Duchenne muscular dystrophy respiratory profiles from real world registry data
Mona Hnaini, Matt Downs, Michael R. Miller, Craig Campbell, Aaron St‐Laurent- Pulmonary and Respiratory Medicine
- Pediatrics, Perinatology and Child Health
Abstract
Introduction
Understanding real‐world profiles from neuromuscular databases is helpful for optimizing clinical care and planning research studies. The Canadian Neuromuscular Disease Registry (CNDR) has respiratory data from a population of boys with Duchenne Muscular Dystrophy (DMD).
Objectives
To describe cross‐sectional respiratory profiles from a national DMD real‐world dataset. To explore the relationship between forced vital capacity percent predicted (FVC%) and disease severity parameters: scoliosis, ambulation and ventilation status.
Methods
Descriptive statistics summarized the respiratory profiles. The CNDR registry enrolls and collects DMD clinic data from 36 Canadian centers.
Results
There were 414 participants enrolled. The age ranged from 2 to 36 years old. Pulmonary function test data were available for 323 participants. The use of ventilatory support was seen in a significant proportion (19.5%) of subjects by age 14–16 years and was used by the majority (69.2%) by age 20–22 years. FVC% declined at a rate of 3.19% per year with every 1‐year increase in age. FVC% declined annually by 2.47% in nonambulatory participants versus by 0.96% in ambulatory participants. FVC% did not significantly change over age with the presence of scoliosis or use of ventilatory technology.
Conclusions
The data from this large cohort are valuable for understanding real‐world patterns of clinical care and disease progression. There is a significant association between the loss of ambulation and the rate of FVC% decline. Further longitudinal studies are needed to better understand the impact of disease parameters on pulmonary function decline and the need for ventilatory support.