Melbourne Neuropsychiatry Centre, Department of Psychiatry, The University of Melbourne and Melbourne Health, Carlton South, VIC, Australia.
Department of Psychiatry, Brigham and Women's Hospital, Harvard Medical School, Boston, MA.
Schizophr Bull. 2021 Mar 16;47(2):542-551. doi: 10.1093/schbul/sbaa134.
Clarifying the role of neuroinflammation in schizophrenia is subject to its detection in the living brain. Free-water (FW) imaging is an in vivo diffusion-weighted magnetic resonance imaging (dMRI) technique that measures water molecules freely diffusing in the brain and is hypothesized to detect inflammatory processes. Here, we aimed to establish a link between peripheral markers of inflammation and FW in brain white matter.
All data were obtained from the Australian Schizophrenia Research Bank (ASRB) across 5 Australian states and territories. We first tested for the presence of peripheral cytokine deregulation in schizophrenia, using a large sample (N = 1143) comprising the ASRB. We next determined the extent to which individual variation in 8 circulating pro-/anti-inflammatory cytokines related to FW in brain white matter, imaged in a subset (n = 308) of patients and controls.
Patients with schizophrenia showed reduced interleukin-2 (IL-2) (t = -3.56, P = .0004) and IL-12(p70) (t = -2.84, P = .005) and increased IL-6 (t = 3.56, P = .0004), IL-8 (t = 3.8, P = .0002), and TNFα (t = 4.30, P < .0001). Higher proinflammatory signaling of IL-6 (t = 3.4, P = .0007) and TNFα (t = 2.7, P = .0007) was associated with higher FW levels in white matter. The reciprocal increases in serum cytokines and FW were spatially widespread in patients encompassing most major fibers; conversely, in controls, the relationship was confined to the anterior corpus callosum and thalamic radiations. No relationships were observed with alternative dMRI measures, including the fractional anisotropy and tissue-related FA.
We report widespread deregulation of cytokines in schizophrenia and identify inflammation as a putative mechanism underlying increases in brain FW levels.
阐明精神分裂症中的神经炎症作用,取决于在活体大脑中对其进行检测。游离水(FW)成像是一种活体弥散磁共振成像(dMRI)技术,可测量大脑中自由扩散的水分子,并假设可检测炎症过程。在此,我们旨在建立外周炎症标志物与脑白质中 FW 之间的联系。
所有数据均来自澳大利亚精神分裂症研究银行(ASRB),涵盖澳大利亚 5 个州和地区。我们首先使用包含 ASRB 的大样本(N = 1143)测试精神分裂症中是否存在外周细胞因子失调。接下来,我们确定患者和对照组亚组(n = 308)中,个体间 8 种循环促炎/抗炎细胞因子的差异与脑白质中 FW 的关系。
精神分裂症患者表现出白细胞介素-2(IL-2)(t = -3.56,P =.0004)和白细胞介素-12(p70)(t = -2.84,P =.005)降低,IL-6(t = 3.56,P =.0004),IL-8(t = 3.8,P =.0002)和 TNFα(t = 4.30,P <.0001)升高。IL-6(t = 3.4,P =.0007)和 TNFα(t = 2.7,P =.0007)的促炎信号升高与脑白质中更高的 FW 水平相关。在患者中,血清细胞因子和 FW 的递增在空间上广泛分布,包含大多数主要纤维;相反,在对照组中,这种关系仅限于胼胝体前部和丘脑辐射。未观察到与替代 dMRI 测量相关的关系,包括分数各向异性和组织相关 FA。
我们报告了精神分裂症中细胞因子的广泛失调,并确定炎症是导致脑 FW 水平升高的潜在机制。