| Literature DB >> 34194306 |
Gemma J Wilton1, Rhodri Woodhouse1, Valldeflors Vinuela-Navarro1,2, Rachel England1, J Margaret Woodhouse1.
Abstract
It is widely recognised that children with Down syndrome have a broad range and a high prevalence of visual deficits and it has been suggested that those with Down syndrome are more likely to exhibit visual perception deficits indicative of cerebral visual impairment. This exploratory study aims to determine the prevalence of behavioural features suggestive of cerebral visual impairment (CVI) occurring with Down syndrome and whether the visual problems can be ascribed to optometric factors. A cohort of 226 families of children with Down syndrome (trisomy 21), aged 4-17, were invited to participate in a validated question inventory, to recognise visual perception issues. The clinical records of the participants were then reviewed retrospectively. A five-question screening instrument was used to indicate suspected CVI. The majority of the 81 families who responded to the questionnaire reported some level of visual perceptual difficulty in their child. Among this cohort, the prevalence of suspected CVI as indicated by the screening questionnaire was 38%. Only ametropia was found to have a significant association with suspected CVI, although this increased the correct prediction of suspected CVI outcome by only a small amount. Results suggest that children with Down syndrome are more likely to experience problems consistent with cerebral visual impairment, and that these may originate from a similar brain dysfunction to that which contributes to high levels of ametropia and failure to emmetropise. It is important that behavioural features of CVI are recognised in children with Down syndrome, further investigations initiated and appropriate management applied.Entities:
Keywords: CVI; Down syndrome; cerebral visual impairment; dorsal stream; refractive error; ventral stream; visual perception
Year: 2021 PMID: 34194306 PMCID: PMC8236883 DOI: 10.3389/fnhum.2021.673342
Source DB: PubMed Journal: Front Hum Neurosci ISSN: 1662-5161 Impact factor: 3.169
The number of responders falling into each refractive error category.
| Emmetropia | −0.75 D to +2.75 D | 20 | 24.7 |
| Hypermetropia only | > +2.75 D | 13 | 16.0 |
| Myopia only | >-0.75 D | 1 | 1.2 |
| Simple astigmatism | One meridian ametropic and the other meridian emmetropic | 20 | 24.7 |
| Hypermetropic Astigmatism | Both meridians hypermetropic | 22 | 27.2 |
| Myopic Astigmatism | Both meridians myopic | 5 | 6.2 |
The refraction is for the least ametropic or fixing eye.
Figure 1The frequency distribution of the total raw scores in 81 children. The x-axis shows total score expressed as a percentage of applicable questions for (A) all children and (B) children divided into “suspected CVI” and “non-CVI” according to whether the child screened positive on the five-question CVI screening tool.
Figure 2The percentage of questions (excluding those reported as “not applicable”) to which each of 81 participants responded positively (a score of four or five on the question inventory) ranked by increasing number of positive responses; crosshatching represents the participants who fitted the screening criteria for suspected CVI and solid fill represents the participants who did not.
Figure 3The number of participants (81 in total) who responded positively to each question; crosshatching represents the participants who fitted the screening criteria for suspected CVI and solid fill represents the participants who did not. Questions 2, 18, 19, 24, and 27 are the diagnostic questions used in the CVI screening tool and are outlined.
Outcome of logistic regression.
| Constant | −1.461 | 0.487 | 9.006 | 1 | 0.003 | NA |
| Refractive error | 0.340 | 0.137 | 6.104 | 1 | 0.013 | 1.404 (1.073–1.839) |
| Test | ||||||
| Overall model | 6.757 | 1 | 0.009 | |||
| Hosmer & Lemeshow (Goodness-of-fit) | 8.700 | 7 | 0.275 |
All statistics were calculated using SPSS v25.0 (IBM Corp. Armonk, NY, USA). Further descriptive measures of goodness-of-fit given by Cox and Snell R.