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Genome-wide analysis in UK Biobank identifies four loci associated with mood instability and genetic correlation with major depressive disorder, anxiety disorder and schizophrenia

机译:英国生物银行的全基因组分析确定了4个与情绪不稳定相关的基因座以及与重度抑郁症,焦虑症和精神分裂症的遗传相关性

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摘要

Mood instability is a core clinical feature of affective and psychotic disorders. In keeping with the Research Domain Criteria approach, it may be a useful construct for identifying biology that cuts across psychiatric categories. We aimed to investigate the biological validity of a simple measure of mood instability and evaluate its genetic relationship with several psychiatric disorders, including major depressive disorder (MDD), bipolar disorder (BD), schizophrenia, attention deficit hyperactivity disorder (ADHD), anxiety disorder and post-traumatic stress disorder (PTSD). We conducted a genome-wide association study (GWAS) of mood instability in 53,525 cases and 60,443 controls from UK Biobank, identifying four independently associated loci (on chromosomes 8, 9, 14 and 18), and a common single-nucleotide polymorphism (SNP)-based heritability estimate of ~8%. We found a strong genetic correlation between mood instability and MDD (rg = 0.60, SE = 0.07, p = 8.95 × 10−17) and a small but significant genetic correlation with both schizophrenia (rg = 0.11, SE = 0.04, p = 0.01) and anxiety disorders (rg = 0.28, SE = 0.14, p = 0.04), although no genetic correlation with BD, ADHD or PTSD was observed. Several genes at the associated loci may have a role in mood instability, including the DCC netrin 1 receptor (DCC) gene, eukaryotic translation initiation factor 2B subunit beta (eIF2B2), placental growth factor (PGF) and protein tyrosine phosphatase, receptor type D (PTPRD). Strengths of this study include the very large sample size, but our measure of mood instability may be limited by the use of a single question. Overall, this work suggests a polygenic basis for mood instability. This simple measure can be obtained in very large samples; our findings suggest that doing so may offer the opportunity to illuminate the fundamental biology of mood regulation.
机译:情绪不稳定是情感和精神疾病的核心临床特征。与“研究领域标准”方法保持一致,它可能是识别跨精神病学类别的生物学的有用结构。我们旨在调查一种简单的情绪不稳测量方法的生物学有效性,并评估其与几种精神疾病的遗传关系,包括重度抑郁症(MDD),双相情感障碍(BD),精神分裂症,注意缺陷多动障碍(ADHD),焦虑症和创伤后应激障碍(PTSD)。我们进行了全基因组关联研究(GWAS),研究了来自UK Biobank的53,525例病例和60,443个对照,确定了四个独立相关的基因座(在8号,9号,14号和18号染色体上)和常见的单核苷酸多态性(SNP) )的遗传力估算值约为8%。我们发现情绪不稳定与MDD之间存在很强的遗传相关性(rg = 0.60,SE = 0.07,p = 8.95×10-17),与两个精神分裂症的遗传相关性均很小但显着(rg = 0.11,SE = 0.04,p = 0.01) )和焦虑症(rg = 0.28,SE = 0.14,p = 0.04),尽管未发现与BD,ADHD或PTSD有遗传相关性。相关基因座上的几个基因可能与情绪不稳定有关,包括DCC netrin 1受体(DCC)基因,真核翻译起始因子2B亚基beta(eIF2B2),胎盘生长因子(PGF)和酪氨酸磷酸酶,D型受体(PTPRD)。这项研究的优势包括非常大的样本量,但是我们对情绪不稳定性的测量可能会受到单个问题的限制。总的来说,这项工作表明了情绪不稳定的多基因基础。可以在非常大的样本中获得这种简单的度量。我们的发现表明,这样做可能为阐明情绪调节的基础生物学提供机会。

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