Keshteli Ammar Hassanzadeh, van den Brand Floris F, Madsen Karen L, Mandal Rupasri, Valcheva Rosica, Kroeker Karen I, Han Beomsoo, Bell Rhonda C, Cole Janis, Hoevers Thomas, Wishart David S, Fedorak Richard N, Dieleman Levinus A
Ammar Hassanzadeh Keshteli, Floris F van den Brand, Karen L Madsen, Rosica Valcheva, Karen I Kroeker, Thomas Hoevers, Richard N Fedorak, Levinus A Dieleman, Department of Medicine, Division of Gastroenterology and CEGIIR, University of Alberta, Edmonton, AB T6G 2X8, Canada.
World J Gastroenterol. 2017 Jun 7;23(21):3890-3899. doi: 10.3748/wjg.v23.i21.3890.
To identify demographic, clinical, metabolomic, and lifestyle related predictors of relapse in adult ulcerative colitis (UC) patients.
In this prospective pilot study, UC patients in clinical remission were recruited and followed-up at 12 mo to assess a clinical relapse, or not. At baseline information on demographic and clinical parameters was collected. Serum and urine samples were collected for analysis of metabolomic assays using a combined direct infusion/liquid chromatography tandem mass spectrometry and nuclear magnetic resolution spectroscopy. Stool samples were also collected to measure fecal calprotectin (FCP). Dietary assessment was performed using a validated self-administered food frequency questionnaire.
Twenty patients were included (mean age: 42.7 ± 14.8 years, females: 55%). Seven patients (35%) experienced a clinical relapse during the follow-up period. While 6 patients (66.7%) with normal body weight developed a clinical relapse, 1 UC patient (9.1%) who was overweight/obese relapsed during the follow-up ( = 0.02). At baseline, poultry intake was significantly higher in patients who were still in remission during follow-up (0.9 oz 0.2 oz, = 0.002). Five patients (71.4%) with FCP > 150 μg/g and 2 patients (15.4%) with normal FCP (≤ 150 μg/g) at baseline relapsed during the follow-up ( = 0.02). Interestingly, baseline urinary and serum metabolomic profiling of UC patients with or without clinical relapse within 12 mo showed a significant difference. The most important metabolites that were responsible for this discrimination were trans-aconitate, cystine and acetamide in urine, and 3-hydroxybutyrate, acetoacetate and acetone in serum.
A combination of baseline dietary intake, fecal calprotectin, and metabolomic factors are associated with risk of UC clinical relapse within 12 mo.
确定成年溃疡性结肠炎(UC)患者复发的人口统计学、临床、代谢组学和生活方式相关预测因素。
在这项前瞻性试点研究中,招募临床缓解期的UC患者,并随访12个月以评估是否发生临床复发。在基线时收集人口统计学和临床参数信息。收集血清和尿液样本,使用直接进样/液相色谱串联质谱和核磁共振波谱联用技术分析代谢组学检测。还收集粪便样本以测量粪便钙卫蛋白(FCP)。使用经过验证的自填式食物频率问卷进行饮食评估。
纳入20例患者(平均年龄:42.7±14.8岁,女性:55%)。7例患者(35%)在随访期间经历临床复发。体重正常的6例患者(66.7%)发生临床复发,1例超重/肥胖的UC患者在随访期间复发(P=0.02)。在基线时,随访期间仍处于缓解期的患者家禽摄入量显著更高(0.9盎司±0.2盎司,P=0.002)。基线时FCP>150μg/g的5例患者(71.4%)和FCP正常(≤150μg/g)的2例患者(15.4%)在随访期间复发(P=0.02)。有趣的是,12个月内有或无临床复发的UC患者的基线尿液和血清代谢组学图谱显示出显著差异。造成这种差异的最重要代谢物是尿液中的反乌头酸、胱氨酸和乙酰胺,以及血清中的3-羟基丁酸、乙酰乙酸和丙酮。
基线饮食摄入量、粪便钙卫蛋白和代谢组学因素的组合与UC患者12个月内临床复发风险相关。