Institute of Neuroscience and Physiology, The Sahlgrenska Academy,University of Gothenburg,Gothenburg,Sweden.
Centre for Ethics, Law and Mental Health (CELAM),University of Gothenburg,Gothenburg,Sweden.
Acta Neuropsychiatr. 2019 Aug;31(4):220-229. doi: 10.1017/neu.2019.18. Epub 2019 Jun 4.
The immune system has been suggested to be associated with neuropsychiatric disorders; for example, elevated levels of cytokines and the inflammation-related transcription factor nuclear factor kappa-B (NF-κB) have been reported in individuals with autism spectrum disorder (ASD). The aim of this study was to investigate possible associations between autistic-like traits (ALTs) and single nucleotide polymorphisms (SNPs) in NFKB1 (encoding a subunit of the NF-κB protein complex) and NF-κB inhibitor-like protein 1 (NFKBIL1).
The study was conducted in a cohort from the general population: The Child and Adolescent Twin Study in Sweden (CATSS, n = 12 319, 9-12 years old). The subjects were assessed by the Autism-Tics, ADHD, and Other Comorbidities Inventory. Five SNPs within the two genes were genotyped (NFKBIL1: rs2857605, rs2239707, rs2230365 and rs2071592; NFKB1: rs4648022).
We found significant associations for two SNPs in NFKBIL1: rs2239707 showed a significant distribution of genotype frequencies in the case-control analysis both for all individuals combined and in boys only, and rs2230365 was significantly associated with the ALTs-module language impairment in boys only. Furthermore, we found nominal association in the case-control study for rs2230365, replicating earlier association between this SNP and ASD in an independent genome-wide association study.
The shown associations between polymorphisms in NFKBIL1 and ALTs are supporting an influence of the immune system on neuropsychiatric symptoms.
免疫系统与神经精神疾病有关;例如,自闭症谱系障碍(ASD)患者的细胞因子和与炎症相关的转录因子核因子 kappa-B(NF-κB)水平升高。本研究旨在探讨 NFKB1(编码 NF-κB 蛋白复合物亚基)和 NF-κB 抑制剂样蛋白 1(NFKBIL1)中的单核苷酸多态性(SNP)与类似自闭症特征(ALT)之间的可能关联。
该研究在瑞典儿童和青少年双胞胎研究(CATSS)的一般人群队列中进行(n = 12319,9-12 岁)。通过自闭症-抽搐-注意缺陷多动障碍及其他共病量表对受试者进行评估。对两个基因中的五个 SNP 进行基因分型(NFKBIL1:rs2857605、rs2239707、rs2230365 和 rs2071592;NFKB1:rs4648022)。
我们发现 NFKBIL1 中的两个 SNP 存在显著关联:rs2239707 在病例对照分析中,无论是所有个体还是仅男孩的基因型频率分布均存在显著差异,rs2230365 仅与男孩的 ALT 模块语言障碍显著相关。此外,我们在病例对照研究中发现 rs2230365 存在名义关联,该 SNP 与之前在独立全基因组关联研究中与 ASD 的关联相吻合。
NFKBIL1 多态性与 ALT 之间的关联表明免疫系统对神经精神症状有影响。