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本文引用的文献

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A comparison of methods to harmonize cortical thickness measurements across scanners and sites.比较跨扫描仪和站点协调皮质厚度测量的方法。
Neuroimage. 2022 Nov 1;261:119509. doi: 10.1016/j.neuroimage.2022.119509. Epub 2022 Jul 30.
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Assessment of brain age in posttraumatic stress disorder: Findings from the ENIGMA PTSD and brain age working groups.创伤后应激障碍的大脑年龄评估:来自 ENIGMA PTSD 和大脑年龄工作组的发现。
Brain Behav. 2022 Jan;12(1):e2413. doi: 10.1002/brb3.2413. Epub 2021 Dec 14.
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Cortical volume abnormalities in posttraumatic stress disorder: an ENIGMA-psychiatric genomics consortium PTSD workgroup mega-analysis.创伤后应激障碍的皮质体积异常:ENIGMA-精神遗传学联盟 PTSD 工作组的 mega 分析。
Mol Psychiatry. 2021 Aug;26(8):4331-4343. doi: 10.1038/s41380-020-00967-1. Epub 2020 Dec 7.
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Klotho, PTSD, and advanced epigenetic age in cortical tissue.衰老抑制蛋白、创伤后应激障碍与皮质组织中的高级表观遗传年龄
Neuropsychopharmacology. 2021 Mar;46(4):721-730. doi: 10.1038/s41386-020-00884-5. Epub 2020 Oct 23.
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Altered large-scale functional brain organization in posttraumatic stress disorder: A comprehensive review of univariate and network-level neurocircuitry models of PTSD.创伤后应激障碍中大脑功能的大规模改变:创伤后应激障碍神经回路模型的单变量和网络水平的综合综述。
Neuroimage Clin. 2020;27:102319. doi: 10.1016/j.nicl.2020.102319. Epub 2020 Jun 23.
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Increased power by harmonizing structural MRI site differences with the ComBat batch adjustment method in ENIGMA.利用 ENIGMA 中的 ComBat 批量调整方法协调结构 MRI 站点差异来提高效能。
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Evaluating the impact of trauma and PTSD on epigenetic prediction of lifespan and neural integrity.评估创伤和创伤后应激障碍对寿命和神经完整性的表观遗传预测的影响。
Neuropsychopharmacology. 2020 Sep;45(10):1609-1616. doi: 10.1038/s41386-020-0700-5. Epub 2020 May 7.
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Inflammation, reward circuitry and symptoms of anhedonia and PTSD in trauma-exposed women.创伤后暴露女性的炎症、奖励回路和快感缺失及创伤后应激障碍症状。
Soc Cogn Affect Neurosci. 2020 Nov 10;15(10):1046-1055. doi: 10.1093/scan/nsz100.
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Diminished responses to bodily threat and blunted interoception in suicide attempters.自杀未遂者对身体威胁的反应减弱及内感受迟钝。
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Effects of stress on the structure and function of the medial prefrontal cortex: Insights from animal models.应激对前额皮质内侧结构和功能的影响:动物模型的研究进展。
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创伤后应激障碍中皮质结构连接组的重塑:ENIGMA-PGC创伤后应激障碍联盟的结果

Remodeling of the Cortical Structural Connectome in Posttraumatic Stress Disorder: Results From the ENIGMA-PGC Posttraumatic Stress Disorder Consortium.

作者信息

Sun Delin, Rakesh Gopalkumar, Clarke-Rubright Emily K, Haswell Courtney C, Logue Mark W, O'Leary Erin N, Cotton Andrew S, Xie Hong, Dennis Emily L, Jahanshad Neda, Salminen Lauren E, Thomopoulos Sophia I, Rashid Faisal M, Ching Christopher R K, Koch Saskia B J, Frijling Jessie L, Nawijn Laura, van Zuiden Mirjam, Zhu Xi, Suarez-Jimenez Benjamin, Sierk Anika, Walter Henrik, Manthey Antje, Stevens Jennifer S, Fani Negar, van Rooij Sanne J H, Stein Murray B, Bomyea Jessica, Koerte Inga, Choi Kyle, van der Werff Steven J A, Vermeiren Robert R J M, Herzog Julia I, Lebois Lauren A M, Baker Justin T, Ressler Kerry J, Olson Elizabeth A, Straube Thomas, Korgaonkar Mayuresh S, Andrew Elpiniki, Zhu Ye, Li Gen, Ipser Jonathan, Hudson Anna R, Peverill Matthew, Sambrook Kelly, Gordon Evan, Baugh Lee A, Forster Gina, Simons Raluca M, Simons Jeffrey S, Magnotta Vincent A, Maron-Katz Adi, du Plessis Stefan, Disner Seth G, Davenport Nicholas D, Grupe Dan, Nitschke Jack B, deRoon-Cassini Terri A, Fitzgerald Jacklynn, Krystal John H, Levy Ifat, Olff Miranda, Veltman Dick J, Wang Li, Neria Yuval, De Bellis Michael D, Jovanovic Tanja, Daniels Judith K, Shenton Martha E, van de Wee Nic J A, Schmahl Christian, Kaufman Milissa L, Rosso Isabelle M, Sponheim Scott R, Hofmann David Bernd, Bryant Richard A, Fercho Kelene A, Stein Dan J, Mueller Sven C, Phan K Luan, McLaughlin Katie A, Davidson Richard J, Larson Christine, May Geoffrey, Nelson Steven M, Abdallah Chadi G, Gomaa Hassaan, Etkin Amit, Seedat Soraya, Harpaz-Rotem Ilan, Liberzon Israel, Wang Xin, Thompson Paul M, Morey Rajendra A

