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炎症性肠病与银屑病之间的因果关联:两样本双向孟德尔随机化研究。

Causal Association Between Inflammatory Bowel Disease and Psoriasis: A Two-Sample Bidirectional Mendelian Randomization Study.

机构信息

Department of Dermatology, Xiangya Hospital, Central South University, Changsha, China.

National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.

出版信息

Front Immunol. 2022 Jun 10;13:916645. doi: 10.3389/fimmu.2022.916645. eCollection 2022.

Abstract

BACKGROUND

Previous observational studies have found an association between inflammatory bowel disease (IBD) and psoriasis. Using the mendelian randomization (MR) approach, we aim to determine whether there was a causal association between IBD and psoriasis.

METHODS

We performed a two-sample MR with the genetic instruments identified for IBD and its main subtypes, Crohn's disease (CD) and ulcerative colitis (UC), from a genome-wide association study (GWAS) involving 25,042 cases with an IBD diagnosis and 34,915 controls. Summarized data for psoriasis were obtained from different GWAS studies which included 4510 cases and 212,242 controls without psoriasis. Causal estimates are presented as odds ratios (ORs) with 95% confidence intervals (CIs).

RESULTS

The overall outcome of MR analysis was to demonstrate that genetic predisposition to IBD was associated with an increased risk of psoriasis (OR: 1.1271; 95% CI: 1.0708 to 1.1864). Psoriatic arthritis (PsA) had a significant association with total IBD (OR: 1.1202; 95% CI: 1.0491 to 1.1961). Casual relationship was also identified for CD-psoriasis (OR: 1.1552; 95% CI: 1.0955 to 1.2182) and CD-PsA (OR: 1.1407; 95% CI: 1.0535 to 1.2350). The bidirectional analysis did not demonstrate that a genetic predisposition to psoriasis was associated with total IBD, although psoriasis showed association with CD (OR: 1.2224; 95% CI: 1.1710 to 1.2760) but not with UC. A genetic predisposition to PsA had a borderline association with IBD (OR: 1.0716; 95% CI: 1.0292 to 1.1157) and a suggestive association with CD (OR: 1.0667; 95% CI: 1.0194 to 1.1162).

CONCLUSION

There appears to be a causal relationship between IBD and psoriasis, especially for PsA, but for psoriasis and IBD, only total psoriasis and PsA were associated with CD. Understanding that specific types of psoriasis and IBD constitute mutual risk factors facilitates the clinical management of two diseases.

摘要

背景

先前的观察性研究发现炎症性肠病(IBD)和银屑病之间存在关联。使用孟德尔随机化(MR)方法,我们旨在确定 IBD 和银屑病之间是否存在因果关系。

方法

我们使用全基因组关联研究(GWAS)中确定的 IBD 及其主要亚型(克罗恩病[CD]和溃疡性结肠炎[UC])的遗传工具进行了两样本 MR。GWAS 研究共纳入 25042 例 IBD 患者和 34915 例对照,总结了银屑病的汇总数据来自不同的 GWAS 研究,包括 4510 例无银屑病的病例和 212242 例对照。因果估计以比值比(OR)及其 95%置信区间(CI)表示。

结果

MR 分析的总体结果表明,IBD 的遗传易感性与银屑病风险增加相关(OR:1.1271;95%CI:1.0708 至 1.1864)。银屑病关节炎(PsA)与总 IBD 有显著关联(OR:1.1202;95%CI:1.0491 至 1.1961)。CD-银屑病(OR:1.1552;95%CI:1.0955 至 1.2182)和 CD-PsA(OR:1.1407;95%CI:1.0535 至 1.2350)也存在因果关系。双向分析并未表明银屑病的遗传易感性与总 IBD 相关,尽管银屑病与 CD 相关(OR:1.2224;95%CI:1.1710 至 1.2760),但与 UC 无关。遗传易感性与 PsA 与 IBD 呈边缘关联(OR:1.0716;95%CI:1.0292 至 1.1157),与 CD 呈提示性关联(OR:1.0667;95%CI:1.0194 至 1.1162)。

结论

IBD 和银屑病之间似乎存在因果关系,尤其是对于 PsA,但对于银屑病和 IBD,只有总银屑病和 PsA 与 CD 相关。了解特定类型的银屑病和 IBD 构成相互危险因素有助于两种疾病的临床管理。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f005/9226443/ee5508780ab3/fimmu-13-916645-g001.jpg

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