• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

原发性胆汁性胆管炎与糖尿病和心血管疾病的相关性:一项双向多变量孟德尔随机化研究。

Association between primary biliary cholangitis with diabetes and cardiovascular diseases: A bidirectional multivariable Mendelian randomization study.

机构信息

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou 325000, Zhejiang, PR China.

The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, Wenzhou 325000, Zhejiang, PR China.

出版信息

Clin Res Hepatol Gastroenterol. 2024 Aug;48(7):102419. doi: 10.1016/j.clinre.2024.102419. Epub 2024 Jul 9.

DOI:10.1016/j.clinre.2024.102419
PMID:38992425
Abstract

BACKGROUND AND AIMS

Primary biliary cholangitis (PBC) is an autoimmune disease often accompanied by multisystem damage. This study aimed to explore the causal association between genetically predicted PBC and diabetes, as well as multiple cardiovascular diseases (CVDs).

METHODS

Genome-wide association studies (GWAS) summary data of PBC in 24,510 individuals of European ancestry from the European Association for the Study of the Liver was used to identify genetically predicted PBC. We conducted 2-sample single-variable Mendelian randomization (SVMR) and multivariable Mendelian randomization (MVMR) to estimate the impacts of PBC on diabetes (N = 17,685 to 318,014) and 20 CVDs from the genetic consortium (N = 171,875 to 1,030,836).

RESULTS

SVMR provided evidence that genetically predicted PBC is associated with an increased risk of type 1 diabetes (T1D), type 2 diabetes (T2D), myocardial infarction (MI), heart failure (HF), hypertension, atrial fibrillation (AF), stroke, ischemic stroke, and small-vessel ischemic stroke. Additionally, there was no evidence of a causal association between PBC and coronary atherosclerosis. In the MVMR analysis, PBC maintained independent effects on T1D, HF, MI, and small-vessel ischemic stroke in most models.

CONCLUSION

Our findings revealed the causal effects of PBC on diabetes and 7 CVDs, and no causal relationship was detected between PBC and coronary atherosclerosis.

摘要

背景和目的

原发性胆汁性胆管炎(PBC)是一种常伴有多系统损害的自身免疫性疾病。本研究旨在探讨遗传预测的 PBC 与糖尿病以及多种心血管疾病(CVDs)之间的因果关联。

方法

利用欧洲肝脏研究协会的 24510 名欧洲血统个体的 PBC 全基因组关联研究(GWAS)汇总数据来识别遗传预测的 PBC。我们进行了两样本单变量 Mendelian 随机化(SVMR)和多变量 Mendelian 随机化(MVMR),以估计 PBC 对糖尿病(N=17685 至 318014)和来自遗传联盟的 20 种 CVD 的影响(N=171875 至 1030836)。

结果

SVMR 提供了证据表明,遗传预测的 PBC 与 1 型糖尿病(T1D)、2 型糖尿病(T2D)、心肌梗死(MI)、心力衰竭(HF)、高血压、心房颤动(AF)、中风、缺血性中风和小血管缺血性中风的风险增加有关。此外,没有证据表明 PBC 与冠状动脉粥样硬化之间存在因果关系。在 MVMR 分析中,在大多数模型中,PBC 对 T1D、HF、MI 和小血管缺血性中风仍具有独立的影响。

