Department of Clinical Sciences, Malmö, Lund University, Malmo, Sweden.
Department of Clinical Neuroscience, Institute of Neuroscience and Physiology, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Int J Immunogenet. 2024 Oct;51(5):310-318. doi: 10.1111/iji.12688. Epub 2024 Jun 19.
Narcolepsy is a sleep disorder caused by an apparent degeneration of orexin/hypocretin neurons in the lateral hypothalamic area and a subsequent decrease in orexin/hypocretin levels in the cerebrospinal fluid. Narcolepsy is classified into type 1 (NT1) and type 2 (NT2). While genetic associations in the human leukocyte antigen (HLA) region and candidate autoantibodies have been investigated in NT1 to imply an autoimmune origin, less is known about the pathogenesis in NT2. Twenty-six NT1 and 15 NT2 patients were included, together with control groups of 24 idiopathic hypersomnia (IH) patients and 778 general population participants. High-resolution sequencing was used to determine the alleles, the extended haplotypes, and the genotypes of HLA-DRB3, -DRB4, -DRB5, -DRB1, -DQA1, -DQB1, -DPA1, and -DPB1. Radiobinding assay was used to determine autoantibodies against hypocretin receptor 2 (anti-HCRTR2 autoantibodies). NT1 was associated with HLA-DRB501:01:01, -DRB115:01:01, -DQA101:02:01, -DQB106:02:01, -DRB501:01:01, -DRB115:01:01, -DQA101:02:01, -DQB106:02:01 (odds ratio [OR]: 9.15; p = 8.31 × 10) and HLA-DRB501:01:01, -DRB115:01:01, -DQA101:02:01, -DQB106:02:01, -DRB401:03:01, -DRB104:01:01, -DQA103:02//03:03:01, -DQB103:01:01 (OR: 23.61; p = 1.58 × 10) genotypes. Lower orexin/hypocretin levels were reported in the NT2 subgroup (n = 5) that was associated with the extended HLA-DQB106:02:01 haplotype (p = .001). Anti-HCRTR2 autoantibody levels were not different between study groups (p = .8524). We confirmed the previous association of NT1 with HLA-DQB106:02:01 extended genotypes. A subgroup of NT2 patients with intermediate orexin/hypocretin levels and association with HLA-DQB1*06:02:01 was identified, indicating a possible overlap between the two distinct narcolepsy subtypes, NT1 and NT2. Low anti-HCRTR2 autoantibody levels suggest that these receptors might not function as autoimmune targets in either NT1 or NT2.
发作性睡病是一种由外侧下丘脑区域的食欲素/下丘脑分泌素神经元明显退化和随后脑脊液中食欲素/下丘脑分泌素水平下降引起的睡眠障碍。发作性睡病分为 1 型(NT1)和 2 型(NT2)。虽然在 NT1 中已经研究了人类白细胞抗原(HLA)区域的遗传关联和候选自身抗体,以暗示自身免疫起源,但对 NT2 的发病机制知之甚少。纳入了 26 名 NT1 患者和 15 名 NT2 患者,以及 24 名特发性嗜睡症(IH)患者和 778 名普通人群参与者的对照组。使用高分辨率测序来确定 HLA-DRB3、-DRB4、-DRB5、-DRB1、-DQA1、-DQB1、-DPA1 和-DPB1 的等位基因、扩展单倍型和基因型。放射配体测定法用于测定下丘脑分泌素受体 2(抗 HCRTR2 自身抗体)的自身抗体。NT1 与 HLA-DRB501:01:01、-DRB115:01:01、-DQA101:02:01、-DQB106:02:01、-DRB501:01:01、-DRB115:01:01、-DQA101:02:01、-DQB106:02:01(比值比 [OR]:9.15;p = 8.31×10)和 HLA-DRB501:01:01、-DRB115:01:01、-DQA101:02:01、-DQB106:02:01、-DRB401:03:01、-DRB104:01:01、-DQA103:02//03:03:01、-DQB103:01:01(OR:23.61;p = 1.58×10)基因型有关。在与扩展 HLA-DQB106:02:01 单倍型相关的 NT2 亚组(n = 5)中报告了较低的食欲素/下丘脑分泌素水平(p =.001)。研究组之间的抗 HCRTR2 自身抗体水平无差异(p =.8524)。我们证实了之前 NT1 与 HLA-DQB106:02:01 扩展基因型的关联。确定了一个具有中间食欲素/下丘脑分泌素水平的 NT2 患者亚组,与 HLA-DQB1*06:02:01 相关,表明两种不同的发作性睡病亚型 NT1 和 NT2 之间可能存在重叠。低抗 HCRTR2 自身抗体水平表明这些受体在 NT1 或 NT2 中可能不作为自身免疫靶标。