Evidence map›Paper›PMID 40353906›Full record

ReviewJournal of neurology2025

New developments in imaging in ALS.

Jana Kleinerova, Giorgia Querin, Pierre-Francois Pradat, We Fong Siah, Peter Bede

Abstract readReview
In one paragraph

Review in Journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Potential Roles of Neuroimaging in Motor Neuron Disease.Current neurology and neuroscience reports · 2026
    Review
  2. Article
  3. Review
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Jana KleinerovaComputational Neuroimaging Group (CNG), School of Medicine, Trinity College Dublin, Room 5.43, Pearse Street, Dublin 2, Dublin, Ireland.
Giorgia QuerinBiomedical Imaging Laboratory, CNRS, INSERM, Sorbonne University, Paris, France.
Pierre-Francois PradatBiomedical Imaging Laboratory, CNRS, INSERM, Sorbonne University, Paris, France.
We Fong SiahComputational Neuroimaging Group (CNG), School of Medicine, Trinity College Dublin, Room 5.43, Pearse Street, Dublin 2, Dublin, Ireland.
Peter BedeComputational Neuroimaging Group (CNG), School of Medicine, Trinity College Dublin, Room 5.43, Pearse Street, Dublin 2, Dublin, Ireland. bedep@tcd.ie.

Funding

Health Research Board HRB EIA-2017-019Health Research Board JPND-Cofund-2-2019-1
6 · The paper itself

Abstract

Neuroimaging in ALS has contributed considerable academic insights in recent years demonstrating genotype-specific topological changes decades before phenoconversion and characterising longitudinal propagation patterns in specific phenotypes. It has elucidated the radiological underpinnings of specific clinical phenomena such as pseudobulbar affect, apathy, behavioural change, spasticity, and language deficits. Academic concepts such as sexual dimorphism, motor reserve, cognitive reserve, adaptive changes, connectivity-based propagation, pathological stages, and compensatory mechanisms have also been evaluated by imaging. The underpinnings of extra-motor manifestations such as cerebellar, sensory, extrapyramidal and cognitive symptoms have been studied by purpose-designed imaging protocols. Clustering approaches have been implemented to uncover radiologically distinct disease subtypes and machine-learning models have been piloted to accurately classify individual patients into relevant diagnostic, phenotypic, and prognostic categories. Prediction models have been developed for survival in symptomatic patients and phenoconversion in asymptomatic mutation carriers. A range of novel imaging modalities have been implemented and 7 Tesla MRI platforms are increasingly being used in ALS studies. Non-ALS MND conditions, such as PLS, SBMA, and SMA, are now also being increasingly studied by quantitative neuroimaging approaches. A unifying theme of recent imaging papers is the departure from describing focal brain changes to focusing on dynamic structural and functional connectivity alterations. Progressive cortico-cortical, cortico-basal, cortico-cerebellar, cortico-bulbar, and cortico-spinal disconnection has been consistently demonstrated by recent studies and recognised as the primary driver of clinical decline. These studies have led the reconceptualisation of ALS as a "network" or "circuitry disease".

Indexed as

Amyotrophic Lateral SclerosisBrainNeuroimagingHumansMagnetic Resonance ImagingAmyotrophic lateral sclerosisBiomarkersCerebellumFrontotemporal dementiaMagnetic resonance imagingMotor neuron diseaseNeuroimagingPrimary lateral sclerosis

Identifiers

PMID40353906
PMCPMC12069492

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.