Evidence map›Paper›PMID 29487115›Full record

ArticleDiabetes2018

Fibroblast Growth Factor 21 Protects Photoreceptor Function in Type 1 Diabetic Mice.

Zhongjie Fu, Zhongxiao Wang, Chi-Hsiu Liu, Yan Gong, Bertan Cakir, Raffael Liegl, Ye Sun, Steven S Meng, Samuel B Burnim, Ivana Arellano and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 10% 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

54 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
  2. Review
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  5. Fenofibrate in ophthalmology: therapeutic efficacy and mechanisms.Journal of pharmacy & pharmaceutical sciences : a publication of the Canadian Society for Pharmaceutical Sciences, Societe canadienne des sciences pharmaceutiques · 2026
    Review
  6. Article
  7. Hepatocyte Piezo1 regulates glycogen metabolism via the FGF21-STAT3 pathway.Cellular and molecular life sciences : CMLS · 2025
    Article
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  14. The N-Methyl-D-Aspartate Receptor Antagonist Dextromethorphan Improves Glucose Homeostasis and Preserves Pancreatic Islets in NOD Mice.Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme · 2024
    Article
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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

18 authors at 3 institutions in 2 countries.

Zhongjie FuDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Zhongxiao WangDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Chi-Hsiu LiuDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Yan GongDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Bertan CakirDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Raffael LieglDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Ye SunDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Steven S MengDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Samuel B BurnimDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Ivana ArellanoDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Elizabeth MoranDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Rubi DuranDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Alexander PobleteDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Steve S ChoDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Saswata TalukdarMerck Research Laboratories, Boston, MA.
James D AkulaDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA.
Ann HellströmSection for Ophthalmology, Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Göteborg, Sweden.
Lois E H SmithDepartment of Ophthalmology, Boston Children's Hospital, Harvard Medical School, Boston, MA lois.smith@childrens.harvard.edu.ORCID 0000-0001-7644-6410
Boston Children's Hospital · USMerck & Co., Inc., Rahway, NJ, USA (United States) · USUniversity of Gothenburg · SE

Funding

Dietary control of angiogenesis in retinopathy modelsR01EY017017 · NEI · BOSTON CHILDREN'S HOSPITAL · PI Zhongjie Fu, Lois Smith · 2006 to 2026
$11.8M
Novel therapies to inhibit Diabetic RetinopathyR24EY024864 · NEI · UNIVERSITY OF CALIFORNIA-IRVINE · PI KERN, TIMOTHY S · 2015 to 2019
$8.1M
Mouse Neurodevelopmental Behavior CoreU54HD090255 · NICHD · BOSTON CHILDREN'S HOSPITAL · PI KUNKEL, LOUIS M · 2016 to 2020
$5.2M
NEI NIH HHS R01 EY017017NEI NIH HHS R24 EY024864NICHD NIH HHS U54 HD090255
6 · The paper itself

Abstract

Retinal neuronal abnormalities occur before vascular changes in diabetic retinopathy. Accumulating experimental evidence suggests that neurons control vascular pathology in diabetic and other neovascular retinal diseases. Therefore, normalizing neuronal activity in diabetes may prevent vascular pathology. We investigated whether fibroblast growth factor 21 (FGF21) prevented retinal neuronal dysfunction in insulin-deficient diabetic mice. We found that in diabetic neural retina, photoreceptor rather than inner retinal function was most affected and administration of the long-acting FGF21 analog PF-05231023 restored the retinal neuronal functional deficits detected by electroretinography. PF-05231023 administration protected against diabetes-induced disorganization of photoreceptor segments seen in retinal cross section with immunohistochemistry and attenuated the reduction in the thickness of photoreceptor segments measured by optical coherence tomography. PF-05231023, independent of its downstream metabolic modulator adiponectin, reduced inflammatory marker interleukin-1β (IL-1β) mRNA levels. PF-05231023 activated the AKT-nuclear factor erythroid 2-related factor 2 pathway and reduced IL-1β expression in stressed photoreceptors. PF-05231023 administration did not change retinal expression of vascular endothelial growth factor A, suggesting a novel therapeutic approach for the prevention of early diabetic retinopathy by protecting photoreceptor function in diabetes.

Indexed as

AnimalsAntibodies, Monoclonal, HumanizedDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Diabetic RetinopathyDisease Models, AnimalElectroretinographyFibroblast Growth FactorsInterleukin-1betaMaleMiceNF-E2-Related Factor 2Photoreceptor Cells, VertebrateProto-Oncogene Proteins c-aktRetinal NeuronsTomography, Optical CoherenceAntibodies, Monoclonal, Humanizedfibroblast growth factor 21Fibroblast Growth FactorsIL1B protein, mouseInterleukin-1betaNfe2l2 protein, mouseNF-E2-Related Factor 2PF-05231023Proto-Oncogene Proteins c-aktVascular Endothelial Growth Factor Avascular endothelial growth factor A, mouse

Identifiers

PMID29487115
PMCPMC5909994
OpenAlexW2790701533

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.