Evidence map›Paper›PMID 25993337›Full record

ArticlePloS one2015

Ceramide as a mediator of non-alcoholic Fatty liver disease and associated atherosclerosis.

Takhar Kasumov, Ling Li, Min Li, Kailash Gulshan, John P Kirwan, Xiuli Liu, Stephen Previs, Belinda Willard, Jonathan D Smith, Arthur McCullough

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed
9.0field-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

126 citing papers in PubMed, 202 citations in OpenAlex.

  1. Trial
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  5. Article
  6. Sphingolipids and Atherosclerosis.Current atherosclerosis reports · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. The Role of Ceramides in Metabolic and Cardiovascular Diseases.Journal of cardiovascular development and disease · 2026
    Review
  11. MASH: the nexus of metabolism, inflammation, and fibrosis.The Journal of clinical investigation · 2025
    Review
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Article

66 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

10 authors at 2 institutions in 1 country.

Takhar KasumovDepartment of Gastroenterology& Hepatology, Cleveland Clinic, Cleveland, OH, United States of America.
Ling LiDepartment of Research Core Services, Cleveland Clinic, Cleveland, OH, United States of America.
Min LiDepartment of Pathobiology, Cleveland Clinic, Cleveland, OH, United States of America.
Kailash GulshanDepartment of Cellular & Molecular Medicine, Cleveland Clinic, Cleveland, OH, United States of America.
John P KirwanDepartment of Pathobiology, Cleveland Clinic, Cleveland, OH, United States of America.
Xiuli LiuDepartment of Anatomic Pathology, Cleveland Clinic, Cleveland, OH, United States of America.
Stephen PrevisDepartment of Nutrition & Medicine, Case Western Reserve University School of Medicine Cleveland Clinic, Cleveland, OH, United States of America.
Belinda WillardDepartment of Research Core Services, Cleveland Clinic, Cleveland, OH, United States of America.
Jonathan D SmithDepartment of Cellular & Molecular Medicine, Cleveland Clinic, Cleveland, OH, United States of America.
Arthur McCulloughDepartment of Gastroenterology& Hepatology, Cleveland Clinic, Cleveland, OH, United States of America; Department of Pathobiology, Cleveland Clinic, Cleveland, OH, United States of America.
Cleveland Clinic · USUniversity School · US

Funding

Clinical and Translational Science Collaborative of ClevelandUL1TR000439 · NCATS · CASE WESTERN RESERVE UNIVERSITY · PI KONSTAN, MICHAEL W. · 2012 to 2016
$50.0M
Vascular Cell function and AtherosclerosisP01HL029582 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI FOX, PAUL L · 1985 to 2019
$32.0M
Regression of Atherosclerosis CoreP01HL098055 · NHLBI · CLEVELAND CLINIC LERNER COM-CWRU · PI FISHER, EDWARD A · 2010 to 2014
$12.1M
Novel computational methods for in vivo proteome dynamics estimation using heavy water metabolic labeling and LC-MSR01GM112044 · NIGMS · UNIVERSITY OF TEXAS MED BR GALVESTON · PI SADYGOV, ROVSHAN G · 2015 to 2023
$2.7M
LTQ-Orbitrap Velos instrumentS10RR031537 · NCRR · CLEVELAND CLINIC LERNER COM-CWRU · PI WILLARD, BELINDA BELLE · 2011 to 2011
$600k
Enabling studies of proteome dynamicsR21RR025346 · NCRR · CASE WESTERN RESERVE UNIVERSITY · PI KASUMOV, TAKHAR · 2009 to 2011
$583k
Mitochondrial Proteome Dynamics in Heart Failure Assessed with Heavy WaterR21HL114407 · NHLBI · UNIVERSITY OF MARYLAND BALTIMORE · PI KASUMOV, TAKHAR · 2012 to 2013
$394k
NCATS NIH HHS UL1 TR000439NCRR NIH HHS 1S10RR031537-01NCRR NIH HHS 5R21RR025346-03NCRR NIH HHS R21 RR025346NCRR NIH HHS S10 RR031537NHLBI NIH HHS P01 HL029582NHLBI NIH HHS P01 HL098055NHLBI NIH HHS R21 HL114407NIGMS NIH HHS R01 GM112044
6 · The paper itself

Abstract

Cardiovascular disease (CVD) is a serious comorbidity in nonalcoholic fatty liver disease (NAFLD). Since plasma ceramides are increased in NAFLD and sphingomyelin, a ceramide metabolite, is an independent risk factor for CVD, the role of ceramides in dyslipidemia was assessed using LDLR(-/-) mice, a diet-induced model of NAFLD and atherosclerosis. Mice were fed a standard or Western diet (WD), with or without myriocin, an inhibitor of ceramide synthesis. Hepatic and plasma ceramides were profiled and lipid and lipoprotein kinetics were quantified. Hepatic and intestinal expression of genes and proteins involved in insulin, lipid and lipoprotein metabolism were also determined. WD caused hepatic oxidative stress, inflammation, apoptosis, increased hepatic long-chain ceramides associated with apoptosis (C16 and C18) and decreased very-long-chain ceramide C24 involved in insulin signaling. The plasma ratio of ApoB/ApoA1 (proteins of VLDL/LDL and HDL) was increased 2-fold due to increased ApoB production. Myriocin reduced hepatic and plasma ceramides and sphingomyelin, and decreased atherosclerosis, hepatic steatosis, fibrosis, and apoptosis without any effect on oxidative stress. These changes were associated with decreased lipogenesis, ApoB production and increased HDL turnover. Thus, modulation of ceramide synthesis may lead to the development of novel strategies for the treatment of both NAFLD and its associated atherosclerosis.

Indexed as

AnimalsApolipoproteins BApoptosisAtherosclerosisBiological TransportBody WeightCeramidesCholesterol, HDLDiet, WesternFastingFatty Acids, MonounsaturatedFeeding BehaviorGene Expression RegulationGlucoseInflammationInsulinApolipoproteins BCeramidesCholesterol, HDLFatty Acids, MonounsaturatedGlucoseInsulinReceptors, LDLRNA, Messengerthermozymocidin

Identifiers

PMID25993337
PMCPMC4439060
OpenAlexW1530661366

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.