Department of Endocrinology and Metabolism, Peking University People's Hospital, Beijing, China.
Department of Endocrinology and Metabolism (Section 1), Tangshan Gongren Hospital, Tangshan, Hebei, China.
Obes Rev. 2024 Jun;25(6):e13725. doi: 10.1111/obr.13725. Epub 2024 Feb 12.
In this meta-analysis, we aim to evaluate the risk of gallbladder and biliary disease of weight management strategies and investigate the association between weight reduction and risk of gallbladder or biliary disease. Randomized controlled trials (RCTs) with a duration of at least 12 weeks that compare antiobesity medications (AOMs) with placebo or bariatric surgery with less intensive weight management strategy were concluded. Weight management strategy was associated with a significant increased risk of gallbladder or biliary disease (OR 1.361, 95% CI 1.147 to 1.614, P < 0.001, I = 3.5%), cholelithiasis, cholecystitis, and cholecystectomy compared with placebo or controls. The increased risk of gallbladder or biliary disease was observed both in pharmacotherapies subgroup and bariatric surgery subgroup. With regards of specific pharmacotherapies, an increased risk of gallbladder or biliary disease was observed in trials with glucagon-like peptide 1 receptor agonist (GLP-1 RA) treatments. In addition, trials with indication of obesity and overweight treatment and trials with higher doses showed significant higher risk of gallbladder or biliary disease compared with placebo or controls. In conclusion, weight management strategy was associated with an increased risk of gallbladder or biliary disease when compared with placebo or control groups.
在这项荟萃分析中,我们旨在评估体重管理策略与胆囊和胆道疾病风险之间的关系,并研究减重与胆囊或胆道疾病风险之间的关联。纳入了至少持续 12 周、比较抗肥胖药物(AOM)与安慰剂或减重手术与非强化体重管理策略的随机对照试验(RCT)。与安慰剂或对照组相比,体重管理策略与胆囊或胆道疾病(OR 1.361,95%CI 1.147 至 1.614,P<0.001,I=3.5%)、胆结石、胆囊炎和胆囊切除术的风险显著增加相关。在药物治疗亚组和减重手术亚组均观察到胆囊或胆道疾病风险增加。关于特定的药物治疗,使用胰高血糖素样肽 1 受体激动剂(GLP-1 RA)治疗的试验中观察到胆囊或胆道疾病风险增加。此外,针对肥胖和超重治疗的适应证和较高剂量的试验与安慰剂或对照组相比,显示出胆囊或胆道疾病的风险显著增加。总之,与安慰剂或对照组相比,体重管理策略与胆囊或胆道疾病风险增加相关。