Salomon Benita, Grännö Olle, Bergemalm Daniel, Strid Hans, Carstens Adam, Hjortswang Henrik, Ling Lundström Maria, Hreinsson Jóhann P, Almer Sven, Bresso Franscesca, Eriksson Carl, Grip Olof, Blomberg André, Marsal Jan, Nikaein Niloofar, Bakhtyar Shoaib, Lindqvist Carl Mårten, Hultgren Hörnquist Elisabeth, Magnusson Maria K, Keita Åsa V, D'Amato Mauro, Repsilber Dirk, Öhman Lena, Söderholm Johan D, Carlson Marie, Hedin Charlotte R H, Kruse Robert, Halfvarson Jonas
School of Medical Sciences, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
Department of Laboratory Medicine, Clinical Microbiology, Faculty of Medicine and Health, Örebro University, Örebro, Sweden.
BMJ Open. 2025 May 6;15(5):e099218. doi: 10.1136/bmjopen-2025-099218.
There is a need for diagnostic and prognostic biosignatures to improve long-term outcomes in inflammatory bowel disease (IBD). Here, we describe the establishment of the Swedish Inception Cohort in IBD (SIC-IBD) and demonstrate its potential for the identification of such signatures.
Patients aged ≥18 years with gastrointestinal symptoms who were referred to the gastroenterology unit due to suspected IBD at eight Swedish hospitals between November 2011 and March 2021 were eligible for inclusion.
In total, 367 patients with IBD (Crohn's disease, n=142; ulcerative colitis, n=201; IBD-unclassified, n=24) and 168 symptomatic controls were included. In addition, 59 healthy controls without gastrointestinal symptoms were recruited as a second control group. Biospecimens and clinical data were collected at inclusion and in patients with IBD also during follow-up to 10 years. Levels of faecal calprotectin and high-sensitivity C-reactive protein were higher in patients with IBD compared with symptomatic controls and healthy controls. Preliminary results highlight the potential of serum protein signatures and autoantibodies, as well as results from faecal markers, to differentiate between IBD and symptomatic controls in the cohort. During the first year of follow-up, 37% (53/142) of the patients with Crohn's disease, 24% (48/201) with ulcerative colitis and 4% (1/24) with IBD-U experienced an aggressive disease course.
We have established an inception cohort enabling ongoing initiatives to collect and generate clinical data and multi-omics datasets. The cohort will allow analyses for translation into candidate biosignatures to support clinical decision-making in IBD. Additionally, the data will provide insights into mechanisms of disease pathogenesis.
需要诊断和预后生物标志物来改善炎症性肠病(IBD)的长期预后。在此,我们描述了瑞典IBD初始队列(SIC-IBD)的建立,并展示了其识别此类标志物的潜力。
2011年11月至2021年3月期间,因疑似IBD被转诊至瑞典8家医院胃肠病科的年龄≥18岁且有胃肠道症状的患者符合纳入条件。
总共纳入了367例IBD患者(克罗恩病,n = 142;溃疡性结肠炎,n = 201;未分类IBD,n = 24)和168例有症状对照。此外,招募了59例无胃肠道症状的健康对照作为第二对照组。在纳入时收集生物标本和临床数据,IBD患者在随访至10年期间也进行收集。与有症状对照和健康对照相比,IBD患者的粪便钙卫蛋白和高敏C反应蛋白水平更高。初步结果突出了血清蛋白标志物和自身抗体以及粪便标志物结果在该队列中区分IBD和有症状对照的潜力。在随访的第一年,37%(53/142)的克罗恩病患者、24%(48/201)的溃疡性结肠炎患者和4%(1/24)的未分类IBD患者经历了侵袭性病程。
我们建立了一个初始队列,支持正在进行的收集和生成临床数据及多组学数据集的项目。该队列将允许进行分析以转化为候选生物标志物,以支持IBD的临床决策。此外,这些数据将提供对疾病发病机制的见解。