Evidence map›Paper›PMID 32666680›Full record

ArticleAnnals of clinical and translational neurology2020

CSF chitinases before and after symptom onset in amyotrophic lateral sclerosis.

Elizabeth Gray, Alexander G Thompson, Joanne Wuu, Joe Pelt, Kevin Talbot, Michael Benatar, Martin R Turner

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
2.6field-weighted citation impact, top 8% 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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it, 42 citations in OpenAlex.

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  15. Chitinase Signature in the Plasticity of Neurodegenerative Diseases.International journal of molecular sciences · 2023
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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

7 authors at 2 institutions in 2 countries.

Elizabeth GrayNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Alexander G ThompsonNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.ORCID 0000-0003-1063-3277
Joanne WuuDepartment of Neurology, University of Miami, Miami, Florida.
Joe PeltNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Kevin TalbotNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.
Michael BenatarDepartment of Neurology, University of Miami, Miami, Florida.ORCID 0000-0003-4241-5135
Martin R TurnerNuffield Department of Clinical Neurosciences, University of Oxford, Oxford, UK.ORCID 0000-0003-0267-3180
University of Oxford · GBUniversity of Miami · US

Funding

Pre-Symptomatic Familial ALS (Pre-fALS) Study - Prelude to a Treatment Trial; Administrative SupplementR01NS105479 · NINDS · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI BENATAR, MICHAEL, WUU, JOANNE · 2018 to 2022
$3.0M
Medical Research Council MR/T006927/1Motor Neurone Disease Association TURNER/OCT18/989-797NINDS NIH HHS R01 NS105479
6 · The paper itself

Abstract

objectiveTo evaluate the CSF levels of chitinase proteins during the presymptomatic and early symptomatic phases of amyotrophic lateral sclerosis (ALS).

methodsCSF samples were obtained from 16 controls, 55 individuals at-risk for ALS (including 18 carrying a mutation in C9ORF72, 33 in SOD1), 12 ALS patients, and 7 phenoconverters (individuals diagnosed with ALS during follow-up). At-risk individuals and phenoconverters were enrolled through the Pre-fALS study, which includes individuals carrying an ALS-associated gene mutation without disease manifestations at initial assessment. Longitudinal CSF collections, where possible, took place every 3-12 months for ALS patients and every 1-2 years for others. CSF levels of chitotriosidase 1 (CHIT1), chitinase-3-like protein 1 (CHI3L1, YKL-40) and chitinase-3-like protein 2 (CHI3L2, YKL-39) were measured by ELISA, along with CHIT1 activity. Longitudinal changes in at-risk individuals and phenoconverters were fitted to linear mixed effects models.

resultsSlowly rising levels of CHIT1 were observed over time in the at-risk individuals (slope 0.059 log

interpretationThe CHIT1 neuroinflammatory response is a feature of the late presymptomatic to early symptomatic phases of ALS. This study does not suggest a long prodrome of upregulated glial activity in ALS pathogenesis, but strengthens the place of CHIT1 as part of a panel of biomarkers to objectively assess the impact of immune-modulatory therapeutic interventions in ALS.

Indexed as

AdultAmyotrophic Lateral SclerosisChitinase-3-Like Protein 1ChitinasesDisease ProgressionFemaleHexosaminidasesHumansLongitudinal StudiesMaleMiddle AgedProdromal SymptomsCHI3L1 protein, humanCHI3L2 protein, humanChitinase-3-Like Protein 1ChitinaseschitotriosidaseHexosaminidases

Identifiers

PMID32666680
PMCPMC7448184
OpenAlexW3033752638

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.