| Literature DB >> 29960818 |
Marika Pane1, Concetta Palermo1, Sonia Messina2, Valeria A Sansone3, Claudio Bruno4, Michela Catteruccia5, Maria Sframeli2, Emilio Albamonte3, Marina Pedemonte4, Adele D'Amico5, Giorgia Brigati4, Roberto de Sanctis1, Giorgia Coratti1, Simona Lucibello1, Enrico Bertini5, Giuseppe Vita2, Francesco Danilo Tiziano6, Eugenio Mercuri7.
Abstract
We report preliminary data on the six month use of Nusinersen in 104 type 1 patients of age ranging from three months to 19 years, 9 months. Ten of the 104 were classified as 1.1, 58 as 1.5 and 36 as 1.9. Three patients had one SMN2 copy, 65 had two and 24 had three copies. In 12 the SMN2 copy number was not available. After six months an improvement of more than two points was found in 58 of the 104 (55.7%) on the CHOP INTEND and in 21 of the 104 (20.19%) on the Hammersmith Infant Neurological Examination (HINE). Changes more than two points were found in 26/71 patients older than two years, and in seven of the 20 older than 10 years. Changes ≥ four points were found in 20/71 older than two years, and in six of the 20 patients older than 10 years. The difference between baseline and six months on both CHOP INTEND and HINE was significant for the whole group (p < 0.001) as well as for the subgroups with two (p < 0.001), and three SMN2 copies (p < 0.001). Our preliminary results suggest that functional improvement can be observed in type 1 patients outside the range of the inclusion criteria used in the Endear study.Entities:
Keywords: CHOP INTEND; Hammersmith Infant Neurological Examination; Nusinersen; Spinal Muscular Atrophy; Werdnig Hoffmann disease
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Year: 2018 PMID: 29960818 DOI: 10.1016/j.nmd.2018.05.010
Source DB: PubMed Journal: Neuromuscul Disord ISSN: 0960-8966 Impact factor: 4.296