Evidence map›Paper›PMID 35213002›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

Analysis of the Sphingolipidome in NAFLD.

David Montefusco, Johana Lambert, Andrea Anderson, Jeremy Allegood, L Ashley Cowart

Open access · greenAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
7.5field-weighted citation impact, top 2% 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

7 citing papers in PubMed, 17 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

5 authors at 1 institution in 1 country.

David MontefuscoDepartment of Biochemistry and Molecular Biology, Virginia Commonwealth University, Richmond, VA, USA. David.montefusco@vcuhealth.org.
Johana LambertDepartment of Biochemistry and Molecular Biology, Virginia Commonwealth University, Richmond, VA, USA.
Andrea AndersonDepartment of Biology, Virginia Commonwealth University, Richmond, VA, USA.
Jeremy AllegoodDepartment of Biochemistry and Molecular Biology, Virginia Commonwealth University, Richmond, VA, USA.
L Ashley CowartDepartment of Biochemistry and Molecular Biology, Virginia Commonwealth University, Richmond, VA, USA.
Virginia Commonwealth University · US

Funding

Virus Vector Shared ResourceP30CA016059 · NCI · VIRGINIA COMMONWEALTH UNIVERSITY · PI Renato Martins · 1985 to 2026
$51.0M
Novel sphingolipid metabolites in myocardial ischemiaR01HL151243 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI COWART, LAUREN ASHLEY · 2020 to 2024
$1.9M
Sphingolipids in Diabetic CardiomyopathyR01HL117233 · NHLBI · VIRGINIA COMMONWEALTH UNIVERSITY · PI COWART, LAUREN ASHLEY · 2014 to 2018
$1.9M
Sphingolipids in the Pathophysiology of Obesity and DiabetesI01BX000200 · VA · VA VETERANS ADMINISTRATION HOSPITAL · PI COWART, LAUREN ASHLEY · 2009 to 2025
–
BLRD VA I01 BX000200BLRD VA IK6 BX006315NCI NIH HHS P30 CA016059NHLBI NIH HHS R01 HL117233NHLBI NIH HHS R01 HL151243
6 · The paper itself

Abstract

The relationship between sphingolipid levels and NAFLD pathology has been recognized for some time. Numerous studies using pharmacological and genetic approaches in vitro and in animal models of NAFLD have demonstrated that modifications to sphingolipid metabolism can attenuate various facets of NAFLD pathology. However, a more precise understanding of the role of sphingolipids and NAFLD pathology is essential to creating therapeutics that target this pathway. This chapter touches on the scale and variety of sphingolipid metabolites at play in NAFLD, which vary widely in their chemical structures and biological functions. With advances in liquid chromatography and tandem mass spectrometry approaches, each of thousands of individual sphingolipid species and sphingolipid metabolites can be identified and precisely quantified. These approaches are beginning to reveal specific sub-classes and species of sphingolipids that change in NAFLD, and as such, enzymes that generate them can be identified and potentially serve as therapeutic targets. Advances in lipidomics technology have been, and will continue to be, critical to these gains in our understanding of NAFLD.

Indexed as

Non-alcoholic Fatty Liver DiseaseAnimalsChromatography, LiquidLipid MetabolismLipidomicsSphingolipidsSphingolipidsAlcoholic fatty liver diseaseCeramideLipidLipidomicsMetabolic syndromeNAFLDNASHNon-alcoholic fatty liver diseaseNon-alcoholic steatohepatitisSphingoidSphingolipidsSphingosineSphingosine-1-phosphate

Identifiers

PMID35213002
PMCPMC9159091
OpenAlexW4214646003

What OpenQuestion holds

Textmetadata
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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.