Evidence map›Paper›PMID 40681735›Full record

Observational studyEye (London, England)2025

Risk factor stratification in early-onset primary angle closure disease.

Shikha Gupta, Suresh Kumar Yadav, Arnav Panigrahi, Shruti Sapkal, Toshit Varshney, Anand Kumar Pathak, Sonam Singh, Rishi Sethi, Viney Gupta

Abstract readObservational Study
In one paragraph

Observational study in Eye (London, England), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Accommodative Demand and Near Addition in Early-Onset Primary Angle-Closure Disease: A Comparative Study.Ophthalmic & physiological optics : the journal of the British College of Ophthalmic Opticians (Optometrists) · 2026
    Article
  2. 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.

Shikha GuptaDr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India. shikhagupta@aiims.edu.ORCID http://orcid.org/0000-0003-2120-3651
Suresh Kumar YadavDr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India.
Arnav PanigrahiDr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India.ORCID http://orcid.org/0000-0002-0036-3624
Shruti SapkalDr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India.
Toshit VarshneyDr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India.ORCID http://orcid.org/0000-0002-5236-1778
Anand Kumar PathakDr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India.ORCID http://orcid.org/0009-0004-2410-387X
Sonam SinghDr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India.
Rishi SethiDivisional Medical Officer, Northern Railway Central Hospital, New Delhi, India.
Viney GuptaDr Rajendra Prasad Centre for Ophthalmic Sciences, All India Institute of Medical Sciences, New Delhi, India.ORCID http://orcid.org/0000-0002-8850-0485

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTo identify the potential biometric associations in patients with early-onset primary angle closure disease (EOPACD), and the relevant biometric cut-offs for distinguishing them.

designA prospective cross-sectional observational study.

participantsThe study included 190 eyes with EOPACD of 128 patients, aged 20-40 years (mean age 34.2 ± 6.0 years).

methodsEOPACD (defined as primary angle closure presenting before 40 years of age) was classified into early-onset primary angle closure suspect (EOPACS), early-onset primary angle closure (EOPAC), and early-onset primary angle closure glaucoma (EOPACG) groups. The participants underwent a baseline clinical examination, including gonioscopy, ultrasound biomicroscopy, anterior segment ocular coherent tomography (ASOCT) and optical biometry (IOL Master). Statistical analysis was performed to identify risk factors associated with EOPACG such as axial length (AL), lens thickness (LT), lens vault (LV), anterior chamber depth (ACD), anterior chamber area (ACA) and other parameters on ASOCT.

main outcome measuresTo identify ocular biometric associations and potential cut-offs for distinguishing glaucoma eyes from suspects.

resultsBiometric measurements showed that the AL was the shortest, while ACD, ACA and ASOCT angle parameters were narrowest in eyes with EOPACG, as compared to EOPACS and EOPAC (p < 0.001; Bonferroni/Dunn test). Similarly, LV and LT were highest in eyes with EOPACG (p < 0.001). Logistic regression analysis revealed that ACD exhibited the highest predictive ability (ACD ≤ 2.73 mm, OR 4.36, AUC 0.72), followed by LT (LT ≥ 4.22 mm, OR 4.2, AUC 0.71) and ACA (ACA ≤ 17.24mm

conclusionsThis study highlights the significance of ocular biometric measurements, especially ACD and LT, which can assist in stratifying individuals with EOPACD for early detection of glaucoma. Thickening of the lens with the resultant crowded anterior chamber seemed to be the most prevalent biometric characteristic in eyes with frank glaucoma.

Indexed as

Glaucoma, Angle-ClosureAdultAge of OnsetAnterior ChamberAxial Length, EyeBiometryCross-Sectional StudiesFemaleGonioscopyHumansIntraocular PressureLens, CrystallineMaleMicroscopy, AcousticProspective StudiesRisk Factors

Identifiers

PMID40681735
PMCPMC12402232

What OpenQuestion holds

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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.