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Lack of response to chenodeoxycholic acid in obese and non-obese patients. Role of cholesterol synthesis and possible response to ursodeoxycholic acid.

机译:肥胖和非肥胖患者对鹅去氧胆酸缺乏反应。胆固醇合成的作用以及对熊去氧胆酸的可能反应。

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摘要

This paper describes seven patients with radiolucent gallstones in functioning gallbladders who did not respond to chenodeoxycholic acid (CDCA). Despite large doses (greater than or equal to 19 mg CDCA/kg/day), CDCA-rich bile (CDCA conjugates 70-97% of total biliary bile acids) and greater than or equal to one year's treatment, their fasting duodenal bile remained supersaturated with cholesterol and their gallstones did not dissolve. Five patients came to cholecystectomy, gallstone analysis and liver biopsy for measurement of hepatic cholesterogenesis (HMGCoAR activity). In three who stopped CDCA before surgery, the mean HMGCoAR (pmol/mg microsomal protein/min) of 50.2 was higher than in our untreated gallstone controls (32.2 +/- SEM 2.0; P less than 0.05). Two patients who took CDCA until surgery had a mean HMGCoAR of 33.5--more than twice that in CDCA-treated gallstone controls. These findings suggest that non-response to CDCA may be related to high or unsuppressed hepatic cholesterogenesis. In one patient who did not respond to CDCA, treatment with 19 mg ursodeoxycholic acid/kg/day did desaturate his bile.
机译:本文描述了7例功能正常的胆囊中放射性不透性胆结石患者,它们对鹅去氧胆酸(CDCA)无反应。尽管大剂量(大于或等于19 mg CDCA / kg /天),富含CDCA的胆汁(CDCA结合了胆汁总胆汁酸的70-97%)且大于或等于一年的治疗,但其空腹十二指肠胆汁仍保留胆固醇过饱和,它们的胆结石没有溶解。五例患者进行了胆囊切除术,胆结石分析和肝活检,以测量肝胆固醇生成(HMGCoAR活性)。在手术前停止CDCA的三名患者中,平均HMGCoAR(pmol / mg微粒体蛋白/分钟)为50.2,高于未治疗的胆结石对照组(32.2 +/- SEM 2.0; P小于0.05)。接受CDCA治疗直至手术的两名患者的平均HMGCoAR为33.5,是CDCA治疗的胆结石对照患者的两倍。这些发现表明,对CDCA的无反应可能与高胆固醇水平或未抑制肝胆固醇生成有关。在一位对CDCA无反应的患者中,用19 mg熊去氧胆酸/ kg /天的治疗确实使他的胆汁去饱和。

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