Evidence map›Paper›PMID 37471052›Full record

ArticleHepatology communications2023

Cytomegalovirus in biliary atresia is associated with increased pretransplant death, but not decreased native liver survival.

Sarah Kemme, Jennifer D Canniff, Amy G Feldman, Krystle M Garth, Shaobing Li, Zhaoxing Pan, Ronald J Sokol, Adriana Weinberg, Cara L Mack

Open access · goldAbstract read
In one paragraph

Article in Hepatology communications, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.5field-weighted citation impact, top 7% 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.

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

8 citing papers in PubMed, 11 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Organoids in biliary atresia.World journal of pediatric surgery · 2025
    Review
  6. Article
  7. Biliary atresia.Nature reviews. Disease primers · 2024
    Review
  8. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 1 country.

Sarah KemmeD.Brent Polk Division of Pediatric Gastroenterology, Hepatology, and Nutrition, Monroe Carrell Jr. Children's Hospital at Vanderbilt, Nashville, Tennessee, USA.ORCID 0000-0002-9524-3288
Jennifer D CanniffDepartment of Pediatrics, Medicine, and Pathology, University of Colorado, Aurora, Colorado, USA.
Amy G FeldmanDigestive Health Institute, Section of Pediatric Gastroenterology, Hepatology and Nutrition, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, Colorado, USA.ORCID 0000-0003-4021-5615
Krystle M GarthDepartment of Pediatrics, Medicine, and Pathology, University of Colorado, Aurora, Colorado, USA.
Shaobing LiPediatric Infectious Diseases, University of Colorado School of Medicine, Aurora, Colorado, USA.
Zhaoxing PanDepartment of Pediatrics, Research Institute, Children's Hospital Colorado, University of Colorado School of Medicine, Aurora, Colorado, USA.
Ronald J SokolDigestive Health Institute, Section of Pediatric Gastroenterology, Hepatology and Nutrition, University of Colorado School of Medicine and Children's Hospital Colorado, Aurora, Colorado, USA.ORCID 0000-0001-7433-4095
Adriana WeinbergDepartment of Pediatrics, Medicine, and Pathology, University of Colorado, Aurora, Colorado, USA.ORCID 0000-0001-6920-0623
Cara L MackDivision of Pediatric Gastroenterology, Department of Pediatrics, Hepatology & Nutrition, Medical College of Wisconsin, Children's Wisconsin, Milwaukee, Wisconsin, USA.ORCID 0000-0002-5760-3836
Children's Hospital Colorado · USUniversity of Colorado Anschutz Medical Campus · USChildren's Hospital of Wisconsin · USMonroe Carell Jr. Children's Hospital · USUniversity of Colorado Denver · US

Funding

NIH Prior Approval Process ProfessionalUL1TR002535 · NCATS · UNIVERSITY OF COLORADO DENVER · PI SOKOL, RONALD J. · 2018 to 2022
$51.1M
Childhood Liver Disease Research Network Data Coordinating CenterU24DK062456 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI JOHN C MAGEE · 2019 to 2026
$18.9M
Institutional Training Grant in Pediatric GastroenterologyT32DK067009 · NIDDK · UNIVERSITY OF COLORADO DENVER · PI RONALD J. SOKOL, Edwin Fulco de Zoeten · 2005 to 2026
$7.1M
Clinical Center for ChiLDREN: Pathogenesis, Biomarkers, and Antifibrotic TherapyU01DK103149 · NIDDK · BAYLOR COLLEGE OF MEDICINE · PI BENJAMIN L SHNEIDER · 2014 to 2026
$4.8M
Improving Immunization Rates in Transplant Candidates Through the Use of a Health Information Technology ToolK08HS026510 · AHRQ · UNIVERSITY OF COLORADO DENVER · PI FELDMAN, AMY · 2019 to 2023
$742k
AHRQ HHS K08 HS026510NCATS NIH HHS UL1 TR002535NIDDK NIH HHS T32 DK067009NIDDK NIH HHS U01 DK103149NIDDK NIH HHS U24 DK062456
6 · The paper itself

Abstract

backgroundBiliary atresia (BA) is likely caused by a common phenotypic response to various triggers; one proposed trigger, cytomegalovirus (CMV), may lead to worse outcomes. The aim of this study was to determine the severity of disease and pretransplant outcomes of infants with BA, who have evidence of CMV (CMV+) at diagnosis compared with CMV-negative (CMV-) infants.

methodsThe study used data and biospecimens from the Childhood Liver Disease Research Network PROBE study of cholestatic infants. Plasma obtained at the time of hepatic portoenterostomy (HPE) of 249 infants with BA was tested for CMV by DNA-PCR and CMV-IgM. Comparisons between CMV+ and CMV- infants were made using Wilcoxon rank sum, Student t test, chi-square, or Fisher exact test. Native liver survival (NLS) outcomes were analyzed using Kaplan-Meier and Cox regression adjusting for age at HPE; pretransplant patient survival outcomes were analyzed using a competing risk model and adjusting for age at HPE.

resultsCMV+ infants (n = 29, 12%) underwent HPE later (67.8±13.6 d vs. 55.1±18.5 d, p = 0.0005) and had higher baseline alkaline phosphatase and aminotransferases. There was no difference between groups in jaundice clearance or NLS. The subdistribution HR of pretransplant death for CMV+ infants adjusted for age at HPE was 3.8 (p = 0.034).

conclusionsCMV infection at the time of HPE in infants with BA is not associated with worse NLS despite the association with worse liver injury, older age at HPE, and increased risk of pretransplant death adjusted for age at HPE. Continued evaluation of the consequences of CMV infection and the effects of antiviral treatment should be explored.

Indexed as

Biliary AtresiaCytomegalovirus InfectionsChildCytomegalovirusHumansInfantLiverPortoenterostomy, Hepatic

Identifiers

PMID37471052
PMCPMC10351947
OpenAlexW4384820669

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.