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强直性脊柱炎的遗传风险与克罗恩病二线治疗需求:一项孟德尔随机化研究

Genetic Risk of Ankylosing Spondylitis and Second-Line Therapy Need in Crohn's Disease: A Mendelian Randomization Study.

作者信息

Omar Mahmud, Omar Mohammad, Patt Yonatan Shneor, Ukashi Offir, Sharif Yousra, Lahat Adi, Selinger Christian Phillip, Sharif Kassem

机构信息

Faculty of Medicine, Tel-Aviv University, Tel-Aviv 6997801, Israel.

School of Medicine, V. N. Karazin Kharkiv National University, 61022 Kharkiv, Ukraine.

出版信息

J Clin Med. 2024 Dec 10;13(24):7496. doi: 10.3390/jcm13247496.

Abstract

Crohn's disease (CD) and Ankylosing Spondylitis (AS) are chronic conditions with overlapping inflammatory pathways. This research investigates the genetic association between AS and the requirement for more aggressive therapeutic interventions in CD, suggesting a likelihood of increased severity in CD progression among individuals diagnosed with AS. This study utilized two-sample Mendelian randomization (TSMR) to analyze GWAS datasets for AS and CD requiring second-line treatment. Instrumental variables were selected based on single-nucleotide polymorphisms of genome-wide significance. Analytical methods included inverse-variance weighted (IVW), MR Egger, and other MR approaches, alongside sensitivity analysis, to validate the findings. Our results indicated a significant association between AS genetic predisposition and the increased need for second-line treatments in CD. The IVW method showed an Odds Ratio (OR) of 2.16, and MR Egger provided an OR of 2.71, both were statistically significant. This association persisted even after the exclusion of influential outlier SNP rs2517655, confirming the robustness of our findings. This study suggests that genetic factors contributing to AS may influence the progression of CD, potentially necessitating more intensive treatment strategies. These findings underscore the importance of early screening in patients with co-existing AS and CD for tailoring treatment approaches, thus advancing personalized medicine in the management of these complex conditions.

摘要

克罗恩病(CD)和强直性脊柱炎(AS)是炎症途径重叠的慢性疾病。本研究调查了AS与CD中更积极治疗干预需求之间的遗传关联,提示在诊断为AS的个体中,CD进展严重程度增加的可能性。本研究利用两样本孟德尔随机化(TSMR)分析AS和需要二线治疗的CD的全基因组关联研究(GWAS)数据集。基于全基因组显著性的单核苷酸多态性选择工具变量。分析方法包括逆方差加权(IVW)、MR Egger和其他MR方法,以及敏感性分析,以验证研究结果。我们的结果表明,AS遗传易感性与CD中二线治疗需求增加之间存在显著关联。IVW方法显示优势比(OR)为2.16,MR Egger方法的OR为2.71,两者均具有统计学意义。即使排除有影响的异常单核苷酸多态性rs2517655后,这种关联仍然存在,证实了我们研究结果的稳健性。本研究表明,导致AS的遗传因素可能影响CD的进展,可能需要更强化的治疗策略。这些发现强调了对同时患有AS和CD的患者进行早期筛查以制定治疗方案的重要性,从而推动这些复杂疾病管理中的个性化医疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bfc/11678710/db6526d577ee/jcm-13-07496-g001.jpg

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