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Publication:
Neurocognitive impairment in patients with ataxia telangiectasia and their unaffected parents: is it similar?

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SCHOOL OF MEDICINE
Upper Org Unit

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Uyar, Emel

Usanmaz, Sevil

Kiykim, Ayca

Tufan, Ali Evren

Alibas, Hande

Aydiner, Omer

Somer, Ayper

Ozen, Ahmet

Baris, Safa

Karakoc-Aydiner, Elif

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Abstract

Background: Ataxia telangiectasia (AT) is a genetic multisystemic disorder affecting the nervous system. Data on neurocognitive functioning in AT are limited and focused on patients at various stages of disease. Because of the genetic nature of the disorder, parents of patients may also display subtle neurological problems. This study aimed to evaluate neurocognitive functioning in patients with AT and their unaffected parents. Methods: The study included 26 patients with AT and 41 parents among which 13 patients and 18 parents were evaluated with neurocognitive tests. Clinical and radiological data were reviewed retrospectively. Data were analyzed with descriptive statistics. Results: The median ages of patients and parents were 12.5 years (interquartile range [IQR] = 9.5) and 38.0 years (IQR = 12.0), respectively. Median intelligence quotients were 62.0 (IQR = 21.3) and 82.5 (IQR = 16.8), respectively, for patients and parents. Rates of intellectual disability for patients and parents were 100.0% and 83.3%, respectively. Areas of impairment in patients in decreasing order of frequency were motor skills, visual perception/memory, visual-manual coordination, spontaneous/focused and sustained attention (100.0% for each), social judgment, as well as vocabulary and arithmetic skills (75.0% for each). Areas of impairment in unaffected parents in decreasing order of frequency were visualmanual coordination (77.8%), working memory (76.5%), and visual perception and motor skills (66.7% for each). Conclusion: Intellectual disabilities, visual-spatial disabilities, and reduced visual-motor coordination seem to be similar in patients with AT and their parents. These results should be replicated with larger samples from multiple centers and may form putative cognitive endophenotypes for the disorder. (c) 2024 Elsevier Inc. All rights reserved.

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Elsevier Inc.

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Pediatric Neurology

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10.1016/j.pediatrneurol.2024.04.010

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