Literature DB >> 33761963

Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophy.

Anna Lusakowska1, Maria Jedrzejowska2, Anna Kaminska1, Katarzyna Janiszewska1, Przemysław Grochowski3, Janusz Zimowski4, Janusz Sierdzinski5, Anna Kostera-Pruszczyk6.   

Abstract

BACKGROUND: Spinal muscular atrophy (SMA) is one of the most frequent and severe genetic diseases leading to premature death or severe motor disability. New therapies have been developed in recent years that change the natural history of the disease. The aim of this study is to describe patients included in the Polish Registry of SMA, with a focus on the course of type 3 SMA (SMA3) before the availability of disease-modifying treatments.
RESULTS: 790 patients with SMA were included in the registry (173 with type 1 [SMA1], 218 with type 2 [SMA2], 393 with SMA3, and six with type 4 SMA [SMA4]), most (52%) of whom were adults. Data on SMN2 gene copy number were available for 672 (85%) patients. The mean age of onset was 5 months for SMA1, 11.5 months for SMA2, and 4.5 years for SMA3. In patients with SMA3, the first symptoms occurred earlier in those with three copies of SMN2 than in those with four copies of SMN2 (3.2 years vs. 6.7 years). The age of onset of SMA3 was younger in girls than in boys (3.1 years vs. 5.7 years), with no new cases observed in women older than 16 years. Male patients outnumbered female patients, especially among patients with SMA3b (49 female vs. 85 male patients) and among patients with SMA3 with four copies of SMN2 (30 female vs. 69 male patients). 44% of patients with SMA3 were still able to walk; in those who were not still able to walk, the mean age of immobilization was 14.0 years. Patients with SMA3a (age of onset < 3 years) and three copies of SMN2 had significantly worse prognosis for remaining ambulant than patients with SMA3b (age of onset ≥ 3 years) and four copies of SMN2.
CONCLUSIONS: The Registry of SMA is an effective tool for assessing the disease course in the real world setting. SMN2 copy number is an important prognostic factor for the age of onset and ambulation in SMA3. Sex and age of disease onset also strongly affect the course of SMA. Data supplied by this study can aid treatment decisions.

Entities:  

Keywords:  Neuromuscular disease; Registry; SMN2 copy number; Spinal muscular atrophy (SMA); TREAT-NMD; Type 3 SMA

Mesh:

Substances:

Year:  2021        PMID: 33761963      PMCID: PMC7992780          DOI: 10.1186/s13023-021-01771-y

Source DB:  PubMed          Journal:  Orphanet J Rare Dis        ISSN: 1750-1172            Impact factor:   4.123


  30 in total

1.  Association of motor milestones, SMN2 copy and outcome in spinal muscular atrophy types 0-4.

Authors:  Renske I Wadman; Marloes Stam; Marleen Gijzen; Henny H Lemmink; Irina N Snoeck; Camiel A Wijngaarde; Kees P J Braun; Marja A G C Schoenmakers; Leonard H van den Berg; Dennis Dooijes; W-Ludo van der Pol
Journal:  J Neurol Neurosurg Psychiatry       Date:  2017-01-20       Impact factor: 10.154

2.  Chronic proximal spinal muscular atrophy of childhood and adolescence: sex influence.

Authors:  I Hausmanowa-Petrusewicz; J Zaremba; J Borkowska; W Szirkowiec
Journal:  J Med Genet       Date:  1984-12       Impact factor: 6.318

3.  Mutation update of spinal muscular atrophy in Spain: molecular characterization of 745 unrelated patients and identification of four novel mutations in the SMN1 gene.

Authors:  Laura Alías; Sara Bernal; Pablo Fuentes-Prior; María Jesus Barceló; Eva Also; Rebeca Martínez-Hernández; Francisco J Rodríguez-Alvarez; Yolanda Martín; Elena Aller; Elena Grau; Ana Peciña; Guillermo Antiñolo; Enrique Galán; Alberto L Rosa; Miguel Fernández-Burriel; Salud Borrego; José M Millán; Concepción Hernández-Chico; Montserrat Baiget; Eduardo F Tizzano
Journal:  Hum Genet       Date:  2008-12-03       Impact factor: 4.132

4.  Phenotype modifiers of spinal muscular atrophy: the number of SMN2 gene copies, deletion in the NAIP gene and probably gender influence the course of the disease.

Authors:  Maria Jedrzejowska; Michał Milewski; Janusz Zimowski; Janina Borkowska; Anna Kostera-Pruszczyk; Danuta Sielska; Marta Jurek; Irena Hausmanowa-Petrusewicz
Journal:  Acta Biochim Pol       Date:  2009-03-14       Impact factor: 2.149

5.  Incidence of spinal muscular atrophy in Poland--more frequent than predicted?

Authors:  Maria Jedrzejowska; Michal Milewski; Janusz Zimowski; Pawel Zagozdzon; Anna Kostera-Pruszczyk; Janina Borkowska; Danuta Sielska; Marta Jurek; Irena Hausmanowa-Petrusewicz
Journal:  Neuroepidemiology       Date:  2010-01-15       Impact factor: 3.282

6.  Identification and characterization of a spinal muscular atrophy-determining gene.

Authors:  S Lefebvre; L Bürglen; S Reboullet; O Clermont; P Burlet; L Viollet; B Benichou; C Cruaud; P Millasseau; M Zeviani
Journal:  Cell       Date:  1995-01-13       Impact factor: 41.582

7.  A multi-source approach to determine SMA incidence and research ready population.

Authors:  Ingrid E C Verhaart; Agata Robertson; Rebecca Leary; Grace McMacken; Kirsten König; Janbernd Kirschner; Cynthia C Jones; Suzanne F Cook; Hanns Lochmüller
Journal:  J Neurol       Date:  2017-06-20       Impact factor: 4.849

Review 8.  Emerging therapies and challenges in spinal muscular atrophy.

Authors:  Michelle A Farrar; Susanna B Park; Steve Vucic; Kate A Carey; Bradley J Turner; Thomas H Gillingwater; Kathryn J Swoboda; Matthew C Kiernan
Journal:  Ann Neurol       Date:  2017-02-17       Impact factor: 10.422

9.  An overview of the Cure SMA membership database: Highlights of key demographic and clinical characteristics of SMA members.

Authors:  Lisa Belter; Suzanne F Cook; Thomas O Crawford; Jill Jarecki; Cynthia C Jones; John T Kissel; Mary Schroth; Kenneth Hobby
Journal:  J Neuromuscul Dis       Date:  2018

10.  The Italian neuromuscular registry: a coordinated platform where patient organizations and clinicians collaborate for data collection and multiple usage.

Authors:  Anna Ambrosini; Daniela Calabrese; Francesco Maria Avato; Felice Catania; Guido Cavaletti; Maria Carmela Pera; Antonio Toscano; Giuseppe Vita; Lucia Monaco; Davide Pareyson
Journal:  Orphanet J Rare Dis       Date:  2018-10-04       Impact factor: 4.123

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