Predicting disease course in ulcerative colitis using stool proteins identified through an aptamer-based screen

利用基于适体筛选鉴定的粪便蛋白预测溃疡性结肠炎的疾病进程

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作者:Sanam Soomro # ,Suresh Venkateswaran # ,Kamala Vanarsa ,Marwa Kharboutli ,Malavika Nidhi ,Ramya Susarla ,Ting Zhang ,Prashanth Sasidharan ,Kyung Hyun Lee ,Joel Rosh ,James Markowitz ,Claudia Pedroza ,Lee A Denson ,Jeffrey Hyams ,Subra Kugathasan ,Chandra Mohan

Abstract

In the search for improved stool biomarkers for inflammatory bowel disease (IBD), an aptamer-based screen of 1129 stool proteins was conducted using stool samples from an IBD cohort. Here we report that of the 20 proteins subsequently validated by ELISA, stool Ferritin, Fibrinogen, Haptoglobin, Hemoglobin, Lipocalin-2, MMP-12, MMP-9, Myeloperoxidase, PGRP-S, Properdin, Resistin, Serpin A4, and TIMP-1 are significantly elevated in both ulcerative colitis (UC) and Crohn's disease (CD) compared to controls. When tested in a longitudinal cohort of 50 UC patients at 4 time-points, fecal Fibrinogen, MMP-8, PGRP-S, and TIMP-2 show the strongest positive correlation with concurrent PUCAI and PGA scores and are superior to fecal calprotectin. Unlike fecal calprotectin, baseline stool Fibrinogen, MMP-12, PGRP-S, TIMP-1, and TIMP-2 can predict clinical remission at Week-4. Here we show that stool proteins identified using the comprehensive aptamer-based screen are superior to fecal calprotectin alone in disease monitoring and prediction in IBD.

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