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Therapeutic effect of melatonin on pediatric functional dyspepsia: A pilot study

机译:褪黑素对小儿功能性消化不良的治疗作用:一项初步研究

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摘要

AIM: To study the effectiveness of melatonin vs placebo in children with functional dyspepsia (FD).METHODS: The study was conducted as a double blind, randomized, placebo controlled crossover trial. Subjects were aged 8-17 years and diagnosed with FD based on Rome III criteria. All subjects had failed to respond to 4 wk of acid suppression. Subjects receive a continuous two weeks of placebo and a continuous two weeks of melatonin in an order blinded to the participant and the study team. A Global Clinical Score was obtained to assess changes in abdominal pain. Pain was self-reported to be worse (grade 1), no change (grade 2), moderate improvement (grade 3), good (grade 4; minimal pain and not interfering with daily activities), or excellent (grade 5; no pain), respectively. A positive clinical response was defined as a grade 3 or greater response. Subjects wore an actigraph to assess sleep during a one week baseline period and during each treatment period. Subjects’ sleep latency and total sleep time were recorded throughout the duration of the study.RESULTS: Fourteen subjects were enrolled and 12 completed the study. One withdrew prior to starting both melatonin and placebo and the other before starting melatonin. A positive clinical response (grade 3-5) was achieved in 42% of subjects on melatonin vs 50% of subjects on placebo (NS). Effect size was calculated and revealed a Cohen’s D of 0.343 which demonstrates a medium effect favoring placebo. A grade 4 or grade 5 response was seen in 4 patients on melatonin and 5 patients on placebo. Baseline sleep parameters were in the healthy range with the longest sleep latency being just over 20 min (mean 7.46 ± 8.53 min) and the shortest sleep duration just over 7 h (mean 10.09 ± 2.72 h). The mean latency did not differ between periods of treatment with melatonin as compared to placebo (4.48 ± 6.45 min vs 3.58 ± 4.24 min; NS). The mean sleep duration did not differ between periods of treatment with melatonin as compared to placebo (9.90 ± 3.53 h vs 9.41 ± 2.70 h; NS).CONCLUSION: Melatonin does not appear to have efficacy in relieving pain in unselected pediatric FD. Future studies should consider FD subtypes, pathophysiologic mechanisms, and baseline sleep disturbances.
机译:目的:研究褪黑激素与安慰剂在功能性消化不良(FD)患儿中的有效性。方法:该研究是一项双盲,随机,安慰剂对照的交叉试验。受试者年龄为8-17岁,并根据罗马III标准诊断为FD。所有受试者均未对4周酸抑制做出反应。受试者接受连续两周的安慰剂和连续两周的褪黑激素,以使参与者和研究小组不知情。获得全球临床评分以评估腹痛的变化。自我报告的疼痛较重(1级),无变化(2级),中度改善(3级),良好(4级;疼痛最小且不影响日常活动)或优异(5级;无疼痛) ), 分别。阳性临床反应定义为3级或更高反应。受试者戴着活动记录仪以评估在一周的基线期间和每个治疗期间的睡眠。在整个研究过程中记录受试者的睡眠潜伏期和总睡眠时间。结果:招募了14名受试者,其中12名完成了研究。一个人在开始褪黑激素和安慰剂之前退出,另一个在开始褪黑激素之前退出。接受褪黑激素治疗的受试者中有42%达到了阳性临床反应(3-5级),而使用安慰剂(NS)则达到了50%。计算了效应大小,并显示了0.343的Cohen D值,这表明有中等效应有利于安慰剂。在4例褪黑素患者和5例安慰剂患者中发现4级或5级反应。基线睡眠参数处于健康范围内,最长的睡眠潜伏期刚好超过20分钟(平均7.46±8.53分钟),而最短的睡眠持续时间刚好超过7小时(平均10.09±2.72小时)。与安慰剂相比,褪黑激素治疗期间的平均潜伏期无差异(4.48±6.45分钟vs 3.58±4.24分钟; NS)。与安慰剂相比,褪黑激素治疗各阶段的平均睡眠时间无差异(9.90±3.53 h vs 9.41±2.70 h; NS)。结论:褪黑素似乎对缓解非选择性儿科FD患者的疼痛没有疗效。未来的研究应考虑FD亚型,病理生理机制和基线睡眠障碍。

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