机构信息

Brain Imaging and Analysis Center, Duke University, Durham, North Carolina; Department of Veteran Affairs Mid-Atlantic Mental Illness Research, Education and Clinical Center, Durham, North Carolina.

National Center for PTSD, VA Boston Healthcare System, Boston, Massachusetts; Department of Psychiatry, Boston University School of Medicine, Boston, Massachusetts; Biomedical Genetics, Boston University School of Medicine, Boston, Massachusetts; Department of Biostatistics, Boston University School of Public Health, Boston, Massachusetts.

出版信息

Biol Psychiatry Cogn Neurosci Neuroimaging. 2022 Sep;7(9):935-948. doi: 10.1016/j.bpsc.2022.02.008. Epub 2022 Mar 15.

DOI:10.1016/j.bpsc.2022.02.008
PMID:35307575
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9835553/
Abstract

BACKGROUND

Posttraumatic stress disorder (PTSD) is accompanied by disrupted cortical neuroanatomy. We investigated alteration in covariance of structural networks associated with PTSD in regions that demonstrate the case-control differences in cortical thickness (CT) and surface area (SA).

METHODS

Neuroimaging and clinical data were aggregated from 29 research sites in >1300 PTSD cases and >2000 trauma-exposed control subjects (ages 6.2-85.2 years) by the ENIGMA-PGC (Enhancing Neuro Imaging Genetics through Meta Analysis-Psychiatric Genomics Consortium) PTSD working group. Cortical regions in the network were rank ordered by the effect size of PTSD-related cortical differences in CT and SA. The top-n (n = 2-148) regions with the largest effect size for PTSD > non-PTSD formed hypertrophic networks, the largest effect size for PTSD < non-PTSD formed atrophic networks, and the smallest effect size of between-group differences formed stable networks. The mean structural covariance (SC) of a given n-region network was the average of all positive pairwise correlations and was compared with the mean SC of 5000 randomly generated n-region networks.

RESULTS

Patients with PTSD, relative to non-PTSD control subjects, exhibited lower mean SC in CT-based and SA-based atrophic networks. Comorbid depression, sex, and age modulated covariance differences of PTSD-related structural networks.

CONCLUSIONS

Covariance of structural networks based on CT and cortical SA are affected by PTSD and further modulated by comorbid depression, sex, and age. The SC networks that are perturbed in PTSD comport with converging evidence from resting-state functional connectivity networks and networks affected by inflammatory processes and stress hormones in PTSD.

摘要

背景

创伤后应激障碍(PTSD)伴有皮质神经解剖结构紊乱。我们研究了与PTSD相关的结构网络协方差在皮质厚度(CT)和表面积(SA)存在病例对照差异的区域中的变化。

方法

通过ENIGMA-PGC(通过荟萃分析增强神经影像遗传学-精神基因组学联盟)PTSD工作组,汇总了来自29个研究地点的>1300例PTSD病例和>2000名有创伤暴露经历的对照受试者(年龄6.2-85.2岁)的神经影像和临床数据。根据PTSD相关皮质差异在CT和SA中的效应大小,对网络中的皮质区域进行排序。PTSD>非PTSD效应大小最大的前n个(n = 2-148)区域形成肥厚网络,PTSD<非PTSD效应大小最大的区域形成萎缩网络,组间差异效应大小最小的区域形成稳定网络。给定n区域网络的平均结构协方差(SC)是所有正成对相关性的平均值,并与5000个随机生成的n区域网络的平均SC进行比较。

结果

与非PTSD对照受试者相比,PTSD患者在基于CT和基于SA的萎缩网络中表现出较低的平均SC。共病抑郁、性别和年龄调节了PTSD相关结构网络的协方差差异。

结论

基于CT和皮质SA的结构网络协方差受PTSD影响,并进一步受到共病抑郁、性别和年龄的调节。PTSD中受到干扰的SC网络与来自静息态功能连接网络以及受PTSD中炎症过程和应激激素影响的网络的汇聚证据一致。