Purpose: The availability of care recommendations has improved survival and delayed the progression of clinical signs in Duchenne muscular dystrophy. The aim of the study was to perform a nationwide survey investigating the prevalence, age distribution, and functional status of Duchenne muscular dystrophyin Italy. Methods: The survey was performed by collecting data from all 31 reference centers for Duchenne muscular dystrophy in Italy using a structured form. We assessed age distribution, motor function, and the need for respiratory and nutritional support to evaluate their prevalence in different age and functional subgroups. Results: The estimated prevalence was 1.65/100,000 (3.4/100,000 males). There were 972 boys and adults with a confirmed diagnosis of Duchenne, of age ranging between 6 months and 48 years (mean = 16.5). Over 59% were below the age of 18 years and the remaining 41% were adults. Over 43% were ambulant and 57% non-ambulant; 14.7% were steroids naive (mean 20.6 years), 75% are currently on steroids (mean 14.6 years) with 604 on the daily regime, 126 intermittent. Nearly 73% did not require any ventilatory support, 16% had NIV ≤ 12 h, 9% > 12 h, and 1.4% had a tracheostomy. More than 82% did not require any nutritional support, 13% required food modification/semisolid and 4.4% had a G-tube. Conclusions: Our findings provide information to be used not only for epidemiological purposes but also for possible trial design to include older non-ambulant patients who until recently have been excluded and for whom clinical information is limited. (Table presented.)

Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey / A. Capasso, G. Cicala, M. Ricci, M. Pane, A. D'Amico, C. Bruno, V.A. Sansone, S. Messina, L. Bello, E. Pegoraro, M.G. D'Angelo, R. Masson, A. Berardinelli, A. Pini, F. Ricci, T.E. Mongini, M. Coccia, V. Nigro, A. Trabacca, M. Filosto, G. Comi, F. Magri, A. Barp, R. Battini, S.C. Previtali, M.L. Valentino, E. Diella, C. Dosi, L. Ruggiero, G. Siciliano, G. Ricci, M. Catteruccia, C. Arpaia, G. Coratti, G. Norcia, S. Bonanno, L. Verriello, C. Agosto, A. Varone, A. Ferlini, M.A. Maioli, C. Brogna, S. Siliquini, I. Bruno, C. Panicucci, C. Allegra, E. Albamonte, E. Mercuri. - In: EUROPEAN JOURNAL OF PEDIATRICS. - ISSN 0340-6199. - 184:1(2024 Dec), pp. 86.1-86.10. [10.1007/s00431-024-05903-x]

Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey

V.A. Sansone;G. Comi;F. Magri;
2024

Abstract

Purpose: The availability of care recommendations has improved survival and delayed the progression of clinical signs in Duchenne muscular dystrophy. The aim of the study was to perform a nationwide survey investigating the prevalence, age distribution, and functional status of Duchenne muscular dystrophyin Italy. Methods: The survey was performed by collecting data from all 31 reference centers for Duchenne muscular dystrophy in Italy using a structured form. We assessed age distribution, motor function, and the need for respiratory and nutritional support to evaluate their prevalence in different age and functional subgroups. Results: The estimated prevalence was 1.65/100,000 (3.4/100,000 males). There were 972 boys and adults with a confirmed diagnosis of Duchenne, of age ranging between 6 months and 48 years (mean = 16.5). Over 59% were below the age of 18 years and the remaining 41% were adults. Over 43% were ambulant and 57% non-ambulant; 14.7% were steroids naive (mean 20.6 years), 75% are currently on steroids (mean 14.6 years) with 604 on the daily regime, 126 intermittent. Nearly 73% did not require any ventilatory support, 16% had NIV ≤ 12 h, 9% > 12 h, and 1.4% had a tracheostomy. More than 82% did not require any nutritional support, 13% required food modification/semisolid and 4.4% had a G-tube. Conclusions: Our findings provide information to be used not only for epidemiological purposes but also for possible trial design to include older non-ambulant patients who until recently have been excluded and for whom clinical information is limited. (Table presented.)
Duchenne muscular dystrophy; Prevalence; Respiratory
Settore MEDS-12/A - Neurologia
dic-2024
Article (author)
File in questo prodotto:
File Dimensione Formato  
s00431-024-05903-x (1).pdf

accesso riservato

Tipologia: Publisher's version/PDF
Licenza: Nessuna licenza
Dimensione 1.23 MB
Formato Adobe PDF
1.23 MB Adobe PDF   Visualizza/Apri   Richiedi una copia
Pubblicazioni consigliate

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1156959
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus 0
  • ???jsp.display-item.citation.isi??? 0
  • OpenAlex ND
social impact