Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2025 Feb;71(2):171-182.
doi: 10.1002/mus.28306. Epub 2024 Nov 29.

Longitudinal Quantitative MRI Provides Responsive Outcome Measures for Early and Late Muscle Changes in ALS

Affiliations

Longitudinal Quantitative MRI Provides Responsive Outcome Measures for Early and Late Muscle Changes in ALS

Frank Diaz et al. Muscle Nerve. 2025 Feb.

Abstract

Introduction/aims: Studies have demonstrated the potential of muscle MRIs to measure disease progression in ALS. However, the responsiveness and utility of quantitative muscle MRIs in an ALS clinical trial remain unknown. This study aimed to determine the responsiveness of quantitative muscle MRIs to measure disease progression in ALS.

Methods: Longitudinal quantitative muscle MRIs were obtained in an ALS study that delivered human neural progenitor cells to the spinal cord (NCT02943850). Participants underwent MRIs at baseline, 1, 3, 6, 9, and 12 months. MRI measures included fat fraction (ff), water T2 (T 2m), cross-sectional area (CSA), and remaining muscle area (RMA). Non-MRI measures included strength via Accurate Test of Limb Isometric Strength (ATLIS) and the ALSFRS-R. Standardized response means (SRM) were calculated at 1, 3, 6, and 12 months.

Results: Significant increases in muscle FF and decreases in CSA and RMA were seen as early as 1 month from baseline. At 6 months, the most responsive measures were muscle FF (SRMthigh = 1.85, SRMcalf = 1.39), T 2m (SRMthigh = 1.2, SRMcalf = 1.71), CSA (SRMthigh = -1.58, SRMcalf = -1.14), RMA (SRMthigh = -1.77, SRMcalf = -1.28), and strength tested via ATLIS (SRMknee extension = -1.79, SRMknee flexion = -1.3). The ALSFRS-R was the least responsive at 6 months (SRM = -0.85). Muscle FF and T 2m correlated with ALSFRS-R leg subscores and MRI measures demonstrated varying degrees of correlation with strength.

Discussion: High responsiveness and low variability make quantitative muscle MRI a novel and complementary outcome measure for ALS clinical trials.

Keywords: ALS; amyotrophic lateral sclerosis; muscle MRI; neuroimaging; outcome measures.

PubMed Disclaimer

References

    1. A. Kriss and T. Jenkins, “Muscle MRI in Motor Neuron Diseases: A Systematic Review,” Amyotroph Lateral Scler Front Degener 23, no. 3–4 (2022): 161–175, https://doi.org/10.1080/21678421.2021.1936062.
    1. J. M. Morrow, C. D. J. Sinclair, A. Fischmann, et al., “MRI Biomarker Assessment of Neuromuscular Disease Progression: A Prospective Observational Cohort Study,” Lancet Neurology 15, no. 1 (2016): 65–77, https://doi.org/10.1016/S1474‐4422(15)00242‐2.
    1. J. M. Morrow, M. R. B. Evans, T. Grider, et al., “Validation of MRC Centre MRI Calf Muscle Fat Fraction Protocol as an Outcome Measure in CMT1A,” Neurology 91, no. 12 (2018): e1125–e1129, https://doi.org/10.1212/WNL.0000000000006214.
    1. C. H. Cha and B. M. Patten, “Amyotrophic Lateral Sclerosis: Abnormalities of the Tongue on Magnetic Resonance Imaging,” Annals of Neurology 25, no. 5 (1989): 468–472, https://doi.org/10.1002/ANA.410250508.
    1. Staff NP, K. K. Amrami, and B. M. Howe, “Magnetic Resonance Imaging Abnormalities of Peripheral Nerve and Muscle Are Common in Amyotrophic Lateral Sclerosis and Share Features With Multifocal Motor Neuropathy,” Muscle and Nerve 52, no. 1 (2015): 137–139, https://doi.org/10.1002/MUS.24630.

LinkOut - more resources