Hayes Jasmeet P, Logue Mark W, Reagan Andrew, Salat David, Wolf Erika J, Sadeh Naomi, Spielberg Jeffrey M, Sperbeck Emily, Hayes Scott M, McGlinchey Regina E, Milberg William P, Verfaellie Mieke, Stone Annjanette, Schichman Steven A, Miller Mark W
From the National Center for PTSD, VA Boston Healthcare System, Boston, Mass. (Hayes, Reagan, Wolf, Sadeh, Miller); the Department of Psychiatry, Boston University School of Medicine, Boston, Mass. (Hayes, Wolf, Sadeh, Spielberg, Sperbeck, Hayes, Verfaellie, Miller); the Neuroimaging Research for Veterans Center, VA Boston Healthcare System, Boston, Mass. (Hayes, Salat, Spielberg, Hayes); the Research Service, VA Boston Healthcare System, Boston, Mass. (Logue); the Biomedical Genetics, Boston University School of Medicine, Boston, Mass. (Logue); the Department of Biostatistics, Boston University School of Public Health, Boston, Mass. (Logue); the Memory Disorders Research Center, VA Boston Healthcare System, Boston, Mass. (Hayes, Verfaellie); the Athinoula A. Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard University, Boston, Mass. (Salat); the Harvard Medical School, Harvard University, Boston, Mass. (Salat); the Translational Research Center for TBI and Stress Disorders and Geriatric Research, Educational and Clinical Center, VA Boston Healthcare System, Boston, Mass. (McGlinchey, Milberg); the Department of Psychiatry, Harvard Medical School, Boston, Mass. (McGlinchey, Milberg); the Pharmacogenomics Analysis Laboratory, Research Service, Central Arkansas Veterans Healthcare System, USA (Stone, Schichman).
J Psychiatry Neurosci. 2017 Mar;42(2):95-102. doi: 10.1503/jpn.150339.
Memory-based alterations are among the hallmark symptoms of posttraumatic stress disorder (PTSD) and may be associated with the integrity of the hippocampus. However, neuroimaging studies of hippocampal volume in individuals with PTSD have yielded inconsistent results, raising the possibility that various moderators, such as genetic factors, may influence this association. We examined whether the catechol-O-methyltransferase (COMT) Val158Met polymorphism, which has previously been shown to be associated with hippocampal volume in healthy individuals, moderates the association between PTSD and hippocampal volume.
Recent war veterans underwent structural MRI on a 3 T scanner. We extracted volumes of the right and left hippocampus using FreeSurfer and adjusted them for individual differences in intracranial volume. We assessed PTSD severity using the Clinician-Administered PTSD Scale. Hierarchical linear regression was used to model the genotype (Val158Met polymorphism) × PTSD severity interaction and its association with hippocampal volume.
We included 146 white, non-Hispanic recent war veterans (90% male, 53% with diagnosed PTSD) in our analyses. A significant genotype × PTSD symptom severity interaction emerged such that individuals with greater current PTSD symptom severity who were homozygous for the Val allele showed significant reductions in left hippocampal volume.
The direction of proposed effects is unknown, thus precluding definitive assessment of whether differences in hippocampal volume reflect a consequence of PTSD, a pre-existing characteristic, or both.
Our findings suggest that the COMT polymorphism moderates the association between PTSD and hippocampal volume. These results highlight the role that the dopaminergic system has in brain structure and suggest a possible mechanism for memory disturbance in individuals with PTSD.
基于记忆的改变是创伤后应激障碍(PTSD)的标志性症状之一,可能与海马体的完整性有关。然而,对PTSD患者海马体体积的神经影像学研究结果并不一致,这增加了各种调节因素(如遗传因素)可能影响这种关联的可能性。我们研究了儿茶酚-O-甲基转移酶(COMT)Val158Met多态性是否会调节PTSD与海马体体积之间的关联,此前已证明该多态性与健康个体的海马体体积有关。
近期退伍军人在3T扫描仪上接受结构MRI检查。我们使用FreeSurfer提取左右海马体的体积,并针对颅内体积的个体差异进行调整。我们使用临床医生管理的PTSD量表评估PTSD严重程度。采用分层线性回归对基因型(Val158Met多态性)×PTSD严重程度相互作用及其与海马体体积的关联进行建模。
我们的分析纳入了146名非西班牙裔白人近期退伍军人(90%为男性,53%被诊断为PTSD)。出现了显著的基因型×PTSD症状严重程度相互作用,即当前PTSD症状严重程度较高且Val等位基因纯合的个体左海马体体积显著减小。
所提出效应的方向未知,因此无法确定海马体体积差异是否反映了PTSD的后果、预先存在的特征或两者兼而有之。
我们的研究结果表明,COMT多态性调节了PTSD与海马体体积之间的关联。这些结果突出了多巴胺能系统在脑结构中的作用,并为PTSD患者的记忆障碍提出了一种可能的机制。