Evidence map›Paper›PMID 29602400›Full record

ReviewSeminars in nephrology2018

Targeting Glucosylceramide Synthesis in the Treatment of Rare and Common Renal Disease.

James A Shayman

Open access · greenAbstract readReview
In one paragraph

Review in Seminars in nephrology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

26 citing papers in PubMed, 37 citations in OpenAlex.

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  11. Role of UDP-glucose ceramide glucosyltransferase in venous malformation.Frontiers in cell and developmental biology · 2023
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  14. Review
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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

1 author at 1 institution in 1 country.

James A ShaymanDepartment of Internal Medicine, University of Michigan, Ann Arbor, Michigan. Electronic address: jshayman@umich.edu.
University of Michigan–Ann Arbor · US

Funding

THE PHARMACOLOGIC TREATMENT OF FABRY DISEASER01DK055823 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHAYMAN, JAMES ALAN · 2000 to 2013
$4.1M
Novel Probes for Studying Treatment of CNS-based Lysosomal Storage DiseasesR01HD076004 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LARSEN, SCOTT D, SHAYMAN, JAMES ALAN · 2013 to 2015
$1.8M
Lysosomal Phospholipase A2 in Autoimmune DiseaseR01AR056991 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SHAYMAN, JAMES ALAN · 2010 to 2014
$1.6M
The Development of Small Molecule Inhibitors for Gaucher Disease Type 3UH3NS092981 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LARSEN, SCOTT D, SHAYMAN, JAMES ALAN · 2016 to 2019
$1.5M
The Development of Small Molecule Inhibitors for Gaucher Disease Type 3UH2NS092981 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LARSEN, SCOTT D, SHAYMAN, JAMES ALAN · 2015 to 2015
$631k
Mechanisms of Drug Induced PhospholipidosisI01BX002021 · VA · VETERANS HEALTH ADMINISTRATION · PI SHAYMAN, JAMES ALAN · 2013 to 2016
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BLRD VA I01 BX002021NIAMS NIH HHS R01 AR056991NICHD NIH HHS R01 HD076004NIDDK NIH HHS R01 DK055823NINDS NIH HHS UH2 NS092981NINDS NIH HHS UH3 NS092981
6 · The paper itself

Abstract

Sphingolipids, including ceramides, glycosphingolipids, sphingomyelin, and sphingosine-1-phosphate, have been recognized as important molecules that regulate critical cellular functions. Although originally studied in the context of lysosomal storage diseases, the roles of these compounds in more common disorders involving metabolism, vascular disease, and aberrant growth has been the focus of recent studies, including in disorders that affect the kidneys. These efforts have led to new insights into Fabry disease, a classic disorder of lysosomal function that results in renal failure as well as in more common renal diseases including diabetic nephropathy and polycystic kidney disease. Pathways for glycosphingolipid synthesis can be targeted with orally available small-molecule inhibitors, creating new opportunities for the treatment of both rare and common kidney diseases.

Indexed as

Signal TransductionAnimalsDiabetic NephropathiesFabry DiseaseGlucosylceramidesGlucosyltransferasesHumansKidney DiseasesPolycystic Kidney DiseasesRare DiseasesSphingolipidsceramide glucosyltransferaseGlucosylceramidesGlucosyltransferasesSphingolipidsdiabetesFabry diseaseglucosylceramideGlycosphingolipidspolycystic kidney diseasesubstrate reduction

Identifiers

PMID29602400
PMCPMC6317906
OpenAlexW2795162597

What OpenQuestion holds

Textmetadata
LicenceTDM
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.