Lee Ju Yup, Kim Nayoung, Park Ji Hyun, Yu Jeong Eun, Song Yun Jeong, Yoon Jung Won, Lee Dong Ho
Department of Internal Medicine, Seoul National University Bundang Hospital, Seoungnam, Gyeonggi-do, Korea.
Department of Internal Medicine, Keimyung University School of Medicine, Daegu, Korea.
J Neurogastroenterol Motil. 2022 Jan 30;28(1):145-158. doi: 10.5056/jnm21047.
BACKGROUND/AIMS: Overlap functional gastrointestinal disorder (FGID) is associated with more severe gastrointestinal symptoms and lower quality of life. The aim of this study is to evaluate clinical features of non-erosive reflux disease (NERD), functional dyspepsia, irritable bowel syndrome, their overlap in terms of sex and gender, and to assess the risk factors, including genetic polymorphisms.
A total of 494 FGIDs and 239 controls were prospectively enrolled between 2004 and 2020. FGIDs were diagnosed based on the Rome III criteria and symptoms were evaluated using a questionnaire. Follow-up questionnaires were conducted to determine the change of symptoms during the 75.8-month mean observation period. Risk factors including genetic polymorphisms in neurotransmitter receptor (, and ) and cytokine ( and ) genes.
NERD was more prevalent in men, and functional dyspepsia in women. Overlap FGIDs (n = 239) were more prevalent than nonoverlap FGIDs (n = 255) in women ( = 0.019). Anxiety and depression scores were higher in the overlaps ( = 0.012 and < 0.001, respectively). Symptoms were more frequent and severe in the overlap FGIDs than in the non-overlaps ( < 0.001). During followup, symptoms progressed more frequently in the overlap FGIDs, especially in patients with the L/S genotype of and anxiety/depression.
Overlap FGID patients need attention given their association with anxiety/depression and more severe symptoms, especially in women. Genetic polymorphisms also may be associated with certain symptoms of overlap FGIDs.
背景/目的:重叠型功能性胃肠病(FGID)与更严重的胃肠道症状及更低的生活质量相关。本研究旨在评估非糜烂性反流病(NERD)、功能性消化不良、肠易激综合征的临床特征,及其在性别方面的重叠情况,并评估包括基因多态性在内的危险因素。
2004年至2020年期间前瞻性纳入了494例FGID患者和239例对照。FGID根据罗马Ⅲ标准进行诊断,症状通过问卷进行评估。进行随访问卷以确定在平均75.8个月的观察期内症状的变化。危险因素包括神经递质受体(、和)及细胞因子(和)基因的基因多态性。
NERD在男性中更常见,而功能性消化不良在女性中更常见。重叠型FGID(n = 239)在女性中比非重叠型FGID(n = 255)更常见(= 0.019)。重叠型患者的焦虑和抑郁评分更高(分别为 = 0.012和<0.001)。重叠型FGID的症状比非重叠型更频繁、更严重(<0.001)。在随访期间,重叠型FGID的症状进展更频繁,尤其是具有和焦虑/抑郁的L/S基因型的患者。
重叠型FGID患者因其与焦虑/抑郁及更严重症状的关联而需要关注,尤其是在女性中。基因多态性也可能与重叠型FGID的某些症状相关。