Department of Chemical and Systems Biology, Stanford University School of Medicine, Stanford, California.
Stanford Inflammatory Bowel Disease Center, Department of Pediatrics, Stanford, California; GastroImmunology, Genentech, South San Francisco, California.
Clin Gastroenterol Hepatol. 2020 Oct;18(11):2618-2619.e1. doi: 10.1016/j.cgh.2019.08.052. Epub 2019 Sep 6.
Fecal calprotectin, the heterodimer of S100A8/S100A9, makes up ∼60% of neutrophil cytoplasmic protein content and is a canonical clinical biomarker of gut inflammation. Fecal calprotectin is commonly used to diagnose inflammatory bowel disease (IBD) and has an average sensitivity of 93% and specificity of 96%. For diagnosing pediatric IBD, calprotectin fecal tests have similar sensitivity (92%) but substantially less specificity (76%). Low specificity, especially in pediatric patients, means a high likelihood of false negative diagnoses, suggesting that a substantial number of active IBD cases remain undiagnosed and untreated. To improve on calprotectin as an effective IBD monitoring tool in pediatric populations, specificity must be increased. To develop an assay with higher specificity in pediatric patients, we identified a panel of multiple proteins that are present in both IBD flare and remission but have distinct abundance ranges between each condition. From a pilot cohort of 10 pediatric patients in states of either active disease or remission, we discovered and relatively quantified hundreds of stool proteins. Of these, our mass spectrometry-based study prioritized at least 5 that have potential to augment negative predictive power of mucosal-level inflammation alongside fecal biomarkers such as calprotectin.
粪便钙卫蛋白是 S100A8/S100A9 的异源二聚体,占中性粒细胞细胞质蛋白含量的 ∼60%,是肠道炎症的经典临床生物标志物。粪便钙卫蛋白常用于诊断炎症性肠病 (IBD),其平均灵敏度为 93%,特异性为 96%。对于诊断儿科 IBD,钙卫蛋白粪便检测具有相似的灵敏度(92%),但特异性显著降低(76%)。特异性低,尤其是在儿科患者中,意味着假阴性诊断的可能性很高,这表明大量活动性 IBD 病例仍未被诊断和治疗。为了提高钙卫蛋白作为儿科人群中有效 IBD 监测工具的效果,必须提高其特异性。为了开发一种在儿科患者中具有更高特异性的检测方法,我们确定了一组存在于 IBD 发作和缓解期的多种蛋白质,但每种情况下的丰度范围不同。在 10 名处于活动期或缓解期的儿科患者的试点队列中,我们发现并相对定量了数百种粪便蛋白。在这些蛋白中,我们基于质谱的研究至少确定了 5 种具有与钙卫蛋白等黏膜水平炎症的粪便生物标志物联合使用时提高阴性预测能力的潜力。