Zhuo Chuanjun, Zhang Qiuyu, Wang Lina, Ma Xiaoyan, Li Ranli, Ping Jing, Zhu Jingjing, Tian Hongjun, Jiang Deguo
Key Laboratory of Sensory Information Processing Abnormalities in Schizophrenia (SIPAS_Lab), Tianjin Fourth Center Hospital, Nankai University Affiliated Tianjin Fourth Center Hospital, Tianjin Medical University Affiliated Tianjin Fourth Center Hospital, No. 1 Zhongshan Road, Hebei District, Tianjin, 300140, China.
Key Laboratory of Multiple Organs Damage in Patients with Metal Disorder (MODMD_Lab), Tianjin Fourth Center Hospital, Nankai University Affiliated Tianjin Fourth Center Hospital, Tianjin Medical University Affiliated Tianjin Fourth Center Hospital, Tianjin, 300140, China.
CNS Drugs. 2024 Jan;38(1):33-44. doi: 10.1007/s40263-023-01057-w. Epub 2023 Dec 14.
Schizophrenia is a complex psychotic disorder with co-occurring conditions, including insulin resistance and type 2 diabetes (T2D). It is well established that T2D and its precursors (i.e., insulin resistance) are more prevalent in patients with schizophrenia who are treated with antipsychotics, as well as in antipsychotic-naïve patients experiencing their first episode of psychosis, compared with the general population. However, the mechanism(s) underlying the increased susceptibility, shared genetics, and possible cause-effect relationship between schizophrenia and T2D remain largely unknown. The objective of this narrative review was to synthesize important studies, including Mendelian randomization (MR) analyses that have integrated genome-wide association studies (GWAS), as well as results from in vitro models, in vivo models, and observational studies of patients with schizophrenia. Both GWAS and MR studies have found that schizophrenia and T2D/insulin resistance share genetic risk factors, and this may mediate a connection between peripheral or brain insulin resistance and T2D with cognition impairment and an increased risk of developing prediabetes and T2D in schizophrenia. Moreover, accumulating evidence supports a causal role for insulin resistance in schizophrenia and emphasizes the importance of a genetic basis for susceptibility to T2D in patients with schizophrenia before they receive psychotic treatment. The present findings and observations may have clinical implications for the development of better strategies to treat patients with schizophrenia, with both pharmacological (i.e., samidorphan, empagliflozin) and/or nonpharmacological (i.e., lifestyle changes) approaches. Additionally, this review may benefit the design of future studies by physicians and clinical investigators.
精神分裂症是一种复杂的精神障碍,常伴有胰岛素抵抗和2型糖尿病(T2D)等共病情况。与普通人群相比,接受抗精神病药物治疗的精神分裂症患者以及首次发作精神病的未使用过抗精神病药物的患者中,T2D及其前驱症状(即胰岛素抵抗)更为普遍,这一点已得到充分证实。然而,精神分裂症与T2D之间易感性增加、共享遗传学以及可能的因果关系背后的机制在很大程度上仍不清楚。本叙述性综述的目的是综合重要研究,包括整合了全基因组关联研究(GWAS)的孟德尔随机化(MR)分析,以及来自体外模型、体内模型和精神分裂症患者观察性研究的结果。GWAS和MR研究均发现,精神分裂症与T2D/胰岛素抵抗共享遗传风险因素,这可能介导外周或大脑胰岛素抵抗与T2D之间的联系,以及精神分裂症患者认知障碍和发生糖尿病前期及T2D风险增加的情况。此外,越来越多的证据支持胰岛素抵抗在精神分裂症中起因果作用,并强调了精神分裂症患者在接受精神病治疗前对T2D易感性的遗传基础的重要性。目前的研究结果和观察结果可能对制定更好的治疗精神分裂症患者的策略具有临床意义,包括药理学方法(即塞美度芬、恩格列净)和/或非药理学方法(即生活方式改变)。此外,本综述可能有助于医生和临床研究人员设计未来的研究。