{"title":"循环微量营养素水平与多种神经免疫疾病之间的潜在因果关系:遗传关联分析","authors":"Longhao Chen, Xuzhou Wu, Kaizheng Wang, Xingchen Zhou, Yika Mou, Zhen Liu, Zhifang Shen, Zhizhen Lv, Lijiang Lv","doi":"10.1002/brb3.70848","DOIUrl":null,"url":null,"abstract":"<div>\n \n \n <section>\n \n <h3> Background</h3>\n \n <p>Growing evidence suggests a close association between circulating micronutrient levels and neuroimmune diseases. Nevertheless, the causal relationship between them remains unclear. Furthermore, due to confounding factors, many micronutrients implicated in these diseases remain unidentified. This study aimed to determine the causal relationship between circulating micronutrients and neuroimmune diseases through genetic association analysis, and to analyze the regulatory role of circulating micronutrients in neuroimmune diseases.</p>\n </section>\n \n <section>\n \n <h3> Method</h3>\n \n <p>In this study, we used a two-sample mendelian randomization (MR) analysis to explore the causal relationship between micronutrients levels and neuroimmune disease. Fourteen micronutrients were screened from a published genome-wide association study (GWAS). Neuroimmune diseases include multiple sclerosis (MS), Guillain–Barre syndrome (GBS), acute disseminated encephalomyelitis (ADEM), acute poliomyelitis (AP), sequelae of poliomyelitis (SP), optic neuritis (ON), and myasthenia gravis (MG). Data on these seven neuroimmune diseases came from the FinnGen database and included 5523 cases and 2,860,006 controls. The inverse variance weighting (IVW) method was used as the main MR analysis method, and sensitivity analysis was performed to determine MR hypotheses.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>Through MR analysis and sensitivity testing, we identified significant causal relationships between four neuroimmune diseases and micronutrient levels. Specifically, MS was causally associated with magnesium levels (OR: 0.467, 95% CI: 0.269–0.809, <i>p</i> = 0.007), ADEM with folate levels (OR: 0.022, 95% CI: 0.001–0.957, <i>p</i> = 0.047), ON with vitamin B6 levels (OR: 0.382, 95% CI: 0.187–0.778, <i>p</i> = 0.008), and MG with iron levels (OR: 0.194, 95% CI: 0.043–0.867, <i>p</i> = 0.032). Sensitivity analysis showed that there was no level pleiotropic or heterogeneity in our study results.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>This study established the causal relationship between micronutrients and neuroimmune diseases. These findings provide new insights into the etiology of neuroimmune diseases and provide a theoretical basis for micronutrient regulation, prevention, and treatment of neuroimmune diseases.</p>\n </section>\n </div>","PeriodicalId":9081,"journal":{"name":"Brain and Behavior","volume":"15 9","pages":""},"PeriodicalIF":2.7000,"publicationDate":"2025-09-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/brb3.70848","citationCount":"0","resultStr":"{\"title\":\"Potential Causal Relationships Between Circulating Micronutrient Levels and Multiple Neuroimmune Diseases: A Genetic Association Analysis\",\"authors\":\"Longhao Chen, Xuzhou Wu, Kaizheng Wang, Xingchen Zhou, Yika Mou, Zhen Liu, Zhifang Shen, Zhizhen Lv, Lijiang Lv\",\"doi\":\"10.1002/brb3.70848\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Growing evidence suggests a close association between circulating micronutrient levels and neuroimmune diseases. Nevertheless, the causal relationship between them remains unclear. Furthermore, due to confounding factors, many micronutrients implicated in these diseases remain unidentified. This study aimed to determine the causal relationship between circulating micronutrients and neuroimmune diseases through genetic association analysis, and to analyze the regulatory role of circulating micronutrients in neuroimmune diseases.