| Frontiers in Genetics | |
| Genetically predicted circulating levels of cytokines and the risk of depression: a bidirectional Mendelian-randomization study | |
| Genetics | |
| Shun-Xian Zhang1  Jinxin Zheng2  Shi-Yang Guan3  Meiti Wang4  Ying Cheng4  Guixiang Jin5  | |
| [1] Clinical Research Center, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, China;School of Global Health, Chinese Center for Tropical Diseases Research—Shanghai Jiao Tong University School of Medicine, Shanghai, China;Second Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China;Shanghai Mental Health Center, Shanghai Jiao Tong University School of Medicine, Shanghai, China;Shanghai Yangpu Mental Health Center, Shanghai, China; | |
| 关键词: major depressive disorder; inflammatory cytokine; Mendelian randomization; GWAS; IL-18; RANTES; IL-1beta; | |
| DOI : 10.3389/fgene.2023.1242614 | |
| received in 2023-06-19, accepted in 2023-07-24, 发布年份 2023 | |
| 来源: Frontiers | |
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【 摘 要 】
Objective: Inflammatory cytokines disturbance is the main result of immune dysregulation, which is widely described in major depressive disorder (MDD). However, the potential causal relationship between these two factors has not been discovered. Therefore, the purpose of this study was to investigate the causal relationship between inflammatory cytokines and MDD risk by using the two-sample Mendelian randomization (MR) analysis.Method: Two genetic instruments obtained from publicly available gene profile data were utilized for the analysis. We obtained the genetic variation data of 41 inflammatory cytokines from genome-wide association studies (GWAS) meta-analysis of 8293 individuals of Finnish descent. The MDD data, including 135,458 MDD cases and 344,901 controls, were obtained from the Psychiatric Genomics Consortium Database. For the Mendelian randomization (MR) estimation, several methods were employed, namely, MR-Egger regression, inverse-variance weighted (IVW), weighted median, and MR-Pleiotropy RESidual Sum and Outlier (MR-PRESSO) methods.Result: A causal relationship was identified between the genetically proxied levels of Interleukin (IL) −18, IL-1β, and Regulated upon activation normal T cell expressed and secreted (RANTES) and the risk of MDD (OR = 0.968, 95%CI = 0.938, 0.998, p = 0.036; OR = 0.875, 95%CI = 0.787, 0.971, p = 0.012; OR = 0.947, 95%CI = 0.902, 0.995, p = 0.03; respectively). However, our Mendelian randomization (MR) estimates provided no causality of MDD on inflammatory cytokines.Conclusion: Our study elucidates the connection between inflammatory cytokines and MDD by using MR analysis, thereby enhancing our comprehension of the potential mechanisms. By identifying these associations, our findings hold substantial implications for the development of more effective treatments aimed at improving patient outcomes. However, further investigation is required to fully comprehend the exact biological mechanisms involved.
【 授权许可】
Unknown
Copyright © 2023 Wang, Jin, Cheng, Guan, Zheng and Zhang.
【 预 览 】
| Files | Size | Format | View |
|---|---|---|---|
| RO202310105937819ZK.pdf | 1258KB |
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