Lee Kwang Jae
Department of Gastroenterology, Ajou University School of Medicine, Suwon, Gyeonggi-do, Korea.
J Neurogastroenterol Motil. 2021 Jul 30;27(3):326-336. doi: 10.5056/jnm21042.
Functional dyspepsia (FD) is considered to be a heterogeneous disorder with different pathophysiological mechanisms or pathogenetic factors. In addition to traditional mechanisms, novel concepts regarding pathophysiologic mechanisms of FD have been proposed. Candidates of therapeutic agents based on novel concepts have also been suggested. FD is a symptom complex and currently diagnosed by symptom-based Rome criteria. In the Rome criteria, symptom-based subtypes of FD including postprandial distress syndrome and epigastric pain syndrome are recommended to be used, based on the assumption that each subtype is more homogenous in terms of underlying pathophysiologic mechanisms than FD as a whole. In this review, the usefulness of symptombased subtypes of FD for predicting underlying pathophysiologic mechanisms and choosing appropriate therapeutic agents was evaluated. Although several classic pathophysiologic mechanisms are suggested to be associated with individual dyspeptic symptoms, symptom-based subtypes of FD are not specific for a certain pathogenetic factor or pathophysiologic mechanism, and may be frequently associated with multiple pathophysiologic abnormalities. Novel concepts on the pathophysiology of FD show complex interactions between pathophysiologic mechanisms and pathogenetic factors, and prediction of underlying mechanisms of individual patients simply by the symptom pattern or symptom-based subtypes may not be accurate in a considerable proportion of cases. Therefore, subtyping by the Rome criteria appears to have limited value to guide therapeutic strategy, suggesting that the addition of objective parameters or subclassification reflecting physiologic or pathologic tests may be necessary for the targeted therapeutic approaches, particularly when therapeutic agents targeting novel mechanisms are available.
功能性消化不良(FD)被认为是一种具有不同病理生理机制或致病因素的异质性疾病。除了传统机制外,关于FD病理生理机制的新概念也已被提出。基于新概念的治疗药物候选物也已被提出。FD是一种症状复合体,目前根据基于症状的罗马标准进行诊断。在罗马标准中,建议使用基于症状的FD亚型,包括餐后不适综合征和上腹痛综合征,其假设是每个亚型在潜在病理生理机制方面比整体FD更具同质性。在本综述中,评估了基于症状的FD亚型对预测潜在病理生理机制和选择合适治疗药物的有用性。尽管有几种经典的病理生理机制被认为与个体消化不良症状相关,但基于症状的FD亚型并非特定于某种致病因素或病理生理机制,并且可能经常与多种病理生理异常相关。关于FD病理生理学的新概念显示了病理生理机制和致病因素之间的复杂相互作用,在相当一部分病例中,仅通过症状模式或基于症状的亚型来预测个体患者的潜在机制可能并不准确。因此,根据罗马标准进行亚型分类似乎对指导治疗策略的价值有限,这表明对于靶向治疗方法而言,添加反映生理或病理检查的客观参数或进一步分类可能是必要的,特别是当有针对新机制的治疗药物时。