Evidence map›Paper›PMID 38027131›Full record

ReviewFrontiers in endocrinology2023

The ideal treatment timing for diabetic retinopathy: the molecular pathological mechanisms underlying early-stage diabetic retinopathy are a matter of concern.

Wen-Jie Sun, Xue-Dong An, Yue-Hong Zhang, Xue-Fei Zhao, Yu-Ting Sun, Cun-Qing Yang, Xiao-Min Kang, Lin-Lin Jiang, Hang-Yu Ji, Feng-Mei Lian

Open access · goldAbstract readReview
In one paragraph

Review in Frontiers in endocrinology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

24 citing papers in PubMed, 36 citations in OpenAlex.

  1. Trial
  2. Article
  3. Short-term natural history of non-perfusion areas in treatment-naive diabetic retinopathy patients using swept-source OCT angiography.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2026
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  6. Review
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  8. Review
  9. Article
  10. Article
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  13. CD44, ACAN, PLVAP, and HBEGF Emerged as Potential Biomarkers in Diabetic Retinopathy.Diabetes, metabolic syndrome and obesity : targets and therapy · 2025
    Article
  14. Article
  15. Therapeutic potential ofFrontiers in nutrition · 2025
    Review
  16. Article
  17. Review
  18. Review
  19. 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

10 authors at 2 institutions in 1 country.

Wen-Jie Sun *Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Xue-Dong An *Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Yue-Hong Zhang *Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Xue-Fei Zhao *Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Yu-Ting SunGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Cun-Qing YangGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Xiao-Min KangGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Lin-Lin JiangGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Hang-Yu JiGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Feng-Mei LianGuang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.
Chinese Academy of Medical Sciences & Peking Union Medical College · CNGuang’anmen Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diabetic retinopathy (DR) is a prevalent complication of diabetes, significantly impacting patients' quality of life due to vision loss. No pharmacological therapies are currently approved for DR, excepted the drugs to treat diabetic macular edema such as the anti-VEGF agents or steroids administered by intraocular route. Advancements in research have highlighted the crucial role of early intervention in DR for halting or delaying disease progression. This holds immense significance in enhancing patients' quality of life and alleviating the societal burden associated with medical care costs. The non-proliferative stage represents the early phase of DR. In comparison to the proliferative stage, pathological changes primarily manifest as microangiomas and hemorrhages, while at the cellular level, there is a loss of pericytes, neuronal cell death, and disruption of components and functionality within the retinal neuronal vascular unit encompassing pericytes and neurons. Both neurodegenerative and microvascular abnormalities manifest in the early stages of DR. Therefore, our focus lies on the non-proliferative stage of DR and we have initially summarized the mechanisms involved in its development, including pathways such as polyols, that revolve around the pathological changes occurring during this early stage. We also integrate cutting-edge mechanisms, including leukocyte adhesion, neutrophil extracellular traps, multiple RNA regulation, microorganisms, cell death (ferroptosis and pyroptosis), and other related mechanisms. The current status of drug therapy for early-stage DR is also discussed to provide insights for the development of pharmaceutical interventions targeting the early treatment of DR.

Indexed as

Diabetes MellitusDiabetic RetinopathyMacular EdemaHumansNeuronsPericytesQuality of Lifeblood-retinal barrierdiabetic retinopathyinflammationneurovascular unitnon-proliferative phasepathological changestreatment

Identifiers

PMID38027131
PMCPMC10680169
OpenAlexW4388636207

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.