Evidence map›Paper›PMID 39947696›Full record

ArticleAmerican journal of physiology. Gastrointestinal and liver physiology2025

Unresolved alterations in bile acid composition and dyslipidemia in maternal and cord blood after UDCA treatment for intrahepatic cholestasis of pregnancy.

Srijani Basu, Sarah G Običan, Enrico Bertaggia, Hannah Staab, M Concepcion Izquierdo, Cynthia Gyamfi-Bannerman, Rebecca A Haeusler

Abstract read
In one paragraph

Article in American journal of physiology. Gastrointestinal and liver physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Srijani BasuNaomi Berrie Diabetes Center, Columbia University, New York, New York, United States.ORCID 0000-0002-6462-1477
Sarah G ObičanDepartment of Obstetrics and Gynecology, Columbia University, New York, New York, United States.
Enrico BertaggiaNaomi Berrie Diabetes Center, Columbia University, New York, New York, United States.
Hannah StaabNaomi Berrie Diabetes Center, Columbia University, New York, New York, United States.
M Concepcion IzquierdoNaomi Berrie Diabetes Center, Columbia University, New York, New York, United States.
Cynthia Gyamfi-BannermanDepartment of Obstetrics and Gynecology, Columbia University, New York, New York, United States.
Rebecca A HaeuslerNaomi Berrie Diabetes Center, Columbia University, New York, New York, United States.ORCID 0000-0002-6973-9845

Funding

Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
Translational Biomarker Analytical Core (TBAC)P30DK063608 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Remi J Creusot · 2003 to 2026
$36.7M
The Organoid and Cell Culture CoreP30DK132710 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Jianwen Que · 2022 to 2026
$7.2M
Bile acids and insulin sensitivityR01DK115825 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Rebecca Anne Haeusler · 2018 to 2026
$5.4M
Mechanisms linking insulin action with lipoprotein metabolismR01HL125649 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI HAEUSLER, REBECCA ANNE · 2015 to 2023
$4.2M
Insulin regulation of hepatic transportR01DK135298 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Rebecca Anne Haeusler · 2023 to 2026
$2.6M
AMA | American Medical Association Foundation (AMAF) Seed GrantHHS | NIH | National Center for Advancing Translational Sciences (NCATS) UL1TR001873HHS | NIH | National Heart, Lung, and Blood Institute (NHLBI) R01HL125649HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) P30DK063608HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) P30DK132710HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) R01DK115825HHS | NIH | National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) R01DK135298NCATS NIH HHS UL1 TR001873NHLBI NIH HHS R01 HL125649NIDDK NIH HHS P30 DK063608NIDDK NIH HHS P30 DK132710NIDDK NIH HHS R01 DK115825NIDDK NIH HHS R01 DK135298Russell Berrie Foundation (RBF)
6 · The paper itself

Abstract

Intrahepatic cholestasis of pregnancy (ICP) is characterized by elevated plasma bile acid levels. ICP is linked to adverse metabolic outcomes, including a reported increased risk of gestational diabetes. The standard therapeutic approach for managing ICP is treatment with ursodeoxycholic acid (UDCA) and induction of labor before 40 wk of gestation. To investigate bile acid and metabolic parameters after UDCA treatment, we enrolled 12 ICP patients with singleton pregnancies-half with and half without gestational diabetes-and 7 controls. Our study reveals that after UDCA treatment, notwithstanding a reduction in total bile acid and alanine aminotransferase levels, imbalances persist in the cholic acid (CA) to chenodeoxycholic acid (CDCA) ratio in maternal and cord blood plasma. This indicates a continued dysregulation of bile acid metabolism despite therapeutic intervention. Maternal plasma lipid analysis showed a distinct maternal dyslipidemia pattern among patients with ICP, marked by elevated cholesterol levels on VLDL particles and heightened triglyceride concentrations on LDL particles, persisting even after UDCA treatment. Cord plasma lipid profiles in patients with ICP exhibited elevated triglyceride and free fatty acid levels alongside a tendency toward increased β-hydroxybutyrate. The changes in lipid metabolism in both maternal and cord blood correlated with the high CA/CDCA ratio but not total bile acid levels or gestational diabetes status. Understanding the imbalances in maternal and cord bile acid and lipid profiles that persist after standard UDCA therapy provides insights for improving management strategies and mitigating the long-term consequences of ICP.

Indexed as

Bile Acids and SaltsCholagogues and CholereticsCholestasis, IntrahepaticDyslipidemiasFetal BloodPregnancy ComplicationsUrsodeoxycholic AcidAdultCase-Control StudiesCholic AcidDiabetes, GestationalFemaleHumansPregnancyBile Acids and SaltsCholagogues and CholereticsCholic AcidUrsodeoxycholic Acidbile acid metabolismcholestasisdyslipidemiaslipoproteinspregnancy

Identifiers

PMID39947696
PMCPMC12053871

What Socratic holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.