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