Open AccessHepatocellular enzyme glutathione S‐transferase alpha and intrahepatic cholestasis of pregnancy
Author(s) -
JOUTSINIEMI TITTA,
LEINO RIITTA,
TIMONEN SUSANNA,
PULKKI KARI,
EKBLAD ULLA
Publication year - 2008
Publication title -
acta obstetricia et gynecologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 102
eISSN - 1600-0412
pISSN - 0001-6349
DOI - 10.1080/00016340802468316
Subject(s) - cholestasis of pregnancy , medicine , bile acid , cholestasis , glutathione s transferase , pregnancy , endocrinology , alanine aminotransferase , immunoassay , gestational age , gamma glutamyltransferase , transferase , glutathione , enzyme , chemistry , biochemistry , fetus , biology , immunology , antibody , genetics
Objective . To evaluate and compare plasma glutathione S‐transferase alpha (GSTA) concentrations in the third trimester of pregnancy in patients with intrahepatic cholestasis of pregnancy (ICP) and in healthy pregnant women. Design . Non‐randomized clinical study. Setting. Maternity unit and Department of Clinical Chemistry, Turku University Central Hospital, Turku, Finland. Population . Twenty‐seven women with ICP and 49 healthy pregnant women. Methods . GSTA concentrations were assessed in plasma samples in the third trimester of pregnancy using an enzyme‐linked immunoassay (HEPKIT™ Alpha, Biotrin, Sinsheim‐Reihen, Germany). Main outcome measures . Plasma GSTA, serum alanine and bile acid concentrations were compared between study and control group. Correlation between plasma GSTA levels and serum alanine aminotransferase and bile acid levels in the ICP patients were tested by Spearman correlation coefficients. Main perinatal outcome was compared between the groups. Results . GSTA concentration in the control group was 1.62 μg/l (range: 0.25–6.1). In the ICP patients, the mean plasma GSTA concentration was 51.0 μg/l (range: 2.1–183.5), the mean serum alanine aminotransferase concentration was 145.70 U/l (range: 6–393) and the mean bile acid concentration was 19.2 μmol/l (range: 3–63). There was a statistically significant correlation in ICP patients between plasma GSTA concentration and serum alanine aminotransferase concentration ( r = 0.694, p = 0.0001), but not with serum bile acid concentration. Nor was there any statistically significant correlation between gestational weeks and plasma GSTA concentration in the study group. Conclusion . Plasma GSTA measurements may provide a more sensitive and specific diagnostic tool for diagnosis of ICP than the evaluation of transaminases or bile acid concentrations alone. Further studies are needed to evaluate the role of GSTA in the follow‐up of patients with ICP and its prognostic value for threatening fetal distress in patients with ICP.