Evidence map›Paper›PMID 30678043›Full record

ReviewInternational journal of molecular sciences2019

Sphingolipid Metabolism: New Insight into Ceramide-Induced Lipotoxicity in Muscle Cells.

Cécile L Bandet, Sophie Tan-Chen, Olivier Bourron, Hervé Le Stunff, Eric Hajduch

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 72 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
72citing papers in PubMed, 2 pooled it
5.3field-weighted citation impact, top 3% 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

72 citing papers in PubMed, 2 syntheses or guidelines pooled it, 114 citations in OpenAlex.

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12 more citing papers are in PubMed but not listed here.

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 4 institutions in 1 country.

Cécile L BandetINSERM UMRS 1138, Sorbonne Université, Institut Hospitalo-Universitaire ICAN, 75013 Paris, France. cecile.bandet@gmail.com.
Sophie Tan-ChenINSERM UMRS 1138, Sorbonne Université, Institut Hospitalo-Universitaire ICAN, 75013 Paris, France. sophie.tan@crc.jussieu.fr.
Olivier BourronINSERM UMRS 1138, Sorbonne Université, Institut Hospitalo-Universitaire ICAN, 75013 Paris, France. olivier.bourron@aphp.fr.
Hervé Le StunffCNRS UMR 9198 Institut des Neurosciences Paris Saclay (Neuro-PSI), Université Paris-Saclay, 91400 Orsay, France. herve.le-stunff@paris7.jussieu.fr.
Eric HajduchINSERM UMRS 1138, Sorbonne Université, Institut Hospitalo-Universitaire ICAN, 75013 Paris, France. eric.hajduch@crc.jussieu.fr.
Sorbonne Paris Cité · FRCentre National de la Recherche Scientifique · FRDélégation Paris 5 · FRInserm · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Insulin-resistance is a characteristic feature of type 2 diabetes (T2D) and plays a major role in the pathogenesis of this disease. Skeletal muscles are quantitatively the biggest glucose users in response to insulin and are considered as main targets in development of insulin-resistance. It is now clear that circulating fatty acids (FA), which are highly increased in T2D, play a major role in the development of muscle insulin-resistance. In healthy individuals, excess FA are stored as lipid droplets in adipocytes. In situations like obesity and T2D, FA from lipolysis and food are in excess and eventually accumulate in peripheral tissues. High plasma concentrations of FA are generally associated with increased risk of developing diabetes. Indeed, ectopic fat accumulation is associated with insulin-resistance; this is called lipotoxicity. However, FA themselves are not involved in insulin-resistance, but rather some of their metabolic derivatives, such as ceramides. Ceramides, which are synthetized de novo from saturated FA like palmitate, have been demonstrated to play a critical role in the deterioration of insulin sensitivity in muscle cells. This review describes the latest progress involving ceramides as major players in the development of muscle insulin-resistance through the targeting of selective actors of the insulin signaling pathway.

Indexed as

Disease SusceptibilityLipid MetabolismAnimalsCeramidesDiabetes Mellitus, Type 2Energy MetabolismHumansInsulinInsulin ResistanceMuscle CellsSignal TransductionSphingolipidsCeramidesInsulinSphingolipidsceramideDAGdiabetesinsulinsphingolipids

Identifiers

PMID30678043
PMCPMC6387241
OpenAlexW2914020526

What Socratic 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 Socratic graph.