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Systematic review: predictive biomarkers of therapeutic response in inflammatory bowel disease—personalised medicine in its infancy

机译:系统评价:其婴儿期炎症性肠病疾病的预测生物标志物

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Summary Background Inflammatory bowel disease (IBD) is characterised by substantial heterogeneity in treatment response. With an expanding number of therapeutic agents, identifying optimal treatment at the patient level remains a major challenge. Aim To systematically review the available literature on predictive biomarkers of therapeutic response in IBD. Methods An electronic literature search was performed on 30 January 2018 using MEDLINE, EMBASE and the Cochrane Library. Retrospective, prospective, uncontrolled and controlled studies reporting on biomarkers predicting therapeutic response in paediatric and adult IBD populations were eligible for inclusion. The methodological quality of the included studies was assessed using the QUIPS tool. Due to anticipated heterogeneity and limited data, a qualitative, rather than quantitative, assessment was planned. Results Of the 10?638 citations identified, 92 articles met the inclusion criteria. Several potential DNA, mRNA and protein markers were evaluated as predictive biomarkers. Most studies focused on predicting response to anti‐TNF agents. Substantial between‐study heterogeneity was identified with respect to both the biomarkers studied and the definition of response. None of the included studies received a low risk of bias rating for all six domains. Currently, none of the biomarkers is sufficiently predictive for clinical use. Conclusions The search for predictive biomarkers is still in its infancy and current evidence is limited. Future research efforts should take into account the high patient heterogeneity within prospective trials with objective response assessment. Predictive models will most likely comprise a combination of several molecular markers from integrated omics‐levels and clinical characteristics.
机译:发明内容背景炎症性肠病(IBD)的特征在于治疗反应中的基本异质性。随着治疗剂的扩大数量,鉴定患者水平的最佳治疗仍然是一个重大挑战。旨在系统地审查IBD治疗反应预测生物标志物的可用文献。方法使用Medline,Embase和Cochrane库于2018年1月30日进行电子文献搜索。关于预测儿科和成人IBD种群预测治疗反应的生物标志物的回顾性,前瞻性,不受控制和对照研究有资格包含。使用Quips工具评估包括的研究的方法论质量。由于预期的异质性和有限的数据,计划的定性而不是定量的评估。结果的结果为10?638引文,92条符合纳入标准。评估几种潜在的DNA,mRNA和蛋白质标记作为预测性生物标志物。大多数研究重点是预测对抗TNF药剂的反应。关于研究的两种生物标志物和响应的定义,确定了研究的实质性异质性。没有包括所有六个域的偏差额定值的风险低。目前,没有一种生物标志物对临床使用充分预测性。结论寻找预测性生物标志物仍处于初期,目前的证据是有限的。未来的研究努力应考虑到客观反应评估的前瞻性试验中的高患者异质性。预测模型最有可能包括来自集成的常规水平和临床特征的几种分子标记的组合。

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    Department of Gastroenterology and HepatologyAmsterdam UMC University of AmsterdamAmsterdam The;

    Department of Gastroenterology and HepatologyAmsterdam UMC University of AmsterdamAmsterdam The;

    Department of Gastroenterology and HepatologyAmsterdam UMC University of AmsterdamAmsterdam The;

    Robarts Clinical Trials IncLondon ON Canada;

    Department of Gastroenterology and HepatologyAmsterdam UMC University of AmsterdamAmsterdam The;

    Department of Gastroenterology and HepatologyAmsterdam UMC University of AmsterdamAmsterdam The;

    Department of Gastroenterology and HepatologyAmsterdam UMC University of AmsterdamAmsterdam The;

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  • 正文语种 eng
  • 中图分类 药理学;
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