Andreas G Chiocchetti
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Professor Andreas G. Chiocchetti is a faculty member at Goethe University Frankfurt, Germany. His research areas encompass CRISPR technology, positive psychology in mental health, and the molecular mechanisms of neurodevelopmental disorders. Recent publications include studies on genetic adaptations in stem cells, ADHD-related gene variants, and the clinical profiles of patients during the COVID-19 pandemic.
Articles (10)
Year:
2024
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2024
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2024
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2024
Year:
2023
Objective The phenotypic and genotypic spectrum of adult patients with epilepsy and intellectual disability (ID) is less clear than in children. We investigated an adult patient cohort to further elucidate this and inform the genetic testing approach. Methods Fifty‐two adult patients (30 male, 22 female) with epilepsy, at least mild ID and no known genetic or acquired cause were included and phenotyped. Variants identified through exome sequencing were evaluated using ACMG criteria. Identified variants were compared with commercially available gene panels. Cluster analysis of two features, age at seizure onset and age at ascertainment of cognitive deficits, was performed. Results Median age was 27 years (range 20‐57 years) with median seizure onset at 3 years and median ascertainment of cognitive deficits at 1 year. Likely pathogenic/pathogenic variants were identified in 16/52 patients (31%) including 14 (27%) single nucleotide variants and 2 (4%) copy number variants. Simulated yield of commercial gene panels varied between 13% in small (≤144 genes) and 27% in large panels (≥1478 genes). Cluster analysis (optimal number 3 clusters) identified a cluster with early seizure onset and early developmental delay (developmental and epileptic encephalopathy, n = 26), a cluster with early developmental delay but late seizure onset (ID with epilepsy, n = 16) and a third cluster with late ascertainment of cognitive deficits and variable seizure onset (n = 7). The smaller gene panels particularly missed the genes identified in the cluster with early ascertainment of cognitive deficits and later onset of epilepsy (0/4) as opposed to the cluster with developmental and epileptic encephalopathy (7/10). Significance Our data indicates that adult patients with epilepsy and ID represent a heterogeneous cohort that includes grown‐up patients with DEE but also patients with primary ID and later onset of epilepsy. To maximize diagnostic yield in this cohort either large gene panels or exome sequencing should be used.
Year:
2023
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2023
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2023
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2023
Year:
2022
Collaborators (11)
Stefan Zielen
Professor for Cystic fibrosis, allergy and pneumology
Educational Research Institute
Katharina Günther
University of Innsbruck
Marie Schaer
University of Geneva
Ermal Aliu
University of Pittsburgh
Karl Martin Klein
-
Ralf Schubert
University Hospital
Silvia De Rubeis
Associate Professor
Icahn School of Medicine at Mount Sinai
Siddharth Banka
The University of Manchester
Andrea Rossi
Group Leader
IUF - Leibniz-Institut für umwelt- medizinische Forschung gGmbH
Jamie Kramer
Associate Professor
Dalhousie University
Matthias Nieberler
University Hospital Würzburg
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