Shiffman M L, Kaplan G D, Brinkman-Kaplan V, Vickers F F
Hepatology Section, Medical College of Virginia, Richmond 23298-0711, USA.
Ann Intern Med. 1995 Jun 15;122(12):899-905. doi: 10.7326/0003-4819-122-12-199506150-00002.
To determine whether prophylactic treatment with ursodeoxycholic acid can prevent gallstone formation in persons participating in a very-low-calorie weight reduction diet program.
Multicenter, double-blind, placebo-controlled, multidose clinical trial. Patients were treated with placebo or with 300 mg/d, 600 mg/d, or 1200 mg/d of ursodeoxycholic acid.
31 Health Management Resources weight management centers.
1004 patients were initially enrolled in a 16-week, 520-kcal/d, Health Management Resources liquid protein diet program. All patients had a body mass index of 38 kg/m2 or more and a normal gallbladder ultrasonogram before study entry. Bile analysis was done in 32 patients.
Body weight and body mass index were measured before the diet was started and at 2-week intervals for 16 weeks. Gallbladder ultrasonography was done before enrollment and after 8 and 16 weeks of dieting. Bile was obtained by endoscopy and analyzed for cholesterol crystals and lipid levels.
Mean body weight for all patients at the start of dieting was 128.2 kg +/- 23.2 kg; mean initial body mass index was 44.2 kg/m2 +/- 6.0 kg/m2. Gallstones developed in 28% (95% CI, 22% to 35%) of patients receiving placebo, in 8% (CI, 5% to 13%) of patients treated with 300 mg/d of ursodeoxycholic acid, in 3% (CI, 1% to 7%) of patients treated with 600 mg/d of ursodeoxycholic acid, and in 2% (CI, 0.5% to 5%) of patients treated with 1200 mg/d of ursodeoxycholic acid. The differences between patients receiving placebo and patients receiving ursodeoxycholic acid were statistically significant. The percentage of ursodeoxycholic acid in bile increased stepwise with increasing doses of ursodeoxycholic acid.
Ursodeoxycholic acid, 600 mg/d, is highly effective in preventing gallstone formation in patients having dietary-induced weight reduction.
确定熊去氧胆酸预防性治疗能否预防参与极低热量减肥饮食计划的人群形成胆结石。
多中心、双盲、安慰剂对照、多剂量临床试验。患者接受安慰剂或300毫克/天、600毫克/天或1200毫克/天的熊去氧胆酸治疗。
31家健康管理资源体重管理中心。
1004例患者最初参加了一项为期16周、每天520千卡的健康管理资源液体蛋白饮食计划。所有患者在研究开始前体重指数均为38千克/平方米或更高,且胆囊超声检查正常。对32例患者进行了胆汁分析。
在饮食开始前以及之后的16周内每2周测量一次体重和体重指数。在入组前以及节食8周和16周后进行胆囊超声检查。通过内镜获取胆汁并分析胆固醇结晶和脂质水平。
所有患者节食开始时的平均体重为128.2千克±23.2千克;平均初始体重指数为44.2千克/平方米±6.0千克/平方米。接受安慰剂治疗的患者中有28%(95%可信区间,22%至35%)出现胆结石,接受300毫克/天熊去氧胆酸治疗的患者中有8%(可信区间,5%至13%)出现胆结石,接受600毫克/天熊去氧胆酸治疗的患者中有3%(可信区间,1%至7%)出现胆结石,接受1200毫克/天熊去氧胆酸治疗的患者中有2%(可信区间,0.5%至5%)出现胆结石。接受安慰剂治疗的患者与接受熊去氧胆酸治疗的患者之间的差异具有统计学意义。胆汁中熊去氧胆酸的百分比随熊去氧胆酸剂量增加而逐步升高。
每天600毫克的熊去氧胆酸在预防因饮食导致体重减轻的患者形成胆结石方面非常有效。