Evidence map›Paper›PMID 26311337›Full record

ReviewInternational journal of obesity (2005)2016

MicroRNAs as regulators of metabolic disease: pathophysiologic significance and emerging role as biomarkers and therapeutics.

J A Deiuliis

Open access · hybridAbstract readReview
In one paragraph

Review in International journal of obesity (2005), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 190 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
190citing papers in PubMed, 5 pooled it
11.8field-weighted citation impact, top 1% 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

190 citing papers in PubMed, 5 syntheses or guidelines pooled it, 340 citations in OpenAlex.

  1. Epigenetic Mechanisms in Childhood Obesity.Annals of the New York Academy of Sciences · 2025
    Pooled it
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  5. A Systematic Study of Dysregulated MicroRNA in Type 2 Diabetes Mellitus.International journal of molecular sciences · 2017
    Pooled it
  6. Trial
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  18. lncRNA SNHG6 improves placental villous cell function in anArchives of medical science : AMS · 2026
    Article
  19. Review
  20. Article

130 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

1 author at 1 institution in 1 country.

J A DeiuliisDepartment of Medicine, University of Maryland Baltimore, Baltimore, MD, USA.
University of Maryland, Baltimore · US

Funding

Adipose microRNAs (miRs) in Insulin ResistanceK01DK099475 · NIDDK · UNIVERSITY OF MARYLAND BALTIMORE · PI DEIULIIS, JEFFREY ALAN · 2014 to 2016
$427k
NIDDK NIH HHS K01 DK099475NIDDK NIH HHS K01DK099475
6 · The paper itself

Abstract

The prevalence of overweight and obesity in developed and developing countries has greatly increased the risk of insulin resistance and type 2 diabetes mellitus. It is evident from human and animal studies that obesity alters microRNA (miRNA) expression in metabolically important organs, and that miRNAs are involved in changes to normal physiology, acting as mediators of disease. miRNAs regulate multiple pathways including insulin signaling, immune-mediated inflammation, adipokine expression, adipogenesis, lipid metabolism, and food intake regulation. Thus, miRNA-based therapeutics represent an innovative and attractive treatment modality, with non-human primate studies showing great promise. In addition, miRNA measures in plasma or bodily fluids may be used as disease biomarkers and predictors of metabolic disease in humans. This review analyzes the role of miRNAs in obesity and insulin resistance, focusing on the miR-17/92, miR-143-145, miR-130, let-7, miR-221/222, miR-200, miR-223, miR-29 and miR-375 families, as well as miRNA changes by relevant tissue (adipose, liver and skeletal muscle). Further, the current and future applications of miRNA-based therapeutics and diagnostics in metabolic disease are discussed.

Indexed as

Insulin ResistanceMolecular Targeted TherapyAdipogenesisAnimalsBiomarkersDiabetes Mellitus, Type 2Disease Models, AnimalHumansLipid MetabolismMetabolic SyndromeMiceMicroRNAsObesityPrevalenceSignal TransductionUnited StatesBiomarkersMicroRNAs

Identifiers

PMID26311337
PMCPMC4722234
OpenAlexW1910286204

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.