Muscle MRI quantifies disease progression in Amyotrophic Lateral Sclerosis

ABSTRACT Importance Quantitative, sensitive and operator-independent biomarkers of disease progression are needed to minimize the size, duration, and cost of clinical trials in amyotrophic lateral sclerosis (ALS) to allow a more effective investigation of promising therapeutic agents.Objective We assess the potential of skeletal muscle magnetic resonance imaging (MRI) as a sensitive and reliable outcome measure for future ALS clinical trials.Design In this longitudinal cohort study, muscle MRI of head-neck, upper, and lower limb regions, along with clinical and functional assessments, were acquired at three timepoints over the individual maximum observation period (iMOP) of 1 year.Participants Twenty consecutive ALS patients were recruited from a motor neuron disease clinic between 2015 and 2017, along with 16 healthy controls.Main outcomes and measures Quantitative MRI parameters CSA (cross-sectional area), VOL (muscle volume), FF (fat fraction), functional rest muscle area (fRMA) and water T2 (T2m) were used to assess progressive muscle degeneration and were correlated with changes in clinical parameters of disease severity (functional rating scales and myometry). Standardized response mean (SRM) was calculated for MRI outcome measures.Results Out of 20 ALS patients, 17 were available for follow-up. A significant decline in VOL of the dominant hand (rs=0.66, p<0.001) and head and neck muscles (partial η²=0.47, p=0.002) as well as CSA of the lower limbs (thighs: partial η²=0.56, p<0.001, calves: partial η²=0.54, p<0.001) was observed over iMOP, with highest responsiveness for progressive atrophy in hand (SRM -1.17) and leg muscles (thigh: SRM -1.09; calf: SRM -1.08). Furthermore, lower limb FF and T2mincreased over time, with distal leg muscles being most affected (FF: partial η²=0.54, p=0.002, SRM 0.81; T2m:partial η²=0.37, p=0.01, SRM 0.74). Finally, longitudinal MRI changes showed correlation with strength in leg muscles (knee extension: r=0.77, p=0.001, 95% CI 0.46–0.91; plantar flexion: r=0.78, p<0.001, 95% CI 0.47 – 0.92), and fRMA decrease at thigh and calf level correlated with global clinical disease progression measured with ALSFRS (r=0.52, p=0.03, and r=0.68, p=0.004 respectively).Conclusions and Relevance Our findings demonstrate the effectiveness of muscle MRI as a sensitive neuroimaging biomarker of disease progression in ALS, highlighting its potential application in clinical trials.Key Points Question:Can quantitative muscle MRI track disease progression over time in patients with amyotrophic lateral sclerosis (ALS)?Findings:Longitudinal quantitative MRI reliably detects progressive intramuscular fat infiltration, oedema and atrophy, which correlate with progressive loss of muscle strength.Meaning:Muscle MRI has the potential to be utilised as a biomarker for ALS disease progression and could contribute to reduce the size and duration of clinical trials facilitating future drug developments..

Medienart:	Preprint

Erscheinungsjahr:	2024
Erschienen:	2024

Enthalten in:	bioRxiv.org - (2024) vom: 16. Apr. Zur Gesamtaufnahme - year:2024

Sprache:	Englisch

Beteiligte Personen:

Klickovic, Uros [VerfasserIn] Zampedri, Luca [VerfasserIn] Zafeiropoulos, Nick [VerfasserIn] Ziff, Oliver J [VerfasserIn] Sinclair, Christopher DJ [VerfasserIn] Wastling, Stephen J [VerfasserIn] Dudziec, Magda [VerfasserIn] Allen, Jodie [VerfasserIn] Trimmel, Karin [VerfasserIn] Howard, Robin S [VerfasserIn] Malaspina, Andrea [VerfasserIn] Sharma, Nikhil [VerfasserIn] Sidle, Katie CL [VerfasserIn] Shah, Sachit [VerfasserIn] Nasel, Christian [VerfasserIn] Yousry, Tarek A [VerfasserIn] Greensmith, Linda [VerfasserIn] Morrow, Jasper M [VerfasserIn] Thornton, John S [VerfasserIn] Fratta, Pietro [VerfasserIn]

Links:	Volltext [kostenfrei]

Themen:	570 Biology

doi:	10.1101/2024.04.10.24305608

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PPN (Katalog-ID):	XBI043256511