Evidence map›Paper›PMID 31947513›Full record

ReviewJournal of clinical medicine2020

Do Genomic Factors Play a Role in Diabetic Retinopathy?

Andrea P Cabrera, Finny Monickaraj, Sampathkumar Rangasamy, Sam Hobbs, Paul McGuire, Arup Das

Open access · goldAbstract readReview
In one paragraph

Review in Journal of clinical medicine, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
6.3field-weighted citation impact, top 2% 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

22 citing papers in PubMed, 54 citations in OpenAlex.

  1. Review
  2. Article
  3. Report of the 2023 Mary Tyler Moore Vision Initiative Workshop.Translational vision science & technology · 2025
    Article
  4. Review
  5. Review
  6. Association of the rs9896052 Polymorphism Upstream ofInternational journal of molecular sciences · 2024
    Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. A Guide to Genome-Wide Association Study Design for Diabetic Retinopathy.Methods in molecular biology (Clifton, N.J.) · 2023
    Review
  12. Article
  13. Article
  14. Article
  15. Epigenetic modifications in diabetes.Metabolism: clinical and experimental · 2022
    Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 2 institutions in 1 country.

Andrea P CabreraDepartment of Surgery/Ophthalmology, University of New Mexico School of Medicine, Albuquerque, NM 87131, USA.
Finny MonickarajDepartment of Surgery/Ophthalmology, University of New Mexico School of Medicine, Albuquerque, NM 87131, USA.
Sampathkumar RangasamyTranslational and Genomics Research Institute (TGen), Phoenix, AZ 85004, USA.ORCID 0000-0003-2151-9162
Sam HobbsDepartment of Surgery/Ophthalmology, University of New Mexico School of Medicine, Albuquerque, NM 87131, USA.ORCID 0000-0002-9587-5162
Paul McGuireDepartment of Cell Biology & Physiology, UNM, Albuquerque, NM 87131, USA.
Arup DasDepartment of Surgery/Ophthalmology, University of New Mexico School of Medicine, Albuquerque, NM 87131, USA.
University of New Mexico · USTranslational Genomics Research Institute · US

Funding

Novel Biomarkers and Genetics of Diabetic RetinopathyR01EY028606 · NEI · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI DAS, ARUP · 2018 to 2022
$2.8M
NEI NIH HHS R01 EY028606NIH HHS EY028606-01A1
6 · The paper itself

Abstract

Although there is strong clinical evidence that the control of blood glucose, blood pressure, and lipid level can prevent and slow down the progression of diabetic retinopathy (DR) as shown by landmark clinical trials, it has been shown that these factors only account for 10% of the risk for developing this disease. This suggests that other factors, such as genetics, may play a role in the development and progression of DR. Clinical evidence shows that some diabetics, despite the long duration of their diabetes (25 years or more) do not show any sign of DR or show minimal non-proliferative diabetic retinopathy (NPDR). Similarly, not all diabetics develop proliferative diabetic retinopathy (PDR). So far, linkage analysis, candidate gene studies, and genome-wide association studies (GWAS) have not produced any statistically significant results. We recently initiated a genomics study, the Diabetic Retinopathy Genetics (DRGen) Study, to examine the contribution of rare and common variants in the development of different phenotypes of DR, as well as their responsiveness to anti-VEGF treatment in diabetic macular edema (DME). Our preliminary findings reveal a novel set of genetic variants involved in the angiogenesis and inflammatory pathways that contribute to DR progression or protection. Further investigation of variants can help to develop novel biomarkers and lead to new therapeutic targets in DR.

Indexed as

blood-retinal barrierdiabetic retinopathygeneticsGWASVEGFwhole exome sequencing

Identifiers

PMID31947513
PMCPMC7019561
OpenAlexW3000559775

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.