Heubi James E, Setchell Kenneth D R, Jha Pinky, Buckley Donna, Zhang Wujuan, Rosenthal Philip, Potter Carol, Horslen Simon, Suskind David
Division of Gastroenterology, Hepatology and Nutrition, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH; Clinical and Translational Research Center, Cincinnati Children's Hospital Medical Center, University of Cincinnati, Cincinnati, OH.
Hepatology. 2015 Jan;61(1):268-74. doi: 10.1002/hep.27401. Epub 2014 Dec 23.
Bile acid amidation defects were predicted to present with fat/fat soluble vitamin malabsorption with minimal cholestasis. We identified and treated five patients (one male, four females) from four families with defective bile acid amidation due to a genetically confirmed deficiency in bile acid CoA:amino acid N-acyl transferase (BAAT) with the conjugated bile acid, glycocholic acid (GCA). Fast atom bombardment-mass spectrometry analysis of urine and bile at baseline revealed predominantly unconjugated cholic acid and absence of the usual glycine and taurine conjugated primary bile acids. Treatment with 15 mg/kg GCA resulted in total duodenal bile acid concentrations of 23.3 ± 19.1 mmol/L (mean ± SD) and 63.5 ± 4.0% of the bile acids were secreted in bile in the conjugated form, of which GCA represented 59.6 ± 9.3% of the total biliary bile acids. Unconjugated cholic acid continued to be present in high concentrations in bile because of partial intestinal deconjugation of orally administered GCA. Serum total bile acid concentrations did not significantly differ between pretreatment and posttreatment samples and serum contained predominantly unconjugated cholic acid. These findings confirmed efficient intestinal absorption, hepatic extraction, and biliary secretion of the administered GCA. Oral tolerance tests for vitamin D2 (1,000 IU vitamin D2/kg) and tocopherol (100 IU/kg tocopherol acetate) demonstrated improvement in fat-soluble vitamin absorption after GCA treatment. Growth improved in 3/3 growth-delayed prepubertal patients.
Oral glycocholic acid therapy is safe and effective in improving growth and fat-soluble vitamin absorption in children and adolescents with inborn errors of bile acid metabolism due to amidation defects.
胆汁酸酰胺化缺陷预计会表现为脂肪/脂溶性维生素吸收不良,且胆汁淤积程度较轻。我们从四个家庭中识别并治疗了五名患者(一名男性,四名女性),这些患者因基因确诊的胆汁酸辅酶A:氨基酸N-酰基转移酶(BAAT)缺乏而存在胆汁酸酰胺化缺陷,并给予其结合型胆汁酸甘氨胆酸(GCA)进行治疗。基线时对尿液和胆汁进行的快原子轰击质谱分析显示,主要为未结合的胆酸,且通常的甘氨酸和牛磺酸结合型初级胆汁酸缺失。给予15mg/kg GCA治疗后,十二指肠胆汁酸总浓度为23.3±19.1mmol/L(平均值±标准差),63.5±4.0%的胆汁酸以结合形式分泌到胆汁中,其中GCA占总胆汁酸的59.6±9.3%。由于口服GCA在肠道内部分去结合,未结合的胆酸在胆汁中仍以高浓度存在。治疗前和治疗后样本的血清总胆汁酸浓度无显著差异,且血清中主要为未结合的胆酸。这些发现证实了所给予的GCA在肠道吸收、肝脏摄取和胆汁分泌方面是有效的。维生素D2(1000IU维生素D2/kg)和生育酚(100IU/kg醋酸生育酚)的口服耐受性试验表明,GCA治疗后脂溶性维生素吸收有所改善。3名青春期前生长发育迟缓的患者生长情况得到改善。
口服甘氨胆酸疗法对于改善因酰胺化缺陷导致胆汁酸代谢先天性异常的儿童和青少年的生长及脂溶性维生素吸收是安全有效的。