Genetic analysis implicates APOE, SNCA and suggests lysosomal dysfunction in the etiology of Dementia with Lewy Bodies.

Forskningsoutput: TidskriftsbidragArtikel i vetenskaplig tidskrift

Abstract

Clinical and neuropathological similarities between Dementia with Lewy Bodies (DLB), ParkinsonÕs and AlzheimerÕs diseases (PD and AD, respectively) suggest that these disorders may share etiology. To test this hypothesis we have performed an association study of 54 genomic regions, previously implicated in PD or AD, in a large cohort of DLB cases and controls. The cohort comprised 788 DLB cases and 2624 controls. To minimize the issue of potential misdiagnosis, we have also performed the analysis including only neuropathologically proven DLB cases (667 cases). Results show that the APOE is a strong genetic risk factor for DLB, confirming previous findings, and that the SNCA and SCARB2 loci are also associated after study-wise Bonferroni correction, although these have a different association profile than the associations reported for the same loci in PD. We have previously shown that the p.N370S variant in GBA is associated with DLB, which, together with the findings at the SCARB2 locus, suggests a role for lysosomal dysfunction in this disease. These results indicate that DLB has a unique genetic risk profile when compared to the two most common neurodegenerative diseases and that the lysosome may play an important role in the etiology of this disorder. We make all these data available.

Detaljer

Författare
  • Jose Bras
  • Rita Guerreiro
  • Lee Darwent
  • Laura Parkkinen
  • Olaf Ansorge
  • Valentina Escott-Price
  • Dena G Hernandez
  • Michael A Nalls
  • Lorraine Clark
  • Lawrence Honig
  • Karen Marder
  • Wiesje van der Flier
  • Afina Lemstra
  • Philip Scheltens
  • Ekaterina Rogaeva
  • Peter St George-Hyslop
  • Henrik Zetterberg
  • Sara Ortega-Cubero
  • Pau Pastor
  • Tanis J Ferman
  • Neill R Graff-Radford
  • Owen A Ross
  • Imelda Barber
  • Anne Braae
  • Kristelle Brown
  • Kevin Morgan
  • Walter Maetzler
  • Daniela Berg
  • Claire Troakes
  • Safa Al-Sarraj
  • Tammaryn Lashley
  • Yarko Compta
  • Tamas Revesz
  • Andrew Lees
  • Nigel Cairns
  • Glenda M Halliday
  • David Mann
  • Stuart Pickering-Brown
  • Dennis Dickson
  • Andrew Singleton
  • John Hardy
Enheter & grupper
Forskningsområden

Ämnesklassifikation (UKÄ) – OBLIGATORISK

  • Medicinsk genetik
Originalspråkengelska
Sidor (från-till)6139-6146
TidskriftHuman Molecular Genetics
Volym23
Utgivningsnummer23
StatusPublished - 2014
PublikationskategoriForskning
Peer review utfördJa

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