Literature DB >> 33547876

Type I SMA "new natural history": long-term data in nusinersen-treated patients.

Marika Pane1,2, Giorgia Coratti1,2, Valeria A Sansone3, Sonia Messina4, Michela Catteruccia5, Claudio Bruno6, Maria Sframeli4, Emilio Albamonte3, Marina Pedemonte6, Adele D'Amico5, Chiara Bravetti2, Beatrice Berti2, Concetta Palermo2, Daniela Leone2, Giorgia Brigati6, Paola Tacchetti6, Francesca Salmin3, Roberto De Sanctis2, Simona Lucibello1,2, Maria Carmela Pera1,2, Marco Piastra7, Orazio Genovese7, Enrico Bertini5, Gianluca Vita4, Francesco Danilo Tiziano8, Eugenio Mercuri1,2.   

Abstract

OBJECTIVE: The aim of this paper was to report the 2-year follow-up in type I patients treated with Nusinersen and to assess whether possible changes in motor function are related to the subtype, age, or SMN2 copy number.
METHODS: Sixty-eight patients, with ages ranging from 0.20 to 15.92 years (mean: 3.96; standard deviation: +3.90) were enrolled in the study. All patients were assessed using the Children's Hospital of Philadelphia Infant Test of Neuromuscular Disorders (CHOP INTEND) and the developmental section of the Hammersmith Infant Neurological Examination (HINE-2) at the time they started treatment and 12 and 24 months after that.
RESULTS: For both CHOP and HINE-2 repeated measures analysis of variance showed a significant difference (P < 0.001) between baseline and 12 months, 12 months and 24 months, and baseline and 24-month scores for the whole group. When age subgroups (<210 days, <2 years, 2-4 years, 5-11 years, 12-18 years) were considered, on the CHOP INTEND the difference was significant between baseline and 24 months in all age subgroups. On the HINE-2, the difference between baseline and 24 months was significant in all the subgroups before the age of 4 years. Age was predictive of changes on both scales (P < 0.05), whereas SMN2 copy number and decimal classification were not.
INTERPRETATION: Our results suggest that some improvement of motor function can be observed even after the first year of treatment. This is more obvious in the infants treated in the first 2 years but some improvement can also be found in older children.
© 2021 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.

Entities:  

Year:  2021        PMID: 33547876     DOI: 10.1002/acn3.51276

Source DB:  PubMed          Journal:  Ann Clin Transl Neurol        ISSN: 2328-9503            Impact factor:   4.511


  9 in total

Review 1.  Disease Modifying Therapies for the Management of Children with Spinal Muscular Atrophy (5q SMA): An Update on the Emerging Evidence.

Authors:  Helgi Thor Hjartarson; Kristofer Nathorst-Böös; Thomas Sejersen
Journal:  Drug Des Devel Ther       Date:  2022-06-16       Impact factor: 4.319

2.  Nusinersen in Adults with 5q Spinal Muscular Atrophy: a Systematic Review and Meta-analysis.

Authors:  Maria Gavriilaki; Maria Moschou; Vasileios Papaliagkas; Konstantinos Notas; Evangelia Chatzikyriakou; Sotirios Papagiannopoulos; Marianthi Arnaoutoglou; Vasilios K Kimiskidis
Journal:  Neurotherapeutics       Date:  2022-02-17       Impact factor: 6.088

3.  Improved upper limb function in non-ambulant children with SMA type 2 and 3 during nusinersen treatment: a prospective 3-years SMArtCARE registry study.

Authors:  Astrid Pechmann; Max Behrens; Katharina Dörnbrack; Adrian Tassoni; Franziska Wenzel; Sabine Stein; Sibylle Vogt; Daniela Zöller; Günther Bernert; Tim Hagenacker; Ulrike Schara-Schmidt; Maggie C Walter; Astrid Bertsche; Katharina Vill; Matthias Baumann; Manuela Baumgartner; Isabell Cordts; Astrid Eisenkölbl; Marina Flotats-Bastardas; Johannes Friese; René Günther; Andreas Hahn; Veronka Horber; Ralf A Husain; Sabine Illsinger; Jörg Jahnel; Jessika Johannsen; Cornelia Köhler; Heike Kölbel; Monika Müller; Arpad von Moers; Annette Schwerin-Nagel; Christof Reihle; Kurt Schlachter; Gudrun Schreiber; Oliver Schwartz; Martin Smitka; Elisabeth Steiner; Regina Trollmann; Markus Weiler; Claudia Weiß; Gert Wiegand; Ekkehard Wilichowski; Andreas Ziegler; Hanns Lochmüller; Janbernd Kirschner
Journal:  Orphanet J Rare Dis       Date:  2022-10-23       Impact factor: 4.303

Review 4.  Facilitations and Hurdles of Genetic Testing in Neuromuscular Disorders.

Authors:  Andrea Barp; Lorena Mosca; Valeria Ada Sansone
Journal:  Diagnostics (Basel)       Date:  2021-04-14

5.  Nusinersen: A Review in 5q Spinal Muscular Atrophy.

Authors:  Sheridan M Hoy
Journal:  CNS Drugs       Date:  2021-11-30       Impact factor: 5.749

6.  Nusinersen efficacy data for 24-month in type 2 and 3 spinal muscular atrophy.

Authors:  Marika Pane; Giorgia Coratti; Maria Carmela Pera; Valeria A Sansone; Sonia Messina; Adele d'Amico; Claudio Bruno; Francesca Salmin; Emilio Albamonte; Roberto De Sanctis; Maria Sframeli; Vincenzo Di Bella; Simone Morando; Concetta Palermo; Anna Lia Frongia; Laura Antonaci; Anna Capasso; Michela Catteruccia; Antonella Longo; Martina Ricci; Costanza Cutrona; Alice Pirola; Chiara Bravetti; Marina Pedemonte; Noemi Brolatti; Enrico Bertini; Eugenio Mercuri
Journal:  Ann Clin Transl Neurol       Date:  2022-02-15       Impact factor: 4.511

7.  Experience and Perspectives in the US on the Evolving Treatment Landscape in Spinal Muscular Atrophy.

Authors:  Leigh Ramos-Platt; Lauren Elman; Perry B Shieh
Journal:  Int J Gen Med       Date:  2022-09-17

8.  Evolution of bulbar function in spinal muscular atrophy type 1 treated with nusinersen.

Authors:  Harriet Weststrate; Georgia Stimpson; Lily Thomas; Mariacristina Scoto; Emily Johnson; Alexandra Stewart; Francesco Muntoni; Giovanni Baranello; Eleanor Conway
Journal:  Dev Med Child Neurol       Date:  2022-02-01       Impact factor: 4.864

Review 9.  Spinal muscular atrophy: From approved therapies to future therapeutic targets for personalized medicine.

Authors:  Helena Chaytow; Kiterie M E Faller; Yu-Ting Huang; Thomas H Gillingwater
Journal:  Cell Rep Med       Date:  2021-07-21
  9 in total

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