Cathepsin D (C224T) polymorphism in sporadic and genetic creutzfeldt-jakob disease

Gabor G. Kovacs, Pascual Sanchez-Juan, Thomas Ströbel, Maaike Schuur, Anna Poleggi, Sara Nocentini, Claudia Giannattasio, Girma Belay, Matthew Bishop, Sabina Capellari, Piero Parchi, Ellen Gelpi, Aniko Gal, Agnes Bakos, Maria J. Molnar, Uta Heinemann, Inga Zerr, Richard S G Knight, Eva Mitrova, Cornelia Van DuijnHerbert Budka

Research output: Contribution to journalArticle

Abstract

Accumulation of cathepsin D immunoreactive lysosomes correlates with tissue pathology in sporadic Creutzfeldt-Jakob disease (CJD) brains. The C-to-T transition within exon 2 of the cathepsin D (CTSD) gene is associated with altered enzymatic activity. Possession of the TT genotype is a risk factor for variant CJD. To verify the association between the CTSD position 224T allele and the risk for and survival in sporadic and genetic CJD, we genotyped 540 sporadic, 101 genetic CJD, and 723 control individuals. Genotype data and duration of illness were compared using multiple logistic regression and Kruskal-Wallis test. Multivariate survival analysis was performed using Cox's regression model. The distribution of CTSD position 224 alleles was approximately the same in all groups. We observed a trend for shorter survival in sporadic CJD patients harboring the T allele at position 224 of the CTSD gene in particular in sporadic CJD patients with the prion protein gene position 129 MM genotype. We conclude that the CTSD position 224 polymorphism alone is not a significant risk or disease-modifying factor in sporadic or genetic CJD.

Original languageEnglish
Pages (from-to)104-107
Number of pages4
JournalAlzheimer Disease and Associated Disorders
Volume24
Issue number1
DOIs
Publication statusPublished - Jan 2010

Keywords

  • Apolipoprotein E
  • Cathepsin D
  • Creutzfeldt-Jakob disease
  • Polymorphism
  • Prion protein gene

ASJC Scopus subject areas

  • Geriatrics and Gerontology
  • Psychiatry and Mental health
  • Gerontology
  • Clinical Psychology

Fingerprint Dive into the research topics of 'Cathepsin D (C224T) polymorphism in sporadic and genetic creutzfeldt-jakob disease'. Together they form a unique fingerprint.

  • Cite this

    Kovacs, G. G., Sanchez-Juan, P., Ströbel, T., Schuur, M., Poleggi, A., Nocentini, S., Giannattasio, C., Belay, G., Bishop, M., Capellari, S., Parchi, P., Gelpi, E., Gal, A., Bakos, A., Molnar, M. J., Heinemann, U., Zerr, I., Knight, R. S. G., Mitrova, E., ... Budka, H. (2010). Cathepsin D (C224T) polymorphism in sporadic and genetic creutzfeldt-jakob disease. Alzheimer Disease and Associated Disorders, 24(1), 104-107. https://doi.org/10.1097/WAD.0b013e3181ad378c