The impact of genotype on age at loss of ambulation in individuals with Duchenne muscular dystrophy treated with corticosteroids: A single‐center study of 555 patients

德菲扎科特 医学 杜氏肌营养不良 队列 强的松 回顾性队列研究 回廊的 发病年龄 基因型 儿科 队列研究 肌营养不良 内科学 物理疗法 疾病 遗传学 生物 基因
作者
A. Zygmunt,Brenda Wong,David Moon,Paul S. Horn,RICHARD M. RATHBUN,Joshua T. Lambert,J. Bange,I. Rybalsky,Lisa Reebals,Cuixia Tian
出处
期刊:Muscle & Nerve [Wiley]
标识
DOI:10.1002/mus.28255
摘要

Abstract Introduction/Aims Studies have demonstrated that certain genotypes in Duchenne muscular dystrophy (DMD) have milder or more severe phenotypes. These studies included individuals treated and not treated with corticosteroids and multiple sites with potentially varying standards of care. We aimed to assess genotype–phenotype correlations for age at loss of ambulation (LoA) in a large cohort of individuals with DMD treated with corticosteroids at one center. Methods In this retrospective review of medical records, encounters were included for individuals diagnosed with DMD if prescribed corticosteroids, defined as daily deflazacort or prednisone or high‐dose weekend prednisone, for 12 consecutive months. Encounters were excluded if the participants were taking disease‐modifying therapy. Data were analyzed using survival analysis for LoA and Fisher's exact tests to assess the percentage of late ambulatory (>14 years old) individuals for selected genotypes. Results Overall, 3948 encounters from 555 individuals were included. Survival analysis showed later age at LoA for exon 44 skip amenable ( p = .004), deletion exons 3–7 ( p < .001) and duplication exon 2 ( p = .043) cohorts and earlier age at LoA for the exon 51 skip amenable cohort ( p < .001) when compared with the rest of the cohort. Individuals with deletions of exons 3–7 had significantly more late ambulatory individuals than other cohorts (75%), while those with exon 51 skip amenable deletions had significantly fewer (11.9%) compared with other cohorts. Discussion This confirms previous observations of genotype–phenotype correlations in DMD and enhances information for trial design and clinical management.
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