von Jochen Maximilian Schmitt ; Thomas Bierbaum ; Max Geraedts ; Holger Gothe ; Martin Härter ; Falk Hoffmann ; Peter Ihle ; Ursula Kramer ; Monika Klinkhammer-Schalke ; Silke Kuske ; Stefanie March ; Jens-Peter Reese ; Olaf Schoffer ; Enno Swart ; Horst Christian Vollmar ; Felix Walther ; Wolfgang Hoffmann
von Christof Veit ; Thomas Bierbaum ; Simone Wesselmann ; Stephanie Stock ; Claus-Dieter Heidecke ; Christian Apfelbacher ; Stefan Rolf Benz ; Karsten Dreinhöfer ; Michael Hauptmann ; Falk Hoffmann ; Wolfgang Hoffmann ; Thomas Kaiser ; Monika Klinkhammer-Schalke ; Michael Koller ; Tanja Kostuj ; Olaf Ortmann ; Jochen Maximilian Schmitt ; Holger J. Schünemann ; Max Geraedts
von Damián Leonardo Arévalo Martínez ; Amir Haroon ; Hermann Werner Bange ; Ercan Erkul ; Marion Jegen ; Nils Moosdorf ; Jens Schneider von Deimling ; Christian Berndt ; Michael Ernst Böttcher ; Jasper Hoffmann ; Volker Liebetrau ; Ulf Mallast ; Gudrun Massmann ; Aaron Micallef ; Holly A. Michael ; Hendrik Paasche ; Wolfgang Rabbel ; Isaac Santos ; Jan Scholten ; Katrin Schwalenberg ; Beata Szymczycha ; Ariel Tremayne Thomas ; Joonas J. Virtasalo ; Hannelore Waska ; Bradley A. Weymer
von Kim M. Thalwitzer ; Jan Henje Driedger ; Julie Xian ; Afshin Saffari ; Pia Zacher ; Bigna K. Bölsterli ; Sarah McKeown Ruggiero ; Katie Rose Sullivan ; Alexandre N. Datta ; Christoph Kellinghaus ; Jürgen Althaus ; Adelheid Wiemer-Kruel ; Andreas van Baalen ; Armin Pampel ; Michael Alber ; Hilde M. H. Braakman ; Otfried Martin Debus ; Jonas Denecke ; Elke Hobbiebrunken ; Ina Breitweg ; Danielle Diehl ; Hans Christian Eitel ; Janina Gburek-Augustat ; Martin Preisel ; Jan-Ulrich Schlump ; Mirjam Laufs ; Dilbar Mammadova ; Carsten Wurst ; Christine Prager ; Christa Löhr-Nilles ; Peter Martin ; Sven Garbade ; Konrad Platzer ; Ira Benkel-Herrenbrueck ; Kerstin Egler ; Walid Fazeli ; Johannes R. Lemke ; Eva Runkel ; Barbara Klein ; Tobias Linden ; Julian Schröter ; Heike Steffeck ; Bastian Thies ; Florian von Deimling ; Sabine Illsinger ; Ingo Borggräfe ; Georg Classen ; Dagmar Wieczorek ; Georgia Ramantani ; Stefan Kölker ; Georg F. Hoffmann ; Markus Ries ; Ingo Helbig ; Steffen Syrbe
BACKGROUND AND OBJECTIVES: Pathogenic variants in STXBP1 are among the major genetic causes of neurodevelopmental disorders. Despite the increasing number of individuals diagnosed without a history of epilepsy, little is known about the natural history and developmental trajectories in this subgroup and endpoints for future therapeutic studies are limited to seizure control. - METHODS: We performed a cross-sectional retrospective study using standardized questionnaires for clinicians and caregivers of individuals with STXBP1-related disorders capturing medical histories, genetic findings, and developmental outcomes. Motor and language function were assessed using Gross Motor Function Classification System scores (GMFCS) and a speech impairment score and were compared within and across clinically defined subgroups. - RESULTS: We collected data of 71 individuals with STXBP1-related disorders, including 44 previously unreported individuals. Median age at inclusion was 5.3 years (IQR = 3.5-9.3) with the oldest individual aged 43.8 years. Epilepsy was absent in 18/71 (25%) of individuals. The range of developmental outcomes was broad, including two individuals presenting with close to age-appropriate motor development. 29/61 (48%) individuals were able to walk unassisted and 24/69 (35%) were able to speak single words. Individuals without epilepsy presented with a similar onset and spectrum of phenotypic features but had lower GMFCS scores (median 3 vs. 4, p < 0.01) than individuals with epilepsy. Individuals with epileptic spasms were less likely to walk unassisted than individuals with other seizure types (6% vs. 58%, p < 0.01). Individuals with early epilepsy onset had higher speech impairment scores (p = 0.02) than individuals with later epilepsy onset. - DISCUSSION: We expand the spectrum of STXBP1-related disorders and provide clinical features and developmental trajectories in individuals with and without a history of epilepsy. Individuals with epilepsy, in particular epileptic spasms, and neonatal or early-onset, presented with less favorable motor and language functional outcomes compared to individuals without epilepsy. These findings identify children at risk for severe disease and can serve as comparator for future interventional studies in STXBP1-related disorders.