Attwells Sophia, Setiawan Elaine, Wilson Alan A, Rusjan Pablo M, Mizrahi Romina, Miler Laura, Xu Cynthia, Richter Margaret Anne, Kahn Alan, Kish Stephen J, Houle Sylvain, Ravindran Lakshmi, Meyer Jeffrey H
Research Imaging Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada2Department of Pharmacology and Toxicology, University of Toronto, Toronto, Ontario, Canada.
Research Imaging Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
JAMA Psychiatry. 2017 Aug 1;74(8):833-840. doi: 10.1001/jamapsychiatry.2017.1567.
For a small percentage of obsessive-compulsive disorder (OCD) cases exhibiting additional neuropsychiatric symptoms, it was proposed that neuroinflammation occurs in the basal ganglia as an autoimmune response to infections. However, it is possible that elevated neuroinflammation, inducible by a diverse range of mechanisms, is important throughout the cortico-striato-thalamo-cortical circuit of OCD. Identifying brain inflammation is possible with the recent advance in positron emission tomography (PET) radioligands that bind to the translocator protein (TSPO). Translocator protein density increases when microglia are activated during neuroinflammation and the TSPO distribution volume (VT) is an index of TSPO density.
To determine whether TSPO VT is elevated in the dorsal caudate, orbitofrontal cortex, thalamus, ventral striatum, dorsal putamen, and anterior cingulate cortex in OCD.
DESIGN, SETTING, AND PARTICIPANTS: This case-control study was conducted at a tertiary care psychiatric hospital from May 1, 2010, to November 30, 2016. Participants with OCD (n = 20) and age-matched healthy control individuals (n = 20) underwent a fluorine F 18-labeled N-(2-(2-fluoroethoxy)benzyl)-N-(4-phenoxypyridin-3-yl)acetamide PET scan. It is a high-quality second-generation TSPO-binding PET radiotracer. All participants were drug and medication free, nonsmoking, and otherwise healthy.
The TSPO VT was measured in the dorsal caudate, orbitofrontal cortex, thalamus, ventral striatum, dorsal putamen, and anterior cingulate cortex. Compulsions were assessed with the Yale-Brown Obsessive Compulsive Scale.
In the OCD and healthy groups, the mean (SD) ages were 27.4 (7.1) years and 27.6 (6.6) years, respectively, and 11 (55%) and 8 (40%) were women, respectively. In OCD, TSPO VT was significantly elevated in these brain regions (mean, 32%; range, 31%-36% except anterior cingulate cortex, 24%; analysis of variance, effect of diagnosis: P < .001 to P = .004). Slightly lower elevations in TSPO VT (22%-29%) were present in other gray matter regions. The Yale-Brown Obsessive Compulsive Scale measure of distress associated with preventing compulsive behaviors significantly correlated with TSPO VT in the orbitofrontal cortex (uncorrected Pearson correlation r = 0.62; P = .005).
To our knowledge, this is the first study demonstrating inflammation within the neurocircuitry of OCD. The regional distribution of elevated TSPO VT argues that the autoimmune/neuroinflammatory theories of OCD should extend beyond the basal ganglia to include the cortico-striato-thalamo-cortical circuit. Immunomodulatory therapies should be investigated in adult OCD, rather than solely childhood OCD, particularly in cases with prominent distress when preventing compulsions.
对于一小部分表现出额外神经精神症状的强迫症(OCD)病例,有人提出基底节区会发生神经炎症,这是对感染的一种自身免疫反应。然而,多种机制诱导的神经炎症水平升高,在强迫症的整个皮质 - 纹状体 - 丘脑 - 皮质回路中可能都很重要。随着正电子发射断层扫描(PET)放射性配体的最新进展,这些配体可与转位蛋白(TSPO)结合,从而有可能识别脑部炎症。当小胶质细胞在神经炎症过程中被激活时,转位蛋白密度会增加,而TSPO分布容积(VT)是TSPO密度的一个指标。
确定强迫症患者的背侧尾状核、眶额皮质、丘脑、腹侧纹状体、背侧壳核和前扣带回皮质中的TSPO VT是否升高。
设计、地点和参与者:这项病例对照研究于2010年5月1日至2016年11月30日在一家三级护理精神病医院进行。强迫症患者(n = 20)和年龄匹配的健康对照个体(n = 20)接受了氟F 18标记的N - (2 - (2 - 氟乙氧基)苄基) - N - (4 - 苯氧基吡啶 - 3 - 基)乙酰胺PET扫描。这是一种高质量的第二代TSPO结合PET放射性示踪剂。所有参与者均未使用药物和其他药物,不吸烟,且在其他方面健康。
测量背侧尾状核、眶额皮质、丘脑、腹侧纹状体、背侧壳核和前扣带回皮质中的TSPO VT。使用耶鲁 - 布朗强迫症量表评估强迫行为。
在强迫症组和健康组中,平均(标准差)年龄分别为27.4(7.1)岁和27.6(6.6)岁,女性分别为11名(55%)和8名(40%)。在强迫症患者中,这些脑区的TSPO VT显著升高(平均为32%;范围为31% - 36%,前扣带回皮质除外,为24%;方差分析,诊断效应:P <.001至P = 0.004)。其他灰质区域的TSPO VT也有稍低程度的升高(22% - 29%)。耶鲁 - 布朗强迫症量表中与预防强迫行为相关的痛苦程度测量值与眶额皮质中的TSPO VT显著相关(未校正的皮尔逊相关系数r = 0.62;P = 0.005)。
据我们所知,这是第一项证明强迫症神经回路内存在炎症的研究。TSPO VT升高的区域分布表明,强迫症的自身免疫/神经炎症理论应扩展到基底节区之外,涵盖皮质 - 纹状体 - 丘脑 - 皮质回路。应在成年强迫症患者中研究免疫调节疗法,而不仅仅是儿童强迫症患者,特别是在预防强迫行为时伴有明显痛苦的病例中。