Evidence map›Paper›PMID 27618014›Full record

ReviewInternational journal of molecular sciences2016

Moving Past Anti-VEGF: Novel Therapies for Treating Diabetic Retinopathy.

Mark T Bolinger, David A Antonetti

2 registry-linked trialsOpen access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 56 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 1 pooled it
11.9field-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.

NCT04378972 completednot on this mapstarted 2019, after this paper: background citation

Analysis of Soluble Mediators of Inflammation and Angiogenesis in the Vitreous of Patients With Diabetic Retinopathy Treated With Curcumin/Homotaurine/Vit. D3

TypeobservationalSponsorUniversity of MoliseRan2019 to 2019Enrolled25ConditionsDiabetic RetinopathyArmscurcumin, homotaurine, vitamin D3, control
NCT05333055 terminatednot on this mapstarted 2022, after this paper: background citation

Aqueous Biomarker Levels in Diabetic Retinopathy and Diabetic Macular Edema

TypeobservationalSponsorGreater Houston Retina ResearchRan2022 to 2024Enrolled107ConditionsDiabetic Retinopathy, Diabetic Macular Edema, Other Retinal Disorders
3 · Its place in the literature

Who cites it

56 citing papers in PubMed, 1 synthesis or guideline pooled it, 103 citations in OpenAlex.

  1. Pooled it
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  7. Review
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  9. Review
  10. Diabetic retinopathy: emerging concepts of current and potential therapy.Naunyn-Schmiedeberg's archives of pharmacology · 2023
    Review
  11. Dysregulated CD200-CD200R signaling in early diabetes modulates microglia-mediated retinopathy.Proceedings of the National Academy of Sciences of the United States of America · 2023
    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

2 authors at 1 institution in 1 country.

Mark T BolingerDepartments of Ophthalmology and Visual Sciences, Kellogg Eye Center, and Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI 48105, USA. bolimark@umich.edu.
David A AntonettiDepartments of Ophthalmology and Visual Sciences, Kellogg Eye Center, and Molecular and Integrative Physiology, University of Michigan, Ann Arbor, MI 48105, USA. dantonet@umich.edu.
University of Michigan–Ann Arbor · US

Funding

Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Mehboob A Hussain · 2013 to 2026
$24.3M
MECHANISMS OF RETINAL VASCULAR PERMEABILITY IN DIABETESR01EY012021 · NEI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ANTONETTI, DAVID · 1998 to 2024
$8.6M
NEI NIH HHS R01 EY012021NIDDK NIH HHS P30 DK020572
6 · The paper itself

Abstract

Diabetic retinopathy is the leading cause of blindness in working age adults, and is projected to be a significant future health concern due to the rising incidence of diabetes. The recent advent of anti-vascular endothelial growth factor (VEGF) antibodies has revolutionized the treatment of diabetic retinopathy but a significant subset of patients fail to respond to treatment. Accumulating evidence indicates that inflammatory cytokines and chemokines other than VEGF may contribute to the disease process. The current review examines the presence of non-VEGF cytokines in the eyes of patients with diabetic retinopathy and highlights mechanistic pathways in relevant animal models. Finally, novel drug targets including components of the kinin-kallikrein system and emerging treatments such as anti-HPTP (human protein tyrosine phosphatase) β antibodies are discussed. Recognition of non-VEGF contributions to disease pathogenesis may lead to novel therapeutics to enhance existing treatments for patients who do not respond to anti-VEGF therapies.

Indexed as

AdalimumabAnimalsBevacizumabDiabetic RetinopathyDrug TherapyHumansKallikreinsPeptidesTumor Necrosis Factor-alphaVascular Endothelial Growth Factor AAdalimumabBevacizumabecallantideKallikreinsPeptidesTumor Necrosis Factor-alphaVascular Endothelial Growth Factor Aangiopoietinblood retinal barriercorticosteroidcytokinediabetic macular edemadiabetic retinopathykinin-kallikrein systemrenin-angiotensin systemTNF-αVEGFvitreomacular adhesion

Identifiers

PMID27618014
PMCPMC5037775
OpenAlexW2510037838

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.