations with longitudinal clinical function. Here we show 318 aptamers (294 proteins) significantly associated with motor performance across the two sites, with most associations found with lower limb functional tests (NSAA, 10MRW, and 6MWT). Thirty-six proteins are associated with milestones including RGMA, ART3, ANTXR2, and DLK1. These proteins show promise as prognostic biomarkers, and could potentially be used for patient stratification in clinical trial design and for monitoring interventions.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2025-10-13
DOI
https://doi.org/10.1038/s41467-025-64146-y
Citations
1
Primary Topic
Muscle Physiology and Disorders
Type
article
Field-Weighted Citation Impact
0.81

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Large-scale serum protein biomarkers discovery associated with function and clinical milestones in Duchenne muscular dystrophy

E. Niks, A. M. Barnard, Krista Vandenborne, Simon Eng et al.
1 citations
Nature Communications
Muscle Physiology and Disorders
0.81
article

Large-scale serum protein biomarkers discovery associated with function and clinical milestones in Duchenne muscular dystrophy

E. Niks, A. M. Barnard, Krista Vandenborne, Simon Eng, Hermien E. Kan, Glenn A. Walter, Nadine A. Ikelaar, Kevin Ha, Pietro Spitali, S. Hosseini Vajargah
article en
1 citations

Abstract

Duchenne muscular dystrophy (DMD) is characterized by progressive muscle wasting and weakness. Serum proteins may offer insight into disease processes and clinical decline. This observational study uses the 7 K SomaScan® assay to discover serum proteins associated with muscle function and disease milestones. In total 702 serum samples from 153 male patients, collected across two centers (2009-2022), are analyzed. Using linear mixed effects modelling, we evaluate age and corticosteroid use as covariates affecting protein levels and assess protein correlations with longitudinal clinical function. Here we show 318 aptamers (294 proteins) significantly associated with motor performance across the two sites, with most associations found with lower limb functional tests (NSAA, 10MRW, and 6MWT). Thirty-six proteins are associated with milestones including RGMA, ART3, ANTXR2, and DLK1. These proteins show promise as prognostic biomarkers, and could potentially be used for patient stratification in clinical trial design and for monitoring interventions.

Nature CommunicationsVol. 16(1)
Huntington University (US), Leiden University Medical Center (NL), University of Florida (US), Duchenne Parent Project (NL)
Parent Project Muscular Dystrophy, National Institutes of Health, Clinical and Translational Science Institute, University of Florida, National Center for Advancing Translational Sciences
Openalex Percentile: Top 23%
Muscle Physiology and Disorders
0.81
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.