Evidence map›Paper›PMID 26351673›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2015

Fibroblast growth factor 9 is a novel modulator of negative affect.

Elyse L Aurbach, Edny Gula Inui, Cortney A Turner, Megan H Hagenauer, Katherine E Prater, Jun Z Li, Devin Absher, Najmul Shah, Peter Blandino, William E Bunney and 5 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. FGF family in health and disease.Molecular biomedicine · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Research progress of fibroblast growth factor in nervous system diseases.Zhejiang da xue xue bao. Yi xue ban = Journal of Zhejiang University. Medical sciences · 2022
    Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Article
  20. Revisiting the Stress Concept: Implications for Affective Disorders.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    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

15 authors at 5 institutions in 1 country.

Elyse L AurbachMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109; Neuroscience Graduate Program, University of Michigan, Ann Arbor, MI 48109;
Edny Gula InuiMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109;
Cortney A TurnerMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109;
Megan H HagenauerMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109;
Katherine E PraterMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109; Neuroscience Graduate Program, University of Michigan, Ann Arbor, MI 48109;
Jun Z LiMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109;
Devin AbsherDepartment of Psychiatry & Human Behavior, University of California, Irvine, CA 92697;
Najmul ShahMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109;
Peter BlandinoMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109;
William E BunneyDepartment of Psychiatry & Human Behavior, University of California, Irvine, CA 92697;
Richard M MyersHudsonAlpha Institute for Biotechnology, Huntsville, AL 35806;
Jack D BarchasDepartment of Psychiatry, Cornell University, New York, NY 10065;
Alan F SchatzbergDepartment of Psychiatry, Stanford University, Stanford, CA 94305.
Stanley J WatsonMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109;
Huda AkilMolecular and Behavioral Neuroscience Institute, University of Michigan, Ann Arbor, MI 48109; akil@umich.edu.
University of Michigan–Ann Arbor · USUniversity of California, Irvine · USCornell University · USHudsonAlpha Institute for Biotechnology · USStanford University · US

Funding

NIDA Training Program in Neuroscience-Administrative SupplementT32DA007281 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Shelly Beth Flagel · 1995 to 2026
$5.7M
Early Stage Training in the NeurosciencesT32NS076401 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Carol Fuzeti Elias, LESLIE S. SATIN · 2011 to 2026
$3.1M
Can Affective Resilience be Enhanced? A Developmental and Epigenetic ApproachR01MH104261 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI AKIL, HUDA, WATSON, STANLEY J · 2014 to 2018
$2.8M
Early Stage Training in the NeurosciencesT32EY017878 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MAREN, STEPHEN · 2006 to 2010
$1.5M
NEI NIH HHS T32 EY017878NIDA NIH HHS T32 DA007281NIMH NIH HHS R01 MH104261NINDS NIH HHS T32 NS076401
6 · The paper itself

Abstract

Both gene expression profiling in postmortem human brain and studies using animal models have implicated the fibroblast growth factor (FGF) family in affect regulation and suggest a potential role in the pathophysiology of major depressive disorder (MDD). FGF2, the most widely characterized family member, is down-regulated in the depressed brain and plays a protective role in rodent models of affective disorders. By contrast, using three microarray analyses followed by quantitative RT-PCR confirmation, we show that FGF9 expression is up-regulated in the hippocampus of individuals with MDD, and that FGF9 expression is inversely related to the expression of FGF2. Because little is known about FGF9's function in emotion regulation, we used animal models to shed light on its potential role in affective function. We found that chronic social defeat stress, an animal model recapitulating some aspects of MDD, leads to a significant increase in hippocampal FGF9 expression, paralleling the elevations seen in postmortem human brain tissue. Chronic intracerebroventricular administration of FGF9 increased both anxiety- and depression-like behaviors. In contrast, knocking down FGF9 expression in the dentate gyrus of the hippocampus using a lentiviral vector produced a decrease in FGF9 expression and ameliorated anxiety-like behavior. Collectively, these results suggest that high levels of hippocampal FGF9 play an important role in the development or expression of mood and anxiety disorders. We propose that the relative levels of FGF9 in relation to other members of the FGF family may prove key to understanding vulnerability or resilience in affective disorders.

Indexed as

AffectAdultAgedAged, 80 and overAnimalsAnxietyAvoidance LearningCase-Control StudiesDemographyDentate GyrusFemaleFibroblast Growth Factor 9Gene Expression RegulationGene Knockdown TechniquesHumansLentivirusFibroblast Growth Factor 9Receptor, Fibroblast Growth Factor, Type 1RNA, Small Interferingaffectanxietyfibroblast growth factor 9hippocampusmajor depression

Identifiers

PMID26351673
PMCPMC4586860
OpenAlexW2138613154

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.