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本文引用的文献

1
Rate of de novo mutations and the importance of father's age to disease risk.新突变率和父亲年龄对疾病风险的重要性。
Nature. 2012 Aug 23;488(7412):471-5. doi: 10.1038/nature11396.
2
Genome wide association studies (GWAS) and copy number variation (CNV) studies of the major psychoses: what have we learnt?全基因组关联研究(GWAS)和主要精神病的拷贝数变异(CNV)研究:我们学到了什么?
Neurosci Biobehav Rev. 2012 Jan;36(1):556-71. doi: 10.1016/j.neubiorev.2011.09.001. Epub 2011 Sep 17.
3
Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism.多种反复出现的新生拷贝数变异,包括 7q11.23 威廉姆斯综合征区域的重复,与自闭症强烈相关。
Neuron. 2011 Jun 9;70(5):863-85. doi: 10.1016/j.neuron.2011.05.002.
4
Paternal age and psychiatric disorders: findings from a Dutch population registry.父亲年龄与精神障碍:来自荷兰人口登记处的研究结果。
Schizophr Res. 2011 Jul;129(2-3):128-32. doi: 10.1016/j.schres.2011.03.021. Epub 2011 Apr 12.
5
Advancing paternal age and risk of autism: new evidence from a population-based study and a meta-analysis of epidemiological studies.高龄父亲与自闭症风险:一项基于人群的研究和流行病学研究荟萃分析的新证据。
Mol Psychiatry. 2011 Dec;16(12):1203-12. doi: 10.1038/mp.2010.121. Epub 2010 Nov 30.
6
Paternal age at birth of first child and risk of schizophrenia.父亲生育第一胎时的年龄与精神分裂症风险。
Am J Psychiatry. 2011 Jan;168(1):82-8. doi: 10.1176/appi.ajp.2010.10020252. Epub 2010 Oct 15.
7
Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.罕见拷贝数变异:双相情感障碍和精神分裂症遗传风险中的一个罕见点。
Arch Gen Psychiatry. 2010 Apr;67(4):318-27. doi: 10.1001/archgenpsychiatry.2010.25.
8
Meta-analysis of paternal age and schizophrenia risk in male versus female offspring.父亲年龄与精神分裂症风险的荟萃分析:子女性别差异。
Schizophr Bull. 2011 Sep;37(5):1039-47. doi: 10.1093/schbul/sbq011. Epub 2010 Feb 25.
9
Advanced paternal age is associated with alterations in discrete behavioural domains and cortical neuroanatomy of C57BL/6J mice.高龄父亲与 C57BL/6J 小鼠离散行为域和皮质神经解剖结构的改变有关。
Eur J Neurosci. 2010 Feb;31(3):556-64. doi: 10.1111/j.1460-9568.2010.07074.x. Epub 2010 Jan 25.
10
Advancing paternal age is associated with deficits in social and exploratory behaviors in the offspring: a mouse model.高龄父亲与后代的社交和探索行为缺陷有关:一个小鼠模型。
PLoS One. 2009 Dec 30;4(12):e8456. doi: 10.1371/journal.pone.0008456.

父母年龄与子女双相情感障碍风险。

Parental age and risk of bipolar disorder in offspring.

机构信息

Department of Psychiatry, Columbia University College of Physicians and Surgeons, New York State Psychiatric Institute, 1051 Riverside Drive, New York, NY 10032, USA.

出版信息

Psychiatry Res. 2013 Aug 15;208(3):225-31. doi: 10.1016/j.psychres.2013.05.024. Epub 2013 Jun 19.

DOI:10.1016/j.psychres.2013.05.024
PMID:23790979
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3725196/
Abstract

We investigated prospectively documented parental age and bipolar disorder (BD) in a multi-ethnic birth cohort. The study was based on a nested case-control design from the Child Health and Development Study (CHDS) birth cohort from 1959 to 1966. Potential cases with BD were ascertained by database linkages between CHDS, Kaiser Permanente Medical Care Plan (KPNC), and Alameda County Behavioral Health Care Services, and mailed questionnaires. Consensus diagnoses with the SCID for DSM-IV-TR were made. The total number of BD cases was 94. Controls (N=746) were selected from the birth cohort and matched on date of birth, sex, and KPNC membership or residence in Alameda County. For every 10-year increment of paternal age, there was no significant association with BD, adjusting for maternal age. There was also no significant association between maternal age, modeled in 10-year increments, and risk of BD after adjustment for paternal age and maternal race, although there was a suggestion for a protective relationship between increasing maternal age and BD with psychotic features. These findings suggest that if advanced paternal age is a risk factor for BD, the strength of the relationship is small.

摘要

我们前瞻性地研究了多民族出生队列中父母年龄与双相情感障碍(BD)的关系。该研究基于 1959 年至 1966 年的儿童健康与发展研究(CHDS)出生队列中的嵌套病例对照设计。通过 CHDS、Kaiser Permanente 医疗保健计划(KPNC)和阿拉米达县行为保健服务之间的数据库链接以及邮寄问卷来确定潜在的 BD 病例。使用 DSM-IV-TR 的 SCID 进行共识诊断。BD 总病例数为 94 例。对照组(N=746)选自出生队列,并根据出生日期、性别以及 KPNC 会员资格或在阿拉米达县的居住情况进行匹配。在调整了母亲年龄后,父亲年龄每增加 10 年,与 BD 无显著关联。在调整了父亲年龄和母亲种族后,母亲年龄每增加 10 年,与 BD 的风险也没有显著关联,但有迹象表明,母亲年龄的增加与伴有精神病特征的 BD 之间存在保护关系。这些发现表明,如果父亲年龄较大是 BD 的一个危险因素,那么这种关系的强度很小。