2017, Number 2
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Ann Hepatol 2017; 16 (2)
Intrahepatic Cholestasis of Pregnancy: New Diagnostic Insights
Chacko KR, Wolkoff AW
Language: English
References: 15
Page: 176-178
PDF size: 103.12 Kb.
Text Extraction
Intrahepatic Cholestasis of Pregnancy (ICP) is the most
common pregnancy-related liver disease and is characterized
by onset of pruritus and elevated serum transaminases
and bile acids (BA) in the third trimester of pregnancy.
Symptoms and abnormal liver tests resolve following delivery
but frequently recur in subsequent pregnancies. Genetic
defects of canalicular transporters have been
associated with the development of ICP, which may be
further influenced by gestational hormones. In particular,
the syndrome has been associated in some patients with
heterozygosity for mutations in the genes encoding familial
intrahepatic cholestasis protein-1 FIC1 (ICP-type 1),
bile salt excretory protein (BSEP) (ICP-type 2), and
multidrug resistance protein 3 (MDR3) (ICP-type 3). Patients
are classified as mild (BA 10-40) or severe (BA ›
40) which has implications with respect to the risk of
perinatal complications.
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