机构地区:[1]江西中医药大学循证医学研究中心,南昌330004 [2]内蒙古农业大学食品科学与工程学院,呼和浩特010018 [3]四川大学华西医院中国循证医学中心,成都610041 [4]江西中医药大学附属医院,南昌330000 [5]南昌大学第一附属医院胃肠病科,南昌330000 [6]南昌大学第二附属医院中医科,南昌330000 [7]南昌中西医结合医院胃肠病科,南昌330000 [8]南昌洪都中医院内科,南昌330000
出 处:《中国循证医学杂志》2020年第10期1142-1149,共8页Chinese Journal of Evidence-based Medicine
基 金:江西省卫生健康委员会科技项目(编号:2016B026);江西省自然科学基金项目(编号:2019ZBAB205095)。
摘 要:目的评价猴姑米稀对非器质性胃肠疾病(nonorganic gastrointestinal disorders,NOGD)脾气虚证(spleen qi deficiency,SQD)患者的有效性和安全性。方法采用随机、盲法、平行、安慰剂对照试验设计,纳入NOGD患者并随机分为猴姑米稀组与安慰剂组,每天食用30g猴姑米稀或安慰剂,于第0、2、4、8、26、52周随访观察,比较两组的不同NOGD类型和不同幽门螺旋杆菌(helicobacter pylori,Hp)类型亚组间SQD症状评估量表得分、体重、体质指数(body mass index,BMI)、胃泌素17及不良事件发生情况。结果共纳入200例患者,其中猴姑米稀组100例,安慰剂组100例。在第4、8、26、52周随访点,猴姑米稀组SQD量表得分(临床症状)显著低于安慰剂组[MD=-9.40,95%CI(-18.53,-0.27),P=0.044]、[MD=-10.07,95%CI(-19.66,-0.48),P=0.04]、[MD=-12.45,95%CI(-22.31,-2.59),P=0.014]和[MD=-17.25,95%CI(-28.53,-5.97),P=0.003]。亚组分析显示,在第8、26、52周3个随访点,猴姑米稀可显著降低Hp阴性患者的SQD量表得分[MD=-15.20,95%CI(-28.16,-2.24),P=0.022]、[MD=-17.91,95%CI(-31.22,-4.59),P=0.009]和[MD=-20.38,95%CI(-35.43,-5.32),P=0.008];但对Hp阳性患者,两组得分差异无统计学意义。在第2、26、52周,猴姑米稀可显著降低慢性非萎缩性胃炎患者的SQD量表得分[MD=-13.02,95%CI(-24.75,-1.29),P=0.03]、[MD=-12.43,95%CI(-24.36,-0.5),P=0.041]和[MD=-15.90,95%CI(-30.72,-1.08),P=0.036],并在第52周时降低功能性胃肠病患者的SQD量表得分[MD=-18.22,95%CI(-35.75,-0.69),P=0.042]。研究和随访期间猴姑米稀组均未发生不良事件。两组患者在体重、BMI、胃泌素17水平方面的差异均无统计学意义。结论猴姑米稀可有效改善非器质性胃肠疾病,特别是Hp阴性患者的脾气虚证症状,且安全性良好。Objectives To investigate the efficacy and safety of Hou Gu Mi Xi(HGMX) in patients with nonorganic gastrointestinal disorders(NOGD) from the aspect of dietary therapy. Methods A randomized, doubleblind, parallel, placebo-controlled trial was performed. Patients with NOGD and spleen qi deficiency(SQD) syndrome were randomly assigned into HGMX or placebo group. Each received 30 g/day HGMX or placebo for one year. The outcomes included SQD scores, body weight, body mass index(BMI), gastrin-17, and adverse events(AEs) between HGMX and placebo groups, or subgroups divided by NOGD type or helicobacter pylori(Hp) infection, at the 0th, 2nd, 4th,8th, 26th, or 52nd weeks’ follow-up. Results The reduction of SQD scale score was found in the HGMX group compared with the placebo group at 4th week(MD=-9.40, 95%CI-18.53 to-0.27, P=0.044), 8th week(MD=-10.07, 95%CI-19.66 to-0.48, P=0.04), 26th week(MD=-12.45, 95%CI-22.31 to-2.59, P=0.014) and 52th week(MD=-17.25, 95%CI-28.53 to-5.97, P=0.003), respectively. In the subgroup analyses, HGMX showed significant efficacy in Hp-negative patients with the detailed reduction of SQD scale score being(MD=-15.20, 95%CI-28.16 to-2.24, P=0.022),(MD=-17.91, 95%CI-31.22 to-4.59, P=0.009) and(MD=-20.38, 95%CI-35.43 to-5.32, P=0.008) at the 8th, 26th and 52nd week, respectively,and in patients with chronic nonatrophic gastritis with the detailed reduction being(MD=-13.02, 95%CI-24.75 to-1.29,P=0.03),(MD=-12.43, 95%CI-24.36 to-0.5, P=0.041) and(MD=-15.90, 95%CI-30.72 to-1.08, P=0.036) at the 2nd, 26th and 52nd week, respectively, and in patients with functional gastrointestinal disease with the reduction being(MD=-18.22,95%CI-35.75 to-0.69, P=0.042) at the 52nd week. However, no significant efficacy was found in Hp-positive patient at any time. HGMX was not associated with changes in weight, BMI, or gastrin-17. No AEs were reported in the HGMX group. Conclusions HGMX improves SQD symptoms in patients with NOGD, especially Hp-negative patients, and has a good safety profile.
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