van Blankenstein M, Frenkel M, van den Berg J W, ten Kate F J, Bosman-Jacobs E P, Touw-Blommesteyn A C
Dig Dis Sci. 1983 Feb;28(2):137-44. doi: 10.1007/BF01315143.
Fasting and postprandial (stimulated) serum conjugated bile acids (CBA) were measured by a solid-phase radioimmunoassay in 329 patients undergoing liver biopsy, and the results were analyzed for 231 who fitted into 10 diagnostic categories. In healthy volunteers the mean fasting CBA of 1.8 +/- 0.7 mumol/liter rose to 3.0 +/- 0.8 mumol/liter postprandially. In patients mean fasting and stimulated CBA were only significantly raised in moderate to severe chronic and acute liver disease. Diagnostic sensitivity was poor in mild liver disease. Individuals with normal results were found in 8 of 11 disease categories. The ratio of stimulated to fasting CBA expressed in a stimulation quotient did not rise in more advanced liver disease. These findings are best explained by a constant fractional clearance of bile acids by the liver. We conclude that the serum conjugated bile acid determination as a test of liver cell function is not sensitive enough to identify all cases of biopsy-proven liver disease.
采用固相放射免疫分析法对329例接受肝活检的患者进行空腹和餐后(刺激后)血清结合胆汁酸(CBA)测定,并对符合10种诊断类别的231例患者的结果进行分析。健康志愿者空腹时CBA的平均值为1.8±0.7μmol/升,餐后升至3.0±0.8μmol/升。在患者中,仅在中度至重度慢性和急性肝病时,空腹和刺激后的CBA平均值才显著升高。轻度肝病的诊断敏感性较差。在11种疾病类别中的8种中发现结果正常的个体。以刺激商表示的刺激后与空腹CBA的比值在更晚期肝病中并未升高。这些发现最好用肝脏对胆汁酸的恒定分数清除率来解释。我们得出结论,血清结合胆汁酸测定作为肝细胞功能检测方法,其敏感性不足以识别所有经活检证实的肝病病例。