Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study
| Autor: | Balendra, Rubika, Uphill, James, Collinson, Claire, Druyeh, Ronald, Adamson, Gary, Hummerich, Holger, Zerr, Inga, Gambetti, Pierluigi, Collinge, John, Mead, Simon |
|---|---|
| Jazyk: | angličtina |
| Rok vydání: | 2016 |
| Předmět: |
PLCXD3
Genotyping Techniques Prions animal diseases PRNP protein human diagnosis [Creutzfeldt-Jakob Syndrome] phosphatidylinositol specific phospholipase C human Polymorphism Single Nucleotide Creutzfeldt-Jakob Syndrome Linkage Disequilibrium Prion Proteins Phosphoinositide Phospholipase C Risk Factors Germany mental disorders Genetics Humans Genetics(clinical) ddc:610 genetics [Phosphoinositide Phospholipase C] genetics [Prions] genetics [Creutzfeldt-Jakob Syndrome] Exons Creutzfeldt-Jakob disease United States nervous system diseases Genetic Loci metabolism [Prions] Human prion diseases Research Article Genome-Wide Association Study |
| Zdroj: | BMC medical genetics 17(1), 28 (2016). doi:10.1186/s12881-016-0278-2 BMC Medical Genetics |
| DOI: | 10.1186/s12881-016-0278-2 |
| Popis: | Background Human prion diseases are relentlessly progressive neurodegenerative disorders which include sporadic Creutzfeldt-Jakob disease (sCJD) and variant CJD (vCJD). Aside from variants of the prion protein gene (PRNP) replicated association at genome-wide levels of significance has proven elusive. A recent association study identified variants in or near to the PLCXD3 gene locus as strong disease risk factors in multiple human prion diseases. This study claimed the first non-PRNP locus to be highly significantly associated with prion disease in genomic studies. Methods A sub-study of a genome-wide association study with imputation aiming to replicate the finding at PLCXD3 including 129 vCJD and 2500 sCJD samples. Whole exome sequencing to identify rare coding variants of PLCXD3. Results Imputation of relevant polymorphisms was accurate based on wet genotyping of a sample. We found no supportive evidence that PLCXD3 variants are associated with disease. Conclusion The marked discordance in vCJD genotype frequencies between studies, despite extensive overlap in vCJD cases, and the finding of Hardy-Weinberg disequilibrium in the original study, suggests possible reasons for the discrepancies between studies. peerReviewed |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|