结论

我们的研究结果揭示了 PBC 对糖尿病和 7 种 CVD 的因果影响,而 PBC 与冠状动脉粥样硬化之间没有因果关系。

相似文献

1
Association between primary biliary cholangitis with diabetes and cardiovascular diseases: A bidirectional multivariable Mendelian randomization study.原发性胆汁性胆管炎与糖尿病和心血管疾病的相关性:一项双向多变量孟德尔随机化研究。
Clin Res Hepatol Gastroenterol. 2024 Aug;48(7):102419. doi: 10.1016/j.clinre.2024.102419. Epub 2024 Jul 9.
2
Causal association between type 1 diabetes and autoimmune cholestasis: A bi-directional Mendelian randomized study.1型糖尿病与自身免疫性胆汁淤积之间的因果关联:一项双向孟德尔随机化研究。
Int J Immunopathol Pharmacol. 2025 Jan-Dec;39:3946320251327621. doi: 10.1177/03946320251327621. Epub 2025 Apr 11.
3
Association between diabetes mellitus and primary biliary cholangitis: a two-sample Mendelian randomization study.糖尿病与原发性胆汁性胆管炎的关联:两样本孟德尔随机化研究。
Front Endocrinol (Lausanne). 2024 May 7;15:1362584. doi: 10.3389/fendo.2024.1362584. eCollection 2024.
4
Causal associations between type 1 diabetes mellitus and cardiovascular diseases: a Mendelian randomization study.1 型糖尿病与心血管疾病之间的因果关联:一项孟德尔随机化研究。
Cardiovasc Diabetol. 2023 Sep 2;22(1):236. doi: 10.1186/s12933-023-01974-6.
5
Investigating the causal relationship between rheumatoid arthritis and cardiovascular disease: A Mendelian randomization study.探究类风湿性关节炎与心血管疾病之间的因果关系:一项孟德尔随机化研究。
Clin Rheumatol. 2025 Mar;44(3):1057-1067. doi: 10.1007/s10067-025-07357-4. Epub 2025 Feb 6.
6
Genetic association and causal relationship between multiple modifiable risk factors and autoimmune liver disease: a two-sample mendelian randomization study.多可调节风险因素与自身免疫性肝病之间的遗传关联和因果关系:两样本孟德尔随机化研究。
J Transl Med. 2024 May 4;22(1):425. doi: 10.1186/s12967-024-05247-y.
7
The bidirectional association between frailty index and cardiovascular disease: A Mendelian randomization study.衰弱指数与心血管疾病之间的双向关联:一项孟德尔随机化研究。
Nutr Metab Cardiovasc Dis. 2024 Mar;34(3):624-632. doi: 10.1016/j.numecd.2023.10.018. Epub 2023 Oct 24.
8
Lipids, Blood Pressure, and Diabetes Mellitus on Risk of Cardiovascular Diseases in East Asians: A Mendelian Randomization Study.血脂、血压和糖尿病与东亚人心血管疾病风险的关系:一项孟德尔随机化研究。
Am J Cardiol. 2023 Oct 15;205:329-337. doi: 10.1016/j.amjcard.2023.08.007. Epub 2023 Aug 24.
9
Causal association between systemic lupus erythematosus and primary biliary cholangitis: A bidirectional Mendelian randomization study.系统性红斑狼疮与原发性胆汁性胆管炎之间的因果关联:一项双向孟德尔随机研究。
Medicine (Baltimore). 2024 May 24;103(21):e38282. doi: 10.1097/MD.0000000000038282.
10
Cardiovascular diseases consequences of type 1, type 2 diabetes mellitus and glycemic traits: A Mendelian randomization study.1 型、2 型糖尿病及血糖特征与心血管疾病后果的关系:一项孟德尔随机化研究。
Diabetes Res Clin Pract. 2024 Feb;208:111094. doi: 10.1016/j.diabres.2024.111094. Epub 2024 Jan 13.

引用本文的文献

1
Primary Biliary Cholangitis: Immunopathogenesis and the Role of Bile Acid Metabolism in Disease Progression.原发性胆汁性胆管炎:免疫发病机制及胆汁酸代谢在疾病进展中的作用
Int J Mol Sci. 2025 Aug 16;26(16):7905. doi: 10.3390/ijms26167905.
2
A study on the genetic comorbidity between autoimmune diseases and pulmonary hypertension: an observational study and POST-GWAS analysis.自身免疫性疾病与肺动脉高压之间的遗传共病研究:一项观察性研究及全基因组关联研究后分析
Int J Med Sci. 2025 Feb 18;22(6):1344-1362. doi: 10.7150/ijms.107884. eCollection 2025.