Center for Addiction Medicine, Massachusetts General Hospital, Boston, MA, USA; Department of Psychiatry, Harvard Medical School, Boston, MA, USA.
Center for Addiction Medicine, Massachusetts General Hospital, Boston, MA, USA.
Psychiatry Res Neuroimaging. 2020 Jan 30;295:111017. doi: 10.1016/j.pscychresns.2019.111017. Epub 2019 Nov 14.
Marijuana (MJ) use and post-traumatic stress disorder (PTSD) have both been associated with abnormalities in brain white matter tracts, including the cingulum and the anterior thalamic radiations (ATR), which project from subcortical regions to frontal cortex. Studies have not assessed the integrity of these tracts in patients with comorbid PTSD and MJ use. To examine effects of PTSD and MJ use on brain structure, we performed diffusion tensor imaging scans on seventy-two trauma-exposed participants, categorized into four groups: those with PTSD who used MJ at least weekly (PTSD+MJ; n = 20), those with PTSD with no regular MJ use (PTSD; n = 19), trauma-exposed controls without PTSD who used MJ (TEC+MJ; n = 14) and trauma-exposed controls with no PTSD or MJ use (TEC; n = 19). White matter integrity was evaluated by calculating fractional anisotropy (FA). Results showed that while FA values in the right ATR and the cingulum differed across groups, there were no significant interactions between PTSD and MJ in any white matter tracts, indicating that MJ exposure neither normalizes nor worsens white matter abnormalities in those with PTSD. Further study is needed to evaluate the impact of MJ use on other neurobiological markers of PTSD.
大麻(MJ)使用和创伤后应激障碍(PTSD)都与脑白质束的异常有关,包括扣带束和前丘脑辐射(ATR),它们从前皮质投射到额叶皮质。研究尚未评估合并 PTSD 和 MJ 使用的患者这些束的完整性。为了研究 PTSD 和 MJ 使用对大脑结构的影响,我们对 72 名创伤暴露的参与者进行了弥散张量成像扫描,将他们分为四组:至少每周使用 MJ 的 PTSD 合并 MJ 组(PTSD+MJ;n=20)、没有定期 MJ 使用的 PTSD 组(PTSD;n=19)、没有 PTSD 或 MJ 使用的创伤暴露对照合并 MJ 组(TEC+MJ;n=14)和没有 PTSD 或 MJ 使用的创伤暴露对照合并 MJ 组(TEC;n=19)。通过计算分数各向异性(FA)来评估白质完整性。结果表明,尽管右侧 ATR 和扣带束的 FA 值在各组之间存在差异,但在任何白质束中 PTSD 和 MJ 之间均无显著相互作用,这表明 MJ 暴露既不会使 PTSD 患者的白质异常正常化,也不会使其恶化。需要进一步研究以评估 MJ 使用对 PTSD 的其他神经生物学标志物的影响。