Potential effect of cyclosporin A in formation of cholesterol gallstones in pediatric liver transplant recipients

被引:20
作者
Cao, S
Cox, K
So, SSK
Berquist, W
Lee, SP
Haigh, WG
Concepcion, W
Monge, H
Esquivel, CO
机构
[1] STANFORD UNIV,MED CTR,DEPT SURG,PALO ALTO,CA 94304
[2] STANFORD UNIV,MED CTR,DEPT PEDIAT,PALO ALTO,CA 94304
[3] STANFORD UNIV,MED CTR,DEPT GASTROENTEROL,PALO ALTO,CA 94304
[4] VET AFFAIRS MED CTR,DIV GASTROENTEROL,SEATTLE,WA 98108
关键词
gallstones; orthotopic liver transplant; cyclosporine A; FK506; ursodiol;
D O I
10.1023/A:1018894005748
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Recent advancements in Liver transplantation have resulted in extended survival both for grafts and recipients. Such improvement, together with the shortage of donor organs has prompted expansion of the donor pool to include less than ideal donors, especially in life-threatening situations. The use of older fiver donors has been associated with lower long-term survival. However, potential morbidity such as gallstone formation has not been explored. We analyzed bile composition in a child who developed cholesterol gallstones in the proximal bile duct two years after undergoing emergency liver transplantation with a liver from a 78-year-old donor. Oral administration of ursodeoxycholic acid (ursodiol) shifted the cholesterol composition of the bile from a supersaturated, potentially crystallized state to a liquid (micellar) state. Unlike cyclosporin A, FK506 showed an increase in the proportion of chenodeoxycholic acid and a decrease in the proportion of cholic acid, and thus may exhibit minimal or no hepatotoxic effect. Thus, in donor livers with factors known to be associated with cholesterol gallstone formation (such as age, sex, or obesity), one may consider analyzing the bile composition at the time of procurement. Depending on cholesterol and bile acid composition, the use of FK506 with or without addition of ursodeoxycholic acid may be warranted.
引用
收藏
页码:1409 / 1415
页数:7
相关论文
共 26 条
[1]  
BARTLETT GR, 1959, J BIOL CHEM, V234, P466
[2]   TRANSPLANTATION FOR FULMINANT AND SUBFULMINANT HEPATIC-FAILURE WITH PRESERVATION OF PORTAL AND CAVAL FLOW [J].
BELGHITI, J ;
NOUN, R ;
SAUVANET, A ;
DURAND, F ;
ASCHEHOUG, J ;
ERLINGER, S ;
BENHAMOU, JP ;
BERNUAU, J .
BRITISH JOURNAL OF SURGERY, 1995, 82 (07) :986-989
[3]  
BOHME M, 1994, GASTROENTEROLOGY, V107, P255
[4]  
BOTLA R, 1995, J PHARMACOL EXP THER, V272, P930
[5]  
CHRISTIE WW, 1985, J LIPID RES, V33, P931
[6]  
CONTRERAS JA, 1992, J LIPID RES, V33, P931
[7]   SELECTIVE-INHIBITION OF MITOCHONDRIAL 27-HYDROXYLATION OF BILE-ACID INTERMEDIATES AND 25-HYDROXYLATION OF VITAMIN-D3 BY CYCLOSPORINE-A [J].
DAHLBACKSJOBERG, H ;
BJORKHEM, I ;
PRINCEN, HMG .
BIOCHEMICAL JOURNAL, 1993, 293 :203-206
[8]  
ERLINGER S, 1994, HEPATOLOGY, V4, P308
[9]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[10]   ACUTE-PANCREATITIS INDUCED BY CYCLOSPORINE-A UNDER STIMULATION OF PANCREAS BY CERULEIN [J].
ITO, T ;
KIMURA, T ;
YAMAGUCHI, H ;
KINJO, M ;
SUMII, T ;
NAKANO, I ;
NAWATA, H .
PANCREAS, 1993, 8 (06) :693-699