Ghadir Mohammad Reza, Poradineh Mehri, Sotodeh Masoud, Ansari Reza, Kolahdoozan Shadi, Hormati Ahmad, Yousefi Mohammad Hosein, Mirzaei Samaneh, Vahedi Homayoon
Associate Professor, Qom Gastroenterology and Hepatology Research Center, ShahidBeheshti Hospital, Qom University of Medical Sciences, Qom, Iran.
Researcher, Digestive Disease Research Institute, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran.
Middle East J Dig Dis. 2017 Jan;9(1):20-25. doi: 10.15171/mejdd.2016.47.
BACKGROUND Intestinal mast cells may cause gastrointestinal symptoms in patients with diarrhea-dominant irritable bowel syndrome (IBS). The objective of this study was to determine the effect of mesalazine on the number of lamina propria mast cells and clinical manifestations of patients with diarrhea-dominant IBS referred to Shariati Hospital affiliated to Tehran University of Medical Sciences. METHODS This was a randomized placebo-controlled double-blind trial conducted on 49 patients with diarrhea-dominant IBS. The patients were randomly assigned to one of the experiment or control groups. The patients in experiment group took 2400 mg mesalazine daily in three divided doses for 8 weeks and the patient in control group took placebo on the same basis. Our first targeted outcome was an assigned downturn of mast cells number to the safe colonic baseline and the next one was a marked palliation of disease symptoms. Data were analyzed conforming intention-to-treat method. We used MANCOVA test to compare our both assigned outcomes in the two groups. We also compared the data with baseline values in both groups.All statistical tests were performed at the significance level of 0.05. RESULTS There was no significant difference between Mesalazine and placebo groups regarding the number of mast cells ( value=0.396), abdominal pain ( value=0.054), bloating ( value=0.365), defecation urgency ( value=0.212), and defecation frequency ( value=0.702). CONCLUSION Mesalazine had no significant effect either on the number of mast cells or on the severity of disease symptoms. This finding seems to be inconsistent with the hypothesis indicating immune mechanisms as potential therapeutic targets in IBS. The possible difference in this effect of Mesalazine should be evaluated in further studies among populations varying in race, ethnic, and geographical characteristics.
背景 肠道肥大细胞可能在腹泻型肠易激综合征(IBS)患者中引发胃肠道症状。本研究的目的是确定美沙拉嗪对德黑兰医科大学附属沙里亚蒂医院收治的腹泻型IBS患者固有层肥大细胞数量及临床表现的影响。方法 这是一项针对49例腹泻型IBS患者进行的随机安慰剂对照双盲试验。患者被随机分配至试验组或对照组。试验组患者每日分三次服用2400毫克美沙拉嗪,共8周,对照组患者在相同基础上服用安慰剂。我们的首要目标结果是将肥大细胞数量降至安全的结肠基线水平,其次是显著缓解疾病症状。数据按照意向性分析方法进行分析。我们使用多变量协方差分析(MANCOVA)检验比较两组的两个目标结果。我们还将两组数据与基线值进行了比较。所有统计检验均在0.05的显著性水平上进行。结果 美沙拉嗪组与安慰剂组在肥大细胞数量(值 = 0.396)、腹痛(值 = 0.054)、腹胀(值 = 0.365)、排便急迫感(值 = 0.212)和排便频率(值 = 0.702)方面无显著差异。结论 美沙拉嗪对肥大细胞数量或疾病症状严重程度均无显著影响。这一发现似乎与将免疫机制作为IBS潜在治疗靶点的假设不一致。美沙拉嗪这种效应的可能差异应在种族、民族和地理特征不同的人群中进行进一步研究评估。