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An Update on Genetic Analysis of Cholestatic Liver Diseases: Digging Deeper
被引:7
|作者:
Muellenbach, Roman
[1
]
Lammert, Frank
[1
]
机构:
[1] Saarland Univ Hosp, Dept Med 2, DE-66424 Homburg, Germany
关键词:
ABC transporters;
Genome-wide scan;
Personalized medicine;
Polygenic disease;
SALT EXPORT PUMP;
FAMILIAL INTRAHEPATIC CHOLESTASIS;
PRIMARY BILIARY-CIRRHOSIS;
INTERINDIVIDUAL VARIABILITY;
HEREDITARY CHOLESTASIS;
ALAGILLE-SYNDROME;
SEVERE FORM;
ABCB4;
GENE;
BILE;
PREGNANCY;
D O I:
10.1159/000324137
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Investigations into the molecular mechanisms of cholestasis have revealed intricate and intriguing details of bile salt metabolism as well as its regulatory mechanisms in health and disease. Extensive studies on genotype-phenotype correlations in monogenic diseases, such as progressive familial and benign recurrent intrahepatic cholestasis, facilitate diagnostics and improve the risk assessment of hepatobiliary transporter gene variants in bile transport pathophysiology. While the comparatively easy targets in monogenic cholestasis have been identified for some time now, progress in complex liver disease is rather laborious but steady. Genome-wide association scans are the next step in gathering information about common contributors towards polygenic (multifactorial) cholestatic diseases. New determinants of bile salt metabolism affecting feedback loops within the liver or the enterohepatic circulation are presently under investigation for their contribution towards complex cholestatic syndromes. Copyright (C) 2011 S. Karger AG, Basel
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页码:72 / 77
页数:6
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