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. 2020;13(4):513-519.
doi: 10.3233/NPM-190276.

Correlation of bile acids and aspartate-aminotransferase with outcomes in cholestasis of pregnancy

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Correlation of bile acids and aspartate-aminotransferase with outcomes in cholestasis of pregnancy

A L Juusela et al. J Neonatal Perinatal Med. 2020.

Abstract

Objective: To identify laboratory data that correlates with poor perinatal outcomes.

Methods: A retrospective chart review of women with intrahepatic cholestasis of pregnancy (ICP), admitted for delivery between January 1, 2013 and December 31, 2017, was performed. Chi-square, student's t-test, and ANOVA statistical analysis was performed. The receiver-operator characteristic curves were plotted for the prediction of each category of perinatal outcome and the areas under the curves were determined. All p-values were two-sided, and p < 0.05 was considered statistically significant.

Results: Analysis of the 61 ICP cases showed no occurrence of the intrauterine fetal demise (IUFD), stillbirth, abruption, or neonatal demise. ROC curve analysis revealed a statistically significant correlation between bile acid and AST levels and perinatal outcomes. A bile acid (BA) level equal to or greater than 37μmol/L strongly predicted spontaneous preterm labor in women affected by ICP with a sensitivity of 100% and specificity of 60.70% (p = 0.002). A BA level equal to or greater than 42μmol/L strongly predicted meconium-stained amniotic fluid with a sensitivity of 85.70% and specificity of 66.70% (p = 0.006). AST levels equal to or greater than 62 IU/L strongly predicted NICU admission with a sensitivity of 81.30% and specificity of 62.20% (p = 0.002). AST levels equal to or greater than 75 IU/L strongly predicted hyperbilirubinemia in the neonates with a sensitivity of 87.50% and specificity of 69.80% (p = 0.001).

Conclusions: There is a statistically significant correlation between elevated BA and elevated AST levels and adverse perinatal outcomes.

Keywords: Cholestasis of pregnancy; gastrointestinal disorders; hepatic function; hypercholanemia; liver diseases; transaminitis.

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