Evidence map›Paper›PMID 29447914›Full record

ArticleAmerican journal of ophthalmology2018

Progression of Primary Open-Angle Glaucoma in Diabetic and Nondiabetic Patients.

Huiyuan Hou, Takuhei Shoji, Linda M Zangwill, Sasan Moghimi, Luke J Saunders, Kyle Hasenstab, Elham Ghahari, Patricia Isabel C Manalastas, Tadamichi Akagi, Mark Christopher and 2 more

Open access · greenAbstract readComparative Study
In one paragraph

Article in American journal of ophthalmology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
4.3field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 46 citations in OpenAlex.

  1. Observational
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  7. Central macular OCTA parameters in glaucoma.The British journal of ophthalmology · 2023
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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

12 authors at 2 institutions in 3 countries.

Huiyuan HouHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California.
Takuhei ShojiHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California; Department of Ophthalmology, Saitama Medical University, Iruma, Saitama, Japan.
Linda M ZangwillHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California.
Sasan MoghimiHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California; Department of Ophthalmology, Tehran University of Medical Sciences, Tehran, Iran.
Luke J SaundersHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California.
Kyle HasenstabHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California.
Elham GhahariHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California.
Patricia Isabel C ManalastasHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California.
Tadamichi AkagiHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California; Department of Ophthalmology and Visual Sciences, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Mark ChristopherHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California.
Rafaella C PenteadoHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California.
Robert N WeinrebHamilton Glaucoma Center and Shiley Eye Institute, Department of Ophthalmology, University of California, San Diego, California. Electronic address: rweinreb@ucsd.edu.
University of San Diego · USUniversity of California, San Diego · US

Funding

African Descent And Glaucoma Evaluation Study (ADAGES)U10EY014267 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZANGWILL, LINDA M · 2002 to 2010
$13.2M
Vision BiostatisticsP30EY022589 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Derek Stuart Welsbie · 2012 to 2026
$10.3M
Diagnostic Innovations in Glaucoma:Structural AssessmentR01EY011008 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZANGWILL, LINDA M · 1995 to 2015
$8.7M
Diagnostic Innovations in Glaucoma Study (DIGS): High Myopia and Advanced DiseaseR01EY027510 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI LINDA M ZANGWILL · 2017 to 2026
$5.3M
African Descent and Glaucoma Evaluation (ADAGES) II: Glaucoma ProgressionR01EY019869 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZANGWILL, LINDA M · 2010 to 2014
$2.8M
Translational Vision Research Training at UCSDT32EY026590 · NEI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZANGWILL, LINDA M · 2016 to 2025
$854k
NEI NIH HHS P30 EY022589NEI NIH HHS R01 EY011008NEI NIH HHS R01 EY019869NEI NIH HHS R01 EY027510NEI NIH HHS T32 EY026590NEI NIH HHS U10 EY014267
6 · The paper itself

Abstract

purposeTo compare the rates of visual field (VF) loss and retinal nerve fiber layer (RNFL) thinning in primary open-angle glaucoma (POAG) patients with or without type 2 diabetes mellitus (DM).

designCohort study.

methodsA total of 197 eyes (55 eyes of 32 POAG patients with DM in POAG/DM group and 142 eyes of 111 age-matched POAG patients without DM in POAG/DM- group) were included from the Diagnostic Innovations in Glaucoma Study (DIGS). Type 2 DM participants were defined by self-report of DM history and use of antidiabetic medication. The rates of VF loss and RNFL loss were compared in POAG eyes with and without DM using univariate and multivariable mixed-effects models.

resultsThe median (interquartile range) follow-up was 5.7 years (4.0, 6.4). The mean rate of global RNFL loss in the POAG/DM group was 2-fold slower than in the POAG/DM- group overall (-0.40 μm/year vs -0.83 μm/year, respectively P = .01). Although a slower rate of VF mean deviation and pattern standard deviation loss was found in the POAG/DM group compared to the POAG/DM- group, the difference was not statistically significant.

conclusionsPOAG patients with treated type 2 DM, who had no detectable diabetic retinopathy, had significantly slower rates of RNFL thinning compared to those without diagnosed DM.

Indexed as

AgedCohort StudiesDiabetes Mellitus, Type 2Diabetic RetinopathyDisease ProgressionFemaleFollow-Up StudiesGlaucoma, Open-AngleHumansIntraocular PressureMaleNerve FibersOptic DiskRetinal Ganglion CellsTomography, Optical CoherenceVision Disorders

Identifiers

PMID29447914
PMCPMC5916320
OpenAlexW2787051427

What OpenQuestion holds

Textmetadata
LicenceTDM
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.