Department of Radiology, Xijing Hospital, Fourth Military Medical University, Xi'an, Shaanxi, China.
School of Medical Psychology, Fourth Military Medical University, Xi'an, Shaanxi, China.
Sci Rep. 2017 Nov 23;7(1):16201. doi: 10.1038/s41598-017-14343-7.
Neural substrates behind schizophrenia (SZ) and its heritability mediated by brain function are largely unknown. Cerebral blood flow (CBF), as a biomarker of activation in the brain, reflects the neuronal metabolism, and is promisingly used to detect cerebral alteration thereby shedding light on the features of individuals at high genetic risk. We performed a cross-sectional functional magnetic resonance imaging (MRI) study enrolling 45 first-episode drug-naïve patients with SZ, 32 unaffected first-degree relatives of these patients, and 51 healthy controls (HCs). We examined CBF, CBF connectivity, and CBF topological properties. SZ patients showed increased CBF in the left medial superior frontal gyrus and right precuneus compared with HCs, and decreased CBF in the left middle temporal gyrus compared with their relatives. Furthermore, unaffected relatives revealed higher level of CBF pronounced in regions within default mode network (DMN). Both SZ patients and their relatives exhibited dysconnectivity patterns. Notably, as for the network properties, unaffected relatives were with an intermediate level between SZ patients and HCs in the local efficiency and global efficiency. Our findings demonstrate the aberrant CBF of areas within DMN and the CBF connectivity pattern might be a familial feature in the brain of first-episode SZ patients and their relatives.
精神分裂症(SZ)背后的神经基础及其受大脑功能介导的遗传性在很大程度上是未知的。脑血流(CBF)作为大脑激活的生物标志物,反映了神经元代谢,有望用于检测大脑的改变,从而揭示高遗传风险个体的特征。我们进行了一项横断面功能磁共振成像(MRI)研究,纳入了 45 名首发、未经药物治疗的 SZ 患者、32 名这些患者的无病一级亲属和 51 名健康对照(HCs)。我们检查了 CBF、CBF 连通性和 CBF 拓扑性质。与 HCs 相比,SZ 患者的左侧额上回和右侧楔前叶的 CBF 增加,左侧颞中回的 CBF 减少。此外,未受影响的亲属在默认模式网络(DMN)内的区域显示出更高水平的 CBF。SZ 患者和他们的亲属都表现出连通性模式的异常。值得注意的是,就网络特性而言,未受影响的亲属在局部效率和全局效率方面处于 SZ 患者和 HCs 之间的中间水平。我们的发现表明,DMN 内区域的异常 CBF 和 CBF 连通性模式可能是首发 SZ 患者及其亲属大脑中的家族特征。