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精神分裂症的基因组研究结果及其意义。

Genomic findings in schizophrenia and their implications.

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 Sep;28(9):3638-3647. doi: 10.1038/s41380-023-02293-8. Epub 2023 Oct 18.

Abstract

There has been substantial progress in understanding the genetics of schizophrenia over the past 15 years. This has revealed a highly polygenic condition with the majority of the currently explained heritability coming from common alleles of small effect but with additional contributions from rare copy number and coding variants. Many specific genes and loci have been implicated that provide a firm basis upon which mechanistic research can proceed. These point to disturbances in neuronal, and particularly synaptic, functions that are not confined to a small number of brain regions and circuits. Genetic findings have also revealed the nature of schizophrenia's close relationship to other conditions, particularly bipolar disorder and childhood neurodevelopmental disorders, and provided an explanation for how common risk alleles persist in the population in the face of reduced fecundity. Current genomic approaches only potentially explain around 40% of heritability, but only a small proportion of this is attributable to robustly identified loci. The extreme polygenicity poses challenges for understanding biological mechanisms. The high degree of pleiotropy points to the need for more transdiagnostic research and the shortcomings of current diagnostic criteria as means of delineating biologically distinct strata. It also poses challenges for inferring causality in observational and experimental studies in both humans and model systems. Finally, the Eurocentric bias of genomic studies needs to be rectified to maximise benefits and ensure these are felt across diverse communities. Further advances are likely to come through the application of new and emerging technologies, such as whole-genome and long-read sequencing, to large and diverse samples. Substantive progress in biological understanding will require parallel advances in functional genomics and proteomics applied to the brain across developmental stages. For these efforts to succeed in identifying disease mechanisms and defining novel strata they will need to be combined with sufficiently granular phenotypic data.

摘要

在过去的 15 年中,人们对精神分裂症的遗传学有了实质性的认识。这揭示了一种高度多基因的疾病,目前解释的大部分遗传性来自常见的、效应较小的等位基因,但也有来自罕见的拷贝数和编码变异的额外贡献。许多具体的基因和基因座已经被牵连进来,为机制研究提供了坚实的基础。这些研究指向神经元,特别是突触功能的紊乱,而不仅仅局限于少数几个脑区和回路。遗传研究还揭示了精神分裂症与其他疾病,特别是双相情感障碍和儿童神经发育障碍的密切关系,并解释了为什么在生育率降低的情况下,常见的风险等位基因仍能在人群中持续存在。目前的基因组方法仅能潜在地解释大约 40%的遗传性,但其中只有一小部分归因于已明确的基因座。这种极端的多基因性给理解生物学机制带来了挑战。高度的多效性表明需要更多的跨诊断研究,以及当前诊断标准作为划分生物学上不同层次的手段的不足。它还对在人类和模型系统中进行观察性和实验性研究推断因果关系提出了挑战。最后,基因组研究的欧洲中心主义偏见需要得到纠正,以最大限度地发挥其效益,并确保不同社区都能从中受益。进一步的进展可能来自于将新技术,如全基因组和长读测序,应用于大型和多样化的样本。在生物学理解方面取得实质性进展,需要在整个发育阶段对大脑进行功能基因组学和蛋白质组学的平行进展。为了使这些努力在识别疾病机制和定义新的层次方面取得成功,它们需要与足够细化的表型数据相结合。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/54b1/10730422/6fdf12ecde2d/41380_2023_2293_Fig1_HTML.jpg

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