Genetic predisposition in anti-LGI1 and anti-NMDA receptor encephalitis

  • Stefanie H Mueller
  • Anna Färber
  • Harald Prüss
  • Nico Melzer
  • Kristin S Golombeck
  • Tania Kümpfel
  • Franziska Thaler
  • Martin Elisak
  • Jan Lewerenz
  • Max Kaufmann
  • Kurt-Wolfram Sühs
  • Marius Ringelstein
  • Christoph Kellinghaus
  • Christian G Bien
  • Andrea Kraft
  • Uwe K Zettl
  • Sven Ehrlich
  • Robert Handreka
  • Kevin Rostásy
  • Florian Then Bergh
  • Jürgen H Faiss
  • Wolfgang Lieb
  • Andre Franke
  • Gregor Kuhlenbäumer
  • Klaus-Peter Wandinger
  • Frank Leypoldt
  • German Network for Research on Autoimmune Encephalitis (GENERATE)

Abstract

We performed a genome-wide association study in 1,194 controls and 150 patients with anti-N-methyl-D-aspartate receptor (anti-NMDAR, n = 96) or anti-leucine-rich glioma-inactivated1 (anti-LGI1, n = 54) autoimmune encephalitis. Anti-LGI1 encephalitis was highly associated with 27 single-nucleotide polymorphisms (SNPs) in the HLA-II region (leading SNP rs2858870 p = 1.22 × 10-17 , OR = 13.66 [7.50-24.87]). Potential associations, below genome-wide significance, were found with rs72961463 close to the doublecortin-like kinase 2 gene (DCLK2) and rs62110161 in a cluster of zinc-finger genes. HLA allele imputation identified association of anti-LGI1 encephalitis with HLA-II haplotypes encompassing DRB1*07:01, DQA1*02:01 and DQB1*02:02 (p < 2.2 × 10-16 ) and anti-NMDAR encephalitis with HLA-I allele B*07:02 (p = 0.039). No shared genetic risk factors between encephalitides were identified. Ann Neurol 2018;83:863-869.

Bibliographical data

Original languageEnglish
ISSN0364-5134
DOIs
Publication statusPublished - 04.2018
PubMed 29572931