Falloon Katherine, Cohen Benjamin L, Ottichilo Ronald, Grove David, Rieder Florian, Qazi Taha
Department of Gastroenterology, Hepatology & Nutrition, Digestive Diseases and Surgery Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.
Department of Inflammation and Immunity; Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, OH, USA.
Crohns Colitis 360. 2022 Nov 24;4(4):otac043. doi: 10.1093/crocol/otac043. eCollection 2022 Oct.
Ileal pouch inflammation is a common problem following ileal pouch-anal anastomosis (IPAA). Despite its prevalence, diagnosis remains multimodal and requires endoscopy. The use of biomarkers in the prediction of and/or association with pouchitis has not been well characterized. We performed a systematic review to summarize the available evidence.
A search of Ovid, MEDLINE, Cochrane Library, EMBASE, and Web of Science was conducted. Inclusion criteria included studies evaluating biomarkers for the evaluation and prediction of inflammation in patients with IPAA utilizing pouchoscopy as the gold standard. Exclusion criteria included studies on the role of the microbiome or genetic markers.
A total of 28 studies, 5 case-control studies, and 23 observational cohort studies were identified. Fecal biomarkers were assessed in 23 studies, of which fecal calprotectin was the most commonly studied with sensitivities ranging from 57% to 92% and specificities from 19% to 92%. Six studies examined serum biomarkers. None of the serum biomarkers demonstrated a high sensitivity or specificity in association with pouch inflammation. Six studies described the longitudinal assessment of biomarkers. Of these studies, only three reported a predictive role of biomarkers in diagnosing endoscopic inflammation.
Biomarkers have emerged as a potential option to improve the management of pouchitis given the relative ease of sampling compared to pouchoscopy. Unfortunately, the evaluated biomarkers have not consistently demonstrated accuracy in predicting inflammation. Moreover, these biomarkers have not been reliably shown to be sensitive or specific in association with endoscopic pouch inflammation to merit their widespread use in clinical practice.
回肠贮袋炎是回肠贮袋肛管吻合术(IPAA)后常见的问题。尽管其发病率较高,但诊断仍需采用多种方法,且需要进行内镜检查。生物标志物在贮袋炎预测和/或关联方面的应用尚未得到充分研究。我们进行了一项系统综述以总结现有证据。
检索了Ovid、MEDLINE、Cochrane图书馆、EMBASE和科学网。纳入标准包括以袋状内镜检查为金标准,评估IPAA患者炎症评估和预测生物标志物的研究。排除标准包括关于微生物组或基因标志物作用的研究。
共识别出28项研究,其中5项病例对照研究,23项观察性队列研究。23项研究评估了粪便生物标志物,其中粪便钙卫蛋白是研究最多的,敏感性范围为57%至92%,特异性为19%至92%。6项研究检测了血清生物标志物。没有一种血清生物标志物在与贮袋炎症的关联中表现出高敏感性或特异性。6项研究描述了生物标志物的纵向评估。在这些研究中,只有3项报告了生物标志物在诊断内镜炎症中的预测作用。
鉴于与袋状内镜检查相比,生物标志物采样相对容易,已成为改善贮袋炎管理的潜在选择。不幸的是,所评估的生物标志物在预测炎症方面并未始终表现出准确性。此外,这些生物标志物在与内镜下贮袋炎症的关联中,尚未可靠地显示出敏感性或特异性,不足以在临床实践中广泛应用。