Functional abilities, respiratory and cardiac function in a large cohort of adults with Duchenne muscular dystrophy treated with glucocorticoids

Author:

Schiava Marianela1ORCID,Lofra Robert Muni1,Bourke John P.1,Díaz‐Manera Jordi1ORCID,James Meredith K.1,Elseed Maha A.1,Malinova Monika1,Michel‐Sodhi Jassi1,Moat Dionne1,Ghimenton Elisabetta1,Mccallum Michelle1,Díaz Carla Florencia Bolaño1,Mayhew Anna1,Wong Karen1,Richardson Mark1,Tasca Giorgio1,Eglon Gail1,Eagle Michelle2,Turner Cathy1ORCID,Heslop Emma1,Straub Volker1,Bettolo Chiara Marini1,Guglieri Michela1ORCID

Affiliation:

1. John Walton Muscular Dystrophy Research Centre Newcastle University and Newcastle Hospitals NHS Foundation Trusts Newcastle Upon Tyne UK

2. ATOM International Limited Gateshead UK

Abstract

AbstractBackground and purposeThe transition to adult services, and subsequent glucocorticoid management, is critical in adults with Duchenne muscular dystrophy. This study aims (1) to describe treatment, functional abilities, respiratory and cardiac status during transition to adulthood and adult stages; and (2) to explore the association between glucocorticoid treatment after loss of ambulation (LOA) and late‐stage clinical outcomes.MethodsThis was a retrospective single‐centre study on individuals with Duchenne muscular dystrophy (≥16 years old) between 1986 and 2022. Logistic regression, Cox proportional hazards models and survival analyses were conducted utilizing data from clinical records.ResultsIn all, 112 individuals were included. Mean age was 23.4 ± 5.2 years and mean follow‐up was 18.5 ± 5.5 years. At last assessment, 47.2% were on glucocorticoids; the mean dose of prednisone was 0.38 ± 0.13 mg/kg/day and of deflazacort 0.43 ± 0.16 mg/kg/day. At age 16 years, motor function limitations included using a manual wheelchair (89.7%), standing (87.9%), transferring from a wheelchair (86.2%) and turning in bed (53.4%); 77.5% had a peak cough flow <270 L/min, 53.3% a forced vital capacity percentage of predicted <50% and 40.3% a left ventricular ejection fraction <50%. Glucocorticoids after LOA reduced the risk and delayed the time to difficulties balancing in the wheelchair, loss of hand to mouth function, forced vital capacity percentage of predicted <30% and forced vital capacity <1 L and were associated with lower frequency of left ventricular ejection fraction <50%, without differences between prednisone and deflazacort. Glucocorticoid dose did not differ by functional, respiratory or cardiac status.ConclusionGlucocorticoids after LOA preserve late‐stage functional abilities, respiratory and cardiac function. It is suggested using functional abilities, respiratory and cardiac status at transition stages for adult services planning.

Publisher

Wiley

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