Bile acid profiles by capillary electrophoresis in intrahepatic cholestasis of pregnancy

被引:85
作者
Castaño, G
Lucangioli, S
Sookoian, S
Mesquida, M
Lemberg, A
Di Scala, M
Franchi, P
Carducci, C
Tripodi, V [1 ]
机构
[1] Univ Buenos Aires, Sch Pharm & Biochem, Dept Analyt Chem, Buenos Aires, DF, Argentina
[2] Consejo Nacl Invest Cient & Tecn, Buenos Aires, DF, Argentina
[3] Hosp JM Penna, Dept Internal Med, Gastroenterol Sect, Buenos Aires, DF, Argentina
[4] Univ Buenos Aires, Sch Pharm & Biochem, Dept Physiopathol, Buenos Aires, DF, Argentina
[5] Hosp JM Penna, Div Obstet & Gynecol, Buenos Aires, DF, Argentina
关键词
asymptomatic hypercholanaemia; bile acid; capillary electrophoresis; intrahepatic cholestasis; pregnancy;
D O I
10.1042/CS20050302
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
ICP (intrahepatic cholestasis of pregnancy) is characterized by pruritus and biochemical cholestasis, including raised SBAs (serum bile acids) and, usually, elevated aminotransferases levels. However, AHP (asymptomatic hypercholanaemia of pregnancy) is defined as the presence of total SBA levels above the cut-off value (11 mu M) in healthy pregnant women, thus elevation of total SBAs do not necessarily reflect an ICP condition. The aim of the present study was to describe clinical, obstetric, perinatal and biochemical findings, as well as the SBA profile, in pregnant women studied in the third trimester of pregnancy in order to define characteristic patterns of individual bile acids that enable women with ICP to be distinguished from AHP and healthy pregnancies. Free and conjugated ursodeoxycholic (UDCA), cholic (CA), lithocholic (LCA), deoxycholic (DCA) and chenodeoxycholic (CDCA) acids were evaluated by CE (capillary electrophoresis) in 41 patients (15 of them simultaneously by HPLC), in 30 healthy pregnant women and in 10 non-pregnant women. A highly significant correlation between CE and HPLC for total SBAs (r = 0.990) and for individual SBAs was found. Normal pregnant women had higher total SBA levels than non-pregnant women (due to an increase in taurine-conjugated dihydroxy SBAs). Women with ICP had higher levels of total SBAs, the free/conjugated ratio, LCA, CA, CDCA and DCA than normal pregnant women. Newborns from women with ICP had lower birth weight and gestational age. Women with AHP had higher levels of conjugated dihydroxy SBAs than normocholanaemic patients, without any evidence of a clinical difference. In conclusion, the present study has shown a clear difference in SBA profiles between ICP and normal pregnancies (including AHP), involving a shift towards a characteristic hydrophobic composition in women with ICP.
引用
收藏
页码:459 / 465
页数:7
相关论文
共 31 条
[1]
APGAR V, 1953, Curr Res Anesth Analg, V32, P260
[2]
Azer SA, 1997, BRIT J BIOMED SCI, V54, P118
[3]
SERUM CONJUGATED BILE-ACID PROFILE DURING INH INTRAHEPATIC CHOLESTASIS OF PREGNANCY [J].
BACQ, Y ;
MYARA, A ;
BRECHOT, MC ;
HAMON, C ;
STUDER, E ;
TRIVIN, F ;
METMAN, EH .
JOURNAL OF HEPATOLOGY, 1995, 22 (01) :66-70
[4]
Brites D, 1994, Acta Med Port, V7, P181
[5]
Relevance of serum bile acid profile in the diagnosis of intrahepatic cholestasis of pregnancy in an high incidence area: Portugal [J].
Brites, D ;
Rodrigues, CMP ;
van-Zeller, H ;
Brito, A ;
Silva, R .
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 1998, 80 (01) :31-38
[6]
Unusual case of severe cholestasis of pregnancy with early onset, improved by ursodeoxycholic acid administration [J].
Brites, D ;
Rodrigues, CMP ;
Cardoso, MD ;
Graça, LM .
EUROPEAN JOURNAL OF OBSTETRICS GYNECOLOGY AND REPRODUCTIVE BIOLOGY, 1998, 76 (02) :165-168
[7]
Brites Dora, 2002, Ann Hepatol, V1, P20
[8]
Differentiated quantification of human bile acids in serum by high-performance liquid chromatography-tandem mass spectrometry [J].
Burkard, I ;
von Eckardstein, A ;
Rentsch, KM .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2005, 826 (1-2) :147-159
[9]
CAPURRO H, 1978, J PEDIATR-US, V93, P120, DOI 10.1016/S0022-3476(78)80621-0
[10]
IS NORMAL-PREGNANCY CHOLESTATIC [J].
FULTON, IC ;
DOUGLAS, JG ;
HUTCHON, DJR ;
BECKETT, GJ .
CLINICA CHIMICA ACTA, 1983, 130 (02) :171-176