遗传变异对成人IBD药物反应的影响:系统综述

IF 1.5 Q3 GASTROENTEROLOGY & HEPATOLOGY
JGH Open Pub Date : 2025-07-22 DOI:10.1002/jgh3.70172
Masomeh Askari, Shaghayegh Baradaran Ghavami, Nayeralsadat Fatemi, Mahya Haghipanah, Nesa Kazemifard, Hamid Asadzadeh Aghdaei, Makan Cheraghpour, Hamid Mahdizadeh, Shabnam Shahrokh, Mehdi Totonchi
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引用次数: 0

摘要

炎症性肠病(IBD)的一个主要特征是治疗反应的显著异质性。尽管治疗药物有所增加,但发现最佳的患者水平治疗仍然是一个重要的里程碑。本研究旨在对IBD治疗反应的预测性生物标志物的现有文献进行系统回顾。方法于2025年4月15日使用PubMed和Scopus数据库进行文献检索,同时进行人工检索。对照试验、病例对照研究、横断面研究和队列研究均符合入选条件,这些研究涉及IBD成人治疗反应的预测性生物标志物。CASP工具用于评估纳入研究中所采用方法的质量。由于缺乏信息和预期的异质性,计划进行定性研究而不是定量研究。结果在鉴定的7570篇文献中,31篇符合纳入标准。评估DNA标记物作为预测性生物标记物。大多数研究试图预测抗肿瘤坏死因子药物的反应。在反应的定义和考虑的生物标志物方面,研究之间存在显著的差异。目前,还没有一种生物标志物能为临床实践提供足够的预测能力。因此,我们仍处于寻找预测性生物标志物的早期阶段,现有文献缺乏。未来的研究应通过进行客观的反应评估来解决前瞻性试验中患者之间的巨大异质性。预测模型可能是通过综合组学水平和临床特征的多个分子标记来开发的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Impact of Genetic Variation on Drug Response in Adult IBD: A Systematic Review

The Impact of Genetic Variation on Drug Response in Adult IBD: A Systematic Review

Background

A major characterization of inflammatory bowel disease (IBD) is significant heterogeneity in treatment responses. Despite the increase in therapeutic agents, discovering an optimal patient-level treatment is still a major milestone. This study aims to provide a systematic review of the existing literature on the predictive biomarkers of the response to IBD treatment.

Methods

On April 15, 2025, a literature search was conducted using the PubMed and Scopus databases, as well as a manual search. Controlled trials, case–control studies, cross-sectional studies, and cohort studies addressing predictive biomarkers for treatment response in adults with IBD were eligible for inclusion. The CASP tool was used to assess the quality of the methodologies employed in the included research. Due to a lack of information and expected heterogeneity, a qualitative study was planned instead of a quantitative one.

Results

Of the 7570 identified articles, 31 met the inclusion criteria. DNA markers were assessed as predictive biomarkers. The majority of studies attempted to predict the response to anti-TNF drugs. There is significant variability across studies in both the definition of response and the considered biomarkers.

Conclusions

At the moment, no biomarker provides sufficient predictive ability for clinical practice. Thus, we are still in the early stages of the quest for predictive biomarkers, and existing literature is lacking. Future studies should address the large heterogeneity among patients within prospective trials by conducting objective response evaluations. Prediction models are likely to be developed by combining multiple molecular markers from integrated omics levels and clinical characteristics.

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来源期刊
JGH Open
JGH Open GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
3.40
自引率
0.00%
发文量
143
审稿时长
7 weeks
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