Evidence map›Paper›PMID 33276032›Full record

ArticleJournal of hepatology2021

Fetal cardiac dysfunction in intrahepatic cholestasis of pregnancy is associated with elevated serum bile acid concentrations.

Tharni Vasavan, Sahil Deepak, Indu Asanka Jayawardane, Maristella Lucchini, Catherine Martin, Victoria Geenes, Joel Yang, Anita Lövgren-Sandblom, Paul Townsend Seed, Jenny Chambers and 12 more

Registry-linked trialOpen access · hybridAbstract read
In one paragraph

Article in Journal of hepatology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07428226 (Serum Bile Acid Profiles in Patients With Intrahepatic Cholestasis of Pregnancy), which is not on this map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
3.6field-weighted citation impact, top 5% of its field
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.

NCT07428226 recruitingnot on this mapstarted 2024, after this paper: background citation

Serum Bile Acid Profiles in Patients With Intrahepatic Cholestasis of Pregnancy

TypeobservationalSponsorJena University HospitalRan2024 to 2027Enrolled74ConditionsIntrahepatic Cholestasis of Pregnancy
3 · Its place in the literature

Who cites it

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 86 citations in OpenAlex.

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  19. Intrahepatic cholestasis of pregnancy.Nature reviews. Disease primers · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

22 authors at 7 institutions in 3 countries.

Tharni VasavanDepartment of Women and Children's Health, King's College London, London, UK.
Sahil DeepakDepartment of Women and Children's Health, King's College London, London, UK.
Indu Asanka JayawardaneUniversity Department of Obstetrics and Gynaecology, Nottingham City Hospital, University of Nottingham, Nottingham, UK; Faculty of Engineering, University of Nottingham, Nottingham, UK.
Maristella LucchiniDepartments of Psychiatry and Pediatrics, Columbia University, New York, USA.
Catherine MartinDepartment of Women and Children's Health, King's College London, London, UK.
Victoria GeenesDepartment of Women and Children's Health, King's College London, London, UK.
Joel YangDepartments of Psychiatry and Pediatrics, Columbia University, New York, USA.
Anita Lövgren-SandblomDepartment of Laboratory Medicine, Karolinska Institute, Stockholm, Sweden.
Paul Townsend SeedDepartment of Women and Children's Health, King's College London, London, UK.
Jenny ChambersWomen's Health Research Centre, Imperial College London, London, UK.
Sophia StoneDepartment of Obstetrics and Gynaecology, Western Sussex Hospitals NHS Foundation Trust, West Sussex, UK.
Lesia KurlakUniversity Department of Obstetrics and Gynaecology, Nottingham City Hospital, University of Nottingham, Nottingham, UK.
Peter Hendy DixonDepartment of Women and Children's Health, King's College London, London, UK.
Hanns-Ulrich MarschallDepartment of Molecular and Clinical Medicine, Sahlgrenska Academy, University of Gothenburg, Sweden.
Julia GorelikImperial College London, National Heart and Lung Institute, Imperial Centre for Experimental and Translational Medicine, London, UK.
Lucy ChappellDepartment of Women and Children's Health, King's College London, London, UK.
Pam LoughnaUniversity Department of Obstetrics and Gynaecology, Nottingham City Hospital, University of Nottingham, Nottingham, UK.
Jim ThorntonUniversity Department of Obstetrics and Gynaecology, Nottingham City Hospital, University of Nottingham, Nottingham, UK.
Fiona Broughton PipkinUniversity Department of Obstetrics and Gynaecology, Nottingham City Hospital, University of Nottingham, Nottingham, UK.
Barrie Hayes-GillFaculty of Engineering, University of Nottingham, Nottingham, UK.
William Paul FiferDepartments of Psychiatry and Pediatrics, Columbia University, New York, USA.
Catherine WilliamsonDepartment of Women and Children's Health, King's College London, London, UK. Electronic address: catherine.williamson@kcl.ac.uk.
King's College London · GBUniversity of Nottingham · GBColumbia University · USImperial College London · GBKarolinska Institutet · SEUniversity Hospitals Sussex NHS Foundation Trust · GBUniversity of Gothenburg · SE

Funding

British Heart Foundation RG/17/13/33173Department of Health 12/164/16Department of Health IS-BRC-1215-20006Department of Health RP-2014-05-019Wellcome Trust 092993/Z/10/Z
6 · The paper itself

Abstract

BACKGROUND &

aimsIntrahepatic cholestasis of pregnancy (ICP) is associated with an increased risk of stillbirth. This study aimed to assess the relationship between bile acid concentrations and fetal cardiac dysfunction in patients with ICP who were or were not treated with ursodeoxycholic acid (UDCA).

methodsBile acid profiles and NT-proBNP, a marker of ventricular dysfunction, were assayed in umbilical venous serum from 15 controls and 76 ICP cases (36 untreated, 40 UDCA-treated). Fetal electrocardiogram traces were obtained from 43 controls and 48 ICP cases (26 untreated, 22 UDCA-treated). PR interval length and heart rate variability (HRV) parameters were measured in 2 behavioral states (quiet and active sleep).

resultsIn untreated ICP, fetal total serum bile acid (TSBA) concentrations (r = 0.49, p = 0.019), hydrophobicity index (r = 0.20, p = 0.039), glycocholate concentrations (r = 0.56, p = 0.007) and taurocholate concentrations (r = 0.44, p = 0.039) positively correlated with fetal NT-proBNP. Maternal TSBA (r = 0.40, p = 0.026) and alanine aminotransferase (r = 0.40, p = 0.046) also positively correlated with fetal NT-proBNP. There were no significant correlations between maternal or fetal serum bile acid concentrations and fetal HRV parameters or NT-proBNP concentrations in the UDCA-treated cohort. Fetal PR interval length positively correlated with maternal TSBA in untreated (r = 0.46, p = 0.027) and UDCA-treated ICP (r = 0.54, p = 0.026). Measures of HRV in active sleep and quiet sleep were significantly higher in untreated ICP cases than controls. HRV values in UDCA-treated cases did not differ from controls.

conclusionsElevated fetal and maternal serum bile acid concentrations in untreated ICP are associated with an abnormal fetal cardiac phenotype characterized by increased NT-proBNP concentration, PR interval length and HRV. UDCA treatment partially attenuates this phenotype. LAY SUMMARY: The risk of stillbirth in intrahepatic cholestasis of pregnancy (ICP) is linked to the level of bile acids in the mother which are thought to disrupt the baby's heart rhythm. We found that babies of women with untreated ICP have abnormally functioning hearts compared to those without ICP, and the degree of abnormality is closely linked to the level of harmful bile acids in the mother and baby's blood. Babies of women with ICP who received treatment with the drug UDCA do not have the same level of abnormality in their hearts, suggesting that UDCA could be a beneficial treatment in some ICP cases, although further clinical trials are needed to confirm this.

Indexed as

Cholestasis, IntrahepaticPregnancy ComplicationsVentricular DysfunctionAdultAlanine TransaminaseBile Acids and SaltsBiomarkersCholagogues and CholereticsCorrelation of DataElectrocardiographyFemaleFetal BloodFetal HeartHumansNatriuretic Peptide, BrainPeptide FragmentsAlanine TransaminaseBile Acids and SaltsBiomarkersCholagogues and CholereticsNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)Ursodeoxycholic AcidBileCholic acidFemaleHeart rateIntrahepatic cholestasis of pregnancyPregnancyStillbirthUrsodeoxycholic acidVentricular dysfunction

Identifiers

PMID33276032
PMCPMC8062912
OpenAlexW3109062196

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Registered trials

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 OpenQuestion graph.