Senbao Xu, Qiuyan Luo, Jian He, Xiling Chen, Simin Li, Yang Bai
{"title":"25-羟基维生素D与功能性胃肠疾病的因果关系:一项双样本孟德尔随机研究。","authors":"Senbao Xu, Qiuyan Luo, Jian He, Xiling Chen, Simin Li, Yang Bai","doi":"10.1186/s12263-023-00734-1","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Previous observational studies have shown associations between vitamin Ds and FGIDS[Including irritable bowel syndrome(IBS) and functional dyspepsia(FD)]. However, the association is controversial and the causality remains unknown. In this study, two-sample MR was cited to explore the causal effect on FGIDS caused by vitamin D level and serum 25-hydroxyvitamin D.</p><p><strong>Method: </strong>The GWASs of vitaminD and 25-hydroxyvitamin D, with 57-99 strongly related SNPs were all obtained from UK biobank. The GWASs of IBS and FD were obtained from FinnGen biobank with respectively 187,028 and 194,071 participants involved. Fixed-effect inverse variance weighted regression was used to evaluate causal estimates. Other statistical methods such as MR Egger, weighted median estimation, maximum likelihood estimation and penalty-weighted median estimation are also used to verify the accuracy of the main results.</p><p><strong>Results: </strong>Measuring by the IVW method, our research indicated that no causal relationship was detected between vitamin D intake and Functional gastrointestinal disorders [IVW, OR(vitamin D-IBS) = 0.909, 95% CI 0.789-1.053, p = 0.2017); OR(vitamin D-FD) = 1.0662, 95% CI 0.9182-1.2380, p = 0.4000]. As for serum 25-hydroxyvitamin D, no causal relationship was detected on FD(IVW, OR(25-hydroxyvitamin D-FD) = 0.9635, 95% CI 0.8039-1.1546, p = 0.6869). Nevertheless, a negative causal relationship was revealed between 25-hydroxyvitamin D and IBS(IVW, OR(25-hydroxyvitamin D-IBS) = 0.832, 95% CI 0.696-0.995, p = 0.0436). Sensitive analysis supported the main findings but did not suggest bias due to pleiotropy.</p><p><strong>Conclusions: </strong>Our Mendelian randomization analyses suggest a negative causal relationship between 25-hydroxyvitamin D and IBS. For each additional SD increase of genetically determined 25-hydroxyvitamin D levels, the risk of IBS decreased by 16.8%.</p>","PeriodicalId":12554,"journal":{"name":"Genes & Nutrition","volume":"18 1","pages":"14"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10494327/pdf/","citationCount":"0","resultStr":"{\"title\":\"Causal associations of 25-hydroxyvitamin D with functional gastrointestinal disorders: a two-sample Mendelian randomization study.\",\"authors\":\"Senbao Xu, Qiuyan Luo, Jian He, Xiling Chen, Simin Li, Yang Bai\",\"doi\":\"10.1186/s12263-023-00734-1\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Previous observational studies have shown associations between vitamin Ds and FGIDS[Including irritable bowel syndrome(IBS) and functional dyspepsia(FD)]. However, the association is controversial and the causality remains unknown. In this study, two-sample MR was cited to explore the causal effect on FGIDS caused by vitamin D level and serum 25-hydroxyvitamin D.</p><p><strong>Method: </strong>The GWASs of vitaminD and 25-hydroxyvitamin D, with 57-99 strongly related SNPs were all obtained from UK biobank. The GWASs of IBS and FD were obtained from FinnGen biobank with respectively 187,028 and 194,071 participants involved. Fixed-effect inverse variance weighted regression was used to evaluate causal estimates. Other statistical methods such as MR Egger, weighted median estimation, maximum likelihood estimation and penalty-weighted median estimation are also used to verify the accuracy of the main results.