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 / Capasso, A., Cicala, G., Ricci, M., Pane, M., D'Amico, A., Bruno, C., Sansone, V.A., Messina, S., Bello, L., Pegoraro, E., D'Angelo, M.G., Masson, R., Berardinelli, A., Pini, A., Ricci, F., Mongini, T.E., Coccia, M., Nigro, V., Trabacca, A., Filosto, M., et al.. - In: EUROPEAN JOURNAL OF PEDIATRICS. - ISSN 0340-6199. - 184:1(2024). [10.1007/s00431-024-05903-x]

Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey

Ricci, Martina;Nigro, Vincenzo;Ruggiero, Lucia;Arpaia, Chiara;
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.)
2024
Prevalence of Duchenne muscular dystrophy in Italy: a nationwide survey / Capasso, A., Cicala, G., Ricci, M., Pane, M., D'Amico, A., Bruno, C., Sansone, V.A., Messina, S., Bello, L., Pegoraro, E., D'Angelo, M.G., Masson, R., Berardinelli, A., Pini, A., Ricci, F., Mongini, T.E., Coccia, M., Nigro, V., Trabacca, A., Filosto, M., et al.. - In: EUROPEAN JOURNAL OF PEDIATRICS. - ISSN 0340-6199. - 184:1(2024). [10.1007/s00431-024-05903-x]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/992264
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