Hall M J, Nelson L M, Russell R I, Howard A N
Atherosclerosis. 1981 Jul;39(4):511-6. doi: 10.1016/0021-9150(81)90008-3.
Clofibrate is known to increase cholesterol saturation of bile and the prevalence of gallstones. We studied 10 healthy volunteer subjects to determine the effect of gemfibrozil (a new lipid-lowering agent) on biliary cholesterol saturation and to compare it with that of clofibrate. Biliary cholesterol saturation indices were calculated on fasting duodenal bile samples collected before and after administration of each drug for 4 weeks using a 4-week "washout" period between each preparation. There was a statistically significant rise in the cholesterol saturation index from a control value, taken as the mean of 2 samples, of 1.226 (0.785--1.526), median (range), to 1.547 (0.807--1.781) after clofibrate, P less than 0.05, but the rise to 1.352 (0.840--2.686) after gemfibrozil was not significant. However, direct comparison of the cholesterol saturation indices on clofibrate and gemfibrozil revealed no statistically significant difference. Only prospective clinical trials will establish definitively the risk of cholelithiasis on gemfibrozil but these results suggest that this drug is unlikely to have an advantage over clofibrate in this respect.
已知氯贝丁酯会增加胆汁中胆固醇的饱和度以及胆结石的患病率。我们研究了10名健康志愿者,以确定吉非贝齐(一种新型降脂药物)对胆汁胆固醇饱和度的影响,并将其与氯贝丁酯进行比较。在每次用药4周前后收集空腹十二指肠胆汁样本,使用每种制剂之间4周的“洗脱期”,计算胆汁胆固醇饱和指数。氯贝丁酯用药后,胆固醇饱和指数从作为2个样本均值的对照值1.226(中位数(范围)0.785 - 1.526)有统计学显著升高至1.547(0.807 - 1.781),P<0.05,但吉非贝齐用药后升至1.352(0.840 - 2.686)无显著意义。然而,氯贝丁酯和吉非贝齐的胆固醇饱和指数直接比较未显示统计学显著差异。只有前瞻性临床试验才能明确确定吉非贝齐导致胆石症的风险,但这些结果表明,在这方面该药物不太可能比氯贝丁酯有优势。