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本文引用的文献

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PKNOX2 is associated with formal thought disorder in schizophrenia: a meta-analysis of two genome-wide association studies.PKNOX2 与精神分裂症的形式思维障碍有关:两项全基因组关联研究的荟萃分析。
J Mol Neurosci. 2012 Sep;48(1):265-72. doi: 10.1007/s12031-012-9787-4. Epub 2012 May 31.
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Childhood adversities increase the risk of psychosis: a meta-analysis of patient-control, prospective- and cross-sectional cohort studies.童年逆境增加精神病发病风险:患者对照、前瞻性和横断面队列研究的荟萃分析。
Schizophr Bull. 2012 Jun;38(4):661-71. doi: 10.1093/schbul/sbs050. Epub 2012 Mar 29.
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Testing the psychopathology of psychosis: evidence for a general psychosis dimension.测试精神病学的精神病学:一般精神病维度的证据。
Schizophr Bull. 2013 Jul;39(4):884-95. doi: 10.1093/schbul/sbr182. Epub 2012 Jan 18.
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THE USE OF AN OBJECT SORTING TEST IN ELUCIDATING THE HEREDITARY FACTOR IN SCHIZOPHRENIA.运用物体分类测试来阐明精神分裂症的遗传因素。
J Neurol Neurosurg Psychiatry. 1959 Aug;22(3):243-6. doi: 10.1136/jnnp.22.3.243.
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The environment and schizophrenia.环境与精神分裂症。
Nature. 2010 Nov 11;468(7321):203-12. doi: 10.1038/nature09563.
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Early intervention services, cognitive-behavioural therapy and family intervention in early psychosis: systematic review.早期干预服务、认知行为疗法和家庭干预在早期精神病中的应用:系统评价。
Br J Psychiatry. 2010 Nov;197(5):350-6. doi: 10.1192/bjp.bp.109.074526.
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Neural Netw. 2010 Oct-Nov;23(8-9):985-97. doi: 10.1016/j.neunet.2010.08.009. Epub 2010 Sep 15.
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FOXP2 gene and language impairment in schizophrenia: association and epigenetic studies.FOXP2 基因与精神分裂症的语言障碍:关联和表观遗传学研究。
BMC Med Genet. 2010 Jul 22;11:114. doi: 10.1186/1471-2350-11-114.
9
Communication Deviance in parents of families with adoptees at a high or low risk of schizophrenia-spectrum disorders and its associations with attributes of the adoptee and the adoptive parents.精神分裂症谱系障碍高风险或低风险收养家庭中父母的交流障碍及其与被收养者和养父母特征的关系。
Psychiatry Res. 2011 Jan 30;185(1-2):66-71. doi: 10.1016/j.psychres.2010.04.018. Epub 2010 May 26.
10
Time to abandon the bio-bio-bio model of psychosis: Exploring the epigenetic and psychological mechanisms by which adverse life events lead to psychotic symptoms.是时候摒弃精神病的生物-生物-生物模型了:探索不良生活事件导致精神病症状的表观遗传和心理机制。
Epidemiol Psichiatr Soc. 2009 Oct-Dec;18(4):299-310.

父母沟通与精神病:一项荟萃分析。

Parental communication and psychosis: a meta-analysis.

作者信息

de Sousa Paulo, Varese Filippo, Sellwood William, Bentall Richard P

机构信息

Institute of Psychology, Health and Society, University of Liverpool, Liverpool, UK;

Division of Clinical Psychology, School of Psychological Sciences, University of Manchester, Manchester, UK.

出版信息

Schizophr Bull. 2014 Jul;40(4):756-68. doi: 10.1093/schbul/sbt088. Epub 2013 Jun 25.

DOI:10.1093/schbul/sbt088
PMID:23800431
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4059429/
Abstract

BACKGROUND

Parental communication deviance (CD) has long been suggested as a potential risk factor for the development of psychosis and thought disorder in genetically sensitive offspring. However, the findings of the studies on the prevalence of CD in parents of psychotic patients have never been submitted to quantitative synthesis.

METHOD

PsycINFO was searched from January 1959 to January 2012 for studies on the prevalence of CD in parents of psychotic patients. This search was supplemented with the results from a much larger systematic search (PsycINFO, PubMed, EMBASE, and Web of Science) on childhood trauma and psychosis.

RESULTS

A total of 20 retrieved studies (n = 1753 parents) yielded a pooled g of large magnitude (0.97; 95% CI [0.76; 1.18]) with a significant amount of heterogeneity (Q = 33.63; P = .014; I (2) = 46.47). Subgroup and sensitivity analysis of methodological features (study's design, comparison group, diagnostic criteria, CD rating method, inter-rater reliability not reported, year of publication, and verbosity) and demographic characteristics (level of education or offspring's age) revealed that pooled effect size was stable and unlikely to have been affected by these features.

CONCLUSION

CD is highly prevalent in parents of psychotic offspring. This is discussed in the broader context of adoption and longitudinal studies that have reported a G × E interaction in the development of psychosis and thought disorder. A potential developmental mechanism is suggested to explain how CD may affect the developing offspring. The importance of further studies on CD and its potential value as a clinical concept are discussed.

摘要

背景

长期以来,父母沟通偏差(CD)一直被认为是遗传易感性后代发生精神病和思维障碍的潜在危险因素。然而,关于精神病患者父母中CD患病率的研究结果从未进行过定量综合分析。

方法

检索了1959年1月至2012年1月的PsycINFO数据库,以查找关于精神病患者父母中CD患病率的研究。此次检索还补充了一项关于儿童期创伤与精神病的规模大得多的系统检索(PsycINFO、PubMed、EMBASE和科学引文索引)的结果。

结果

总共检索到20项研究(n = 1753名父母),合并效应量g值较大(0.97;95%可信区间[0.76;1.18]),且存在显著异质性(Q = 33.63;P = 0.014;I² = 46.47)。对方法学特征(研究设计、对照组、诊断标准、CD评分方法、未报告的评分者间信度、发表年份和详细程度)和人口统计学特征(教育水平或后代年龄)进行亚组分析和敏感性分析后发现,合并效应量稳定,不太可能受这些特征影响。

结论

CD在患有精神病后代的父母中高度流行。这在收养研究和纵向研究的更广泛背景下进行了讨论,这些研究报告了精神病和思维障碍发展过程中的基因×环境相互作用。提出了一种潜在的发育机制来解释CD可能如何影响发育中的后代。讨论了对CD进一步研究的重要性及其作为临床概念的潜在价值。