Evidence map›Paper›PMID 28491898›Full record

ArticleAnnals of clinical and translational neurology2017

A Cross-sectional population-based investigation into behavioral change in amyotrophic lateral sclerosis: subphenotypes, staging, cognitive predictors, and survival.

Tom Burke, Marta Pinto-Grau, Katie Lonergan, Peter Bede, Meabhdh O'Sullivan, Mark Heverin, Alice Vajda, Russell L McLaughlin, Niall Pender, Orla Hardiman

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed, 4 pooled it
5.3field-weighted citation impact, top 4% of its field
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

36 citing papers in PubMed, 4 syntheses or guidelines pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  4. Pooled it
  5. Article
  6. Article
  7. The spectrum of behavioral disorders in amyotrophic lateral sclerosis: current view.Journal of neural transmission (Vienna, Austria : 1996) · 2025
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Sensory Involvement in Amyotrophic Lateral Sclerosis.International journal of molecular sciences · 2022
    Review
  13. Review
  14. Article
  15. Article
  16. Extra-motor manifestations in post-polio syndrome (PPS): fatigue, cognitive symptoms and radiological features.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
    Article
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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 at 2 institutions in 1 country.

Tom BurkeAcademic Unit of Neurology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland.
Marta Pinto-GrauAcademic Unit of Neurology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland.
Katie LonerganAcademic Unit of Neurology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland.
Peter BedeAcademic Unit of Neurology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland.
Meabhdh O'SullivanAcademic Unit of Neurology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland.
Mark HeverinAcademic Unit of Neurology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland.
Alice VajdaAcademic Unit of Neurology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland.
Russell L McLaughlinSmurfit Institute of Genetics Trinity College Dublin Dublin Ireland.
Niall PenderAcademic Unit of Neurology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland.
Orla HardimanAcademic Unit of Neurology Trinity Biomedical Sciences Institute Trinity College Dublin Dublin Ireland.
Trinity College Dublin · IEBeaumont Hospital · IE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveAmyotrophic Lateral Sclerosis (ALS) is a clinically heterogeneous neurodegenerative disorder associated with cognitive and behavioral impairment. The primary aim of this study was to identify behavioral subphenotypes in ALS using a custom designed behavioral assessment tool (Beaumont Behavioural Inventory, BBI). Secondary aims were to (1) investigate the predictive nature of cognitive assessment on behavioral change, (2) report the behavioral profile associated with the C9

methodsA cross-sectional population-based research design was applied to examine behavioral data from ALS patients (

resultsNo behavioral changes were reported in 180 patients (57%); 95 patients had mild-moderate behavioral change (30%); 42 patients met the cut-off for Clinically Severe Behavioral Change (13%), suggestive of a bvFTD diagnosis. The most frequently endorsed behaviors in ALS were reduced concern for hygiene (36.8%), irritability (36.2%), new unusual habits (33.4%), and increased apathy (31.1%). Five independent factors were identified through factor analysis. Social cognitive performance was predictive of behavior change (

interpretationThese data imply the presence of distinct subphenotypes of behavioral change in ALS, which most likely reflect subcategories of extramotor network disruption.

Identifiers

PMID28491898
PMCPMC5420811
OpenAlexW2607324914

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

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.