Aldars-García Laila, Gisbert Javier P, Chaparro María
Gastroenterology Department, Hospital Universitario de La Princesa, Instituto de Investigación Sanitaria Princesa (IIS-IP), Universidad Autónoma de Madrid (UAM), Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), 28006 Madrid, Spain.
Pharmaceuticals (Basel). 2021 Nov 20;14(11):1190. doi: 10.3390/ph14111190.
Inflammatory bowel disease (IBD) is a chronic, complex relapsing disorder characterised by immune dysregulation, gut microbiota alteration, and disturbed intestinal permeability. The diagnosis and the management of IBD are challenging due to the recurrent nature and complex evolution of the disease. Furthermore, the molecular mechanism underlying the aetiology and pathogenesis of IBD is still poorly understood. There is an unmet need for novel, reliable, and noninvasive tools for diagnosing and monitoring IBD. In addition, metabolomic profiles may provide a priori determination of optimal therapeutics and reveal novel targets for therapies. This review tries to gather scientific evidence to summarise the emerging contribution of metabolomics to elucidate the mechanisms underlying IBD and changes associated with disease phenotype and therapies, as well as to identify biomarkers with metabolic imbalance in those patients. Metabolite changes during health and disease could provide insights into the disease pathogenesis and the discovery of novel indicators for the diagnosis and prognosis assessment of IBD. Metabolomic studies in IBD have shown changes in tricarboxylic acid cycle intermediates, amino-acid and fatty-acid metabolism, and oxidative pathways. Metabolomics has made progress towards identifying metabolic alterations that may provide clinically useful biomarkers and a deeper understanding of the disease. However, at present, there is insufficient evidence evaluating the predictive accuracy of these molecular signatures and their diagnostic ability, which is necessary before metabolomic data can be translated into clinical practice.
炎症性肠病(IBD)是一种慢性、复杂的复发性疾病,其特征为免疫失调、肠道微生物群改变和肠道通透性紊乱。由于该疾病具有复发性和复杂的演变过程,IBD的诊断和管理具有挑战性。此外,IBD病因和发病机制的分子机制仍知之甚少。对于诊断和监测IBD的新型、可靠且非侵入性工具存在未满足的需求。此外,代谢组学图谱可能有助于预先确定最佳治疗方法,并揭示新的治疗靶点。本综述试图收集科学证据,总结代谢组学在阐明IBD潜在机制、与疾病表型和治疗相关的变化方面的新贡献,以及识别那些患者中存在代谢失衡的生物标志物。健康和疾病期间的代谢物变化可以为疾病发病机制以及IBD诊断和预后评估新指标的发现提供见解。IBD的代谢组学研究显示三羧酸循环中间体、氨基酸和脂肪酸代谢以及氧化途径发生了变化。代谢组学在识别可能提供临床有用生物标志物并更深入了解疾病的代谢改变方面取得了进展。然而,目前,评估这些分子特征的预测准确性及其诊断能力的证据不足,而这是代谢组学数据转化为临床实践之前所必需的。