Evidence map›Paper›PMID 35392792›Full record

ReviewEndocrine, metabolic & immune disorders drug targets2022

Inflammasomes as Potential Therapeutic Targets in Atherosclerotic Cardiovascular Disease.

Ping Wang, Jun Ma, Ru Zhang

Abstract readReview
PubMed Publisher
In one paragraph

Review in Endocrine, metabolic & immune disorders drug targets, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

3 authors at 1 institution in 1 country.

Ping WangDepartment of Geriatrics, The General Hospital of Western Theater Command, Chengdu, Sichuan, 610083; P.R. China.
Jun MaDepartment of Cardiology, West China Hospital, Sichuan University, 610083; P.R. China.
Ru ZhangDepartment of Geriatrics, The General Hospital of Western Theater Command, Chengdu, Sichuan, 610083; P.R. China.
West China Hospital of Sichuan University · CN

Funding

National Natural Science Foundation of China 81900404
6 · The paper itself

Abstract

Recent studies have shown that interleukin 1β monoclonal antibody improves the prognosis of patients with coronary artery disease independently of lipid levels, providing the first evidence of the effectiveness of anti-inflammatory treatment for atherosclerotic disease. However, there is still a significant risk of residual inflammation with interleukin 1β monoclonal antibody therapy alone. Activation of the inflammasome, an intracellular protein complex composed of pattern recognition receptors and other inflammatory molecules, is a critical step in the development of the inflammatory response, and targeting the inflammasome to reduce residual inflammation has emerged as a new idea in the anti-inflammatory treatment of atherosclerotic disease. This review discusses the role and mechanisms of inflammasomes in atherosclerotic disease and lists drugs that are currently thought to potentially treat atherosclerosis through antiinflammasomes, hoping to provide insight into the development of new anti-inflammatory therapies for the prevention and treatment of atherosclerotic disease.

Indexed as

AtherosclerosisCardiovascular DiseasesAntibodies, MonoclonalAnti-Inflammatory AgentsHumansInflammasomesInflammationInterleukin-1betaAntibodies, MonoclonalAnti-Inflammatory AgentsInflammasomesInterleukin-1beta1β monoclonal antibodyAtherosclerotic diseasecoronary artery diseaseinflammasomesinterleukin 18interleukin 1β

Identifiers

PMID35392792
OpenAlexW4226307921

What OpenQuestion holds

Textmetadata
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.