Evidence map›Paper›PMID 39728692›Full record

ArticleInvestigative ophthalmology & visual science2024

Retinal Docosahexaenoic Acid Is Significantly Reduced in Diabetic Humans and Mice: Possible Relationship to Diabetic Retinopathy.

Dhavamani Sugasini, Poorna C R Yalagala, Jason C Park, Guangying Ma, Zeenat Farooq, Basma Baccouche, Onkar B Sawant, J Jason McAnany, Xincheng Yao, Andrius Kazlauskas and 2 more

Abstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Observational
  6. Diabetic retinal disease.Nature reviews. Disease primers · 2025
    Review
  7. 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

12 authors.

Dhavamani SugasiniDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States.
Poorna C R YalagalaDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States.
Jason C ParkDepartment of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois, United States.
Guangying MaDepartment of Biomedical Engineering, University of Illinois at Chicago, Chicago, Illinois, United States.
Zeenat FarooqDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States.
Basma BaccoucheDepartment of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois, United States.
Onkar B SawantCenter for Vision and Eye Banking Research, Eversight, Cleveland, Ohio, United States.
J Jason McAnanyDepartment of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois, United States.
Xincheng YaoDepartment of Biomedical Engineering, University of Illinois at Chicago, Chicago, Illinois, United States.
Andrius KazlauskasDepartment of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, Illinois, United States.
Brian T LaydenDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States.
Papasani V SubbaiahDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Illinois at Chicago, Chicago, Illinois, United States.

Funding

Translational Core for Therapeutic and Diagnostic DevelopmentP30EY001792 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SHUKLA, DEEPAK · 1985 to 2025
$14.8M
Mechanisms of Early Functional Loss in Diabetic Eye DiseaseR01EY026004 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI James JASON McAnany · 2016 to 2026
$4.2M
Functional imaging of retinal photoreceptorsR01EY023522 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI YAO, XINCHENG · 2014 to 2024
$3.5M
Anti-VEGF-mediated barrier closureR01EY031350 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KAZLAUSKAS, ANDRIUS · 2020 to 2024
$1.9M
Differential artery-vein analysis in OCT angiography for objective classification of diabetic retinopathyR01EY030842 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LIM, JENNIFER IRENE, YAO, XINCHENG · 2020 to 2023
$1.7M
Functional tomography of neurovascular coupling interactions in healthy and diseased retinasR01EY030101 · NEI · UNIVERSITY OF ILLINOIS AT CHICAGO · PI YAO, XINCHENG · 2019 to 2022
$1.4M
Purchase of AB Sciex QTRAP 5500 SystemS10OD010660 · OD · UNIVERSITY OF ILLINOIS AT CHICAGO · PI SUBBAIAH, PAPASANI V · 2012 to 2012
$440k
Novel strategy to enrich brain DHA through diet: Potential application for the prevention of Alzheimer's diseaseI01BX004315 · VA · JESSE BROWN VA MEDICAL CENTER · PI SUBBAIAH, PAPASANI V · 2019 to 2023
–
PPAR gamma Agonists for Lung Cancer ChemopreventionI01BX000382 · VA · VA EASTERN COLORADO HEALTH CARE SYSTEM · PI KEITH, ROBERT · 2011 to 2020
–
BLRD VA I01 BX000382BLRD VA I01 BX004315NEI NIH HHS P30 EY001792NEI NIH HHS R01 EY023522NEI NIH HHS R01 EY026004NEI NIH HHS R01 EY030101NEI NIH HHS R01 EY030842NEI NIH HHS R01 EY031350NIH HHS S10 OD010660
6 · The paper itself

Abstract

Purpose: The retina contains the highest concentration of the omega 3 fatty acid, docosahexaenoic acid (DHA), in the body. Although epidemiologic studies showed an inverse correlation between the consumption of omega 3 fatty acids and the prevalence of diabetic retinopathy, there are no data showing the effect of diabetes on retinal DHA in humans. In this study, we measured the DHA content of the retina in diabetic and non-diabetic humans as well as mice and determined the effect of diabetes on retinal thickness and function in mice. Methods: Fatty acid composition was determined by gas chromatography/mass spectroscopy. Retinal thickness in mice was measured by optical coherence tomography and retinal function was measured by electroretinogram (ERG). Expression of selected genes involved in inflammation and lipid metabolism was determined by quantitative real-time PCR (qRT-PCR). Results: We found a 40% reduction of DHA in peripheral retina and a 25% reduction in the macula of diabetic humans compared with nondiabetic controls. There was a 24% reduction in retinal DHA of type 2 diabetic mice (db/db) compared with the controls (db/+). The retinal thickness was significantly decreased in db/db mice, especially in the inner retina, and the ERG b-wave amplitudes were significantly attenuated. Increased expression of proinflammatory genes was observed in both human and mouse diabetic retinas. Conclusions: Retinal DHA is reduced in diabetic humans and mice, which is associated with a thinning of retina and functional defects in diabetic mice. Enriching retinal DHA through diet may be beneficial in the prevention and treatment of diabetic retinopathy.

Indexed as

Diabetes Mellitus, ExperimentalDiabetic RetinopathyDocosahexaenoic AcidsElectroretinographyMice, Inbred C57BLRetinaTomography, Optical CoherenceAdultAgedAnimalsDiabetes Mellitus, Type 2FemaleGas Chromatography-Mass SpectrometryHumansMaleMiceDocosahexaenoic Acids

Identifiers

PMID39728692
PMCPMC11684127

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Registered trials

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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.