Dyslexia and cognitive impairment in adult patients with myotonic dystrophy type 1: a clinical prospective analysis

التفاصيل البيبلوغرافية
العنوان: Dyslexia and cognitive impairment in adult patients with myotonic dystrophy type 1: a clinical prospective analysis
المؤلفون: Federica Montagnese, Kristina Gutschmidt, Stephan Wenninger, Benedikt Schoser
المصدر: Journal of Neurology
بيانات النشر: Springer Berlin Heidelberg, 2020.
سنة النشر: 2020
مصطلحات موضوعية: 0301 basic medicine, Adult, medicine.medical_specialty, Neurology, Adolescent, media_common.quotation_subject, Audiology, Neurodegenerative, Dyslexia, 03 medical and health sciences, 0302 clinical medicine, Reading (process), Germany, medicine, Humans, Myotonic Dystrophy, Cognitive Dysfunction, Prospective Studies, Prospective cohort study, Child, Neuroradiology, media_common, Original Communication, business.industry, Cognition, medicine.disease, Spelling, 030104 developmental biology, Cognitive impairment, IQ, Cohort, Neurology (clinical), Reading disorder, business, 030217 neurology & neurosurgery
الوصف: Background Cognitive impairments in patients with myotonic dystrophy type 1 (DM1) have often been described, however, there are only few studies differentiating between partial performance disorders and mental retardation in common. This study focused on the evaluation of reading performance and the frequency of dyslexia in adult DM1 patients. Methods We performed a prospective cohort study including genetically confirmed adult DM1 patients registered in the DM registry of Germany or the internal database of the Friedrich-Baur-Institute, Munich, Germany. For the assessment of the patients’ reading and spelling performance, we used the standardized and validated test ‚Salzburger Lese- und Rechtschreibtest‘ (SLRT II). The ‚CFT-20 R Grundintelligenztest Skala 2‘ in revised ("R") version (CFT 20-R), determining the intelligence level, was appropriate to differentiate between dyslexia and general mental retardation. The diagnosis of dyslexia, the combined reading and spelling disorder, was based on the guidelines for diagnosis and therapy of children and adolescents with dyslexia 2015 (S3-guideline) providing (1) the criterion of the divergence from age level and (2) the criterion of IQ-divergence. Results Fifty-seven DM1 patients participated in our study. Evaluating the reading performance, 16 patients fulfilled the divergence criteria of the age level and 2 patients the IQ-divergence criteria. In total, the diagnosis of a reading disorder was given in 18 DM1 patients (31.6 %). In 11 out of these 18 patients with a reading disorder, a relevant impairment of spelling performance was observed with at least three spelling errors. As there are no normative values for adults in spelling performance, we assume a combined reading disorder and dyslexia, in those 11 DM1 patients (19.3 %). Regarding the separate analyses of the test procedures, in the SLRT II the performance was below average in 40.4 % of all patients for ‘word reading’ and in 61.4 % of all patients for ‘pseudoword reading’. There was a significant positive correlation between the CTG expansion size and a reading disorder (p=0.027). The average IQ of 17 examined DM1 patients was in the lower normal range (86.1 ± 19.1). 54.5 % of patients with reading disorder had a normal IQ. Conclusion The calculated prevalence of dyslexia in the DM1 study cohort was 19.3 % and thus considerably increased compared to the normal German population. As dyslexia is not equivalent to a general cognitive impairment, it is important not to miss dyslexic features in cognitive inconspicuous DM1 patients. Case-by-case one should consider a differential diagnostic approach, as individualized therapies can be offered to support dyslexic patients in their performance.
اللغة: English
تدمد: 1432-1459
0340-5354
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ebe56a36504c595047fff886f31331eTest
http://europepmc.org/articles/PMC7880941Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....0ebe56a36504c595047fff886f31331e
قاعدة البيانات: OpenAIRE