Evidence map›Paper›PMID 37549818›Full record

Trial reportAmerican journal of ophthalmology2023

Role of Static and Dynamic Ocular Biometrics Measured in the Dark and Light as Risk Factors for Angle Closure Progression.

Austin Cho, Benjamin Y Xu, David S Friedman, Paul J Foster, Yu Jiang, Anmol A Pardeshi, Yuzhen Jiang, Tin Aung, Mingguang He

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in American journal of ophthalmology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
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

9 authors.

Austin ChoRoski Eye Institute (A.C., B.Y.X., A.A.P.), Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Benjamin Y XuRoski Eye Institute (A.C., B.Y.X., A.A.P.), Keck School of Medicine, University of Southern California, Los Angeles, California, USA. Electronic address: benjamin.xu@med.usc.edu.
David S FriedmanGlaucoma Center of Excellence (D.S.F.), Massachusetts Eye and Ear, Harvard University, Boston, Massachusetts, USA.
Paul J FosterNIHR Biomedical Research Centre at Moorfields Eye Hospital and UCL Institute of Ophthalmology (P.J.F.), London, England.
Yu JiangState Key Laboratory of Ophthalmology (Y.J., Y.J., M.H.), Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, People's Republic of China.
Anmol A PardeshiRoski Eye Institute (A.C., B.Y.X., A.A.P.), Keck School of Medicine, University of Southern California, Los Angeles, California, USA.
Yuzhen JiangState Key Laboratory of Ophthalmology (Y.J., Y.J., M.H.), Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, People's Republic of China.
Tin AungSingapore Eye Research Institute and Singapore National Eye Centre (T.A.), Yong Loo Lin School of Medicine, National University of Singapore, Singapore.
Mingguang HeState Key Laboratory of Ophthalmology (Y.J., Y.J., M.H.), Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, People's Republic of China.

Funding

Development and Validation of Quantitative Anterior Segment OCT-based Methods to Evaluate Patients with Primary Angle Closure DiseaseK23EY029763 · NEI · UNIVERSITY OF SOUTHERN CALIFORNIA · PI XU, BENJAMIN Y. · 2019 to 2023
$1.1M
NEI NIH HHS K23 EY029763
6 · The paper itself

Abstract

purposeTo assess the role of static and dynamic ocular biometric parameters measured in the dark and light for predicting progression of primary angle closure suspect (PACS) to primary angle closure (PAC).

designRetrospective cohort study using prospective randomized controlled trial data from untreated, control eyes.

methodsZhongshan Angle Closure Prevention Trial subjects underwent anterior segment optical coherence tomography (AS-OCT) imaging in the dark and light. Static biometric parameters were measured, consisting of angle, iris, lens, and anterior chamber parameters. Dynamic change parameters were calculated by subtracting light measurements from dark measurements. Cox proportional hazards regression models were developed to assess risk factors for PACD progression.

resultsA total of 861 eyes of 861 participants were analyzed (36 progressors). On univariable analysis, TISA500 measurements in the light and dark were associated with progression (P < .001), whereas dynamic change parameters were not (P ≥ .08). In the primary multivariable model, older age (hazard ratio [HR] = 1.09 per year), higher intraocular pressure (IOP) (HR = 1.13 per mm Hg), and smaller TISA500 in the light (HR = 1.28 per 0.01 mm

conclusionStatic parameters measured in the light are as predictive, and possibly more so, of angle closure progression as those measured in the dark. Ocular biometrics measured under light and dark conditions may provide additional information for risk-stratifying patients for angle closure progression.

Indexed as

Glaucoma, Angle-ClosureIntraocular PressureAnterior Eye SegmentBiometryGonioscopyHumansIrisProspective StudiesRetrospective StudiesRisk FactorsTomography, Optical Coherence

Identifiers

PMID37549818
PMCPMC10840898

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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.