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The association of a novel haplotype in the dopamine transporter with preschool age posttraumatic stress disorder.多巴胺转运体中一种新型单倍型与学龄前创伤后应激障碍的关联。
J Child Adolesc Psychopharmacol. 2013 May;23(4):236-43. doi: 10.1089/cap.2012.0072. Epub 2013 May 6.
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Serotonin transporter genotype 5HTTLPR as a marker of differential susceptibility? A meta-analysis of child and adolescent gene-by-environment studies.5-HTTLPR 基因型作为易感性差异的标志物?儿童和青少年基因-环境研究的荟萃分析。
Transl Psychiatry. 2012 Aug 7;2(8):e147. doi: 10.1038/tp.2012.73.
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Diagnosing PTSD in early childhood: an empirical assessment of four approaches.早期儿童创伤后应激障碍的诊断:四种方法的实证评估。
J Trauma Stress. 2012 Aug;25(4):359-67. doi: 10.1002/jts.21723. Epub 2012 Jul 17.
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Molecular variation at the SLC6A3 locus predicts lifetime risk of PTSD in the Detroit Neighborhood Health Study.SLC6A3 基因座的分子变异可预测底特律社区健康研究中 PTSD 的终生发病风险。
PLoS One. 2012;7(6):e39184. doi: 10.1371/journal.pone.0039184. Epub 2012 Jun 26.
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Higher FKBP5, COMT, CHRNA5, and CRHR1 allele burdens are associated with PTSD and interact with trauma exposure: implications for neuropsychiatric research and treatment.较高的 FKBP5、COMT、CHRNA5 和 CRHR1 等位基因负担与 PTSD 相关,并与创伤暴露相互作用:对神经精神研究和治疗的影响。
Neuropsychiatr Dis Treat. 2012;8:131-9. doi: 10.2147/NDT.S29508. Epub 2012 Mar 23.
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The role of the dopamine transporter (DAT) in the development of PTSD in preschool children.多巴胺转运蛋白(DAT)在学龄前儿童 PTSD 发展中的作用。
J Trauma Stress. 2009 Dec;22(6):534-9. doi: 10.1002/jts.20475.
7
The risk of posttraumatic stress disorder after trauma depends on traumatic load and the catechol-o-methyltransferase Val(158)Met polymorphism.创伤后发生创伤后应激障碍的风险取决于创伤负荷和儿茶酚氧位甲基转移酶 Val(158)Met 多态性。
Biol Psychiatry. 2010 Feb 15;67(4):304-8. doi: 10.1016/j.biopsych.2009.10.009. Epub 2009 Nov 27.
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PTSD and stress sensitisation: a tale of brain and body Part 1: human studies.创伤后应激障碍与应激致敏作用:大脑与身体的故事 第1部分:人体研究
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The use of racial, ethnic, and ancestral categories in human genetics research.人类遗传学研究中种族、民族和祖先类别的使用。
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种族因素调节了学龄前儿童儿茶酚-O-甲基转移酶基因型与创伤后应激障碍之间的关联。

Race moderates the association of Catechol-O-methyltransferase genotype and posttraumatic stress disorder in preschool children.

作者信息

Humphreys Kathryn L, Scheeringa Michael S, Drury Stacy S

机构信息

Tulane University School of Medicine , New Orleans, Louisiana.

出版信息

J Child Adolesc Psychopharmacol. 2014 Oct;24(8):454-7. doi: 10.1089/cap.2014.0077.

DOI:10.1089/cap.2014.0077
PMID:25329975
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4202908/
Abstract

OBJECTIVE

The present study sought to replicate previous findings of an association between the Catechol-O-methyltransferase (COMT) val158met polymorphism with posttraumatic stress disorder (PTSD) and symptomatology in a novel age group, preschool children.

METHODS

COMT genotype was determined in a sample of 171 3-6-year-old trauma-exposed children. PTSD was assessed with a semistructured interview. Accounting for sex, trauma type, and age, genotype was examined in relation to categorical and continuous measures of PTSD both controlling for race and within the two largest racial categories (African American [AA] and European American [EA]).

RESULTS

Race significantly moderated the association between genotype and PTSD. Specifically, the genotype associated with increased PTSD symptoms in one racial group had the opposite association in the other racial group. For AA children the met/met genotype was associated with more PTSD symptoms. However, for EA children, val allele carriers had more PTSD symptoms. Whereas every AA child with the met/met genotype met criteria for PTSD, none of the EA children with the met/met genotype did. This genetic association with COMT genotype, in both races but in opposite directions, was most associated with increased arousal symptoms.

CONCLUSIONS

These findings replicate previous findings in participants of African descent, highlight the moderating effect of race on the association between COMT genotype and PTSD, and provide direct evidence that consideration of population stratification within gene-by-environment studies is valuable to prevent false negative findings.

摘要

目的

本研究旨在在一个新的年龄组——学龄前儿童中,重复先前关于儿茶酚-O-甲基转移酶(COMT)val158met多态性与创伤后应激障碍(PTSD)及症状之间关联的研究结果。

方法

在171名3至6岁遭受创伤的儿童样本中确定COMT基因型。通过半结构化访谈评估PTSD。在控制种族的情况下,并在两个最大的种族类别(非裔美国人[AA]和欧裔美国人[EA])中,考虑性别、创伤类型和年龄,检查基因型与PTSD的分类和连续测量指标之间的关系。

结果

种族显著调节了基因型与PTSD之间的关联。具体而言,在一个种族组中与PTSD症状增加相关的基因型,在另一个种族组中有相反的关联。对于非裔美国儿童,met/met基因型与更多的PTSD症状相关。然而,对于欧裔美国儿童,val等位基因携带者有更多的PTSD症状。虽然每个具有met/met基因型的非裔美国儿童都符合PTSD标准,但没有一个具有met/met基因型的欧裔美国儿童符合标准。在两个种族中,这种与COMT基因型的遗传关联方向相反,且与觉醒症状增加最为相关。

结论

这些发现重复了先前在非洲裔参与者中的研究结果,突出了种族对COMT基因型与PTSD之间关联的调节作用,并提供了直接证据,表明在基因-环境研究中考虑人群分层对于防止假阴性结果是有价值的。