Evidence map›Paper›PMID 41188584›Full record

ArticleEuropean radiology experimental2025

DTI changes of brachial plexus nerve roots in amyotrophic lateral sclerosis and their correlation with electrophysiology.

Shanshan Wang, Yuxin Li, Xuewen Xing, Xiao Man, Yufan Chen, Guangbin Wang

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Article in European radiology experimental, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

6 authors.

Shanshan WangDepartment of Radiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Yuxin LiShandong First Medical University, Jinan, Shandong, China.
Xuewen XingShandong First Medical University, Jinan, Shandong, China.
Xiao ManDepartment of Neurology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Yufan ChenDepartment of Radiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China.
Guangbin WangDepartment of Radiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Jinan, Shandong, China. wgb7932596@hotmail.com.ORCID http://orcid.org/0000-0001-7410-5540

Funding

Jinan Clinical Research Center for Neurological Disease Imaging Monitoring 201912004Scientific Research Incubation Fund of Shandong Provincial Hospital 2024FY135
6 · The paper itself

Abstract

backgroundAmyotrophic lateral sclerosis (ALS) is a progressive motor neuron disease with peripheral nerve involvement, but current diagnostics are limited. Diffusion tensor imaging (DTI) may improve microstructural assessment and correlate with clinical markers. We investigated the diffusion properties of the brachial plexus in ALS and examined their relationships with electrophysiological parameters of upper limb nerves. MATERIALS AND

methodsWe enrolled 25 ALS patients and 22 age- and sex-matched healthy controls. DTI of the brachial plexus was conducted to measure fractional anisotropy (FA), mean diffusivity (MD), axial diffusivity (AD), and radial diffusivity (RD). Differences in DTI parameters between the two groups were analyzed. Correlations between DTI parameters and ALS Functional Rating Scale-Revised (ALSFRS-R) scores, along with electrophysiological measurements, were assessed.

resultsIn ALS patients compared to controls, FA and AD values were significantly lower (p ≤ 0.002), while the RD value was significantly higher (p = 0.002). There were no statistically significant differences in MD (p = 0.540). Both FA and AD showed a positive correlation with ALSFRS-R score, ALSFRS-upper limb score, and compound muscle action potential amplitude of median, ulnar, and radial nerves (r ≥ 0.480; p ≤ 0.015). The RD values showed a negative correlation with ALSFRS-upper limb score and motor nerve conduction velocity of median, ulnar, and radial nerves (r ≤ -0.415; p ≤ 0.039).

conclusionFA, AD, and RD values of DTI showed the potential to identify microstructural changes in the brachial plexus nerve roots of ALS patients and may serve as potential indicators of nerve conduction function in the upper extremities. RELEVANCE STATEMENT: DTI may reveal microstructural changes in ALS brachial plexus, correlating with nerve dysfunction, offering novel biomarkers for evaluation of upper limb neurodegeneration. KEY POINTS: Lower Fractional anisotropy (FA) and axial diffusivity (AD), and higher radial diffusivity (RD) were shown in amyotrophic lateral sclerosis (ALS) brachial plexus. Diffusion tensor imaging (DTI) parameters correlated with clinical and electrophysiological parameters. FA, AD, and RD detected ALS nerve microstructural changes, indicating abnormal conduction function.

Indexed as

Amyotrophic Lateral SclerosisBrachial PlexusDiffusion Tensor ImagingAdultAgedAnisotropyCase-Control StudiesFemaleHumansMaleMiddle AgedNeural ConductionAmyotrophic lateral sclerosisBrachial plexusDiffusion tensor imagingElectrophysiologyMagnetic resonance imaging.

Identifiers

PMID41188584
PMCPMC12586801

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