Chu Xiaomeng, Ye Jing, Wen Yan, Li Ping, Cheng Bolun, Cheng Shiqiang, Zhang Lu, Liu Li, Qi Xin, Ma Mei, Liang Chujun, Kafle Om Prakash, Wu Cuiyan, Wang Sen, Wang Xi, Ning Yujie, Zhang Feng
Key Laboratory of Trace Elements and Endemic Diseases, National Health and Family Planning Commission, School of Public Health, Health Science Center, Xi'an Jiaotong University, Xi'an, China.
Key Laboratory of Trace Elements and Endemic Diseases, National Health and Family Planning Commission, School of Public Health, Health Science Center, Xi'an Jiaotong University, Xi'an, China.
J Psychiatr Res. 2021 Aug;140:149-158. doi: 10.1016/j.jpsychires.2021.05.067. Epub 2021 May 27.
Maternal smoking during pregnancy (MSDP) has been reported to be associated with increased anxiety and depression behaviors in offspring. However, there is still scant evidence to support the link between MSDP and anxiety/depression.
Using the subjects from the UK Biobank cohort (n = 371,903-432,881). Logistic regression analyses were first conducted to test the correlation between MSDP and anxiety/depression in offspring. Second, genome-wide gene-environment interaction study (GWGEIS) analyses were conducted by PLINK, using MSDP as environmental factor. Genetic correlation analysis of anxiety/depression and smoking was conducted by the LDSC software using the published genome-wide association study (GWAS) summary data of four smoking traits (n = 337,334-1,232,091), anxiety (n = 31,880) and depression (n = 490,359). Finally, pathway enrichment analysis was carried out to detect the pathway involved in the development of offspring anxiety caused by the interaction of MSDP × SNPs.
Observational analyses showed that anxiety and depression status in offspring were significantly associated with MSDP (all p < 0.0001). Further GWEGI analyses observed significant MSDP-gene interaction effects at UNC80 gene for anxiety (p = 9.09 × 10). LDSC did not detect significant genetic correlation between anxiety and smoking traits. Pathway analysis identified 19 significant pathways for anxiety, such as MANALO_HYPOXIA_UP (FDR = 5.50 × 10), REACTOME_ADHERENS_JUNCTIONS_INTERACTIONS (FDR = 0.0304) and ONDER_CDH1_TARGETS_2_UP (FDR = 0.0371).
Our study results suggested the important impact of MDSP on the risk of anxiety in offspring, partly attributing to environment-gene interactions effects.
据报道,孕期母亲吸烟(MSDP)与后代焦虑和抑郁行为增加有关。然而,仍缺乏足够证据支持MSDP与焦虑/抑郁之间的联系。
使用英国生物银行队列中的受试者(n = 371,903 - 432,881)。首先进行逻辑回归分析,以检验MSDP与后代焦虑/抑郁之间的相关性。其次,使用PLINK进行全基因组基因 - 环境相互作用研究(GWGEIS)分析,将MSDP作为环境因素。使用LDSC软件,利用已发表的四种吸烟性状(n = 337,334 - 1,232,091)、焦虑(n = 31,880)和抑郁(n = 490,359)的全基因组关联研究(GWAS)汇总数据,进行焦虑/抑郁与吸烟的遗传相关性分析。最后,进行通路富集分析,以检测MSDP×单核苷酸多态性(SNP)相互作用导致后代焦虑发生所涉及的通路。
观察性分析表明,后代的焦虑和抑郁状态与MSDP显著相关(所有p < 0.0001)。进一步的GWEGI分析在UNC80基因处观察到MSDP与基因的显著相互作用效应与焦虑有关(p = 9.09×10)。LDSC未检测到焦虑与吸烟性状之间的显著遗传相关性。通路分析确定了19条与焦虑相关的显著通路,如MANALO_HYPOXIA_UP(错误发现率[FDR] = 5.50×10)、REACTOME_ADHERENS_JUNCTIONS_INTERACTIONS(FDR = 0.0304)和ONDER_CDH1_TARGETS_2_UP(FDR = 0.0371)。
我们的研究结果表明,MSDP对后代焦虑风险有重要影响,部分归因于环境 - 基因相互作用效应。