Evidence map›Paper›PMID 32757967›Full record

ReviewExpert opinion on therapeutic targets2020

Inflammasomes: a preclinical assessment of targeting in atherosclerosis.

Jeremiah Stitham, Astrid Rodriguez-Velez, Xiangyu Zhang, Se-Jin Jeong, Babak Razani

Open access · greenAbstract readReview
In one paragraph

Review in Expert opinion on therapeutic targets, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
0.7field-weighted citation impact, top 32% 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

11 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Review
  3. Review
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  5. Review
  6. Targeted drug delivery systems for atherosclerosis.Journal of nanobiotechnology · 2025
    Review
  7. Correlation between Complement C1q A Chain (Iranian journal of public health · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Review
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.

Jeremiah StithamDepartment of Medicine, Division of Endocrinology, Metabolism, and Lipid Research, Washington University School of Medicine , St. Louis, MO, USA.
Astrid Rodriguez-VelezDepartment of Medicine, Cardiovascular Division, Washington University School of Medicine , St. Louis, MO, USA.
Xiangyu ZhangDepartment of Medicine, Cardiovascular Division, Washington University School of Medicine , St. Louis, MO, USA.
Se-Jin JeongDepartment of Medicine, Cardiovascular Division, Washington University School of Medicine , St. Louis, MO, USA.
Babak RazaniDepartment of Medicine, Cardiovascular Division, Washington University School of Medicine , St. Louis, MO, USA.ORCID 0000-0002-7172-9240
Washington University in St. Louis · US

Funding

THE ROLE OF MACROPHAGE LYSOSOMAL BIOGENESIS IN ATHEROSCLEROSISR01HL125838 · NHLBI · WASHINGTON UNIVERSITY · PI RAZANI, BABAK · 2015 to 2025
$4.6M
Training in Integrative and Systems Biology of Cardiovascular DiseaseT32HL134635 · NHLBI · WASHINGTON UNIVERSITY · PI NERBONNE, JEANNE M. · 2017 to 2021
$1.8M
Harnessing the Autophagy-Lysosomal Biogenesis Response in Macrophages to Treat AtherosclerosisI01BX003415 · VA · VETERANS HEALTH ADMINISTRATION · PI RAZANI, BABAK · 2018 to 2025
–
BLRD VA I01 BX003415NHLBI NIH HHS R01 HL125838NHLBI NIH HHS T32 HL134635
6 · The paper itself

Abstract

introductionInflammasomes are central to atherosclerotic vascular dysfunction with regulatory effects on inflammation, immune modulation, and lipid metabolism. The NLRP3 inflammasome is a critical catalyst for atherogenesis thus highlighting its importance in understanding the pathophysiology of atherosclerosis and for the identification of novel therapeutic targets and biomarkers for the treatment of cardiovascular disease. AREAS COVERED: This review includes an overview of macrophage lipid metabolism and the role of NLRP3 inflammasome activity in cardiovascular inflammation and atherosclerosis. We highlight key activators, signal transducers and major regulatory components that are being considered as putative therapeutic targets for inhibition of NLRP3-mediated cardiovascular inflammation and atherosclerosis. EXPERT OPINION: NLRP3 inflammasome activity lies at the nexus between inflammation and cholesterol metabolism; it offers unique opportunities for understanding atherosclerotic pathophysiology and identifying novel modes of treatment. As such, a host of NLRP3 signaling cascade components have been identified as putative targets for drug development. We catalog these current discoveries in therapeutic targeting of the NLRP3 inflammasome and, utilizing the CANTOS trial as the translational (bench-to-bedside) archetype, we examine the complexities, challenges, and ultimate goals facing the field of atherosclerosis research.

Indexed as

Molecular Targeted TherapyAnimalsAtherosclerosisBiomarkersCardiovascular DiseasesHumansInflammasomesInflammationLipid MetabolismMacrophagesNLR Family, Pyrin Domain-Containing 3 ProteinBiomarkersInflammasomesNLR Family, Pyrin Domain-Containing 3 ProteinNLRP3 protein, humanatherosclerosiscardiovascular diseaseinflammationinterleukin-1bmacrophageNLRP3 inflammasome

Identifiers

PMID32757967
PMCPMC7554266
OpenAlexW3047193884

What OpenQuestion 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 OpenQuestion graph.