Evidence map›Paper›PMID 36632187›Full record

ArticleBrain communications2023

Multiple pathways of lipid dysregulation in amyotrophic lateral sclerosis.

Katherine Phan, Ying He, Surabhi Bhatia, Russell Pickford, Gordon McDonald, Srestha Mazumder, Hannah C Timmins, John R Hodges, Olivier Piguet, Nicolas Dzamko and 3 more

Open access · goldAbstract read
In one paragraph

Article in Brain communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.1field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 29 citations in OpenAlex.

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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

13 authors at 2 institutions in 1 country.

Katherine PhanThe University of Sydney, Brain and Mind Centre, Sydney, NSW, Australia.
Ying HeThe University of Sydney, Brain and Mind Centre, Sydney, NSW, Australia.
Surabhi BhatiaThe University of Sydney, Brain and Mind Centre, Sydney, NSW, Australia.
Russell PickfordBioanalytical Mass Spectrometry Facility, University of New South Wales, Sydney, NSW, Australia.
Gordon McDonaldThe University of Sydney, Sydney Informatics Hub, Sydney, NSW, Australia.
Srestha MazumderThe University of Sydney, Brain and Mind Centre, Sydney, NSW, Australia.
Hannah C TimminsThe University of Sydney, Brain and Mind Centre, Sydney, NSW, Australia.
John R HodgesThe University of Sydney, Brain and Mind Centre, Sydney, NSW, Australia.
Olivier PiguetThe University of Sydney, Brain and Mind Centre, Sydney, NSW, Australia.ORCID https://orcid.org/0000-0002-6696-1440
Nicolas DzamkoThe University of Sydney, Brain and Mind Centre, Sydney, NSW, Australia.ORCID https://orcid.org/0000-0002-9121-0294
Glenda M HallidayThe University of Sydney, Brain and Mind Centre, Sydney, NSW, Australia.ORCID https://orcid.org/0000-0003-0422-8398
Matthew C KiernanThe University of Sydney, Brain and Mind Centre, Sydney, NSW, Australia.ORCID https://orcid.org/0000-0001-9054-026X
Woojin Scott KimThe University of Sydney, Brain and Mind Centre, Sydney, NSW, Australia.ORCID https://orcid.org/0000-0002-4707-933X
The University of Sydney · AUUNSW Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Amyotrophic lateral sclerosis is a rapidly progressing neurodegenerative disease characterized by the degeneration of motor neurons and loss of various muscular functions. Dyslipidaemia is prevalent in amyotrophic lateral sclerosis with aberrant changes mainly in cholesterol ester and triglyceride. Despite this, little is known about global lipid changes in amyotrophic lateral sclerosis or in relation to disease progression. The present study incorporated a longitudinal lipidomic analysis of amyotrophic lateral sclerosis serum with a comparison with healthy controls using advanced liquid chromatography-mass spectrometry. The results established that diglyceride, the precursor of triglyceride, was enriched the most, while ceramide was depleted the most in amyotrophic lateral sclerosis compared with controls, with the diglyceride species (18:1/18:1) correlating significantly to neurofilament light levels. The prenol lipid CoQ

Indexed as

amyotrophic lateral sclerosisbiomarkerslipidomics

Identifiers

PMID36632187
PMCPMC9825811
OpenAlexW4312219875

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.