Evidence map›Paper›PMID 32931575›Full record

ArticleInvestigative ophthalmology & visual science2020

Clinical Characteristics of Neuronal Intranuclear Inclusion Disease-Related Retinopathy With CGG Repeat Expansions in the NOTCH2NLC Gene.

Natsuko Nakamura, Kazushige Tsunoda, Akihiko Mitsutake, Shota Shibata, Tatsuo Mano, Yu Nagashima, Hiroyuki Ishiura, Atsushi Iwata, Tatsushi Toda, Shoji Tsuji and 1 more

Open access · goldAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
1.6field-weighted citation impact, top 13% 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

23 citing papers in PubMed, 29 citations in OpenAlex.

  1. Neurology. Genetics · 2026
    Article
  2. Article
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  6. Neuronal intranuclear inclusion disease in one family: clinical diversity and diagnostic challenges.Canadian journal of ophthalmology. Journal canadien d'ophtalmologie · 2025
    Article
  7. Article
  8. CGG Repeat Expansion inJournal of clinical neurology (Seoul, Korea) · 2024
    Article
  9. Article
  10. Prevalence and Characterization ofNeurology. Genetics · 2024
    Article
  11. Article
  12. Review
  13. Article
  14. Clinical features ofJournal of neurology, neurosurgery, and psychiatry · 2022
    Observational
  15. Article
  16. Characteristics of ocular findings of patients with neuronal intranuclear inclusion disease.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2022
    Article
  17. Review
  18. Review
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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

11 authors at 2 institutions in 1 country.

Natsuko NakamuraDepartment of Ophthalmology, The University of Tokyo, Tokyo, Japan.
Kazushige TsunodaDivision of Vision Research, National Institute of Sensory Organs, National Hospital Organization Tokyo Medical Center, Tokyo, Japan.
Akihiko MitsutakeDepartment of Neurology, The University of Tokyo, Tokyo, Japan.
Shota ShibataDepartment of Neurology, The University of Tokyo, Tokyo, Japan.
Tatsuo ManoDepartment of Neurology, The University of Tokyo, Tokyo, Japan.
Yu NagashimaDepartment of Neurology, The University of Tokyo, Tokyo, Japan.
Hiroyuki IshiuraDepartment of Neurology, The University of Tokyo, Tokyo, Japan.
Atsushi IwataDepartment of Neurology, The University of Tokyo, Tokyo, Japan.
Tatsushi TodaDepartment of Neurology, The University of Tokyo, Tokyo, Japan.
Shoji TsujiDepartment of Neurology, The University of Tokyo, Tokyo, Japan.
Hiromasa SawamuraDepartment of Ophthalmology, The University of Tokyo, Tokyo, Japan.
The University of Tokyo · JPNational Hospital Organization · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: To report the ocular characteristics of neuronal intranuclear inclusion disease (NIID)-related retinopathy with expansion of the CGG repeats in the NOTCH2NLC gene. Methods: Seven patients from six families (aged 66-81 years) diagnosed with adult-onset NIID were studied. Ophthalmologic examinations, including the best-corrected visual acuity (BCVA), Goldmann perimetry, fundus photography, fundus autofluorescence (FAF) imaging, optical coherence tomography (OCT), and full-field electroretinography (ERGs), were performed. The expansion of the CGG repeats in the NOTCH2NLC gene was determined. Results: All patients had an expansion of the CGG repeats (length approximately from 330-520 bp) in the NOTCH2NLC gene. The most common symptoms of the five symptomatic cases were reduced BCVA and night blindness. The other two cases did not have any ocular symptoms. The decimal BCVA varied from 0.15 to 1.2. Goldmann perimetry was constricted in all four cases tested; physiological blind spot was enlarged in two of the cases. The FAF images showed an absence of autofluorescence (AF) around the optic disc in all cases and also showed mild hypo-AF or extinguished AF in the midperiphery. In all cases, the OCT images showed an absence of the ellipsoid zone of the photoreceptors in the peripapillary region, and hyperreflective dots were also present between the retinal ganglion cell layer and outer nuclear layer. The macular region was involved in the late stage of the retinopathy. The full-field ERGs showed rod-cone dysfunction. Conclusions: Patients with adult-onset NIID with CGG repeats expansions in the NOTCH2NLC gene had similar ophthalmologic features, including rod-cone dysfunction with progressive retinal degeneration in the peripapillary and midperipheral regions. The primary site is most likely the photoreceptors. Because the ocular symptoms are often overlooked due to dementia and occasionally precede the onset of dementia, detailed ophthalmological examinations are important for the early diagnosis of NIID-related retinopathy.

Indexed as

Gene Expression RegulationAgedAged, 80 and overElectroretinographyFemaleFluorescein AngiographyFollow-Up StudiesFundus OculiHumansIntranuclear Inclusion BodiesMaleNeurodegenerative DiseasesReceptor, Notch2RetinaRetinal DiseasesRetrospective StudiesNOTCH2 protein, humanReceptor, Notch2RNA

Identifiers

PMID32931575
PMCPMC7500143
OpenAlexW3087164803

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.