Evidence map›Paper›PMID 28948716›Full record

ArticleCNS neuroscience & therapeutics2017

Fibroblast growth factor 22 is a novel modulator of depression through interleukin-1β.

Yu-Hao Xu, Ming Yu, Hong Wei, Shun Yao, Si-Yuan Chen, Xiao-Lan Zhu, Yue-Feng Li

Open access · bronzeAbstract read
In one paragraph

Article in CNS neuroscience & therapeutics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

16 citing papers in PubMed, 25 citations in OpenAlex.

  1. Article
  2. FGF family in health and disease.Molecular biomedicine · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Review
  9. Stress, hypoglycemia, and the autonomic nervous system.Autonomic neuroscience : basic & clinical · 2022
    Review
  10. Review
  11. Review
  12. Animal models for the study of depressive disorder.CNS neuroscience & therapeutics · 2021
    Review
  13. Review
  14. Article
  15. Fibroblast Growth Factors in Depression.Frontiers in pharmacology · 2019
    Review
  16. Article
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.

Yu-Hao XuAffiliated Hospital of Jiangsu University, Zhenjiang, China.
Ming YuAffiliated Hospital of Jiangsu University, Zhenjiang, China.
Hong WeiAffiliated Hospital of Jiangsu University, Zhenjiang, China.
Shun YaoAffiliated Hospital of Jiangsu University, Zhenjiang, China.
Si-Yuan ChenAffiliated Hospital of Jiangsu University, Zhenjiang, China.
Xiao-Lan ZhuThe Forth Affiliated Hospital of Jiangsu University, Zhenjiang, China.
Yue-Feng LiAffiliated Hospital of Jiangsu University, Zhenjiang, China.ORCID http://orcid.org/0000-0001-8875-3610
Jiangsu University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsEmerging evidence shows that fibroblast growth factor 22 (FGF22) plays a critical role in the etiology of depression. However, the molecular mechanisms of FGF22 are not fully comprehended. Here, the effect of FGF22 in depression and its relationship with interleukin-1β (IL-1β) were investigated in clinical, animal, and cell experiments.

methodsSerum from depressive patients was collected, and the levels of FGF22 and IL-1β were analyzed by ELISA. The chronic unpredictable mild stress (CUMS) model was established, and primary hippocampal neuronal cells were cultured to examine changes in FGF22 and IL-1β levels in rat hippocampus.

resultsThe results revealed a negative correlation between serum FGF22 levels and serum IL-1β levels. The expression of IL-1β in the CUMS rat hippocampus decreased, and the apoptosis of hippocampal cells improved after the injection of lentiviral vector-mediated FGF22 (LV-FGF22). Further tests in primary hippocampal neuronal cells also showed a reduction in IL-1β and the cell apoptosis rate after treatment with FGF22.

conclusionIn conclusion, the results revealed that FGF22 plays a role in alleviating depression, which may be mediated by reduced expression of IL-1β.

Indexed as

AdultAnimalsApoptosisCells, CulturedChronic DiseaseDepressive DisorderDisease Models, AnimalFemaleFibroblast Growth FactorsHippocampusHumansInterleukin-1betaMaleNeuronsRats, WistarStress, PsychologicalFGF22 protein, humanFGF22 protein, ratFibroblast Growth FactorsIL1B protein, humanIL1B protein, ratInterleukin-1betadepressionfibroblast growth factor 22hippocampusinterleukin-1β

Identifiers

PMID28948716
PMCPMC6492756
OpenAlexW2757401382

What OpenQuestion holds

Textmetadata
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.