A comprehensive screening of copy number variability in dementia with Lewy bodies

Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

Abstract

The role of genetic variability in dementia with Lewy bodies (DLB) is now indisputable; however, data regarding copy number variation (CNV) in this disease has been lacking. Here, we used whole-genome genotyping of 1454 DLB cases and 1525 controls to assess copy number variability. We used 2 algorithms to confidently detect CNVs, performed a case-control association analysis, screened for candidate CNVs previously associated with DLB-related diseases, and performed a candidate gene approach to fully explore the data. We identified 5 CNV regions with a significant genome-wide association to DLB; 2 of these were only present in cases and absent from publicly available databases: one of the regions overlapped LAPTM4B, a known lysosomal protein, whereas the other overlapped the NME1 locus and SPAG9. We also identified DLB cases presenting rare CNVs in genes previously associated with DLB or related neurodegenerative diseases, such as SNCA, APP, and MAPT. To our knowledge, this is the first study reporting genome-wide CNVs in a large DLB cohort. These results provide preliminary evidence for the contribution of CNVs in DLB risk. © 2018

Detaljer

Författare
Enheter & grupper
Externa organisationer
  • University College London
  • University of Aveiro
Forskningsområden

Ämnesklassifikation (UKÄ) – OBLIGATORISK

  • Medicinsk genetik
  • Neurovetenskaper

Nyckelord

Originalspråkengelska
Sidor (från-till)223.e1-223.e10
TidskriftNeurobiology of Aging
Volym75
Tidigt onlinedatum2018 okt 24
StatusPublished - 2019
PublikationskategoriForskning
Peer review utfördJa