Cattarinussi Giulia, Kubera Katharina M, Hirjak Dusan, Wolf Robert C, Sambataro Fabio
Department of Neuroscience, Università degli studi di Padova, Padova, Italy; Padova Neuroscience Center, Università degli studi di Padova, Padova, Italy.
Department of General Psychiatry, Center for Psychosocial Medicine, Heidelberg University, Heidelberg, Germany.
Biol Psychiatry. 2022 Sep 1;92(5):375-384. doi: 10.1016/j.biopsych.2022.02.960. Epub 2022 Mar 4.
Clinical features and genetics overlap in schizophrenia (SCZ) and bipolar disorder (BD). Identifying brain alterations associated with genetic vulnerability for SCZ and BD could help to discover intermediate phenotypes, quantifiable biological traits with greater prevalence in unaffected relatives (RELs), and early recognition biomarkers in ultrahigh risk populations. However, a comprehensive meta-analysis of structural and functional magnetic resonance imaging (MRI) studies examining relatives of patients with SCZ and BD has not been performed yet.
We systematically searched PubMed, Scopus, and Web of Science for structural and functional MRI studies investigating relatives and healthy control subjects. A total of 230 eligible neuroimaging studies (6274 SCZ-RELs, 1900 BD-RELs, 10,789 healthy control subjects) were identified. We conducted coordinate-based activation likelihood estimation meta-analyses on 26 structural MRI and 81 functional MRI investigations, including stratification by task type. We also meta-analyzed regional and global volumetric changes. Finally, we performed a meta-analysis of all MRI studies combined.
Reduced thalamic volume was present in both SCZ and BD RELs. Moreover, SCZ-RELs showed alterations in corticostriatal-thalamic networks, spanning the dorsolateral prefrontal cortex and temporal regions, while BD-RELs showed altered thalamocortical and limbic regions, including the ventrolateral prefrontal, superior parietal, and medial temporal cortices, with frontoparietal alterations in RELs of BD type I.
Familiarity for SCZ and BD is associated with alterations in the thalamocortical circuits, which may be the expression of the shared genetic mechanism underlying both disorders. Furthermore, the involvement of different prefrontocortical and temporal nodes may be associated with a differential symptom expression in the two disorders.
精神分裂症(SCZ)和双相情感障碍(BD)在临床特征和遗传学方面存在重叠。识别与SCZ和BD遗传易感性相关的脑结构改变,有助于发现中间表型,即在未患病亲属(RELs)中更普遍的可量化生物学特征,以及超高风险人群中的早期识别生物标志物。然而,尚未对检查SCZ和BD患者亲属的结构和功能磁共振成像(MRI)研究进行全面的荟萃分析。
我们系统检索了PubMed、Scopus和Web of Science数据库,查找研究亲属和健康对照受试者的结构和功能MRI研究。共识别出230项符合条件的神经影像学研究(6274名SCZ亲属、1900名BD亲属、10789名健康对照受试者)。我们对26项结构MRI和81项功能MRI研究进行了基于坐标的激活可能性估计荟萃分析,包括按任务类型分层。我们还对区域和整体体积变化进行了荟萃分析。最后,我们对所有MRI研究进行了综合荟萃分析。
SCZ和BD亲属均存在丘脑体积减小。此外,SCZ亲属的皮质纹状体 - 丘脑网络出现改变,涉及背外侧前额叶皮质和颞叶区域,而BD亲属的丘脑皮质和边缘区域出现改变,包括腹外侧前额叶、顶上叶和内侧颞叶皮质,I型BD亲属的额顶叶有改变。
SCZ和BD的家族易感性与丘脑皮质回路的改变有关,这可能是两种疾病共同遗传机制的表现。此外,不同前额叶皮质和颞叶节点的参与可能与两种疾病的不同症状表现有关。