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威尔逊病患者胆汁中的胆汁酸成分

Biliary bile acid composition in Wilson's disease.

作者信息

Cowen A E, Korman M G, Hofmann A F, Goldstein N P

出版信息

Mayo Clin Proc. 1975 May;50(5):229-33.

PMID:1127989
Abstract

Biliary bile acid composition and pattern of bile acid conjugation with glycine or taurine were found to be within normal limits in six patients with documented Wilson's disease. Four patients had previous biopsy evidence of cirrhosis (three with active hepatitis), but most conventional liver function tests gave normal results at the time of the study. Serum levels of conjugates of cholic acid, measured by radioimmunoassay, were not increased. However, plasma disappearance if intravenously injected glycine conjugate of cholic acid was significantly delayed in all subjects, suggesting that this is a more sensitive test of hepatic excretory function and may be of value for assessing hepatic function in patients with this rare genetic disorder. No evidence of a primary disturbance in bile acid metabolism was found in these patients.

摘要

在六名确诊为威尔逊氏病的患者中,发现胆汁胆汁酸组成以及胆汁酸与甘氨酸或牛磺酸结合的模式均在正常范围内。四名患者先前有肝硬化的活检证据(三名患有活动性肝炎),但在研究时大多数常规肝功能检查结果正常。通过放射免疫测定法测得的胆酸结合物血清水平并未升高。然而,所有受试者静脉注射胆酸甘氨酸结合物后的血浆清除明显延迟,这表明这是一种更敏感的肝排泄功能测试,可能对评估这种罕见遗传疾病患者的肝功能有价值。在这些患者中未发现胆汁酸代谢存在原发性紊乱的证据。

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