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一般人群中女性和男性的拷贝数变异与神经精神问题。

Copy number variation and neuropsychiatric problems in females and males in the general population.

机构信息

Department of Medical Epidemiology & Biostatistics, Karolinska Institutet, Stockholm, Sweden.

MRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Cardiff, United Kingdom.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2019 Sep;180(6):341-350. doi: 10.1002/ajmg.b.32685. Epub 2018 Oct 11.

Abstract

Neurodevelopmental problems (NPs) are more common in males, whereas anxiety and depression are more common in females. Rare copy number variants (CNVs) have been implicated in neurodevelopmental disorders. The aim of this study was to characterize the relationship between rare CNVs with NPs, anxiety, and depression in a childhood population sample, as well as to examine sex-specific effects. We analyzed a sample of N = 12,982 children, of whom 5.3% had narrowly defined NPs (clinically diagnosed), 20.9% had broadly defined NPs (based on validated screening measures, but no diagnosis), and 3.0% had clinically diagnosed anxiety or depression. Rare (<1% frequency) CNVs were categorized by size (100-500 kb or > 500 kb), type, and putative relevance to NPs. We tested for association of CNV categories with outcomes and examined sex-specific effects. Medium deletions (OR[CI] = 1.18[1.05-1.33], p = .0053) and large duplications (OR[CI] = 1.45[1.19-1.75], p = .00017) were associated with broadly defined NPs. Large deletions (OR[CI] = 1.85[1.14-3.01], p = .013) were associated with narrowly defined NPs. There were no significant sex differences in CNV burden in individuals with NPs. Although CNVs were not associated with anxiety/depression in the whole sample, in individuals diagnosed with these disorders, females were more likely to have large CNVs (OR[CI] = 3.75[1.45-9.68], p = .0064). Rare CNVs are associated with both narrowly and broadly defined NPs in a general population sample of children. Our results also suggest that large, rare CNVs may show sex-specific phenotypic effects.

摘要

神经发育问题(NPs)在男性中更为常见,而焦虑和抑郁在女性中更为常见。罕见的拷贝数变异(CNVs)与神经发育障碍有关。本研究的目的是描述儿童人群样本中罕见 CNVs 与 NPs、焦虑和抑郁之间的关系,并检查性别特异性影响。我们分析了一个样本,共 12982 名儿童,其中 5.3%有狭义定义的 NPs(临床诊断),20.9%有广义定义的 NPs(基于经过验证的筛查措施,但没有诊断),3.0%有临床诊断的焦虑或抑郁。罕见(频率<1%)CNVs 按大小(100-500kb 或>500kb)、类型和与 NPs 的潜在相关性进行分类。我们测试了 CNV 类别与结果的关联,并检查了性别特异性影响。中等缺失(OR[CI]=1.18[1.05-1.33],p=0.0053)和大重复(OR[CI]=1.45[1.19-1.75],p=0.00017)与广义 NPs 相关。大缺失(OR[CI]=1.85[1.14-3.01],p=0.013)与狭义 NPs 相关。在有 NPs 的个体中,CNV 负担没有显著的性别差异。尽管 CNVs 在整个样本中与焦虑/抑郁无关,但在被诊断为这些疾病的个体中,女性更有可能存在大的 CNVs(OR[CI]=3.75[1.45-9.68],p=0.0064)。罕见 CNVs 与儿童一般人群样本中的狭义和广义 NPs 均相关。我们的结果还表明,大的罕见 CNVs 可能表现出性别特异性的表型效应。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31a4/6767107/611a870c4b5c/AJMG-180-341-g001.jpg

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