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产后精神病的遗传结构:从常见到罕见的基因变异

Genetic Architecture of Postpartum Psychosis: From Common to Rare Genetic Variation.

作者信息

Jung Seulgi, Caballero Madison, Kępińska Adrianna, Smout Shelby, Munk-Olsen Trine, Robakis Thalia K, Bergink Veerle, Mahjani Behrang

机构信息

Seaver Autism Center for Research and Treatment, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Department of Psychiatry, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

出版信息

medRxiv. 2024 Dec 10:2024.12.09.24318732. doi: 10.1101/2024.12.09.24318732.

DOI:10.1101/2024.12.09.24318732
PMID:39711717
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11661424/
Abstract

Postpartum psychosis is a severe psychiatric condition marked by the abrupt onset of psychosis, mania, or psychotic depression following childbirth. Despite evidence for a strong genetic basis, the roles of common and rare genetic variation remain poorly understood. Leveraging data from Swedish national registers and genomic data from the All of Us Research Program, we estimated family-based heritability at 55% and WGS-based heritability at 37%, with an overrepresentation on the X chromosome. Rare coding variant analysis identified and as potential risk genes (q < 0.1). Analysis of 240,009 samples from All of Us demonstrated significant associations between these genes and multiple psychiatric disorders, supporting their biological relevance. Additionally, 17% of bipolar disorder, 21% of schizophrenia, and 16-25% of multiple autoimmune disorder risk genes overlapped with postpartum psychosis. These findings reveal unique genetic contributions and shared pathways, providing a foundation for understanding pathophysiology and advancing therapeutic strategies.

摘要

产后精神病是一种严重的精神疾病,其特征是在分娩后突然出现精神病、躁狂症或精神病性抑郁症。尽管有证据表明其有很强的遗传基础,但常见和罕见基因变异的作用仍知之甚少。利用瑞典国家登记数据和“我们所有人”研究计划的基因组数据,我们估计基于家系的遗传率为55%,基于全基因组测序的遗传率为37%,在X染色体上的比例过高。罕见编码变异分析确定了 和 为潜在风险基因(q < 0.1)。对“我们所有人”项目的240,009个样本的分析表明,这些基因与多种精神疾病之间存在显著关联,支持了它们的生物学相关性。此外,17%的双相情感障碍、21%的精神分裂症以及16 - 25%的多种自身免疫性疾病风险基因与产后精神病重叠。这些发现揭示了独特的遗传贡献和共同途径,为理解病理生理学和推进治疗策略提供了基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af36/11661424/e26cd0de2daf/nihpp-2024.12.09.24318732v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af36/11661424/977cf3492e00/nihpp-2024.12.09.24318732v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af36/11661424/af915b752264/nihpp-2024.12.09.24318732v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af36/11661424/e26cd0de2daf/nihpp-2024.12.09.24318732v1-f0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af36/11661424/977cf3492e00/nihpp-2024.12.09.24318732v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af36/11661424/af915b752264/nihpp-2024.12.09.24318732v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/af36/11661424/e26cd0de2daf/nihpp-2024.12.09.24318732v1-f0003.jpg

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本文引用的文献

1
Familial Risk of Postpartum Psychosis.产后精神病的家族风险。
Am J Psychiatry. 2025 Jun 1;182(6):542-550. doi: 10.1176/appi.ajp.20230576. Epub 2025 May 19.
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Large-scale whole-exome sequencing analyses identified protein-coding variants associated with immune-mediated diseases in 350,770 adults.大规模全外显子测序分析鉴定了 350770 名成年人中与免疫介导性疾病相关的蛋白编码变异。
Nat Commun. 2024 Jul 15;15(1):5924. doi: 10.1038/s41467-024-49782-0.
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Rare de novo damaging DNA variants are enriched in attention-deficit/hyperactivity disorder and implicate risk genes.
新出现的具有破坏性的 DNA 变异在注意力缺陷多动障碍中更为丰富,并暗示了风险基因。
Nat Commun. 2024 Jul 12;15(1):5870. doi: 10.1038/s41467-024-50247-7.
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Whole-exome sequencing in UK Biobank reveals rare genetic architecture for depression.英国生物库全外显子组测序揭示了抑郁症的罕见遗传结构。
Nat Commun. 2024 Feb 26;15(1):1755. doi: 10.1038/s41467-024-45774-2.
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DNMT1 downregulation as well as its overexpression distinctly affect mostly overlapping genes implicated in schizophrenia, autism spectrum, epilepsy, and bipolar disorders.DNMT1的下调及其过表达均明显影响大多数与精神分裂症、自闭症谱系障碍、癫痫和双相情感障碍相关的重叠基因。
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Epigenomic dissection of Alzheimer's disease pinpoints causal variants and reveals epigenome erosion.阿尔茨海默病的表观基因组剖析确定了因果变异,并揭示了表观基因组的侵蚀。
Cell. 2023 Sep 28;186(20):4422-4437.e21. doi: 10.1016/j.cell.2023.08.040.
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Rheumatoid arthritis and the risk of postpartum psychiatric disorders: a Nordic population-based cohort study.类风湿关节炎与产后精神障碍风险:一项基于北欧人群的队列研究。
BMC Med. 2023 Apr 3;21(1):126. doi: 10.1186/s12916-023-02837-3.
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Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.罕见编码变异为自闭症的遗传结构和表型背景提供了深入了解。
Nat Genet. 2022 Sep;54(9):1320-1331. doi: 10.1038/s41588-022-01104-0. Epub 2022 Aug 18.
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Single nucleus multi-omics identifies human cortical cell regulatory genome diversity.单核多组学技术揭示人类皮质细胞调控基因组多样性。
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Exome sequencing in bipolar disorder identifies AKAP11 as a risk gene shared with schizophrenia.外显子组测序在双相情感障碍中发现 AKAP11 是与精神分裂症共享的风险基因。
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