</p><p><strong>Results: </strong>Measuring by the IVW method, our research indicated that no causal relationship was detected between vitamin D intake and Functional gastrointestinal disorders [IVW, OR(vitamin D-IBS) = 0.909, 95% CI 0.789-1.053, p = 0.2017); OR(vitamin D-FD) = 1.0662, 95% CI 0.9182-1.2380, p = 0.4000]. As for serum 25-hydroxyvitamin D, no causal relationship was detected on FD(IVW, OR(25-hydroxyvitamin D-FD) = 0.9635, 95% CI 0.8039-1.1546, p = 0.6869). Nevertheless, a negative causal relationship was revealed between 25-hydroxyvitamin D and IBS(IVW, OR(25-hydroxyvitamin D-IBS) = 0.832, 95% CI 0.696-0.995, p = 0.0436). Sensitive analysis supported the main findings but did not suggest bias due to pleiotropy.</p><p><strong>Conclusions: </strong>Our Mendelian randomization analyses suggest a negative causal relationship between 25-hydroxyvitamin D and IBS. 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引用次数: 0
摘要
背景:先前的观察性研究表明维生素d与FGIDS(包括肠易激综合征(IBS)和功能性消化不良(FD))之间存在关联。然而,这种联系是有争议的,因果关系仍然未知。本研究采用双样本MR,探讨维生素D水平和血清25-羟基维生素D对FGIDS的因果关系。方法:维生素ind和25-羟基维生素D的GWASs,其中57 ~ 99个snp均来自UK biobank。IBS和FD的GWASs分别来自FinnGen生物银行,分别涉及187,028和194,071名参与者。采用固定效应反方差加权回归评估因果估计。其他统计方法如MR Egger、加权中位数估计、最大似然估计和惩罚加权中位数估计也被用来验证主要结果的准确性。结果:通过IVW方法测量,我们的研究表明维生素D摄入与功能性胃肠道疾病之间没有因果关系[IVW, OR(维生素D- ibs) = 0.909, 95% CI 0.789-1.053, p = 0.2017];或(维生素D-FD) = 1.0662, 95% CI 0.9182 - -1.2380, p = 0.4000)。血清25-羟基维生素D与FD无因果关系(IVW, OR(25-羟基维生素D-FD) = 0.9635, 95% CI 0.8039 ~ 1.1546, p = 0.6869)。然而,25-羟基维生素D与IBS之间显示负因果关系(IVW, OR(25-羟基维生素D-IBS) = 0.832, 95% CI 0.696-0.995, p = 0.0436)。敏感性分析支持主要发现,但未发现多效性导致的偏倚。结论:我们的孟德尔随机分析表明25-羟基维生素D与IBS之间存在负相关的因果关系。基因决定的25-羟基维生素D水平每增加1 SD, IBS的风险降低16.8%。
Causal associations of 25-hydroxyvitamin D with functional gastrointestinal disorders: a two-sample Mendelian randomization study.
Background: Previous observational studies have shown associations between vitamin Ds and FGIDS[Including irritable bowel syndrome(IBS) and functional dyspepsia(FD)]. However, the association is controversial and the causality remains unknown. In this study, two-sample MR was cited to explore the causal effect on FGIDS caused by vitamin D level and serum 25-hydroxyvitamin D.
Method: The GWASs of vitaminD and 25-hydroxyvitamin D, with 57-99 strongly related SNPs were all obtained from UK biobank. The GWASs of IBS and FD were obtained from FinnGen biobank with respectively 187,028 and 194,071 participants involved. Fixed-effect inverse variance weighted regression was used to evaluate causal estimates. Other statistical methods such as MR Egger, weighted median estimation, maximum likelihood estimation and penalty-weighted median estimation are also used to verify the accuracy of the main results.
Results: Measuring by the IVW method, our research indicated that no causal relationship was detected between vitamin D intake and Functional gastrointestinal disorders [IVW, OR(vitamin D-IBS) = 0.909, 95% CI 0.789-1.053, p = 0.2017); OR(vitamin D-FD) = 1.0662, 95% CI 0.9182-1.2380, p = 0.4000]. As for serum 25-hydroxyvitamin D, no causal relationship was detected on FD(IVW, OR(25-hydroxyvitamin D-FD) = 0.9635, 95% CI 0.8039-1.1546, p = 0.6869). Nevertheless, a negative causal relationship was revealed between 25-hydroxyvitamin D and IBS(IVW, OR(25-hydroxyvitamin D-IBS) = 0.832, 95% CI 0.696-0.995, p = 0.0436). Sensitive analysis supported the main findings but did not suggest bias due to pleiotropy.
Conclusions: Our Mendelian randomization analyses suggest a negative causal relationship between 25-hydroxyvitamin D and IBS. For each additional SD increase of genetically determined 25-hydroxyvitamin D levels, the risk of IBS decreased by 16.8%.