Evidence mapPaperPMID 38532071Full record

ReviewNature metabolism2024

Dysregulated cellular metabolism in atherosclerosis: mediators and therapeutic opportunities.

Chad Stroope, Felix Sebastian Nettersheim, Brian Coon, Alexandra C Finney, Martin A Schwartz, Klaus Ley, Oren Rom, Arif Yurdagul

Open access · greenAbstract readReview
In one paragraph

Review in Nature metabolism, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
12.0field-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.

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

38 citing papers in PubMed, 50 citations in OpenAlex.

  1. Review
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  18. Review
  19. Anti-Atherogenic Mechanisms and Therapies.Current atherosclerosis reports · 2025
    Review
  20. Article
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

8 authors at 4 institutions in 2 countries.

Chad Stroope *Department of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, LA, USA.
Felix Sebastian Nettersheim *La Jolla Institute for Immunology, La Jolla, CA, USA.ORCID http://orcid.org/0000-0002-4090-3357
Brian Coon *Yale Cardiovascular Research Center, Division of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-4516-0193
Alexandra C FinneyDepartment of Pathology and Translational Pathobiology, Louisiana State University Health Sciences Center, Shreveport, LA, USA.ORCID http://orcid.org/0000-0003-1575-4975
Martin A SchwartzYale Cardiovascular Research Center, Division of Cardiovascular Medicine, Department of Internal Medicine, Yale School of Medicine, New Haven, CT, USA.ORCID http://orcid.org/0000-0002-2071-1243
Klaus LeyLa Jolla Institute for Immunology, La Jolla, CA, USA.ORCID http://orcid.org/0000-0001-9339-3672
Oren RomDepartment of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, LA, USA.ORCID http://orcid.org/0000-0002-9272-086X
Arif YurdagulDepartment of Molecular and Cellular Physiology, Louisiana State University Health Sciences Center, Shreveport, LA, USA. arif.yurdagul@lsuhs.edu.ORCID http://orcid.org/0000-0002-7613-6313
Louisiana State University Health Sciences Center Shreveport · USLa Jolla Institute for Immunology · USOklahoma Medical Research Foundation · USYale University · US

Funding

Project 4: APOB-specific CD4 and CD8 T cells exacerbate atherosclerosisP01HL136275 · NHLBI · LA JOLLA INSTITUTE FOR IMMUNOLOGY · 2022 to 2025
$5.3M
Endothelial-to-mesenchymal transition and atherosclerosisR01HL135582 · NHLBI · YALE UNIVERSITY · PI Martin A Schwartz, Michael Simons · 2021 to 2023
$2.5M
Vascular macrophages and T cells in atherosclerosisR35HL145241 · AUGUSTA UNIVERSITY · 2025 to 2025
$770k
Dysregulations in Polyamine Metabolism During AtherosclerosisR01HL167758 · LOUISIANA STATE UNIV HSC SHREVEPORT · 2025 to 2025
$567k
Lipidated Amino Acids in Cardiometabolic DiseasesR01DK134011 · LOUISIANA STATE UNIV HSC SHREVEPORT · 2025 to 2025
$430k
Dysregulated Oxalate Metabolism in Cardiometabolic DiseasesR01DK136685 · LOUISIANA STATE UNIV HSC SHREVEPORT · 2025 to 2025
$429k
NHLBI NIH HHS P01 HL107205NHLBI NIH HHS P01 HL136275NHLBI NIH HHS R00 HL145131NHLBI NIH HHS R00 HL150233NHLBI NIH HHS R01 HL135582NHLBI NIH HHS R01 HL167758NHLBI NIH HHS R35 HL145241NIDDK NIH HHS R01 DK134011NIDDK NIH HHS R01 DK136685
6 · The paper itself

Abstract

Accumulating evidence over the past decades has revealed an intricate relationship between dysregulation of cellular metabolism and the progression of atherosclerotic cardiovascular disease. However, an integrated understanding of dysregulated cellular metabolism in atherosclerotic cardiovascular disease and its potential value as a therapeutic target is missing. In this Review, we (1) summarize recent advances concerning the role of metabolic dysregulation during atherosclerosis progression in lesional cells, including endothelial cells, vascular smooth muscle cells, macrophages and T cells; (2) explore the complexity of metabolic cross-talk between these lesional cells; (3) highlight emerging technologies that promise to illuminate unknown aspects of metabolism in atherosclerosis; and (4) suggest strategies for targeting these underexplored metabolic alterations to mitigate atherosclerosis progression and stabilize rupture-prone atheromas with a potential new generation of cardiovascular therapeutics.

Indexed as

AtherosclerosisAnimalsEndothelial CellsHumansMacrophagesMuscle, Smooth, VascularT-Lymphocytes

Identifiers

PMID38532071
PMCPMC11055680
OpenAlexW4393200149

What Socratic 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 Socratic graph.