Pediatric Neurology and Nemo Clinical Centre, Fondazione Policlinico Universitario "A. Gemelli IRCSS", Università Cattolica del Sacro Cuore, Rome, Italy.
John Walton Muscular Dystrophy Research Centre, Institute of Genetic Medicine, International Centre for Life, Newcastle Upon Tyne, United Kingdom.
PLoS One. 2018 Jun 20;13(6):e0199223. doi: 10.1371/journal.pone.0199223. eCollection 2018.
The aim of the study was to establish 24 month changes in upper limb function using a revised version of the performance of upper limb test (PUL 2.0) in a large cohort of ambulant and non-ambulant boys with Duchenne muscular dystrophy and to identify possible trajectories of progression. Of the 187 patients studied, 87 were ambulant (age range: 7-15.8 years), and 90 non-ambulant (age range: 9.08-24.78). The total scores changed significantly over time (p<0.001). Non-ambulant patients had lower total scores at baseline (mean 19.7) when compared to the ambulant ones (mean 38.4). They also had also a bigger decrease in total scores over 24 months compared to the ambulant boys (4.36 vs 2.07 points). Multivariate model analysis showed that the Performance of Upper Limb changes reflected the entry level and ambulation status, that were independently associated to the slope of Performance of Upper Limb changes. This information will be of help both in clinical practice and at the time of designing clinical trials.
研究目的是利用上肢功能测试(PUL 2.0)的修订版,在一个患有杜氏肌营养不良的大型可走动和不可走动男孩队列中,确定 24 个月上肢功能的变化,并确定可能的进展轨迹。在研究的 187 名患者中,87 名可走动(年龄范围:7-15.8 岁),90 名不可走动(年龄范围:9.08-24.78)。总分随时间显著变化(p<0.001)。与可走动的患者相比,不可走动的患者基线时总分数较低(平均 19.7)。与可走动的男孩相比,他们在 24 个月内总分数的下降也更大(4.36 分比 2.07 分)。多变量模型分析表明,上肢功能的表现变化反映了进入水平和可走动状态,这与上肢功能变化的斜率独立相关。这些信息将在临床实践和临床试验设计时都有帮助。