Longitudinal natural history in young boys with Duchenne muscular dystrophy

Marika Pane, Eugenio Maria Mercuri, Giorgia Coratti, Claudia Brogna, Adele D'Amico, Simona Lucibello, Giovanni Baranello, Enrico Silvio Bertini, Valeria Ricotti, Lianne Abbott, Angela Berardinelli, Gian Luca Vita, Sonia Messina, Valeria Sansone, Giulia Colia, Francesca Salmin, Alice Gardani, Adnan Manzur, Marion Main, Maria Teresa ArnoldiJulie Parsons, Terri Carry, Anne M. Connolly, Francesco Muntoni

Risultato della ricerca: Contributo in rivistaArticolo in rivista

Abstract

The aim of this prospective multicentric study was to document disease progression in young boys affected by Duchenne muscular dystrophy (DMD) between age 3 and 6 years (±3 months) using the North Star Ambulatory Assessment scale. One hundred fifty-three DMD boys (573 assessments) younger than 6 years (mean: 4.68, SD: 0.84) with a genetically proven DMD diagnoses were included. Our results showed North Star Ambulatory Assessment scores progressively increased with age. The largest increase was observed between age 3 and 4 years but further increase was steadily observed until age of 6 years. Using a multiple linear regression analysis, we found that both the use of corticosteroids and the site of mutation significantly contributed to the North Star Ambulatory Assessment changes (p < 0.001). At each age point, boys on corticosteroid treatment had higher scores than corticosteroid naïve ones (p < 0.001). Similarly, patients with mutations downstream exon 44, had lower baseline scores and lower magnitude of changes compared to those with mutations located at the 5′ end of the gene (p < 0,001). Very few boys achieved the age appropriate maximum score. These results provide useful information for the assessment and counselling of young DMD boys and for the design of clinical trials in this age group.
Lingua originaleEnglish
pagine (da-a)857-862
Numero di pagine6
RivistaNeuromuscular Disorders
Volume29
DOI
Stato di pubblicazionePubblicato - 2019

Keywords

  • Duchenne Muscular dystrophy
  • Outcome measure
  • North Star Ambulatory Assessment
  • Neuromuscular disorders

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