Evidence map›Paper›PMID 31396538›Full record

ArticleJournal of diabetes research2019

Visfatin Induces Inflammation and Insulin Resistance via the NF-

Yu Jung Heo, Sung-E Choi, Ja Young Jeon, Seung Jin Han, Dae Jung Kim, Yup Kang, Kwan Woo Lee, Hae Jin Kim

Open access · goldAbstract read
In one paragraph

Article in Journal of diabetes research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
9.3field-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

87 citing papers in PubMed, 152 citations in OpenAlex.

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  12. Foods (Basel, Switzerland) · 2025
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  18. Impact of 4-Environment & health (Washington, D.C.) · 2025
    Article
  19. Observational
  20. Review

27 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

8 authors at 1 institution in 1 country.

Yu Jung HeoDepartment of Biomedical Sciences, Graduate School of Ajou University, Suwon, Republic of Korea.
Sung-E ChoiDepartment of Physiology, Ajou University School of Medicine, Suwon, Republic of Korea.
Ja Young JeonDepartment of Endocrinology and Metabolism, Ajou University School of Medicine, Suwon, Republic of Korea.
Seung Jin HanDepartment of Endocrinology and Metabolism, Ajou University School of Medicine, Suwon, Republic of Korea.
Dae Jung KimDepartment of Endocrinology and Metabolism, Ajou University School of Medicine, Suwon, Republic of Korea.
Yup KangDepartment of Physiology, Ajou University School of Medicine, Suwon, Republic of Korea.
Kwan Woo LeeDepartment of Endocrinology and Metabolism, Ajou University School of Medicine, Suwon, Republic of Korea.ORCID https://orcid.org/0000-0002-7965-9662
Hae Jin KimDepartment of Endocrinology and Metabolism, Ajou University School of Medicine, Suwon, Republic of Korea.ORCID https://orcid.org/0000-0002-8958-7164
Ajou University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIt has been suggested that visfatin, which is an adipocytokine, exhibits proinflammatory properties and is associated with insulin resistance. Insulin resistance and inflammation are the principal pathogeneses of nonalcoholic fatty liver disease (NAFLD), but the relationship, if any, between visfatin and NAFLD remains unclear. Here, we evaluated the effects of visfatin on hepatic inflammation and insulin resistance in HepG2 cells and examined the molecular mechanisms involved.

methodsAfter treatment with visfatin, the inflammatory cytokines IL-6, TNF-

resultsIn HepG2 cells, visfatin significantly increased the levels of proinflammatory cytokines, reduced the levels of proteins (e.g., phospho-IR, phospho-IRS-1 (Tyr612), phospho-AKT, and phospho-GSK-3

conclusionVisfatin induced proinflammatory cytokine production and inhibited insulin signaling via the STAT3 and NF-

Indexed as

Insulin ResistanceCytokinesHepatocytesHep G2 CellsHumansInflammationInflammation MediatorsInsulin Receptor Substrate ProteinsNF-kappa BNicotinamide PhosphoribosyltransferaseSignal TransductionSTAT3 Transcription FactorUp-RegulationCytokinesInflammation MediatorsInsulin Receptor Substrate ProteinsNF-kappa BNicotinamide PhosphoribosyltransferaseSTAT3 protein, humanSTAT3 Transcription Factor

Identifiers

PMID31396538
PMCPMC6664505
OpenAlexW2958041724

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.