ROLE OF HYPERBILIRUBINEMIA IN THE IMPAIRMENT OF OSTEOBLAST PROLIFERATION-ASSOCIATED WITH CHOLESTATIC JAUNDICE

被引:144
作者
JANES, CH
DICKSON, ER
OKAZAKI, R
BONDE, S
MCDONAGH, AF
RIGGS, BL
机构
[1] MAYO CLIN & MAYO FDN,ENDOCRINE RES UNIT,ROCHESTER,MN 55905
[2] MAYO CLIN & MAYO FDN,DEPT INTERNAL MED,DIV GASTROENTEROL,ROCHESTER,MN 55905
[3] UNIV CALIF SAN FRANCISCO,MED CTR,DEPT MED,SAN FRANCISCO,CA 94143
[4] UNIV CALIF SAN FRANCISCO,MED CTR,CTR LIVER,SAN FRANCISCO,CA 94143
关键词
BILIRUBIN; PRIMARY BILIARY CIRRHOSIS; CHOLESTASIS; OSTEOPOROSIS; LIVER DISEASE;
D O I
10.1172/JCI117959
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Because the osteoporosis occurring in chronic cholestatic liver disease (CCLD) is associated with decreased bone formation and is reversible by liver transplantation, substances retained in plasma during cholestasis may impair osteoblast function, This hypothesis was tested using a new bioassay that measures plasma mitogenic activity (PMA) for normal human osteoblast-like (hOB) cells, In 29 jaundiced patients, mean PMA was 56.4% (P < 0.001) of that in 29 age- and sex-matched normal subjects, and the decrease in PMA was similar in the 14 with CCLD and the 15 with other causes of jaundice. Bile acids and bilirubin are the two major groups of products retained during cholestasis. The common conjugated bile acids and bilirubin were added to normal human plasma in concentrations simulating those found in patients with CCLD. Various bile salts had no effect on PMA whereas unconjugated bilirubin decreased PMA in a dose-dependent fashion (r = -0.98, P < 0.0001) without affecting cell viability, Relatively selective removal of bilirubin from the plasma by photobleaching normalized the decreased PMA in five jaundiced patients but produced no apparent change in five normal subjects, These data support the hypothesis that hyperbilirubinemia or possibly other photolabile substances impair osteoblast proliferative capacity and thus may play a major role in the pathogenesis of the osteoporosis associated with CCLD.
引用
收藏
页码:2581 / 2586
页数:6
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