Popperud T H, Viken M K, Kerty E, Lie B A
Department of Neurology, Oslo University Hospital, Oslo, Norway.
Institute of Clinical Medicine, University of Oslo, Oslo, Norway.
PLoS One. 2017 Oct 16;12(10):e0186383. doi: 10.1371/journal.pone.0186383. eCollection 2017.
Juvenile myasthenia gravis (MG) is a rare autoantibody mediated autoimmune disorder targeting the neuromuscular endplate. The clinical hallmark is muscle weakness and fatigability. Disease aetiology is complex, including both genetic and environmental factors. The involvement of genes in the human leukocyte antigen (HLA) is well established in adult MG. However, HLA associations in European juvenile MG have not been studied. This case-control study aimed to investigate and characterize genetic risk factors in prepubertal and postpubertal onset juvenile MG.
METHODOLOGY/PRINCIPAL FINDINGS: A population based Norwegian cohort of 43 juvenile MG patients (17 with prepubertal onset, 26 with postpubertal onset) and 368 controls were included. Next generation sequencing of five HLA loci (HLA-A, -B, -C, -DRB1 and -DQB1) was performed, and a positive association was seen with HLA-B08 (OR (95% CI) = 3.27 (2.00-5.36), Pc = 0.00003) and HLA-DRB104:04 (OR (95% CI) = 2.65 (1.57-4.24), Pc = 0.03). Stratified in postpubertal and prepubertal onset, HLA-DRB104:04 was only positively associated with the latter (P = 0.01). The HLA-B08 allele (12.9% in the controls), previously described associated with early onset adult MG, was most frequently observed in postpubertal onset MG (40.4%, P = 0.0002) but also increased among prepubertal onset MG (23.5%, P = 0.05).
This study provides novel information about HLA susceptibility alleles in Norwegian juvenile MG where HLA-DRB1*04:04 was associated with prepubertal onset.
青少年型重症肌无力(MG)是一种罕见的自身抗体介导的自身免疫性疾病,其靶点为神经肌肉终板。临床特征为肌肉无力和易疲劳。疾病病因复杂,包括遗传和环境因素。基因在成人MG中与人类白细胞抗原(HLA)的关联已得到充分证实。然而,欧洲青少年MG中的HLA关联尚未得到研究。本病例对照研究旨在调查和表征青春期前和青春期后发病的青少年MG中的遗传危险因素。
方法/主要发现:纳入了一个基于挪威人群的队列,其中包括43例青少年MG患者(17例青春期前发病,26例青春期后发病)和368例对照。对五个HLA位点(HLA-A、-B、-C、-DRB1和-DQB1)进行了下一代测序,发现与HLA-B08呈正相关(比值比(95%可信区间)=3.27(2.00-5.36),Pc=0.00003)以及与HLA-DRB104:04呈正相关(比值比(95%可信区间)=2.65(1.57-4.24),Pc=0.03)。按青春期后和青春期前发病分层,HLA-DRB104:04仅与青春期前发病呈正相关(P=0.01)。HLA-B08等位基因(在对照中为12.9%),先前描述与成人MG早发相关,在青春期后发病的MG中最常观察到(40.4%,P=0.0002),但在青春期前发病的MG中也有所增加(23.5%,P=0.05)。
本研究提供了关于挪威青少年MG中HLA易感等位基因的新信息,其中HLA-DRB1*04:04与青春期前发病相关。