| Literature DB >> 32979048 |
Darius Ebrahimi-Fakhari1, Julian Teinert1,2, Robert Behne1,3, Miriam Wimmer1, Angelica D'Amore1,4, Kathrin Eberhardt1, Barbara Brechmann1, Marvin Ziegler1, Dana M Jensen5, Premsai Nagabhyrava1,6, Gregory Geisel1,6, Erin Carmody1,6, Uzma Shamshad1,6, Kira A Dies1,6, Christopher J Yuskaitis1, Catherine L Salussolia1, Daniel Ebrahimi-Fakhari7,8, Toni S Pearson9, Afshin Saffari2, Andreas Ziegler2, Stefan Kölker2, Jens Volkmann3, Antje Wiesener10, David R Bearden11, Shenela Lakhani12, Devorah Segal12,13, Anaita Udwadia-Hegde14, Andrea Martinuzzi15, Jennifer Hirst16, Seth Perlman17, Yoshihisa Takiyama18, Georgia Xiromerisiou19, Katharina Vill20, William O Walker21, Anju Shukla22, Rachana Dubey Gupta23, Niklas Dahl24, Ayse Aksoy25, Helene Verhelst26, Mauricio R Delgado27, Radka Kremlikova Pourova28, Abdelrahim A Sadek29, Nour M Elkhateeb30, Lubov Blumkin31, Alejandro J Brea-Fernández32, David Dacruz-Álvarez33, Thomas Smol34, Jamal Ghoumid34, Diego Miguel35, Constanze Heine36, Jan-Ulrich Schlump37, Hendrik Langen38, Jonathan Baets39, Saskia Bulk40, Hossein Darvish41, Somayeh Bakhtiari42, Michael C Kruer42, Elizabeth Lim-Melia43, Nur Aydinli44, Yasemin Alanay45, Omnia El-Rashidy46, Sheela Nampoothiri47, Chirag Patel48, Christian Beetz49, Peter Bauer49, Grace Yoon50, Mireille Guillot51, Steven P Miller51, Thomas Bourinaris52, Henry Houlden52, Laura Robelin53, Mathieu Anheim53, Abdullah S Alamri54, Adel A H Mahmoud55, Soroor Inaloo56, Parham Habibzadeh57, Mohammad Ali Faghihi57,58, Anna C Jansen59, Stefanie Brock59, Agathe Roubertie60, Basil T Darras1, Pankaj B Agrawal61, Filippo M Santorelli4, Joseph Gleeson62, Maha S Zaki63, Sarah I Sheikh64, James T Bennett5, Mustafa Sahin1,6.
Abstract
Bi-allelic loss-of-function variants in genes that encode subunits of the adaptor protein complex 4 (AP-4) lead to prototypical yet poorly understood forms of childhood-onset and complex hereditary spastic paraplegia: SPG47 (AP4B1), SPG50 (AP4M1), SPG51 (AP4E1) and SPG52 (AP4S1). Here, we report a detailed cross-sectional analysis of clinical, imaging and molecular data of 156 patients from 101 families. Enrolled patients were of diverse ethnic backgrounds and covered a wide age range (1.0-49.3 years). While the mean age at symptom onset was 0.8 ± 0.6 years [standard deviation (SD), range 0.2-5.0], the mean age at diagnosis was 10.2 ± 8.5 years (SD, range 0.1-46.3). We define a set of core features: early-onset developmental delay with delayed motor milestones and significant speech delay (50% non-verbal); intellectual disability in the moderate to severe range; mild hypotonia in infancy followed by spastic diplegia (mean age: 8.4 ± 5.1 years, SD) and later tetraplegia (mean age: 16.1 ± 9.8 years, SD); postnatal microcephaly (83%); foot deformities (69%); and epilepsy (66%) that is intractable in a subset. At last follow-up, 36% ambulated with assistance (mean age: 8.9 ± 6.4 years, SD) and 54% were wheelchair-dependent (mean age: 13.4 ± 9.8 years, SD). Episodes of stereotypic laughing, possibly consistent with a pseudobulbar affect, were found in 56% of patients. Key features on neuroimaging include a thin corpus callosum (90%), ventriculomegaly (65%) often with colpocephaly, and periventricular white-matter signal abnormalities (68%). Iron deposition and polymicrogyria were found in a subset of patients. AP4B1-associated SPG47 and AP4M1-associated SPG50 accounted for the majority of cases. About two-thirds of patients were born to consanguineous parents, and 82% carried homozygous variants. Over 70 unique variants were present, the majority of which are frameshift or nonsense mutations. To track disease progression across the age spectrum, we defined the relationship between disease severity as measured by several rating scales and disease duration. We found that the presence of epilepsy, which manifested before the age of 3 years in the majority of patients, was associated with worse motor outcomes. Exploring genotype-phenotype correlations, we found that disease severity and major phenotypes were equally distributed among the four subtypes, establishing that SPG47, SPG50, SPG51 and SPG52 share a common phenotype, an 'AP-4 deficiency syndrome'. By delineating the core clinical, imaging, and molecular features of AP-4-associated hereditary spastic paraplegia across the age spectrum our results will facilitate early diagnosis, enable counselling and anticipatory guidance of affected families and help define endpoints for future interventional trials.Entities:
Keywords: SPG47; SPG50; SPG51; SPG52; neurodegeneration
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Year: 2020 PMID: 32979048 PMCID: PMC7780481 DOI: 10.1093/brain/awz307
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 15.255