Department of Medicine, Section of Gastroenterology, Hepatology, and Nutrition, University of Chicago Medicine, Chicago, IL, United States.
Division of Gastroenterology, Washington University in St. Louis, St. Louis, MO, United States.
Inflamm Bowel Dis. 2018 Jun 8;24(7):1471-1480. doi: 10.1093/ibd/izy103.
Mucosal appearance on endoscopy is an important indicator of inflammatory burden and determines prognosis in ulcerative colitis (UC). Inflammation induces tryptophan metabolism along the kynurenine pathway (KP) and yields immunologically relevant metabolites. We sought to examine whether changes in serum tryptophan metabolites and tissue expression of KP enzymes are associated with UC endoscopic and histologic disease severity.
Serum and mucosal samples were prospectively obtained at colonoscopy in patients with UC. Mayo disease activity scores, demographics, smoking status, medications, and outcomes were collected. Serum tryptophan metabolites were analyzed using ultra-high performance liquid chromatography (uHPLC), and gas chromatography-mass spectrometry (GC-MS), and enzyme expression was determined by quantitative real-time polymerase chain reaction. Metabolite and enzyme levels were compared by endoscopic subscore, clinical disease activity, time to surgery, and hospitalization.
This study included 99 patients with Mayo endoscopic subscores 0-3. Kynurenic acid/tryptophan ratio (KYNA/T) and expression of indolamine 2,3-dioxygenase 1 (IDO1), tryptophan 2,3-dioxygenase, kynurinase, and kynurenine monooxygenase correlated positively with endoscopic subscore. Adjusting for age of diagnosis, smoking status, disease extent, and medications yielded significant odds of endoscopic inflammation with increasing KYNA/T (OR 1.0015, P = 0.0186) and IDO1 expression (OR 1.0635, P = 0.0215). The highest tertile ratio of KYNA/T had shorter time to surgery (P = 0.009) and hospitalization (P = 0.01) than the lowest.
Increasing KYNA/T is closely associated with endoscopic inflammation and predictive of disease outcomes in patients with UC. These findings identify this novel metabolic association and further support the role of the KP in regulating mucosal inflammation in UC. 10.1093/ibd/izy103_video1izy103.video15788135676001.
内镜下黏膜表现是炎症负担的重要指标,并决定溃疡性结肠炎(UC)的预后。炎症沿犬尿氨酸途径(KP)诱导色氨酸代谢,并产生具有免疫相关性的代谢物。我们旨在研究血清色氨酸代谢物的变化以及 KP 酶的组织表达是否与 UC 的内镜和组织学疾病严重程度相关。
前瞻性地在 UC 患者的结肠镜检查时采集血清和黏膜样本。收集 Mayo 疾病活动评分、人口统计学、吸烟状况、药物使用情况和结局等数据。使用超高效液相色谱(uHPLC)和气相色谱-质谱联用(GC-MS)分析血清色氨酸代谢物,通过定量实时聚合酶链反应(qRT-PCR)测定酶表达。通过内镜亚评分、临床疾病活动、手术时间和住院时间比较代谢物和酶水平。
本研究纳入了 99 例 Mayo 内镜亚评分 0-3 的患者。犬尿酸/色氨酸比值(KYNA/T)和吲哚胺 2,3-双加氧酶 1(IDO1)、色氨酸 2,3-双加氧酶、犬尿氨酸酶和犬尿氨酸单加氧酶的表达与内镜亚评分呈正相关。在校正诊断年龄、吸烟状况、疾病范围和药物使用后,KYNA/T(比值比 [OR] 1.0015,P = 0.0186)和 IDO1 表达(OR 1.0635,P = 0.0215)与内镜炎症的显著比值比相关。KYNA/T 比值最高的 tertile 组手术时间(P = 0.009)和住院时间(P = 0.01)更短。
KYNA/T 的增加与内镜炎症密切相关,并可预测 UC 患者的疾病结局。这些发现确定了这种新的代谢关联,并进一步支持 KP 在调节 UC 黏膜炎症中的作用。