Evidence map›Paper›PMID 35418088›Full record

ArticleBMC ophthalmology2022

Multifocal pupillographic objective perimetry for assessment of early diabetic retinopathy and generalised diabetes-related tissue injury in persons with type 1 diabetes.

Faran Sabeti, Corinne F Carle, Christopher J Nolan, Alicia J Jenkins, Andrew C James, Lauren Baker, Caitlin E Coombes, Veronica Cheung, Melody Chiou, Ted Maddess

Open access · goldAbstract read
In one paragraph

Article in BMC ophthalmology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 15% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Diagnostic performance of pupil perimetry in detecting hemianopia under standard and virtual reality viewing conditions.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2025
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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 3 institutions in 1 country.

Faran SabetiEccles Institute for Neuroscience, The John Curtin School of Medical Research, The Australian National University, Canberra, ACT, 2601, Australia. faran.sabeti@anu.edu.au.
Corinne F CarleEccles Institute for Neuroscience, The John Curtin School of Medical Research, The Australian National University, Canberra, ACT, 2601, Australia.
Christopher J NolanAustralian National University Medical School, The Australian National University, Canberra, ACT, Australia.
Alicia J JenkinsUniversity of Sydney, NHMRC Clinical Trials Centre, Camperdown, Sydney, NSW, Australia.
Andrew C JamesEccles Institute for Neuroscience, The John Curtin School of Medical Research, The Australian National University, Canberra, ACT, 2601, Australia.
Lauren BakerDivision of Immunity, Inflammation and Infection, The John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia.
Caitlin E CoombesAustralian National University Medical School, The Australian National University, Canberra, ACT, Australia.
Veronica CheungAustralian National University Medical School, The Australian National University, Canberra, ACT, Australia.
Melody ChiouAustralian National University Medical School, The Australian National University, Canberra, ACT, Australia.
Ted MaddessEccles Institute for Neuroscience, The John Curtin School of Medical Research, The Australian National University, Canberra, ACT, 2601, Australia.
Australian National University · AUCanberra Hospital · AUNational Health and Medical Research Council · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo examine the potential utility of five multifocal pupillographic objective perimetry (mfPOP) protocols, in the assessment of early diabetic retinopathy (DR) and generalised diabetes-related tissue injury in subjects with type 1 diabetes (T1D).

methodsTwenty-five T1D subjects (age 41.8 ± 12.1 (SD) years, 13 male) with either no DR (n = 13) or non-proliferative DR (n = 12), and 23 age and gender-matched control subjects (age 39.7 ± 12.9 years, 9 male) were examined by mfPOP using five different stimulus methods differing in visual field eccentricity (central 30° and 60°), and colour (blue, yellow or green test-stimuli presented on, respectively, a blue, yellow or red background), each assessing 44 test-locations per eye. In the T1D subjects, we assessed 16 metabolic status and diabetes complications variables. These were summarised as three principal component analysis (PCA) factors. DR severity was assessed using Early Treatment of Diabetic Retinopathy Study (ETDRS) scores. Area under the curve (AUC) from receiver operator characteristic analyses quantified the diagnostic power of mfPOP response sensitivity and delay deviations for differentiating: (i) T1D subjects from control subjects, (ii) T1D subjects according to three levels of the identified PCA-factors from control subjects, and (iii) TID subjects with from those without non-proliferative DR.

resultsThe two largest PCA-factors describing the T1D subjects were associated with metabolic variables (e.g. body mass index, HbA1c), and tissue-injury variables (e.g. serum creatinine, vibration perception). Linear models showed that mfPOP per-region response delays were more strongly associated than sensitivities with the metabolic PCA-factor and ETDRS scores. Combined mfPOP amplitude and delay measures produced AUCs of 90.4 ± 8.9% (mean ± SE) for discriminating T1D subjects with DR from control subjects, and T1D subjects with DR from those without of 85.9 ± 8.8%. The yellow and green stimuli performed better than blue on most measures. CONCLUSIONS/

interpretationIn T1D subjects, mfPOP testing was able to identify localised visual field functional abnormalities (retinal/neural reflex) in the absence or presence of mild DR. mfPOP responses were also associated with T1D metabolic status, but less so with early stages of non-ophthalmic diabetes complications.

Indexed as

Diabetes Mellitus, Type 1Diabetic RetinopathyAdultFemaleHumansMaleMiddle AgedPupilVisual FieldsVisual Field TestsMetabolic variablesObjective perimetryPupillometryTissue injuryType 1 diabetes

Identifiers

PMID35418088
PMCPMC9008936
OpenAlexW4224036548

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.