Department of Psychiatry, Cheng-Hsin General Hospital, Taipei, Taiwan, ROC.
Department of Psychiatry, Taipei Veterans General Hospital, Taipei, Taiwan, ROC.
J Chin Med Assoc. 2022 Feb 1;85(2):139-144. doi: 10.1097/JCMA.0000000000000675.
Psychiatric disorders in first-degree relatives (FDRs) often differ from the index patient's diagnosis, suggesting that there is genetic contribution to psychiatric disorders in which related cases do not all map to the same diagnosis as the index case. Our aim is to look for psychiatric comorbidities across major mental illnesses using three approaches, genetics, clinical diagnosis, and brain imaging to address common associations and pathology among mental illnesses. Genome-wide association studies from the Psychiatric Genomics Consortium showed single gene polymorphisms are common across 5 major psychiatric disorders, including schizophrenia (SZ), bipolar disorder (BD), major depressive disorder (MDD), autism spectrum disorder (ASD), and attention deficit hyperactivity disorder (ADHD). Clinically, results of Taiwan's nationwide population studies showed that other major psychiatric disorders were more likely to coaggregate in families with an index case of an individual with a psychiatric disorder, compared to control families. Finally, resting functional connectivity (FC) magnetic resonance imaging (MRI) and whole-brain connectomic analysis of SZ, BD I, BD II, MDD, and healthy controls revealed that the four groups of patients shared similar patterns of abnormal neural substrate in the brain that differed from controls. In conclusion, using big data from genetics, administrative health claims, and brain imaging, we identified concordance, indicating dimensional coherence of genetic heritability, clinical mutual associations, and common neurobiological substrates across major psychiatric disorders. These results will challenge the current diagnostic classification system and possibly move psychiatry beyond descriptive syndromes towards a nosology informed by disease cause.
一级亲属(FDRs)中的精神障碍通常与索引患者的诊断不同,这表明精神障碍存在遗传贡献,相关病例并不都与索引病例的同一诊断相符。我们的目的是使用三种方法(遗传学、临床诊断和脑成像)寻找主要精神疾病之间的精神共病,以解决精神疾病之间的常见关联和病理学。来自精神疾病基因组学联盟的全基因组关联研究表明,单一基因多态性在 5 种主要精神障碍中很常见,包括精神分裂症(SZ)、双相情感障碍(BD)、重度抑郁症(MDD)、自闭症谱系障碍(ASD)和注意缺陷多动障碍(ADHD)。临床上,台湾全国性人群研究的结果表明,与对照家庭相比,精神障碍索引病例的家庭中,其他主要精神障碍更有可能共同聚集。最后,对 SZ、BD I、BD II、MDD 和健康对照组的静息功能连通性(FC)磁共振成像(MRI)和全脑连接组学分析表明,这四组患者的大脑中存在相似的异常神经基质模式,与对照组不同。总之,我们利用来自遗传学、行政健康索赔和大脑成像的大数据,确定了一致性,表明遗传遗传性、临床相互关联和主要精神障碍中常见神经生物学基质的维度连贯性。这些结果将挑战当前的诊断分类系统,并可能使精神病学从描述性综合征发展到基于疾病原因的分类学。