Evidence map›Paper›PMID 36561027›Full record

ArticleAnnals of Indian Academy of Neurology

Retinal Degeneration in Patients with Wilson's Disease: An OCT Study in Asian Indian Population.

Amitabh Bhattacharya, Albert Stezin, Nitish Kamble, P M Mohammed Shereef, Bakula Kashyap, Pramod Kumar Pal

Open access · diamondAbstract read
In one paragraph

Article in Annals of Indian Academy of Neurology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 59% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Epidemiology of Wilson's Disease and Pathogenic Variants of theInternational journal of molecular sciences · 2024
    Review
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

6 authors at 1 institution in 1 country.

Amitabh BhattacharyaDepartment of Neurology, National Institute of Mental Health and Neuro Sciences, Bangalore, Karnataka, India.
Albert StezinDepartment of Neurology, National Institute of Mental Health and Neuro Sciences, Bangalore, Karnataka, India.
Nitish KambleDepartment of Neurology, National Institute of Mental Health and Neuro Sciences, Bangalore, Karnataka, India.
P M Mohammed ShereefDepartment of Neurology, National Institute of Mental Health and Neuro Sciences, Bangalore, Karnataka, India.
Bakula KashyapKashyap Eye Clinic, Bangalore, Karnataka, India.
Pramod Kumar PalDepartment of Neurology, National Institute of Mental Health and Neuro Sciences, Bangalore, Karnataka, India.
National Institute of Mental Health and Neurosciences · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Wilson's disease (WD) is an autosomal recessive disorder of copper metabolism. We aimed to study the abnormalities in the retinal layers in patients with WD using optical coherence tomography (OCT). Methods: The study is a chart review of 16 patients with WD (six females) who underwent OCT at our hospital during follow-up visits. Spectral-domain OCT was performed in all subjects to assess the thickness of macula and retinal nerve fiber layer (RNFL) and the data was compared with 14 healthy controls (three females). Results: The mean age of the patients was 20.81 ± 7.47 years and controls was 26.86 ± 9.95 years. The mean age at the onset of the illness was 16.25 ± 5.57 years (range 11-28 years) with the mean duration of illness being 4.81 ± 3.31 years at the final follow-up examination. The mean macular thickness was found to be significantly reduced in patients (232.13 ± 19.39) when compared to controls (271.30 ± 17.32 μm; Conclusions: Abnormalities of the retinal layers were observed in the patients with WD. OCT is a non-invasive tool to identify and quantify the abnormalities of the retinal layers.

Indexed as

Ganglion cell layermacular thicknessoptical coherence tomographyretinal degenerationretinal nerve fiber layerWilson's disease

Identifiers

PMID36561027
PMCPMC9764930
OpenAlexW4285411832

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.