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DOI 10.1371/journal.pone.0083400

Медицинская библиотека · PloS one · 2014

6 Minute walk test in Duchenne MD patients with different mutations: 12 month changes.

Pane Marika, Mazzone Elena S, Sormani Maria Pia, Messina Sonia, Vita Gian Luca, Fanelli Lavinia, Berardinelli Angela, Torrente Yvan, D'Amico Adele, Lanzillotta Valentina, Viggiano Emanuela, D'Ambrosio Paola, Cavallaro Filippo, Frosini Silvia, Bello Luca, Bonfiglio Serena, Scalise Roberta, De Sanctis Roberto, Rolle Enrica, Bianco Flaviana, Van der Haawue Marlene, Magri Francesca, Palermo Concetta, Rossi Francesca, Donati Maria Alice, Alfonsi Chiara, Sacchini Michele, Arnoldi Maria Teresa, Baranello Giovanni, Mongini Tiziana, Pini Antonella, Battini Roberta, Pegoraro Elena, Previtali Stefano C, Napolitano Sara, Bruno Claudio, Politano Luisa, Comi Giacomo P, Bertini Enrico, Morandi Lucia, Gualandi Francesca, Ferlini Alessandra, Goemans Nathalie, Mercuri Eugenio

СтатьяНаблюдательное исследованиеПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

In the last few years some of the therapeutical approaches for Duchenne muscular dystrophy (DMD) are specifically targeting distinct groups of mutations, such as deletions eligible for skipping of individual exons. The aim of this observational study was to establish whether patients with distinct groups of mutations have different profiles of changes on the 6 minute walk test (6MWT) over a 12 month period.

METHODS

The 6MWT was performed in 191 ambulant DMD boys at baseline and 12 months later. The results were analysed using a test for heterogeneity in order to establish possible differences among different types of mutations (deletions, duplications, point mutations) and among subgroups of deletions eligible to skip individual exons.

RESULTS

At baseline the 6MWD ranged between 180 and 560,80 metres (mean 378,06, SD 74,13). The 12 month changes ranged between -325 and 175 (mean -10.8 meters, SD 69.2). Although boys with duplications had better results than those with the other types of mutations, the difference was not significant. Similarly, boys eligible for skipping of the exon 44 had better baseline results and less drastic changes than those eligible for skipping exon 45 or 53, but the difference was not significant.

CONCLUSIONS

even if there are some differences among subgroups, the mean 12 month changes in each subgroup were all within a narrow Range: from the mean of the whole DMD cohort. This information will be of help at the time of designing clinical trials with small numbers of eligible patients.

Для цитирования: Pane Marika, Mazzone Elena S, Sormani Maria Pia, Messina Sonia, Vita Gian Luca, Fanelli Lavinia, Berardinelli Angela, Torrente Yvan, D'Amico Adele, Lanzillotta Valentina, Viggiano Emanuela, D'Ambrosio Paola, Cavallaro Filippo, Frosini Silvia, Bello Luca, Bonfiglio Serena, Scalise Roberta, De Sanctis Roberto, Rolle Enrica, Bianco Flaviana, Van der Haawue Marlene, Magri Francesca, Palermo Concetta, Rossi Francesca, Donati Maria Alice, Alfonsi Chiara, Sacchini Michele, Arnoldi Maria Teresa, Baranello Giovanni, Mongini Tiziana, Pini Antonella, Battini Roberta, Pegoraro Elena, Previtali Stefano C, Napolitano Sara, Bruno Claudio, Politano Luisa, Comi Giacomo P, Bertini Enrico, Morandi Lucia, Gualandi Francesca, Ferlini Alessandra, Goemans Nathalie, Mercuri Eugenio. 6 Minute walk test in Duchenne MD patients with different mutations: 12 month changes.. PloS one. 2014. DOI: 10.1371/journal.pone.0083400.

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