Department of Biochemistry, School of Medicine, Ewha Womans University, Seoul, Korea.
Center for Cohort Studies, Total Healthcare Center, Kangbuk Samsung Hospital, School of Medicine, Sungkyunkwan University, Seoul, Korea.
J Hum Genet. 2017 Oct;62(10):903-909. doi: 10.1038/jhg.2017.61. Epub 2017 Jun 15.
Neuroticism is a heritable personality trait that is comprised of distinct sub-factors, or facets. Sub-factors of neuroticism are linked to different emotional states or psychiatric symptoms and studying the genetic variants associated with these facets may help reveal the biological mechanisms underlying psychiatric disorders. In the present study, a meta-analysis of genome-wide association studies for six facets of neuroticism was performed in 5584 participants from three cohorts. Additionally, a Gene Set Enrichment Analysis was conducted to find biological pathways associated with each facet. Six neuroticism facets (N1: anxiety, N2: angry hostility, N3: depression, N4: self-consciousness, N5: impulsivity and N6: vulnerability) were assessed using the Korean version of the Revised NEO Personality Inventory. In the single-nucleotide polymorphism-based analysis, results showed genome-wide significance for N2 within the MIR548H3 gene (rs1360001, P=4.14 × 10). Notable genes with suggestive associations (P<1.0 × 10) were ITPR1 for N1, WNT7A for N2, FGF10 and FHIT for N3, DDR1 for N4, VGLL4 for N5 and PTPRD for N6. In the pathway-based analysis, the axon guidance pathway was identified to be associated with multiple facets of neuroticism (N2, N4 and N6). The focal adhesion and extracellular matrix receptor interaction pathways were significantly associated with N2 and N3. Our findings revealed genetic influences and biological pathways that are associated with facets of neuroticism.
神经质是一种可遗传的人格特质,由不同的子因素或方面组成。神经质的子因素与不同的情绪状态或精神症状有关,研究与这些方面相关的遗传变异可能有助于揭示精神障碍的生物学机制。在本研究中,对来自三个队列的 5584 名参与者的六个神经质方面进行了全基因组关联研究的荟萃分析。此外,还进行了基因集富集分析,以找到与每个方面相关的生物学途径。使用修订后的 NEO 人格量表的韩语版本评估了六个神经质方面(N1:焦虑,N2:愤怒敌意,N3:抑郁,N4:自我意识,N5:冲动和 N6:脆弱)。在基于单核苷酸多态性的分析中,结果显示在 MIR548H3 基因内的 N2 具有全基因组显著性(rs1360001,P=4.14×10)。具有提示关联(P<1.0×10)的显著基因包括 N1 的 ITPR1、N2 的 WNT7A、N3 的 FGF10 和 FHIT、N4 的 DDR1、N5 的 VGLL4 和 N6 的 PTPRD。在基于途径的分析中,发现轴突导向途径与神经质的多个方面(N2、N4 和 N6)相关。粘着斑和细胞外基质受体相互作用途径与 N2 和 N3 显著相关。我们的研究结果揭示了与神经质方面相关的遗传影响和生物学途径。