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Serum and Urine Metabolomic Profiling of Newly Diagnosed Treatment-Naïve Inflammatory Bowel Disease Patients

溃疡性结肠炎 医学 炎症性肠病 胃肠病学 内科学 尿 代谢组学 克罗恩病 单变量分析 疾病 队列 多元分析 生物信息学 生物
作者
Laila Aldars‐García,Rubén Gil‐Redondo,Nieves Embade,Sabino Riestra,Montserrat Rivero,Ana Gutiérrez,Iago Rodríguez‐Lago,Luis Fernández‐Salazar,Daniel Ceballos,J M Benítez,Mariam Aguas,Iria Bastón‐Rey,Fernando Bermejo,María José Casanova,Rufo Lorente,Yolanda Ber,Daniel Ginard,María Esteve,Ruth de Francisco,María José García
出处
期刊:Inflammatory Bowel Diseases [Oxford University Press]
卷期号:30 (2): 167-182 被引量:18
标识
DOI:10.1093/ibd/izad154
摘要

Abstract Background and Aims Inflammatory bowel disease (IBD) is a prevalent chronic noncurable disease associated with profound metabolic changes. The discovery of novel molecular indicators for unraveling IBD etiopathogenesis and the diagnosis and prognosis of IBD is therefore pivotal. We sought to determine the distinctive metabolic signatures from the different IBD subgroups before treatment initiation. Methods Serum and urine samples from newly diagnosed treatment-naïve IBD patients and age and sex-matched healthy control (HC) individuals were investigated using proton nuclear magnetic resonance spectroscopy. Metabolic differences were identified based on univariate and multivariate statistical analyses. Results A total of 137 Crohn’s disease patients, 202 ulcerative colitis patients, and 338 HC individuals were included. In the IBD cohort, several distinguishable metabolites were detected within each subgroup comparison. Most of the differences revealed alterations in energy and amino acid metabolism in IBD patients, with an increased demand of the body for energy mainly through the ketone bodies. As compared with HC individuals, differences in metabolites were more marked and numerous in Crohn’s disease than in ulcerative colitis patients, and in serum than in urine. In addition, clustering analysis revealed 3 distinct patient profiles with notable differences among them based on the analysis of their clinical, anthropometric, and metabolomic variables. However, relevant phenotypical differences were not found among these 3 clusters. Conclusions This study highlights the molecular alterations present within the different subgroups of newly diagnosed treatment-naïve IBD patients. The metabolomic profile of these patients may provide further understanding of pathogenic mechanisms of IBD subgroups. Serum metabotype seemed to be especially sensitive to the onset of IBD.
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