Evidence map›Paper›PMID 36355127›Full record

ReviewMetabolites2022

Circulating microRNA Related to Cardiometabolic Risk Factors for Metabolic Syndrome: A Systematic Review.

Paula N Brandão-Lima, Gabrielli B de Carvalho, Tanyara B Payolla, Flavia M Sarti, Marcelo M Rogero

Abstract readReview
In one paragraph

Review in Metabolites, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–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

8 citing papers in PubMed.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. miR-92a aggravates metabolic syndrome via KLF2/miR-483 axis.Journal of diabetes investigation · 2025
    Article
  6. Article
  7. Article
  8. 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.

Paula N Brandão-LimaDepartment of Nutrition, School of Public Health, University of Sao Paulo, 715 Dr Arnaldo Avenue, Pacaembu, Sao Paulo 01246-904, SP, Brazil.ORCID 0000-0002-0949-361X
Gabrielli B de CarvalhoDepartment of Nutrition, School of Public Health, University of Sao Paulo, 715 Dr Arnaldo Avenue, Pacaembu, Sao Paulo 01246-904, SP, Brazil.
Tanyara B PayollaDepartment of Nutrition, School of Public Health, University of Sao Paulo, 715 Dr Arnaldo Avenue, Pacaembu, Sao Paulo 01246-904, SP, Brazil.
Flavia M SartiSchool of Arts, Sciences and Humanities, University of Sao Paulo, 1000 Arlindo Bettio Avenue, Sao Paulo 03828-000, SP, Brazil.
Marcelo M RogeroDepartment of Nutrition, School of Public Health, University of Sao Paulo, 715 Dr Arnaldo Avenue, Pacaembu, Sao Paulo 01246-904, SP, Brazil.ORCID 0000-0003-0517-1645

Funding

National Council for Scientific and Technological Development 150834/2020-9National Council for Scientific and Technological Development 301109/2019-2São Paulo Research Foundation 2019/22934-1São Paulo Research Foundation 2020/03104-5
6 · The paper itself

Abstract

MicroRNA regulates multiple pathways in inflammatory response, adipogenesis, and glucose and lipid metabolism, which are involved in metabolic syndrome (MetS). Thus, this systematic review aimed at synthesizing the evidence on the relationships between circulating microRNA and risk factors for MetS. The systematic review was registered in the PROSPERO database (CRD42020168100) and included 24 case-control studies evaluating microRNA expression in serum/plasma of individuals ≥5 years old. Most of the studies focused on 13 microRNAs with higher frequency and there were robust connections between miR-146a and miR-122 with risk factors for MetS, based on average weighted degree. In addition, there was an association of miR-222 with adiposity, lipid metabolism, glycemic metabolism, and chronic inflammation and an association of miR-126, miR-221, and miR-423 with adiposity, lipid, and glycemic metabolism. A major part of circulating microRNA was upregulated in individuals with risk factors for MetS, showing correlations with glycemic and lipid markers and body adiposity. Circulating microRNA showed distinct expression profiles according to the clinical condition of individuals, being particularly linked with increased body fat. However, the exploration of factors associated with variations in microRNA expression was limited by the variety of microRNAs investigated by risk factor in diverse studies identified in this systematic review.

Indexed as

metabolic syndromemiRNAobesityplasmaserumtype 2 diabetes

Identifiers

PMID36355127
PMCPMC9692352

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.