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Nizatidine improves clinical symptoms and gastric emptying in patients with functional dyspepsia accompanied by impaired gastric emptying

机译:尼扎替丁改善功能性消化不良并伴有胃排空障碍的患者的临床症状和胃排空

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Background/Aims: In this crossover study, we investigated whether nizatidine, a H 2-receptor antagonist, can alleviate clinical symptoms and gastric emptying in patients with Rome III-based functional dyspepsia (FD) with or without impaired gastric emptying. Methods: We enrolled 30 patients presenting with FD symptoms (epigastric pain syndrome, n = 6; postprandial distress syndrome, n = 24). Rome III-based FD patients were treated with nizatidine (300 mg/day) or placebo for 4 weeks in a crossover trial. Gastric motility was mainly evaluated with the T max value using the 13C-acetate breath test. Meal-related symptoms were defined as postprandial fullness and early satiation. Gastroesophageal symptom was defined as a burning feeling rising from the stomach or lower chest up toward the neck. Acylated-and desacylated ghrelin levels were evaluated by the ELISA method. Clinical symptoms, gastric emptying and ghrelin levels were evaluated at three different points during the study (pretreatment, after 4 weeks former treatment and after 4 weeks later treatment). The primary end point of this study was to determine whether nizatidine would improve clinical symptoms and gastric emptying in FD patients with or without impaired gastric emptying via affecting ghrelin levels. Results: Meal-related symptoms of the patients treated with nizatidine improved significantly (21/30; 70%) compared to those treated with placebo (3/30; 10%). In addition, nizatidine treatment also significantly improved gastroesophageal symptoms (16/30; 53%) compared to those treated with placebo (0/30; 0%). Nizatidine treatment in patients with FD accompanied by impaired gastric emptying significantly improved clinical symptoms and T max value as a marker of gastric emptying (10/11, 91%; 9/11, 82%) compared to placebo therapy, respectively. There were no significant differences in ghrelin levels between nizatidine treatment and placebo therapy. Conclusion: Nizatidine administration significantly improved both gastric emptying and clinical symptoms in FD patients with impaired gastric emptying.
机译:背景/目的:在这项交叉研究中,我们研究了H 2受体拮抗剂尼扎替丁是否可以缓解以罗马III型功能性消化不良(FD)为伴或不伴有胃排空障碍的患者的临床症状和胃排空。方法:我们招募了30名出现FD症状的患者(室痛综合征,n = 6;餐后窘迫综合征,n = 24)。基于罗马III的FD患者在交叉试验中接受尼扎替丁(300 mg /天)或安慰剂治疗4周。胃动力主要通过13 C-乙酸呼气试验以T max值进行评估。与膳食有关的症状定义为餐后饱胀和早饱。胃食管症状的定义是从胃或下胸部向颈部上升的烧灼感。通过ELISA方法评估酰化和去酰化的生长素释放肽水平。在研究期间的三个不同点(治疗前,治疗前4周和治疗后4周)评估了临床症状,胃排空和生长素释放肽水平。这项研究的主要目的是确定尼扎替丁是否会通过影响生长素释放肽水平来改善有或没有胃排空障碍的FD患者的临床症状和胃排空。结果:与安慰剂治疗的患者(3/30; 10%)相比,尼扎替丁治疗的患者与膳食有关的症状明显改善(21/30; 70%)。此外,与使用安慰剂治疗的患者(0/30; 0%)相比,尼扎替丁治疗还显着改善了胃食管症状(16/30; 53%)。与安慰剂治疗相比,尼扎替丁治疗FD并伴有胃排空障碍的患者显着改善了临床症状和T max值,作为胃排空的标志物(10/11,91%; 9/11,82%)。尼扎替丁治疗和安慰剂治疗之间的生长激素释放肽水平无显着差异。结论:尼扎替丁给药可显着改善FD胃排空障碍患者的胃排空和临床症状。

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