Evidence map›Paper›PMID 37278422›Full record

ArticleBMJ open ophthalmology2023

Is the prolongation latency of visual evoked potentials a pathological sign in children with Down's syndrome without ocular abnormalities? Case-control study of children with Down's syndrome.

Dobrila Karlica Utrobičić, Hana Karlica, Ana Jerončić, Ivan Borjan, Ivana Mudnić

Open access · goldAbstract read
In one paragraph

Article in BMJ open ophthalmology, 2023. 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
–field-weighted citation impact, top 95% of its field
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 0 citations in OpenAlex.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Dobrila Karlica UtrobičićDepartment of Ophthalmology, Klinički bolnički centar Split, Split, Split-Dalmatia, Croatia dobrila.karlica@gmail.com.ORCID 0000-0002-9104-509X
Hana KarlicaDepartment of Ophthalmology, Klinički bolnički centar Split, Split, Split-Dalmatia, Croatia.
Ana JerončićDepartment of Research in Biomedicine and Health, Sveuciliste u Splitu Medicinski fakultet, Split, Croatia.
Ivan BorjanDepartment of Ophthalmology, Klinički bolnički centar Split, Split, Split-Dalmatia, Croatia.
Ivana MudnićDepartment of Basic and Clinical Pharmacology, Sveuciliste u Splitu Medicinski fakultet, Split, Croatia.
Klinički Bolnički Centar Split · HRUniversity of Split · HR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo evaluate retino-cortical function in children with Down's syndrome (DS) and no evident ocular abnormalities beyond mild refractive error, by recording visual evoked potentials (VEP) in response to pattern-reversal stimuli and comparing to those of age-matched healthy controls. METHODS AND ANALYSIS: All the children with DS registered at Split-Dalmatia County who met inclusion criteria of no ocular abnormalities and with refraction error between -0.5 and +2.0 D, and their age-matched healthy controls were included in the study (n=36 children, N=72 eyes, for both groups, respectively, with the same age of 9±2 years). Transient VEP was recorded and the waves with a positive peak as a response to a pattern-reversal stimulus, were analysed. The peak P100 latency, defined as the time from the stimulus onset to the main positive peak, and peak to peak amplitudes were measured.

resultsWhile P100 wave amplitudes were comparable between two groups (p=0.804), P100 latencies were from 4.3 to 28.5 ms longer in children with DS (p<0.001). Interocular latency difference between a VEP dominant and an inferior eye was pronounced in healthy (1.2 ms (0.2-4.0), but was almost diminished in children with DS (0.3 ms (0.1-0.5), p<0.001).

conclusionOur study has demonstrated that VEP response is divergent in children with DS compared with their age-matched healthy controls, indicating possible structural or functional abnormalities of the visual cortex. As VEP results are helpful in the diagnosis and treatment planning of vision-related disorders, we should reconsider the use of common VEP diagnostic criteria in subpopulation of children with DS.

Indexed as

Down SyndromeRefractive ErrorsCase-Control StudiesChildEvoked Potentials, VisualHumansNeurologic ExaminationVision DisordersChild health (paediatrics)Clinical TrialDiagnostic tests/InvestigationElectrophysiology

Identifiers

PMID37278422
PMCPMC10069582
OpenAlexW4360999962

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