Iser J H, Maton P N, Murphy G M, Dowling R H
Br Med J. 1978 Jun 10;1(6126):1509-12. doi: 10.1136/bmj.1.6126.1509.
In most patients with radiolucent gall stones who were given chenodeoxycholic acid (CDCA) in doses of 13-15 mg/kg body weight/day the bile became unsaturated in cholesterol, and their gall stones dissolved. The patients whose stones did not dissolve were significantly heavier and fatter than the responders, which suggested that obese patients might be "resistant" to the effects of CDCA. To test this hypothesis, 32 consecutive patients presenting for medical treatment of gall stones had their ideal body weight (IBW) and estimated body fat mass calculated. The eight most obese and the eight least obese patients were then selected, and their fasting bile lipid responses to CDCA 13-15 mg/kg/day were measured. The very obese patients were also given larger doses, and any changes in bile lipid composition were studied in relation to subsequent gall-stone dissolution.Before treatment the obese patients had a higher mean biliary cholesterol saturation index than the non-obese patients, and this difference was maintained during treatment with the normal dose of CDCA: the bile in the obese patients remained supersaturated while that in the non-obese became unsaturated with cholesterol. When the obese patients were given larger doses of CDCA their bile ultimately became unsaturated in cholesterol. Gall stones dissolved partially or completely in five of the eight non-obese patients after 6-18 months of 13-15 mg CDCA/kg/day, but none of the obese patients showed any response after comparable periods of treatment with this standard dose. With increased doses and unsaturated bile, however, three of the obese patients showed partial gall-stone dissolution after 3-12 months' treatment and one showed complete gall-stone dissolution after three years' treatment.These results suggest that when giving CDCA to patients with gall stones, larger than normal doses (some 18-20 mg/kg/day) should be prescribed. Alternatively the lipid composition of the patients' bile should be monitored by duodenal intubation and the CDCA dose increased until the bile becomes unsaturated in cholesterol.
在大多数接受鹅去氧胆酸(CDCA)治疗的X线透光性胆结石患者中,给予13 - 15mg/(kg体重/天)的剂量时,胆汁中的胆固醇变为不饱和状态,其胆结石溶解。结石未溶解的患者比有反应的患者明显更重、更胖,这表明肥胖患者可能对CDCA的作用“有抗性”。为了验证这一假设,对32例因胆结石前来就医的连续患者计算其理想体重(IBW)和估计体脂量。然后挑选出8例最肥胖和8例最不肥胖的患者,测量他们对13 - 15mg/(kg/天)CDCA的空腹胆汁脂质反应。对非常肥胖的患者也给予更大剂量,并研究胆汁脂质成分的任何变化与随后胆结石溶解的关系。治疗前,肥胖患者的平均胆汁胆固醇饱和指数高于非肥胖患者,在使用正常剂量的CDCA治疗期间这种差异持续存在:肥胖患者的胆汁仍处于过饱和状态,而非肥胖患者的胆汁胆固醇变为不饱和状态。当肥胖患者给予更大剂量的CDCA时,他们的胆汁最终胆固醇变为不饱和状态。在13 - 15mg CDCA/(kg/天)治疗6 - 18个月后,8例非肥胖患者中有5例的胆结石部分或完全溶解,但在使用该标准剂量进行相当长时间的治疗后,肥胖患者均未出现任何反应。然而,随着剂量增加和胆汁变为不饱和状态,3例肥胖患者在治疗3 - 12个月后胆结石出现部分溶解,1例在治疗三年后胆结石完全溶解。这些结果表明,给胆结石患者使用CDCA时,应开具高于正常剂量(约18 - 20mg/(kg/天))的药物。或者,应通过十二指肠插管监测患者胆汁的脂质成分,并增加CDCA剂量,直至胆汁中的胆固醇变为不饱和状态。