| Literature DB >> 30196823 |
Stefan Blum1, Ying Ji2, David Pennisi3, Zhixiu Li3, Paul Leo3, Pamela McCombe1, Matthew A Brown4.
Abstract
Guillain-Barré syndrome (GBS) is considered to have an immune-mediated basis, but the genetic contribution to GBS is unclear. We conducted a GWAS involving 215 GBS patients and 1,105 healthy controls. No significant associations of individual SNPs or imputed HLA types were observed. We performed a genome-wide complex trait analysis for evaluation of the heritability of GBS, and found that common SNPs contribute up to 25% of susceptibility to the disease. Genetic risk score analysis showed no evidence of overlap in genetic susceptibility factors of GBS and multiple sclerosis. Given the unexplained heritability of the trait further larger GWAS are indicated.Entities:
Keywords: Case-control study; Genetic risk score; Genome-wide association study; Guillain-Barré syndrome; Heritability; Human leukocyte antigen (HLA) genes
Mesh:
Year: 2018 PMID: 30196823 DOI: 10.1016/j.jneuroim.2018.07.016
Source DB: PubMed Journal: J Neuroimmunol ISSN: 0165-5728 Impact factor: 3.478