Department of Ultrasound, Tianjin Medical University General Hospital Airport Hospital, Tianjin, China.
Department of Radiology and Tianjin Key Laboratory of Functional Imaging, Tianjin Medical University General Hospital, Tianjin, China.
CNS Neurosci Ther. 2024 Mar;30(3):e14430. doi: 10.1111/cns.14430. Epub 2023 Aug 31.
Previous studies have indicated that smoking is linked to an increased risk of developing schizophrenia, and that individuals with schizophrenia are more prone to engaging in antisocial behavior. However, the causal effects of smoking behaviors on antisocial behavior and the potential mediating role of schizophrenia remains largely unclear.
In the present study, using the summary data from genome wide association studies of smoking phenotypes (N = 323,386-805,431), schizophrenia (Ncases = 53,386, Ncontrols = 77,258), and antisocial behavior (N = 85,359), we assessed bidirectional causality between smoking phenotypes and schizophrenia by the Mendelian randomization (MR) approach. Using a two-step MR approach, we further examined whether causal effects of smoking phenotypes/schizophrenia on antisocial behavior were mediated by schizophrenia/smoking phenotypes.
The results showed that smoking initiation (SmkInit) and age of smoking initiation (AgeSmk) causally increase the risk of schizophrenia (SmkInit: OR = 2.06, 95% CI = 1.77-2.39, p = 4.36 × 10 ; AgeSmk: OR = 0.32, 95% CI = 0.16-0.62, p = 8.11 × 10 , Bonferroni corrected). However, there was no causal effect that liability to schizophrenia leads to smoking phenotypes. MR evidence also revealed causal influences of SmkInit and the amount smoked (CigDay) on antisocial behavior (SmkInit: OR = 1.28, 95% CI = 1.17-1.41, p = 2.53 × 10 ; CigDay: OR = 1.16, 95% CI = 1.06-1.27, p = 1.60 × 10 , Bonferroni corrected). Furthermore, the mediation analysis indicated that the relationship between SmkInit and antisocial behavior was partly mediated by schizophrenia (mediated proportion = 6.92%, 95% CI = 0.004-0.03, p = 9.66 × 10 ).
These results provide compelling evidence for taking smoking interventions as a prevention strategy for schizophrenia and its related antisocial behavior.
先前的研究表明,吸烟与精神分裂症风险增加有关,而精神分裂症患者更容易出现反社会行为。然而,吸烟行为对反社会行为的因果效应以及精神分裂症的潜在中介作用在很大程度上仍不清楚。
本研究使用来自吸烟表型(N=323386-805431)、精神分裂症(Ncases=53386,Ncontrols=77258)和反社会行为(N=85359)的全基因组关联研究汇总数据,采用孟德尔随机化(MR)方法评估吸烟表型与精神分裂症之间的双向因果关系。采用两步 MR 方法,进一步检验了吸烟表型/精神分裂症对反社会行为的因果效应是否由精神分裂症/吸烟表型介导。
结果显示,吸烟起始(SmkInit)和吸烟起始年龄(AgeSmk)会导致精神分裂症的发病风险升高(SmkInit:OR=2.06,95%CI=1.77-2.39,p=4.36×10;AgeSmk:OR=0.32,95%CI=0.16-0.62,p=8.11×10,Bonferroni 校正)。然而,并没有精神分裂症易感性导致吸烟表型的因果效应。MR 证据还揭示了 SmkInit 和吸烟量(CigDay)对反社会行为的因果影响(SmkInit:OR=1.28,95%CI=1.17-1.41,p=2.53×10;CigDay:OR=1.16,95%CI=1.06-1.27,p=1.60×10,Bonferroni 校正)。此外,中介分析表明,SmkInit 与反社会行为之间的关系部分由精神分裂症介导(中介比例=6.92%,95%CI=0.004-0.03,p=9.66×10)。
这些结果为将吸烟干预作为精神分裂症及其相关反社会行为的预防策略提供了有力证据。