Evidence map›Paper›PMID 29777212›Full record

ReviewNature immunology2018

Regulation of macrophage immunometabolism in atherosclerosis.

Graeme J Koelwyn, Emma M Corr, Ebru Erbay, Kathryn J Moore

Abstract readReview
In one paragraph

Review in Nature immunology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 299 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
299citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

299 citing papers in PubMed, 1 synthesis or guideline pooled it.

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239 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

4 authors.

Graeme J KoelwynDepartment of Medicine, Marc and Ruti Bell Program for Vascular Biology and Disease, Leon H. Charney Division of Cardiology, New York University School of Medicine, New York, NY, USA.
Emma M CorrDepartment of Medicine, Marc and Ruti Bell Program for Vascular Biology and Disease, Leon H. Charney Division of Cardiology, New York University School of Medicine, New York, NY, USA.
Ebru ErbayDepartment of Medicine, Heart Institute & Department of Biomedical Sciences, Cedars Sinai Medical Center, Los Angeles, CA, USA.ORCID http://orcid.org/0000-0001-9584-1803
Kathryn J MooreDepartment of Medicine, Marc and Ruti Bell Program for Vascular Biology and Disease, Leon H. Charney Division of Cardiology, New York University School of Medicine, New York, NY, USA. kathryn.moore@nyumc.org.

Funding

Resolving Macrophage Inflammation in Atherosclerotic Plaques and Other Sites in Insulin ResistanceP01HL131481 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ANN MARIE SCHMIDT · 2017 to 2026
$27.3M
Non-coding RNA regulation of cholesterol homeostasis and atherosclerosisR35HL135799 · NHLBI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI MOORE, KATHRYN J · 2017 to 2023
$6.7M
NHLBI NIH HHS P01 HL131481NHLBI NIH HHS R35 HL135799
6 · The paper itself

Abstract

After activation, cells of the myeloid lineage undergo robust metabolic transitions, as well as discrete epigenetic changes, that can dictate both ongoing and future inflammatory responses. In atherosclerosis, in which macrophages play central roles in the initiation, growth, and ultimately rupture of arterial plaques, altered metabolism is a key feature that dictates macrophage function and subsequent disease progression. This Review explores how factors central to the plaque microenvironment (for example, altered cholesterol metabolism, oxidative stress, hypoxia, apoptotic and necrotic cells, and hyperglycemia) shape the metabolic rewiring of macrophages in atherosclerosis as well as how these metabolic shifts in turn alter macrophage immune-effector and tissue-reparative functions. Finally, this overview offers insight into the challenges and opportunities of harnessing metabolism to modulate aberrant macrophage responses in disease.

Indexed as

AnimalsAtherosclerosisHumansMacrophages

Identifiers

PMID29777212
PMCPMC6314674

What OpenQuestion holds

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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.