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基于家系的分析:罕见和常见遗传变异对精神分裂症患者学习成绩的影响。

Family-based analysis of the contribution of rare and common genetic variants to school performance in schizophrenia.

机构信息

Centre for Neuropsychiatric Genetics and Genomics, Division of Psychological Medicine and Clinical Neurosciences, Cardiff University, Cardiff, UK.

出版信息

Mol Psychiatry. 2023 May;28(5):2081-2087. doi: 10.1038/s41380-023-02013-2. Epub 2023 Mar 13.

Abstract

Impaired cognition in schizophrenia is associated with worse functional outcomes. While genetic factors are known to contribute to variation in cognition in schizophrenia, few rare coding variants with strong effects have been identified, and the relative effects from de novo, inherited and non-transmitted alleles are unknown. We used array and exome sequencing data from 656 proband-parent trios to examine the contribution of common and rare variants to school performance, and by implication cognitive function, in schizophrenia. Parental transmission of common alleles contributing to higher educational attainment (p value = 0.00015; OR = 2.63) and intelligence (p value = 0.00009; OR = 2.80), but not to schizophrenia, were associated with higher proband school performance. No significant effects were seen for non-transmitted parental common alleles. Probands with lower school performance were enriched for damaging de novo coding variants in genes associated with developmental disorders (DD) (p value = 0.00026; OR = 11.6). Damaging, ultra-rare coding variants in DD genes that were transmitted or non-transmitted from parents, had no effects on school performance. Among probands with lower school performance, those with damaging de novo coding variants in DD genes had a higher rate of comorbid mild intellectual disability (p value = 0.0002; OR = 15.6). Overall, we provide evidence for rare and common genetic contributions to school performance in schizophrenia. The strong effects for damaging de novo coding variants in DD genes provide further evidence that cognitive impairment in schizophrenia has a shared aetiology with developmental disorders. Furthermore, we report no evidence in this sample that non-transmitted parental common alleles for cognitive traits contributed to school performance in schizophrenia via indirect effects on the environment.

摘要

精神分裂症患者的认知障碍与较差的功能结果有关。虽然遗传因素已知会导致精神分裂症患者认知能力的差异,但很少有具有强效应的罕见编码变异被鉴定出来,并且无法确定新生成的、遗传的和未传递的等位基因的相对效应。我们使用来自 656 个先证者-父母三体型的阵列和外显子测序数据,来检查常见和罕见变异对精神分裂症中学校表现(间接反映认知功能)的贡献。常见等位基因的父系传递与更高的教育程度(p 值=0.00015;OR=2.63)和智力(p 值=0.00009;OR=2.80)有关,但与精神分裂症无关,与先证者更高的学校表现有关。未传递的常见父系等位基因没有显著影响。学校表现较差的先证者在与发育障碍(DD)相关的基因中富集了低功能的新生编码变异(p 值=0.00026;OR=11.6)。从父母传递或未传递的 DD 基因中的有害、超罕见编码变异对学校表现没有影响。在学校表现较差的先证者中,那些在 DD 基因中具有新生破坏性编码变异的人,共患轻度智力障碍的比率更高(p 值=0.0002;OR=15.6)。总的来说,我们为精神分裂症中学校表现的罕见和常见遗传贡献提供了证据。DD 基因中破坏性新生编码变异的强效应进一步表明,精神分裂症中的认知障碍与发育障碍具有共同的病因。此外,我们在这个样本中没有发现证据表明,认知特征的未传递的常见父系等位基因通过对环境的间接影响,导致精神分裂症中的学校表现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e573/10575776/d8fe10134da2/41380_2023_2013_Fig1_HTML.jpg

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