Evidence map›Paper›PMID 36054734›Full record

ArticleAnnals of neurology2022

MRI Clustering Reveals Three ALS Subtypes With Unique Neurodegeneration Patterns.

Harold H G Tan, Henk-Jan Westeneng, Abram D Nitert, Kevin van Veenhuijzen, Jil M Meier, Hannelore K van der Burgh, Martine J E van Zandvoort, Michael A van Es, Jan H Veldink, Leonard H van den Berg

Abstract read
In one paragraph

Article in Annals of neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing 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

33 citing papers in PubMed.

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  12. Association between cardiac autonomic dysfunction, cognitive impairment, and survival in patients with amyotrophic lateral sclerosis.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2025
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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

10 authors.

Harold H G TanDepartment of Neurology, UMC Utrecht Brain Center University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0002-2981-9680
Henk-Jan WestenengDepartment of Neurology, UMC Utrecht Brain Center University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Abram D NitertDepartment of Neurology, UMC Utrecht Brain Center University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Kevin van VeenhuijzenDepartment of Neurology, UMC Utrecht Brain Center University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0002-4386-2351
Jil M MeierDepartment of Neurology, UMC Utrecht Brain Center University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.ORCID 0000-0001-5196-1627
Hannelore K van der BurghDepartment of Neurology, UMC Utrecht Brain Center University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Martine J E van ZandvoortDepartment of Neurology, UMC Utrecht Brain Center University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Michael A van EsDepartment of Neurology, UMC Utrecht Brain Center University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Jan H VeldinkDepartment of Neurology, UMC Utrecht Brain Center University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.
Leonard H van den BergDepartment of Neurology, UMC Utrecht Brain Center University Medical Center Utrecht, Utrecht University, Utrecht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThe purpose of this study was to identify subtypes of amyotrophic lateral sclerosis (ALS) by comparing patterns of neurodegeneration using brain magnetic resonance imaging (MRI) and explore their phenotypes.

methodsWe performed T1-weighted and diffusion tensor imaging in 488 clinically well-characterized patients with ALS and 338 control subjects. Measurements of whole-brain cortical thickness and white matter connectome fractional anisotropy were adjusted for disease-unrelated variation. A probabilistic network-based clustering algorithm was used to divide patients into subgroups of similar neurodegeneration patterns. Clinical characteristics and cognitive profiles were assessed for each subgroup. In total, 512 follow-up scans were used to validate clustering results longitudinally.

resultsThe clustering algorithm divided patients with ALS into 3 subgroups of 187, 163, and 138 patients. All subgroups displayed involvement of the precentral gyrus and are characterized, respectively, by (1) pure motor involvement (pure motor cluster [PM]), (2) orbitofrontal and temporal involvement (frontotemporal cluster [FT]), and (3) involvement of the posterior cingulate cortex, parietal white matter, temporal operculum, and cerebellum (cingulate-parietal-temporal cluster [CPT]). These subgroups had significantly distinct clinical profiles regarding male-to-female ratio, age at symptom onset, and frequency of bulbar symptom onset. FT and CPT revealed higher rates of cognitive impairment on the Edinburgh cognitive and behavioral ALS screen (ECAS). Longitudinally, clustering remained stable: at 90.4% of their follow-up visits, patients clustered in the same subgroup as their baseline visit.

interpretationALS can manifest itself in 3 main patterns of cerebral neurodegeneration, each associated with distinct clinical characteristics and cognitive profiles. Besides the pure motor and frontotemporal dementia (FTD)-like variants of ALS, a new neuroimaging phenotype has emerged, characterized by posterior cingulate, parietal, temporal, and cerebellar involvement. ANN NEUROL 2022;92:1030-1045.

Indexed as

Amyotrophic Lateral SclerosisFrontotemporal DementiaCluster AnalysisDiffusion Tensor ImagingFemaleHumansMagnetic Resonance ImagingMale

Identifiers

PMID36054734
PMCPMC9826424

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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.