4.7 Article

Genetic modifiers of upper limb function in Duchenne muscular dystrophy

Journal

JOURNAL OF NEUROLOGY
Volume 269, Issue 9, Pages 4884-4894

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00415-022-11133-8

Keywords

Duchenne muscular dystrophy; Genetic modifiers; Upper limb function; SPP1-osteopontin; CD40

Funding

  1. Fondazione Telethon [GUP1002]
  2. Cariparo Foundation (Progetto di Eccellenza GenMod)
  3. Telethon Genetic BioBank [GTB12001D]
  4. U.S. Department of Education/NIDRR [H133B031118, H133B090001]
  5. U.S. Department of Defense [W81XWH-12-1-0417]
  6. National Institutes of Health/NIAMS [R01AR061875]
  7. Parent Project Muscular Dystrophy
  8. Eurobiobank Network

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This study investigates the impact of modifiers on upper limb function in patients with DMD. The CD40 gene variant rs1883832 is found to be associated with upper limb functionality. These findings are important for the design and interpretation of clinical trials in DMD, especially for non-ambulatory patients.
Genetic modifiers of Duchenne muscular dystrophy (DMD) are variants located in genes different from the disease-causing gene DMD, but associated with differences in disease onset, progression, or response to treatment. Modifiers described so far have been tested mainly for associations with ambulatory function, while their effect on upper limb function, which is especially relevant for quality of life and independence in non-ambulatory patients, is unknown. We tested genotypes at several known modifier loci (SPP1, LTBP4, CD40, ACTN3) for association with Performance Upper Limb version 1.2 score in an Italian multicenter cohort, and with Brooke scale score in the Cooperative International Neuromuscular Group Duchenne Natural History Study (CINRG-DNHS), using generalized estimating equation (GEE) models of longitudinally collected data, with age and glucocorticoid treatment as covariates. CD40 rs1883832, previously linked to earlier loss of ambulation, emerged as a modifier of upper limb function, negatively affecting shoulder and distal domains of PUL (p = 0.023 and 0.018, respectively) in the Italian cohort, as well as of Brooke score (p = 0.018) in the CINRG-DNHS. These findings will be useful for the design and interpretation of clinical trials in DMD, especially for non-ambulatory populations.

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