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Method</h3>\\n \\n <p>In this study, we used a two-sample mendelian randomization (MR) analysis to explore the causal relationship between micronutrients levels and neuroimmune disease. Fourteen micronutrients were screened from a published genome-wide association study (GWAS). Neuroimmune diseases include multiple sclerosis (MS), Guillain–Barre syndrome (GBS), acute disseminated encephalomyelitis (ADEM), acute poliomyelitis (AP), sequelae of poliomyelitis (SP), optic neuritis (ON), and myasthenia gravis (MG). Data on these seven neuroimmune diseases came from the FinnGen database and included 5523 cases and 2,860,006 controls. The inverse variance weighting (IVW) method was used as the main MR analysis method, and sensitivity analysis was performed to determine MR hypotheses.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Through MR analysis and sensitivity testing, we identified significant causal relationships between four neuroimmune diseases and micronutrient levels. Specifically, MS was causally associated with magnesium levels (OR: 0.467, 95% CI: 0.269–0.809, <i>p</i> = 0.007), ADEM with folate levels (OR: 0.022, 95% CI: 0.001–0.957, <i>p</i> = 0.047), ON with vitamin B6 levels (OR: 0.382, 95% CI: 0.187–0.778, <i>p</i> = 0.008), and MG with iron levels (OR: 0.194, 95% CI: 0.043–0.867, <i>p</i> = 0.032). Sensitivity analysis showed that there was no level pleiotropic or heterogeneity in our study results.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>This study established the causal relationship between micronutrients and neuroimmune diseases. These findings provide new insights into the etiology of neuroimmune diseases and provide a theoretical basis for micronutrient regulation, prevention, and treatment of neuroimmune diseases.</p>\\n </section>\\n </div>\",\"PeriodicalId\":9081,\"journal\":{\"name\":\"Brain and Behavior\",\"volume\":\"15 9\",\"pages\":\"\"},\"PeriodicalIF\":2.7000,\"publicationDate\":\"2025-09-09\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/brb3.70848\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Brain and Behavior\",\"FirstCategoryId\":\"102\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/brb3.70848\",\"RegionNum\":3,\"RegionCategory\":\"心理学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"BEHAVIORAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Brain and Behavior","FirstCategoryId":"102","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/brb3.70848","RegionNum":3,"RegionCategory":"心理学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
引用次数: 0
摘要
背景越来越多的证据表明,循环微量营养素水平与神经免疫疾病之间存在密切联系。然而,它们之间的因果关系仍不清楚。此外,由于混杂因素,许多与这些疾病有关的微量营养素仍未查明。本研究旨在通过遗传关联分析确定循环微量营养素与神经免疫疾病之间的因果关系,并分析循环微量营养素在神经免疫疾病中的调节作用。方法采用双样本孟德尔随机化(MR)分析方法,探讨微量营养素水平与神经免疫疾病之间的因果关系。从已发表的全基因组关联研究(GWAS)中筛选了14种微量营养素。神经免疫性疾病包括多发性硬化症(MS)、格林-巴利综合征(GBS)、急性播散性脑脊髓炎(ADEM)、急性脊髓灰质炎(AP)、脊髓灰质炎后遗症(SP)、视神经炎(ON)和重症肌无力(MG)。这7种神经免疫疾病的数据来自FinnGen数据库,包括5523例病例和2860006例对照。采用方差反加权法(IVW)作为MR分析的主要方法,并通过敏感性分析确定MR假设。结果通过MR分析和敏感性测试,我们确定了四种神经免疫疾病与微量营养素水平之间的显著因果关系。具体来说,MS与镁水平(OR: 0.467, 95% CI: 0.269-0.809, p = 0.007)、ADEM与叶酸水平(OR: 0.022, 95% CI: 0.001-0.957, p = 0.047)、ON与维生素B6水平(OR: 0.382, 95% CI: 0.187-0.778, p = 0.008)、MG与铁水平(OR: 0.194, 95% CI: 0.043-0.867, p = 0.032)呈正相关。敏感性分析显示,我们的研究结果不存在水平多效性或异质性。结论本研究建立了微量营养素与神经免疫疾病之间的因果关系。这些发现为神经免疫疾病的病因学提供了新的认识,并为神经免疫疾病的微量营养素调控、预防和治疗提供了理论依据。
Potential Causal Relationships Between Circulating Micronutrient Levels and Multiple Neuroimmune Diseases: A Genetic Association Analysis
Background
Growing evidence suggests a close association between circulating micronutrient levels and neuroimmune diseases. Nevertheless, the causal relationship between them remains unclear. Furthermore, due to confounding factors, many micronutrients implicated in these diseases remain unidentified. This study aimed to determine the causal relationship between circulating micronutrients and neuroimmune diseases through genetic association analysis, and to analyze the regulatory role of circulating micronutrients in neuroimmune diseases.
