Smaller hippocampal CA1 subfield volume in posttraumatic stress disorder

被引:53
作者
Chen, Lyon W. [1 ,2 ,3 ]
Sun, Delin [1 ,2 ]
Davis, Sarah L. [1 ,2 ]
Haswell, Courtney C. [1 ,2 ]
Dennis, Emily L. [5 ]
Swanson, Chelsea A. [1 ,2 ]
Whelan, Christopher D. [5 ]
Gutman, Boris [5 ]
Jahanshad, Neda [5 ]
Iglesias, Juan Eugenio [6 ]
Thompson, Paul [5 ]
Wagner, H. Ryan [1 ,4 ]
Saemann, Philipp [7 ]
LaBar, Kevin S. [1 ,2 ,4 ]
Morey, Rajendra A. [1 ,2 ,4 ]
机构
[1] Durham VA Med Ctr, Midatlantic Mental Illness Res & Clin Ctr, Durham, NC USA
[2] Duke UNC Brain Imaging & Anal Ctr, 40 Duke Med Circle,Room 414, Durham, NC 27710 USA
[3] Duke Univ, Dept Biomed Engn, Durham, NC 27706 USA
[4] Duke Univ, Dept Psychiat, Durham, NC 27706 USA
[5] USC, Keck Sch Med, Imaging Genet Ctr, Los Angeles, CA USA
[6] UCL, Translat Imaging Grp, London, England
[7] Max Planck Inst Psychiat, Munich, Germany
基金
欧盟地平线“2020”;
关键词
IN-VIVO MRI; DENTATE GYRUS; PATTERN SEPARATION; SEXUAL-ABUSE; MEMORY; FEAR; EXTINCTION; AMYGDALA; PTSD; SEGMENTATION;
D O I
10.1002/da.22833
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Background Methods Smaller hippocampal volume in patients with posttraumatic stress disorder (PTSD) represents the most consistently reported structural alteration in the brain. Subfields of the hippocampus play distinct roles in encoding and processing of memories, which are disrupted in PTSD. We examined PTSD-associated alterations in 12 hippocampal subfields in relation to global hippocampal shape, and clinical features. Case-control cross-sectional studies of U.S. military veterans (n = 282) from the Iraq and Afghanistan era were grouped into PTSD (n = 142) and trauma-exposed controls (n = 140). Participants underwent clinical evaluation for PTSD and associated clinical parameters followed by MRI at 3 T. Segmentation with FreeSurfer v6.0 produced hippocampal subfield volumes for the left and right CA1, CA3, CA4, DG, fimbria, fissure, hippocampus-amygdala transition area, molecular layer, parasubiculum, presubiculum, subiculum, and tail, as well as hippocampal meshes. Covariates included age, gender, trauma exposure, alcohol use, depressive symptoms, antidepressant medication use, total hippocampal volume, and MRI scanner model. Results Conclusions Significantly lower subfield volumes were associated with PTSD in left CA1 (P = 0.01; d = 0.21; uncorrected), CA3 (P = 0.04; d = 0.08; uncorrected), and right CA3 (P = 0.02; d = 0.07; uncorrected) only if ipsilateral whole hippocampal volume was included as a covariate. A trend level association of L-CA1 with PTSD (F-4,F- 221 = 3.32, P = 0.07) is present and the other subfield findings are nonsignificant if ipsilateral whole hippocampal volume is not included as a covariate. PTSD-associated differences in global hippocampal shape were nonsignificant. The present finding of smaller hippocampal CA1 in PTSD is consistent with model systems in rodents that exhibit increased anxiety-like behavior from repeated exposure to acute stress. Behavioral correlations with hippocampal subfield volume differences in PTSD will elucidate their relevance to PTSD, particularly behaviors of associative fear learning, extinction training, and formation of false memories.
引用
收藏
页码:1018 / 1029
页数:12
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