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Early life trauma, post-traumatic stress disorder, and allostatic load in a sample of American Indian adults.美国印第安成年人样本中的早期生活创伤、创伤后应激障碍和应激负荷
Am J Hum Biol. 2017 May 6;29(3). doi: 10.1002/ajhb.22943. Epub 2016 Nov 30.
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Chronic subordinate colony housing paradigm: A mouse model for mechanisms of PTSD vulnerability, targeted prevention, and treatment-2016 Curt Richter Award Paper.慢性从属群体饲养范式:一种用于创伤后应激障碍易感性机制、靶向预防和治疗的小鼠模型——2016年柯特·里希特奖论文
Psychoneuroendocrinology. 2016 Dec;74:221-230. doi: 10.1016/j.psyneuen.2016.08.031. Epub 2016 Sep 9.
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A new view of the tree of life.生命之树的新视角。
Nat Microbiol. 2016 Apr 11;1:16048. doi: 10.1038/nmicrobiol.2016.48.
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The Microbiota, Immunoregulation, and Mental Health: Implications for Public Health.微生物群、免疫调节与心理健康:对公共卫生的启示。
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Akkermansia muciniphila: a novel functional microbe with probiotic properties.黏蛋白阿克曼氏菌:一种具有益生菌特性的新型功能微生物。
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Immunization with a heat-killed preparation of the environmental bacterium Mycobacterium vaccae promotes stress resilience in mice.用环境细菌母牛分枝杆菌的热灭活制剂进行免疫可增强小鼠的应激恢复力。
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Genome-wide Association Studies of Posttraumatic Stress Disorder in 2 Cohorts of US Army Soldiers.美国陆军士兵两个队列中创伤后应激障碍的全基因组关联研究
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MUCOSAL IMMUNOLOGY. Individual intestinal symbionts induce a distinct population of RORγ⁺ regulatory T cells.黏膜免疫学。个体肠道共生菌诱导出不同群体的RORγ⁺调节性T细胞。
Science. 2015 Aug 28;349(6251):993-7. doi: 10.1126/science.aaa9420. Epub 2015 Aug 13.

创伤后应激障碍和创伤暴露对照者中的微生物组:一项探索性研究。

The Microbiome in Posttraumatic Stress Disorder and Trauma-Exposed Controls: An Exploratory Study.

机构信息

From the Department of Psychiatry (Hemmings, Malan-Müller, van den Heuvel, Seedat), Faculty of Medicine and Health Sciences, Stellenbosch University, Tygerberg, South Africa; Departments of Molecular, Cellular and Developmental Biology (Demmitt, Krauter), Chemistry and Biochemistry (Smith), and Integrative Physiology (Bohr, Stamper, Siebler, McQueen, Lowry), Institute for Behavioral Genetics (Demmitt, Bohr, McQueen, Krauter), and Center for Neuroscience (Lowry), University of Colorado Boulder, Boulder; Departments of Epidemiology (Stanislawski), Psychiatry and Neurology (Brenner), and Physical Medicine and Rehabilitation (Brenner, Lowry), and Center for Neuroscience (Lowry), University of Colorado Anschutz Medical Campus, Aurora; US Department of Veterans Affairs (Stanislawski), Denver, CO; Departments of Pediatrics (Hyde, Marotz, Knight) and Computer Science & Engineering (Morton, Knight), and Center for Microbiome Innovation (Knight), University of California San Diego, La Jolla, CA; NXT-Dx (Braspenning); Department of Mathematical Modelling (Van Criekinge), Statistics and Bio-informatics, Ghent University, Gent, Belgium; Department of Civil and Environmental Engineering (Hoisington), United States Air Force Academy, Colorado Springs; Military and Veteran Microbiome Consortium for Research and Education (MVM-CoRE) (Hoisington, Brenner, Postolache, Lowry); VA Rocky Mountain Mental Illness Research, Education, and Clinical Center (MIRECC) (Brenner, Postolache, Lowry), Denver, CO; and Department of Psychiatry (Postolache), School of Medicine, University of Maryland, Baltimore, MD.

出版信息

Psychosom Med. 2017 Oct;79(8):936-946. doi: 10.1097/PSY.0000000000000512.

DOI:10.1097/PSY.0000000000000512
PMID:28700459
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5763914/
Abstract

OBJECTIVE

Inadequate immunoregulation and elevated inflammation may be risk factors for posttraumatic stress disorder (PTSD), and microbial inputs are important determinants of immunoregulation; however, the association between the gut microbiota and PTSD is unknown. This study investigated the gut microbiome in a South African sample of PTSD-affected individuals and trauma-exposed (TE) controls to identify potential differences in microbial diversity or microbial community structure.

METHODS

The Clinician-Administered PTSD Scale for DSM-5 was used to diagnose PTSD according to Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition criteria. Microbial DNA was extracted from stool samples obtained from 18 individuals with PTSD and 12 TE control participants. Bacterial 16S ribosomal RNA gene V3/V4 amplicons were generated and sequenced. Microbial community structure, α-diversity, and β-diversity were analyzed; random forest analysis was used to identify associations between bacterial taxa and PTSD.

RESULTS

There were no differences between PTSD and TE control groups in α- or β-diversity measures (e.g., α-diversity: Shannon index, t = 0.386, p = .70; β-diversity, on the basis of analysis of similarities: Bray-Curtis test statistic = -0.033, p = .70); however, random forest analysis highlighted three phyla as important to distinguish PTSD status: Actinobacteria, Lentisphaerae, and Verrucomicrobia. Decreased total abundance of these taxa was associated with higher Clinician-Administered PTSD Scale scores (r = -0.387, p = .035).

CONCLUSIONS

In this exploratory study, measures of overall microbial diversity were similar among individuals with PTSD and TE controls; however, decreased total abundance of Actinobacteria, Lentisphaerae, and Verrucomicrobia was associated with PTSD status.

摘要

目的

免疫调节不足和炎症升高可能是创伤后应激障碍(PTSD)的危险因素,而微生物的输入是免疫调节的重要决定因素;然而,肠道微生物群与 PTSD 之间的关联尚不清楚。本研究调查了南非 PTSD 患者和创伤暴露(TE)对照个体的肠道微生物组,以确定微生物多样性或微生物群落结构是否存在潜在差异。

方法

根据《精神障碍诊断与统计手册》第五版(DSM-5)的标准,使用临床医生管理的 PTSD 量表来诊断 PTSD。从 18 名 PTSD 患者和 12 名 TE 对照参与者的粪便样本中提取微生物 DNA。生成和测序细菌 16S 核糖体 RNA 基因 V3/V4 扩增子。分析微生物群落结构、α多样性和β多样性;使用随机森林分析来识别细菌分类群与 PTSD 之间的关联。

结果

在α或β多样性测量方面(例如,α多样性:Shannon 指数,t = 0.386,p =.70;β多样性,基于相似性分析:Bray-Curtis 检验统计量 = -0.033,p =.70),PTSD 组和 TE 对照组之间没有差异;然而,随机森林分析突出了三个门对区分 PTSD 状态很重要:放线菌门、 Lentisphaerae 门和 Verrucomicrobia 门。这些类群的总丰度降低与更高的临床医生管理的 PTSD 量表评分相关(r = -0.387,p =.035)。

结论

在这项探索性研究中,PTSD 患者和 TE 对照组的总体微生物多样性测量相似;然而,放线菌门、 Lentisphaerae 门和 Verrucomicrobia 门的总丰度降低与 PTSD 状态相关。

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