Method
In this study, we used a two-sample mendelian randomization (MR) analysis to explore the causal relationship between micronutrients levels and neuroimmune disease. Fourteen micronutrients were screened from a published genome-wide association study (GWAS). Neuroimmune diseases include multiple sclerosis (MS), Guillain–Barre syndrome (GBS), acute disseminated encephalomyelitis (ADEM), acute poliomyelitis (AP), sequelae of poliomyelitis (SP), optic neuritis (ON), and myasthenia gravis (MG). Data on these seven neuroimmune diseases came from the FinnGen database and included 5523 cases and 2,860,006 controls. The inverse variance weighting (IVW) method was used as the main MR analysis method, and sensitivity analysis was performed to determine MR hypotheses.
Results
Through MR analysis and sensitivity testing, we identified significant causal relationships between four neuroimmune diseases and micronutrient levels. Specifically, MS was causally associated with magnesium levels (OR: 0.467, 95% CI: 0.269–0.809, p = 0.007), ADEM with folate levels (OR: 0.022, 95% CI: 0.001–0.957, p = 0.047), ON with vitamin B6 levels (OR: 0.382, 95% CI: 0.187–0.778, p = 0.008), and MG with iron levels (OR: 0.194, 95% CI: 0.043–0.867, p = 0.032). Sensitivity analysis showed that there was no level pleiotropic or heterogeneity in our study results.
Conclusion
This study established the causal relationship between micronutrients and neuroimmune diseases. These findings provide new insights into the etiology of neuroimmune diseases and provide a theoretical basis for micronutrient regulation, prevention, and treatment of neuroimmune diseases.
期刊介绍:
Brain and Behavior is supported by other journals published by Wiley, including a number of society-owned journals. The journals listed below support Brain and Behavior and participate in the Manuscript Transfer Program by referring articles of suitable quality and offering authors the option to have their paper, with any peer review reports, automatically transferred to Brain and Behavior.
* [Acta Psychiatrica Scandinavica](https://publons.com/journal/1366/acta-psychiatrica-scandinavica)
* [Addiction Biology](https://publons.com/journal/1523/addiction-biology)
* [Aggressive Behavior](https://publons.com/journal/3611/aggressive-behavior)
* [Brain Pathology](https://publons.com/journal/1787/brain-pathology)
* [Child: Care, Health and Development](https://publons.com/journal/6111/child-care-health-and-development)
* [Criminal Behaviour and Mental Health](https://publons.com/journal/3839/criminal-behaviour-and-mental-health)
* [Depression and Anxiety](https://publons.com/journal/1528/depression-and-anxiety)
* Developmental Neurobiology
* [Developmental Science](https://publons.com/journal/1069/developmental-science)
* [European Journal of Neuroscience](https://publons.com/journal/1441/european-journal-of-neuroscience)
* [Genes, Brain and Behavior](https://publons.com/journal/1635/genes-brain-and-behavior)
* [GLIA](https://publons.com/journal/1287/glia)
* [Hippocampus](https://publons.com/journal/1056/hippocampus)
* [Human Brain Mapping](https://publons.com/journal/500/human-brain-mapping)
* [Journal for the Theory of Social Behaviour](https://publons.com/journal/7330/journal-for-the-theory-of-social-behaviour)
* [Journal of Comparative Neurology](https://publons.com/journal/1306/journal-of-comparative-neurology)
* [Journal of Neuroimaging](https://publons.com/journal/6379/journal-of-neuroimaging)
* [Journal of Neuroscience Research](https://publons.com/journal/2778/journal-of-neuroscience-research)
* [Journal of Organizational Behavior](https://publons.com/journal/1123/journal-of-organizational-behavior)
* [Journal of the Peripheral Nervous System](https://publons.com/journal/3929/journal-of-the-peripheral-nervous-system)
* [Muscle & Nerve](https://publons.com/journal/4448/muscle-and-nerve)
* [Neural Pathology and Applied Neurobiology](https://publons.com/journal/2401/neuropathology-and-applied-neurobiology)