Creutzfeldt-Jakob disease (CJD) with a mutation at codon 148 of prion protein gene: Relationship with sporadic CJD

Academic Article

Abstract

  • Creutzfeldt-Jakob disease (CJD), the most common human prion disease, includes sporadic (s) and familial (f) forms. Regardless of etiology, both forms are thought to share the pathogenic mechanism whereby the cellular prion protein (PrPC) converts into its pathogenic isoform (PrP Sc). While PrPC conversion is thought to be random in sCJD, conversion in fCJD is facilitated by the congenital presence of mutated PrP. Differences in PrP genotype (PRNP) and in conversion circumstances lead to PrPSc with distinct characteristics that elicit different disease phenotypes. Here, we describe a case of fCJD with a substitution of histidine (H) for arginine (R) at codon 148 (R148H) and heterozygosity of the methionine/valine (M/V) polymorphic codon 129, with the 129M allele coupled with the mutation. The disease phenotype and all major characteristics of PrP Sc of fCJDR148H were virtually indistinguishable from those of SCJDMV2, which has features different from those of any other sCJD. Therefore, despite the differences in etiology, PRNP, and conversion process, the two forms of PrPSc had similar characteristics. Furthermore, comparison of fCJDR148H with a recently reported case carrying R148H and homozygosity at codon 129 suggests that codon 129 coupled with the mutation as well as that located on the normal allele can modify major phenotypic and PrPSc features of fCJDR148H. Copyright © American Society for Investigative Pathology.
  • Authors

    Published In

    Digital Object Identifier (doi)

    Pubmed Id

  • 26361245
  • Author List

  • Pastore M; Chin SS; Bell KL; Dong Z; Yang Q; Yang L; Yuan J; Chen SG; Gambetti P; Zou WQ
  • Start Page

  • 1729
  • End Page

  • 1738
  • Volume

  • 167
  • Issue

  • 6