Evidence map›Paper›PMID 33772258›Full record

ReviewNature reviews. Cardiology2021

Ceramides and other sphingolipids as drivers of cardiovascular disease.

Ran Hee Choi, Sean M Tatum, J David Symons, Scott A Summers, William L Holland

2 registry-linked trialsOpen access · greenAbstract readReview
In one paragraph

Review in Nature reviews. Cardiology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 243 papers.

0numbers the graph read from it
0cells of the map it votes in
243citing papers in PubMed
21.8field-weighted citation impact, top 1% 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.

NCT05390866 nacompletednot on this mapstarted 2022, after this paper: background citation

A Monocentric Randomised Controlled Trial to Investigate Changes in the Circulating Sphingolipidome Composition of Young and Healthy Individuals in Response to a Single Session of High-intensity Interval Training: the SphingoHIIT Study

TypeinterventionalSponsorUniversity of BaselRan2022 to 2023Enrolled36ConditionsPhysiological Response of Sphingolipids to a Single HIIT SessionArmsHIIT
NCT06024291 nacompletednot on this mapstarted 2023, after this paper: background citation

Reducing Circulating Sphingolipid Levels to Optimise Cardiometabolic Health - The SphingoFIT Randomised Controlled Exercise Trial

TypeinterventionalSponsorUniversity of BaselRan2023 to 2025Enrolled88ConditionsOverweight and Obesity, Dyslipidemias, Blood Pressure, Cardiovascular DiseasesArms8-week HIIT programme, Physical activity recommendation
3 · Its place in the literature

Who cites it

243 citing papers in PubMed, 368 citations in OpenAlex.

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  8. Sphingomyelin as a key negative mediator in atrial fibrillation via lipid profiling analysis and functional identification.Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology · 2026
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  20. Sphingolipids and Mortality in Hemodialysis: Innocent Bystanders or Causal Culprits?Journal of the American Society of Nephrology : JASN · 2026
    Article

183 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 1 institution in 1 country.

Ran Hee Choi *Department of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT, USA.
Sean M Tatum *Department of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT, USA.
J David SymonsDepartment of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT, USA.
Scott A SummersDepartment of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT, USA. scott.a.summers@health.utah.edu.ORCID http://orcid.org/0000-0002-4919-0592
William L HollandDepartment of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, UT, USA.
University of Utah · US

Funding

Interdisciplinary Training Program in MetabolismT32DK091317 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI SCOTT A SUMMERS · 2011 to 2026
$4.8M
University of Utah Interdisciplinary Training Program in Computational Approaches to Diabetes and Metabolism ResearchT32DK110966 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Karen Louise Eilbeck, Marcus Guy Pezzolesi · 2016 to 2026
$2.6M
The Role of Ceramides in Skeletal MuscleR01DK115824 · NIDDK · UNIVERSITY OF UTAH · PI SUMMERS, SCOTT A · 2018 to 2021
$2.6M
The Role of Ceramides in the Intestinal Stem CellR01DK131609 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI EDGAR, BRUCE ALEXANDER, SUMMERS, SCOTT A · 2021 to 2025
$2.5M
The Role of Ceramides in the Pancreatic Beta CellR01DK130296 · NIDDK · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI HOLLAND, WILLIAM L, SUMMERS, SCOTT A · 2022 to 2025
$2.2M
Targeting a Ceramide Double Bond to Treat Cardiometabolic DisordersR01DK122001 · NIDDK · UNIVERSITY OF UTAH · PI SUMMERS, SCOTT A · 2019 to 2022
$1.9M
Autophagy maintains vascular function through a novel glycolysis-linked pathway regulating eNOS.R01HL141540 · NHLBI · UNIVERSITY OF UTAH · PI SYMONS, JOHN DAVID · 2018 to 2021
$1.7M
NHLBI NIH HHS R01 HL141540NIDDK NIH HHS R01 DK115824NIDDK NIH HHS R01 DK122001NIDDK NIH HHS R01 DK130296NIDDK NIH HHS R01 DK131609NIDDK NIH HHS T32 DK091317NIDDK NIH HHS T32 DK110966
6 · The paper itself

Abstract

Increases in calorie consumption and sedentary lifestyles are fuelling a global pandemic of cardiometabolic diseases, including coronary artery disease, diabetes mellitus, cardiomyopathy and heart failure. These lifestyle factors, when combined with genetic predispositions, increase the levels of circulating lipids, which can accumulate in non-adipose tissues, including blood vessel walls and the heart. The metabolism of these lipids produces bioactive intermediates that disrupt cellular function and survival. A compelling body of evidence suggests that sphingolipids, such as ceramides, account for much of the tissue damage in these cardiometabolic diseases. In humans, serum ceramide levels are proving to be accurate biomarkers of adverse cardiovascular disease outcomes. In mice and rats, pharmacological inhibition or depletion of enzymes driving de novo ceramide synthesis prevents the development of diabetes, atherosclerosis, hypertension and heart failure. In cultured cells and isolated tissues, ceramides perturb mitochondrial function, block fuel usage, disrupt vasodilatation and promote apoptosis. In this Review, we discuss the body of literature suggesting that ceramides are drivers - and not merely passengers - on the road to cardiovascular disease. Moreover, we explore the feasibility of therapeutic strategies to lower ceramide levels to improve cardiovascular health.

Indexed as

Cardiovascular DiseasesCeramidesSphingolipidsAnimalsMiceRatsCeramidesSphingolipids

Identifiers

PMID33772258
PMCPMC8978615
OpenAlexW3136668199

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

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.