Evidence mapPaperPMID 38085578Full record

ArticleThe Journal of clinical investigation2023

Itaconate suppresses atherosclerosis by activating a Nrf2-dependent antiinflammatory response in macrophages in mice.

Jianrui Song, Yanling Zhang, Ryan A Frieler, Anthony Andren, Sherri Wood, Daniel J Tyrrell, Peter Sajjakulnukit, Jane C Deng, Costas A Lyssiotis, Richard M Mortensen and 2 more

Open access · goldAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
11.7field-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

49 citing papers in PubMed, 71 citations in OpenAlex.

  1. Article
  2. Intercellular transfer of LncRNABiochemistry and biophysics reports · 2026
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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

12 authors at 3 institutions in 3 countries.

Jianrui SongDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Yanling ZhangDepartment of Biochemistry and Molecular Biology, Soochow University Medical College, Suzhou, Jiangsu, China.
Ryan A FrielerDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Anthony AndrenDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Sherri WoodDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Daniel J TyrrellDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of Michigan, Ann Arbor, Michigan, USA.
Peter SajjakulnukitDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Jane C DengGraduate Program in Immunology, and.
Costas A LyssiotisDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Richard M MortensenDepartment of Molecular and Integrative Physiology, University of Michigan, Ann Arbor, Michigan, USA.
Morgan SalmonDepartment of Cardiac Surgery.
Daniel R GoldsteinDepartment of Internal Medicine, Division of Cardiovascular Medicine, University of Michigan, Ann Arbor, Michigan, USA.
University of Michigan · USSoochow University · CNUniversity of Alabama at Birmingham · US

Funding

Univ. Michigan Comprehensive Cancer Center Support GrantP30CA046592 · UNIVERSITY OF MICHIGAN AT ANN ARBOR · 1988 to 2025
$35.8M
Role of mitophagy in age-related respiratory and vascular diseasesR35HL155169 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Daniel Robert Goldstein · 2022 to 2023
$1.2M
Novel mechanisms of age-enhanced vasculopathy after heart transplantationR01AI138347 · NIAID · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Daniel Robert Goldstein · 2022 to 2022
$497k
NCI NIH HHS P30 CA046592NCI NIH HHS R01 CA244931NHLBI NIH HHS R35 HL155169NIAID NIH HHS R01 AI138347NIA NIH HHS R00 AG068309NIA NIH HHS R01 AG028082
6 · The paper itself

Abstract

Itaconate has emerged as a critical immunoregulatory metabolite. Here, we examined the therapeutic potential of itaconate in atherosclerosis. We found that both itaconate and the enzyme that synthesizes it, aconitate decarboxylase 1 (Acod1, also known as immune-responsive gene 1 [IRG1]), are upregulated during atherogenesis in mice. Deletion of Acod1 in myeloid cells exacerbated inflammation and atherosclerosis in vivo and resulted in an elevated frequency of a specific subset of M1-polarized proinflammatory macrophages in the atherosclerotic aorta. Importantly, Acod1 levels were inversely correlated with clinical occlusion in atherosclerotic human aorta specimens. Treating mice with the itaconate derivative 4-octyl itaconate attenuated inflammation and atherosclerosis induced by high cholesterol. Mechanistically, we found that the antioxidant transcription factor, nuclear factor erythroid 2-related factor 2 (Nrf2), was required for itaconate to suppress macrophage activation induced by oxidized lipids in vitro and to decrease atherosclerotic lesion areas in vivo. Overall, our work shows that itaconate suppresses atherogenesis by inducing Nrf2-dependent inhibition of proinflammatory responses in macrophages. Activation of the itaconate pathway may represent an important approach to treat atherosclerosis.

Indexed as

Aortic DiseasesAtherosclerosisSuccinatesAnimalsHumansInflammationMacrophagesMiceNF-E2-Related Factor 2itaconic acidNF-E2-Related Factor 2SuccinatesAtherosclerosisCardiologyCardiovascular diseaseInflammationMacrophages

Identifiers

PMID38085578
PMCPMC10849764
OpenAlexW4389614151

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.