Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study

Author:

Brogna Claudia12,Pane Marika12,Coratti Giorgia2ORCID,D’Amico Adele3ORCID,Pegoraro Elena4ORCID,Bello Luca4ORCID,Sansone Valeria5,Albamonte Emilio5,Messina Sonia6ORCID,Pini Antonella7ORCID,D’Angelo Maria8,Bruno Claudio9,Mongini Tiziana10,Ricci Federica10ORCID,Berardinelli Angela11ORCID,Battini Roberta1213,Masson Riccardo14ORCID,Bertini Enrico3ORCID,Politano Luisa15ORCID,Mercuri Eugenio1,

Affiliation:

1. Pediatric Neurology, Università Cattolica del Sacro Cuore, 00168 Rome, Italy

2. Centro Clinico Nemo, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, 00168 Rome, Italy

3. Unit of Neuromuscular and Neurodegenerative Disorders, Bambino Gesù Children’s Hospital, IRCCS, 00165 Rome, Italy

4. Department of Neurosciences, University of Padua, 35128 Padua, Italy

5. The NEMO Center in Milan, Neurorehabilitation Unit, University of Milan, ASST Niguarda Hospital, 20162 Milan, Italy

6. Department of Clinical and Experimental Medicine, University of Messina, 98122 Messina, Italy

7. Neuromuscular Pediatric Unit, IRCCS Istituto delle Scienze Neurologiche di Bologna, 40139 Bologna, Italy

8. NeuroMuscular Unit IRCCS Eugenio Medea, Bosisio Parini, 23842 Lecco, Italy

9. Center of Translational and Experimental Myology and Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, IRCCS Istituto Giannina Gaslini and University of Genoa, 16132 Genoa, Italy

10. Neuromuscular Center, AOU Città della Salute e della Scienza, University of Torino, 10100 Turin, Italy

11. National Neurological Institute C. Mondino Foundation, IRCCS, 27100 Pavia, Italy

12. Department of Developmental Neuroscience, IRCCS Stella Maris, 56018 Pisa, Italy

13. Department of Clinical and Experimental Medicine, University of Pisa, 56126 Pisa, Italy

14. Developmental Neurology Unit, Fondazione IRCCS Istituto Neurologico Carlo Besta, 20133 Milan, Italy

15. Cardiomiology and Medical Genetics, Department of Experimental Medicine, Università della Campania Luigi Vanvitelli, 80138 Naples, Italy

Abstract

Introduction: The Performance of Upper Limb version 2.0 (PUL 2.0) is increasingly used in Duchenne Muscular Dystrophy (DMD) to study longitudinal functional changes of motor upper limb function in ambulant and non-ambulant patients. The aim of this study was to evaluate changes in upper limb functions in patients carrying mutations amenable to skipping exons 44, 45, 51 and 53. Methods: All DMD patients were assessed using the PUL 2.0 for at least 2 years, focusing on 24-month paired visits in those with mutations eligible for skipping exons 44, 45, 51 and 53. Results: 285 paired assessments were available. The mean total PUL 2.0 12-month change was −0.67 (2.80), −1.15 (3.98), −1.46 (3.37) and −1.95 (4.04) in patients carrying mutations amenable to skipping exon 44, 45, 51 and 53, respectively. The mean total PUL 2.0 24-month change was −1.47 (3.73), −2.78 (5.86), −2.95 (4.56) and −4.53 (6.13) in patients amenable to skipping exon 44, 45, 51 and 53, respectively. The difference in PUL 2.0 mean changes among the type of exon skip class for the total score was not significant at 12 months but was significant at 24 months for the total score (p < 0.001), the shoulder (p = 0.01) and the elbow domain (p < 0.001), with patients amenable to skipping exon 44 having smaller changes compared to those amenable to skipping exon 53. There was no difference within ambulant or non-ambulant cohorts when subdivided by exon skip class for the total and subdomains score (p > 0.05). Conclusions: Our results expand the information on upper limb function changes detected by the PUL 2.0 in a relatively large group of DMD patients with distinct exon-skipping classes. This information can be of help when designing clinical trials or in the interpretation of the real world data including non-ambulant patients.

Funder

Italian Ministry of Health

Publisher

MDPI AG

Subject

Pediatrics, Perinatology and Child Health

Cited by 1 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3