Congenital muscular dystrophies with defective glycosylation of dystroglycan: a population study

Neurology. 2009 May 26;72(21):1802-9. doi: 10.1212/01.wnl.0000346518.68110.60. Epub 2009 Mar 18.

Abstract

Background: Congenital muscular dystrophies (CMD) with reduced glycosylation of alpha-dystroglycan (alpha-DG) are a heterogeneous group of conditions associated with mutations in six genes encoding proven or putative glycosyltransferases.

Objectives: The aim of the study was to establish the prevalence of mutations in the six genes in the Italian population and the spectrum of clinical and brain MRI findings.

Methods: As part of a multicentric study involving all the tertiary neuromuscular centers in Italy, FKRP, POMT1, POMT2, POMGnT1, fukutin, and LARGE were screened in 81 patients with CMD and alpha-DG reduction on muscle biopsy (n = 76) or with a phenotype suggestive of alpha-dystroglycanopathy but in whom a muscle biopsy was not available for alpha-DG immunostaining (n = 5).

Results: Homozygous and compound heterozygous mutations were detected in a total of 43/81 patients (53%), and included seven novel variants. Mutations in POMT1 were the most prevalent in our cohort (21%), followed by POMT2 (11%), POMGnT1 (10%), and FKRP (9%). One patient carried two heterozygous mutations in fukutin and one case harbored a new homozygous variant in LARGE. No clear-cut genotype-phenotype correlation could be observed with each gene, resulting in a wide spectrum of clinical phenotypes. The more severe phenotypes, however, appeared to be consistently associated with mutations predicted to result in a severe disruption of the respective genes.

Conclusions: Our data broaden the clinical spectrum associated with mutations in glycosyltransferases and provide data on their prevalence in the Italian population.

Publication types

  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Brain / pathology
  • Child
  • Child, Preschool
  • Cohort Studies
  • Dystroglycans / analysis
  • Dystroglycans / metabolism*
  • Female
  • Glycosylation
  • Glycosyltransferases / genetics*
  • Humans
  • Infant
  • Italy
  • Magnetic Resonance Imaging
  • Mannosyltransferases / genetics
  • Membrane Proteins / genetics
  • Muscle, Skeletal / chemistry
  • Muscle, Skeletal / pathology
  • Muscular Dystrophies / congenital*
  • Muscular Dystrophies / genetics*
  • Muscular Dystrophies / metabolism
  • Muscular Dystrophies / pathology
  • Mutation
  • N-Acetylglucosaminyltransferases / genetics
  • Pentosyltransferases
  • Phenotype
  • Prevalence
  • Proteins / genetics

Substances

  • DAG1 protein, human
  • FKTN protein, human
  • Membrane Proteins
  • Proteins
  • Dystroglycans
  • Glycosyltransferases
  • LARGE1 protein, human
  • Mannosyltransferases
  • N-Acetylglucosaminyltransferases
  • protein O-mannose beta-1,2-N-acetylglucosaminyltransferase
  • protein O-mannosyltransferase
  • FKRP protein, human
  • Pentosyltransferases