Evidence map›Paper›PMID 33172097›Full record

ReviewMetabolites2020

NLRP3 Inflammasome Biomarker-Could Be the New Tool for Improved Cardiometabolic Syndrome Outcome.

Andra-Iulia Suceveanu, Laura Mazilu, Niki Katsiki, Irinel Parepa, Felix Voinea, Anca Pantea-Stoian, Manfredi Rizzo, Florin Botea, Vlad Herlea, Dragos Serban and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Metabolites, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.9field-weighted citation impact, top 13% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

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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

11 authors at 4 institutions in 4 countries.

Andra-Iulia SuceveanuGastroenterology Department, Ovidius University, 900470 Constanta, Romania.
Laura MaziluOncology Department, Ovidius University, 900470 Constanta, Romania.ORCID 0000-0001-6195-4500
Niki Katsiki1st Department of Internal Medicine, Diabetes Center, Division of Endocrinology and Metabolism, AHEPA University Hospital, 546 21 Thessaloniki, Greece.
Irinel ParepaCardiology Department, Ovidius University, 900470 Constanta, Romania.
Felix VoineaUrology Department, Ovidius University, 900470 Constanta, Romania.
Anca Pantea-StoianDiabetes Mellitus Department, University of Medicine and Pharmacy Carol Davila, 050474 Bucharest, Romania.ORCID 0000-0003-0555-526X
Manfredi RizzoDepartment of Medicine, University of South Carolina, Columbia, SC 29208, USA.ORCID 0000-0002-9549-8504
Florin BoteaLiver Transplant and General Surgery Centre, Fundeni Institute, 022328 Bucharest, Romania.
Vlad HerleaDepartment of Pathology, Fundeni Institute, 022328 Bucharest, Romania.
Dragos SerbanIVth Department of Surgery, University of Medicine and Pharmacy Carol Davila, 050474 Bucharest, Romania.ORCID 0000-0002-1380-2112
Adrian-Paul SuceveanuInternal Medicine Department, Ovidius University, 900470 Constanta, Romania.
Ovidius University · ROUniversity of South Carolina · USCarol Davila University of Medicine and Pharmacy · ROInstitutul Clinic Fundeni · RO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolomics, the research area studying chemical processes involving metabolites, finds its utility in inflammasome biomarker discovery, thus representing a novel approach for cardiometabolic syndrome pathogeny acknowledgements. Metabolite biomarkers discovery is expected to improve the disease evolution and outcome. The activation of abundantly expressed NLRP3 inflammasome represents the background process of the diabetes mellitus disturbances like hyperglycemia and insulin resistance, as well as for myocardial cell death and fibrosis, all of them being features characteristic for cardiometabolic syndrome. Many molecules like troponins, brain natriuretic protein (BNP), ST2/IL-33, C-reactive protein (CRP), TNF, IL-1β, and IL-18 cytokines have been already examined as molecular markers for diagnosing or predicting different cardiac disturbances like myocardial infarction, heart failure, or myocarditis. In addition, metabolomics research comes with new findings arguing that NLRP3 inflammasome becomes a promising molecular tool to use for clinical and therapeutical management providing new targets for therapies in cardiometabolic syndrome. Inflammasome markers analyses, along with other molecular or genetic biomarkers, will result in a better understanding of cardiometabolic syndrome pathogenesis and therapeutic targets. Screening, diagnostic, and prognostic biomarkers resulted from inflammasome biomarker research will become standard of care in cardiometabolic syndrome management, their utility becoming the first magnitude.

Indexed as

biomarkerscardiometabolic syndromeinflammasomemetabolomicsNLRP3 inflammasomeoutcometargeted therapy

Identifiers

PMID33172097
PMCPMC7694742
OpenAlexW3095171706

What OpenQuestion 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 OpenQuestion graph.