Assessment of the fetal thymic-thoracic ratio in pregnant women with intrahepatic cholestasis: a prospective case-control study

Author:

Agaoglu Zahid1ORCID,Tanacan Atakan2ORCID,Bozkurt Ozdal Burcu1,Basaran Ezgi1,Serbetci Hakkı1,Ozturk Agaoglu Merve1ORCID,Okutucu Gulcan1ORCID,Kara Ozgur1,Sahin Dilek2

Affiliation:

1. Department of Obstetrics and Gynecology , Ministry of Health, Ankara City Hospital , Ankara , Türkiye

2. Department of Obstetrics and Gynecology , Ministry of Health, Ankara City Hospital, University of Health Sciences , Ankara , Türkiye

Abstract

Abstract Objectives To examine the fetal thymic-thoracic ratio (TTR) in intrahepatic cholestasis of pregnancy (ICP). Methods This prospective case-control study was conducted in a single tertiary center. The sample consisted of 86 pregnant women at 28–37 weeks of gestation, including 43 women with ICP and 43 healthy controls. TTR was calculated for each patient using the anterior-posterior measurements of the thymus and intrathoracic mediastinal measurements. Results The median TTR value was found to be smaller in the ICP group compared to the control group (0.32 vs. 0.36, p<0.001). The ICP group had a greater rate of admission to the neonatal intensive care unit (NICU) (p<0.001). Univariate regression analysis revealed that lower TTR values increased the possibility of NICU admission six times (95 % confidence interval: 0.26–0.39, p=0.01). A statistically significant negative correlation was detected between TTR and the NICU requirement (r: −0.435, p=0.004). As a result of the receiver operating characteristic analysis, in predicting NICU admission, the optimal cut-off value of TTR was determined to be 0.31 with 78 % sensitivity and 67 % specificity (area under the curve=0.819; p<0.001). Conclusions We determined that the fetal TTR may be affected by the inflammatory process caused by the maternal-fetal immune system and increased serum bile acid levels in fetal organs in the presence of ICP. We consider that TTR can be used to predict adverse pregnancy outcomes in patients with ICP.

Publisher

Walter de Gruyter GmbH

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