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本文引用的文献

1
Perinatal oxytocin increases the risk of offspring bipolar disorder and childhood cognitive impairment.围产期使用催产素会增加后代患双相情感障碍和儿童认知障碍的风险。
J Affect Disord. 2015 Mar 1;173:65-72. doi: 10.1016/j.jad.2014.10.052. Epub 2014 Nov 8.
2
Neonatal levels of inflammatory markers and later risk of schizophrenia.新生儿时期炎症标志物水平与后期精神分裂症风险的关系。
Biol Psychiatry. 2015 Mar 15;77(6):548-55. doi: 10.1016/j.biopsych.2014.07.013. Epub 2014 Jul 22.
3
Searching across diagnostic boundaries.跨越诊断界限进行搜索。
Schizophr Bull. 2014 Sep;40(5):946-8. doi: 10.1093/schbul/sbu112. Epub 2014 Aug 5.
4
Finnish Prenatal Study of Bipolar Disorders (FIPS-B): overview, design and description of the sample.芬兰双相情感障碍产前研究(FIPS-B):样本概述、设计与描述
Nord J Psychiatry. 2014 Apr;68(3):169-79. doi: 10.3109/08039488.2013.789073. Epub 2013 May 13.
5
Serological documentation of maternal influenza exposure and bipolar disorder in adult offspring.母体流感暴露与成年后代双相障碍的血清学证据。
Am J Psychiatry. 2014 May;171(5):557-63. doi: 10.1176/appi.ajp.2013.13070943.
6
Perinatal factors and the risk of bipolar disorder in Finland.围生期因素与芬兰双相障碍的风险。
J Affect Disord. 2014 Feb;155:75-80. doi: 10.1016/j.jad.2013.10.026. Epub 2013 Oct 26.
7
Gestational influenza and bipolar disorder in adult offspring.妊娠期流感与成年后代的双相障碍。
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8
Neonatal levels of acute phase proteins and later risk of non-affective psychosis.新生儿期急性期蛋白水平与后期非情感性精神病风险的关系。
Transl Psychiatry. 2013 Feb 19;3(2):e228. doi: 10.1038/tp.2013.5.
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Perinatal choline effects on neonatal pathophysiology related to later schizophrenia risk.围产期胆碱对新生儿发病机制的影响与后期精神分裂症风险相关。
Am J Psychiatry. 2013 Mar;170(3):290-8. doi: 10.1176/appi.ajp.2012.12070940.
10
Maternal antibodies to infectious agents and risk for non-affective psychoses in the offspring--a matched case-control study.母体对传染性病原体的抗体与后代非情感性精神病的风险——一项匹配的病例对照研究。
Schizophr Res. 2012 Sep;140(1-3):25-30. doi: 10.1016/j.schres.2012.06.035. Epub 2012 Jul 21.

从产前感染和免疫损伤角度看克雷佩林二分法

The Kraepelinian Dichotomy From the Perspective of Prenatal Infectious and Immunologic Insults.

作者信息

Brown Alan S

机构信息

Department of Psychiatry, Columbia University Medical Center, New York State Psychiatric Institute, New York, NY

出版信息

Schizophr Bull. 2015 Jul;41(4):786-91. doi: 10.1093/schbul/sbv063. Epub 2015 May 11.

DOI:10.1093/schbul/sbv063
PMID:25964504
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4466196/
Abstract

The "Kraepelinian dichotomy" between schizophrenia (SZ) and bipolar disorder (BD) has been a dominant force in our thinking on the classification of these mental disorders. Emerging evidence indicates that these 2 disorders overlap significantly with regard to epidemiology, clinical presentation, genetic susceptibility, structural neuroanatomy, and treatment. Prenatal infection and immunologic dysfunction appear to be risk factors for both SZ and BD; some of these gestational exposures are present in both disorders while others may be specific to 1 or the other of the 2 syndromes. In this paper, we shall review prior studies of prenatal infections and immunologic insults in schizophrenia and BD, including exposures which overlap and which differ between these disorders, discuss the potential utility of maternal infection as one strategy toward developing a more biologically meaningful diagnostic classification system, and propose new recommendations for future research aimed at dissecting these 2 disorders from one another at the etiologic level.

摘要

精神分裂症(SZ)和双相情感障碍(BD)之间的“克雷佩林二分法”一直是我们对这些精神障碍分类思考中的主导力量。新出现的证据表明,这两种障碍在流行病学、临床表现、遗传易感性、结构神经解剖学和治疗方面存在显著重叠。产前感染和免疫功能障碍似乎是SZ和BD的危险因素;其中一些孕期暴露在两种障碍中都存在,而其他一些可能特定于这两种综合征中的一种。在本文中,我们将回顾先前关于精神分裂症和双相情感障碍中产前感染和免疫损伤的研究,包括这些障碍之间重叠和不同的暴露情况,讨论母体感染作为制定更具生物学意义的诊断分类系统的一种策略的潜在效用,并针对未来旨在从病因层面区分这两种障碍的研究提出新的建议。