Clinical Enteric Neuroscience Translational and Epidemiological Research (CENTER), College of Medicine, Mayo Clinic, Rochester, MN, United States; Division of Gastroenterology and Hepatology, College of Medicine, Mayo Clinic, Rochester, MN, United States.
Clinical Enteric Neuroscience Translational and Epidemiological Research (CENTER), College of Medicine, Mayo Clinic, Rochester, MN, United States; Division of Gastroenterology and Hepatology, College of Medicine, Mayo Clinic, Rochester, MN, United States.
Dig Liver Dis. 2014 Feb;46(2):113-8. doi: 10.1016/j.dld.2013.09.002. Epub 2013 Oct 4.
In prior studies, pregabalin reduced rectal or colonic pain in patients with irritable bowel syndrome and healthy adults, suggesting reduction of afferent function.
To assess effects of pregabalin on colonic compliance, sensory and motor functions in patients with constipation-predominant irritable bowel syndrome.
In a pilot, double-blind, placebo-controlled, parallel-group study, we tested oral pregabalin, 200mg, in 18 patients with constipation-predominant irritable bowel syndrome. With a barostatically controlled polyethylene balloon in the left colon, we assessed sensation thresholds and colonic compliance using ascending method of limits, sensation ratings over 4 levels of distension, fasting and postprandial colonic tone and phasic motility. Analysis of covariance (adjusted for the corresponding pre-drug response) was used to compare placebo and pregabalin. After 45% participants completed studies, we conducted an interim analysis to assess the conditional power to detect pre-specified treatment effects given the observed variation and treatment group differences based on the planned sample size for the trial.
Pregabalin did not significantly affect colonic compliance, sensation thresholds, sensation ratings, fasting or postprandial tone or motility index. The study was stopped for futility to detect an effect on visceral pain with the planned design and sample size.
Pregabalin, 200mg, might not reduce distension-related colonic pain in constipation-predominant irritable bowel syndrome patients.
在之前的研究中,普瑞巴林可减轻肠易激综合征患者和健康成年人的直肠或结肠疼痛,提示传入功能降低。
评估普瑞巴林对便秘型肠易激综合征患者结肠顺应性、感觉和运动功能的影响。
在一项先导性、双盲、安慰剂对照、平行组研究中,我们测试了便秘型肠易激综合征患者口服普瑞巴林 200mg 的效果。采用球囊控压法,将聚乙稀球囊置于左半结肠,通过升序极限法评估感觉阈值和结肠顺应性,通过 4 级充盈度评估感觉评分、空腹和餐后结肠张力以及时相性运动。采用协方差分析(调整相应的预用药反应)比较安慰剂和普瑞巴林的差异。在 45%的参与者完成研究后,我们进行了中期分析,根据观察到的变异和基于试验计划样本量的治疗组差异,评估在既定设计和样本量下检测预定治疗效果的条件效力。
普瑞巴林对结肠顺应性、感觉阈值、感觉评分、空腹或餐后张力或运动指数均无显著影响。由于计划设计和样本量,该研究因无效而停止,无法检测到对内脏疼痛的影响。
普瑞巴林 200mg 可能不会减轻便秘型肠易激综合征患者的扩张相关结肠疼痛。