Evidence map›Paper›PMID 38312833›Full record

ReviewFrontiers in immunology2024

Critical role of FGF21 in diabetic kidney disease: from energy metabolism to innate immunity.

Yingnan Liang, Qi Chen, Yue Chang, Junsong Han, Jiaxin Yan, Zhenjie Chen, Jingwei Zhou

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 14 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

7 authors at 1 institution in 1 country.

Yingnan LiangDepartment of Nephrology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Qi ChenDepartment of Nephrology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Yue ChangDepartment of Nephrology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Junsong HanDepartment of Nephrology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Jiaxin YanDepartment of Nephrology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Zhenjie ChenDepartment of Nephrology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Jingwei ZhouDepartment of Nephrology, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, China.
Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic kidney disease (DKD) stands as the predominant cause of chronic kidney disease (CKD) on a global scale, with its incidence witnessing a consistent annual rise, thereby imposing a substantial burden on public health. The pathogenesis of DKD is primarily rooted in metabolic disorders and inflammation. Recent years have seen a surge in studies highlighting the regulatory impact of energy metabolism on innate immunity, forging a significant area of research interest. Within this context, fibroblast growth factor 21 (FGF21), recognized as an energy metabolism regulator, assumes a pivotal role. Beyond its role in maintaining glucose and lipid metabolism homeostasis, FGF21 exerts regulatory influence on innate immunity, concurrently inhibiting inflammation and fibrosis. Serving as a nexus between energy metabolism and innate immunity, FGF21 has evolved into a therapeutic target for diabetes, nonalcoholic steatohepatitis, and cardiovascular diseases. While the relationship between FGF21 and DKD has garnered increased attention in recent studies, a comprehensive exploration of this association has yet to be systematically addressed. This paper seeks to fill this gap by summarizing the mechanisms through which FGF21 operates in DKD, encompassing facets of energy metabolism and innate immunity. Additionally, we aim to assess the diagnostic and prognostic value of FGF21 in DKD and explore its potential role as a treatment modality for the condition.

Indexed as

Diabetes MellitusDiabetic NephropathiesFibroblast Growth FactorsEnergy MetabolismHumansImmunity, InnateInflammationfibroblast growth factor 21Fibroblast Growth Factorsdiabetic kidney diseaseenergy metabolismfibroblast growth factor 21inflammationinnate immunity

Identifiers

PMID38312833
PMCPMC10834771
OpenAlexW4391033638

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.