Neurocognitive markers of childhood abuse in individuals with PTSD: Findings from the INTRuST Clinical Consortium.

Neurocognitive markers of childhood abuse in individuals with PTSD: Findings from the INTRuST Clinical Consortium.
复制标题

DOI:
10.1016/j.jpsychires.2019.11.012
复制
发表时间:
2020-02
影响因子:
4.8
通讯作者:
INTRuST consortium
INTRuST consortium
中科院分区:
医学2区
文献类型:
--
作者:
Bomyea J;Simmons AN;Shenton ME;Coleman MJ;Bouix S;Rathi Y;Pasternak O;Coimbra R;Shutter L;George MS;Grant G;Zafonte RD;McAllister TW;Stein MB;INTRuST consortium

文献摘要

参考文献

被引文献

相似文献

To date, few studies have evaluated the contribution of early life experiences to neurocognitive abnormalities observed in posttraumatic stress disorder (PTSD). Childhood maltreatment is common among individuals with PTSD and is thought to catalyze stress-related biobehavioral changes that might impact both brain structure and function in adulthood. The current study examined differences in brain morphology (brain volume, cortical thickness) and neuropsychological performance in individuals with PTSD characterized by low or high self-reported childhood maltreatment, compared with healthy comparison participants. Data were drawn from the INjury and TRaUmatic STress (INTRuST) Clinical Consortium imaging repository, which contains MRI and self-report data for individuals classified as PTSD positive (with and without a history of mild traumatic brain injury [mTBI]), individuals with mTBI only, and healthy comparison participants. The final sample included 36 individuals with PTSD without childhood maltreatment exposure (PTSD, n = 30 with mTBI), 31 individuals with PTSD and childhood maltreatment exposure (PTSD + M, n = 26 with mTBI), and 114 healthy comparison participants without history of childhood maltreatment exposure (HC). The PTSD + M and PTSD groups demonstrated cortical thinning in prefrontal and occipital regions, and poorer verbal memory and processing speed compared to the HC group. PTSD + M participants demonstrated cortical thinning in frontal and cingulate regions, and poorer executive functioning relative to the PTSD and HC groups. Thus, neurocognitive features varied between individuals with PTSD who did versus did not have exposure to childhood maltreatment, highlighting the need to assess developmental history of maltreatment when examining biomarkers in PTSD.
DOI: 10.1016/j.neuropharm.2011.02.008
发表时间: 2012-02
期刊: Neuropharmacology
影响因子: 4.7
作者:
Aupperle RL;Melrose AJ;Stein MB;Paulus MP
通讯作者: Paulus MP
DOI: 10.1016/s0145-2134(02)00541-0
发表时间: 2003-02-01
影响因子: 4.8
作者:
Bernstein, DP;Stein, JA;Zule, W
通讯作者: Zule, W
DOI: 10.1111/j.2517-6161.1995.tb02031.x
发表时间: 1995-01-01
影响因子: 5.8
作者:
BENJAMINI, Y;HOCHBERG, Y
通讯作者: HOCHBERG, Y
DOI: 10.1006/nimg.1998.0395
发表时间: 1999-02-01
期刊: NEUROIMAGE
影响因子: 5.7
作者:
Dale, AM;Fischl, B;Sereno, MI
通讯作者: Sereno, MI
DOI: 10.1016/j.biopsych.2011.10.021
发表时间: 2012-02-15
影响因子: 10.6
作者:
Dannlowski, Udo;Stuhrmann, Anja;Kugel, Harald
通讯作者: Kugel, Harald