Wu Zi-Yu, Zhang Meng-Han, Li Yue, Deng Jin-Yan, Liu Lan-Yue, Chen Chen, Du Hong-Bo, Guo Yi
Gastroenterology Department, Dongzhimen Hospital, Beijing University of Chinese Medicine, Beijing, 100700, China.
Institute of Liver Diseases, Beijing University of Chinese Medicine, Beijing, 100700, China.
Dig Dis Sci. 2025 Aug 24. doi: 10.1007/s10620-025-09334-y.
Bile reflux gastritis (BRG) may lead to precancerous lesions of gastric cancer and gastric cancer. Although ursodeoxycholic acid (UDCA) has been used to treat BRG, its clinical efficacy remains unknown. Therefore, we systematically evaluated the efficacy and safety of UDCA compared with conventional therapy for BRG.
We selected candidate studies and generated a forest plot to evaluate outcomes. Metaregression analysis was conducted to identify possible explanations for heterogeneity. Study quality was evaluated using the Cochrane Risk of Bias 2 tool and the Newcastle-Ottawa scale. The quality of evidence for the outcomes of the meta-analysis was assessed using the Grading of Recommendations Assessment, Development and Evaluation approach.
A total of 14 studies including 1605 patients were identified. Compared with control groups, medication combined with UDCA significantly reduced the number of reflux episodes [mean difference (MD) = - 17.99 times, 95% CI (- 19.84, - 16.14)], shortened the longest duration of reflux [MD = - 9.21 min, 95% CI (- 12.63, - 5.80)], decreased the number of long reflux episodes [MD = - 3.21 times, 95% CI (- 3.76, - 2.66)], increased the clinical response rate [risk ratio = 1.15, 95% CI (1.10, 1.19)], decreased the gastrin content [MD = - 18.03 ng/L, 95% CI (- 33.88, - 2.18)] and alleviated symptoms.
UDCA demonstrates significant therapeutic efficacy for BRG, particularly with 8-week regimens, supporting its potential as a first-line therapy.
胆汁反流性胃炎(BRG)可能导致胃癌的癌前病变及胃癌。尽管熊去氧胆酸(UDCA)已用于治疗BRG,但其临床疗效仍不明确。因此,我们系统评价了UDCA与BRG传统治疗方法相比的疗效和安全性。
我们筛选了候选研究并绘制森林图以评估结果。进行Meta回归分析以确定异质性的可能原因。使用Cochrane偏倚风险2工具和纽卡斯尔-渥太华量表评估研究质量。采用推荐分级的评估、制定与评价方法评估Meta分析结果的证据质量。
共纳入14项研究,涉及1605例患者。与对照组相比,UDCA联合用药显著减少反流发作次数[平均差(MD)=-17.99次,95%可信区间(CI)(-19.84,-16.14)],缩短最长反流持续时间[MD=-9.21分钟,95%CI(-12.63,-5.80)],减少长时间反流发作次数[MD=-3.21次,95%CI(-3.76,-2.66)],提高临床缓解率[风险比=1.15,95%CI(1.10,1.19)],降低胃泌素含量[MD=-18.03 ng/L,95%CI(-33.88,-2.18)]并缓解症状。
UDCA对BRG显示出显著的治疗效果,尤其是8周疗程,支持其作为一线治疗的潜力。