乳糜泻与甲状腺功能因果关系的遗传预测:一项双样本孟德尔随机研究。

IF 2
Xiaoshun He, Hanxin Lv, Wangjianfei Yu, Jun He, Yuyang Xie, Lihao Zhou, Hua Wu, Lingchuan Guo, Xiaoqin Yang
{"title":"乳糜泻与甲状腺功能因果关系的遗传预测:一项双样本孟德尔随机研究。","authors":"Xiaoshun He, Hanxin Lv, Wangjianfei Yu, Jun He, Yuyang Xie, Lihao Zhou, Hua Wu, Lingchuan Guo, Xiaoqin Yang","doi":"10.2174/0118715303364014250713045734","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>Observational studies have suggested an association between celiac disease and thyroid dysfunction, but their causal relationship has not yet been established.</p><p><strong>Methods: </strong>Summary statistics for celiac disease were retrieved from the FinnGen Consortium, thyroid hormone and antibody data were obtained from the ThyroidOmics Consortium, and genetic variants associated with hyperthyroidism and hypothyroidism were sourced from the UK Biobank. MR statistical analyses used the inverse variance weighted algorithm, followed by various sensitivity analyses and reliability evaluations.</p><p><strong>Results: </strong>Genetic proxied celiac disease was significantly associated with increased free thyroxine (FT4) and thyroid peroxidase antibody (TPOAb) levels and decreased free triiodothyronine (FT3)/FT4 ratio, whereas the causality of this common enteropathy on thyroid stimulating hormone (TSH), FT3, total triiodothyronine (TT3), and TT3/FT4 ratio (and vice versa) is unfounded. Moreover, the findings of MR analysis tend to favor the causality of celiac disease for hyperthyroidism, but not hypothyroidism.</p><p><strong>Conclusion: </strong>By leveraging large GWAS consortia datasets, our MR study indicates that the genetic liability to celiac disease is suggestively detrimental to the homeostasis of FT4 and TPOAb levels and FT3/FT4 ratio. Our findings provide caution regarding the risk of hyperthyroidism but not hypothyroidism for individuals suffering from celiac disease.</p>","PeriodicalId":94316,"journal":{"name":"Endocrine, metabolic & immune disorders drug targets","volume":" ","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2025-07-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Genetic Prediction of Causal Association Between Celiac Disease and Thyroid Function: A Two-Sample Mendelian Randomized Study.\",\"authors\":\"Xiaoshun He, Hanxin Lv, Wangjianfei Yu, Jun He, Yuyang Xie, Lihao Zhou, Hua Wu, Lingchuan Guo, Xiaoqin Yang\",\"doi\":\"10.2174/0118715303364014250713045734\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aim: </strong>Observational studies have suggested an association between celiac disease and thyroid dysfunction, but their causal relationship has not yet been established.</p><p><strong>Methods: </strong>Summary statistics for celiac disease were retrieved from the FinnGen Consortium, thyroid hormone and antibody data were obtained from the ThyroidOmics Consortium, and genetic variants associated with hyperthyroidism and hypothyroidism were sourced from the UK Biobank. MR statistical analyses used the inverse variance weighted algorithm, followed by various sensitivity analyses and reliability evaluations.</p><p><strong>Results: </strong>Genetic proxied celiac disease was significantly associated with increased free thyroxine (FT4) and thyroid peroxidase antibody (TPOAb) levels and decreased free triiodothyronine (FT3)/FT4 ratio, whereas the causality of this common enteropathy on thyroid stimulating hormone (TSH), FT3, total triiodothyronine (TT3), and TT3/FT4 ratio (and vice versa) is unfounded. Moreover, the findings of MR analysis tend to favor the causality of celiac disease for hyperthyroidism, but not hypothyroidism.</p><p><strong>Conclusion: </strong>By leveraging large GWAS consortia datasets, our MR study indicates that the genetic liability to celiac disease is suggestively detrimental to the homeostasis of FT4 and TPOAb levels and FT3/FT4 ratio. Our findings provide caution regarding the risk of hyperthyroidism but not hypothyroidism for individuals suffering from celiac disease.</p>\",\"PeriodicalId\":94316,\"journal\":{\"name\":\"Endocrine, metabolic & immune disorders drug targets\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-07-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Endocrine, metabolic & immune disorders drug targets\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2174/0118715303364014250713045734\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Endocrine, metabolic & immune disorders drug targets","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2174/0118715303364014250713045734","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

目的:观察性研究表明乳糜泻与甲状腺功能障碍之间存在关联,但其因果关系尚未确定。方法:乳糜泻的汇总统计数据来自FinnGen Consortium,甲状腺激素和抗体数据来自ThyroidOmics Consortium,与甲状腺功能亢进和甲状腺功能减退相关的遗传变异来自UK Biobank。MR统计分析采用方差反加权算法,然后进行各种敏感性分析和可靠性评估。结果:遗传性乳糜泻与游离甲状腺素(FT4)和甲状腺过氧化物酶抗体(TPOAb)水平升高和游离三碘甲状腺原氨酸(FT3)/FT4比值降低显著相关,而这种常见的肠病与促甲状腺激素(TSH)、FT3、总三碘甲状腺原氨酸(TT3)和TT3/FT4比值(反之亦然)的因果关系是没有根据的。此外,磁共振分析的结果倾向于支持乳糜泻与甲状腺功能亢进的因果关系,而不是甲状腺功能减退。结论:通过利用大型GWAS联盟数据集,我们的MR研究表明,乳糜泻的遗传倾向性对FT4和TPOAb水平以及FT3/FT4比率的稳态不利。我们的研究结果为乳糜泻患者提供了甲状腺功能亢进的风险,而不是甲状腺功能减退的风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Genetic Prediction of Causal Association Between Celiac Disease and Thyroid Function: A Two-Sample Mendelian Randomized Study.

Aim: Observational studies have suggested an association between celiac disease and thyroid dysfunction, but their causal relationship has not yet been established.

Methods: Summary statistics for celiac disease were retrieved from the FinnGen Consortium, thyroid hormone and antibody data were obtained from the ThyroidOmics Consortium, and genetic variants associated with hyperthyroidism and hypothyroidism were sourced from the UK Biobank. MR statistical analyses used the inverse variance weighted algorithm, followed by various sensitivity analyses and reliability evaluations.

Results: Genetic proxied celiac disease was significantly associated with increased free thyroxine (FT4) and thyroid peroxidase antibody (TPOAb) levels and decreased free triiodothyronine (FT3)/FT4 ratio, whereas the causality of this common enteropathy on thyroid stimulating hormone (TSH), FT3, total triiodothyronine (TT3), and TT3/FT4 ratio (and vice versa) is unfounded. Moreover, the findings of MR analysis tend to favor the causality of celiac disease for hyperthyroidism, but not hypothyroidism.

Conclusion: By leveraging large GWAS consortia datasets, our MR study indicates that the genetic liability to celiac disease is suggestively detrimental to the homeostasis of FT4 and TPOAb levels and FT3/FT4 ratio. Our findings provide caution regarding the risk of hyperthyroidism but not hypothyroidism for individuals suffering from celiac disease.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信