Evidence map›Paper›PMID 31436702›Full record

ArticleJournal of pediatric gastroenterology and nutrition2019

Phenotypes of Chronic Hepatitis B in Children From a Large North American Cohort.

Kathleen B Schwarz, Manuel Lombardero, Adrian M Di Bisceglie, Karen F Murray, Philip Rosenthal, Simon C Ling, Yona Keich Cloonan, Norberto Rodriguez-Baez, Sarah Jane Schwarzenberg, Jay H Hoofnagle and 2 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of pediatric gastroenterology and nutrition, 2019. 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
–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

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Observational
  6. Article
  7. Review
  8. Article
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

12 authors.

Kathleen B SchwarzJohn Hopkins University, Baltimore, MD.
Manuel LombarderoUniversity of Pittsburgh, Pittsburgh, PA.
Adrian M Di BisceglieSaint Louis University, Saint Louis, MO.
Karen F MurrayUniversity of Washington, Seattle, WA.
Philip RosenthalUniversity of California, San Francisco, CA.
Simon C LingUniversity of Toronto, Toronto, Ontario, Canada.
Yona Keich CloonanUniversity of Pittsburgh, Pittsburgh, PA.
Norberto Rodriguez-BaezUniversity of Texas Southwestern Medical Center, Dallas, TX.
Sarah Jane SchwarzenbergUniversity of Minnesota, Minneapolis, MN.
Jay H HoofnagleNational Institute of Diabetes and Digestive Diseases, National Institutes of Health, Bethesda, MD.
Jeffrey TeckmanSaint Louis University, Saint Louis, MO.
Hepatitis B Research Network (HBRN)

Funding

Transform Dissemination and Implementation Science in CTSA ProgramsUL1TR002319 · NCATS · UNIVERSITY OF WASHINGTON · PI John K. Amory · 2017 to 2026
$100.0M
Engaging University of California Stakeholders for Biorespository ResearchUL1TR000004 · NCATS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GRANDIS, JENNIFER RUBIN · 2012 to 2015
$78.0M
Institute of Translational Health SciencesUL1TR000423 · NCATS · UNIVERSITY OF WASHINGTON · PI DISIS, MARY L. · 2012 to 2016
$49.4M
Hepatitis B Research Network - Data Coordination CenterU01DK082864 · NIDDK · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI BELLE, STEVEN H. · 2008 to 2019
$25.3M
Hepatitis B Research Network (HBRN): Natural History and Treatment StudiesU01DK082944 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI COOPER, STEWART, KHALILI, MANDANA · 2008 to 2019
$10.0M
Observation Study of Persons with Chronic Hepatitis B Virus infection in North AmericaU01DK082874 · NIDDK · UNIVERSITY HEALTH NETWORK · PI JANSSEN, HARRY · 2008 to 2019
$6.9M
Immunologic and Virologic Correlates of the Age-Related Decrease in HBV DNA in ChildrenU01DK082916 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI MURRAY, KAREN F, RODRIGUEZ BAEZ, NORBERTO · 2008 to 2019
$5.0M
Midwest Hepatitis B ConsortiumU01DK082871 · NIDDK · SAINT LOUIS UNIVERSITY · PI DI BISCEGLIE, ADRIAN MICHAEL · 2008 to 2019
$4.7M
Optimal Long-term Outcome of Chronic Hepatitis BU01DK082843 · NIDDK · MAYO CLINIC ROCHESTER · PI ROBERTS, LEWIS R · 2008 to 2014
$2.0M
NCATS NIH HHS UL1 TR000004NCATS NIH HHS UL1 TR000423NCATS NIH HHS UL1 TR002319NIDDK NIH HHS U01 DK082843NIDDK NIH HHS U01 DK082864NIDDK NIH HHS U01 DK082871NIDDK NIH HHS U01 DK082874NIDDK NIH HHS U01 DK082916NIDDK NIH HHS U01 DK082944
6 · The paper itself

Abstract

objectiveThe aim of the study was to define chronic HBV phenotypes in a large, cohort of United States and Canadian children utilizing recently published population-based upper limit of normal alanine aminotransferase levels (ULN ALT), compared with local laboratory ULN; identify relationships with host and viral factors.

backgroundChronic hepatitis B virus (HBV) infection has been characterized by phases or phenotypes, possibly associated with prognosis and indications for therapy.

methodsBaseline enrollment data of children in the Hepatitis B Research Network were examined. Phenotype definitions were inactive carrier: HBeAg-negative with low HBV DNA and normal ALT levels; immune-tolerant: HBeAg-positive with high HBV DNA but normal ALT levels; or chronic hepatitis B: HBeAg-positive or -negative with high HBV DNA and abnormal ALT levels.

resultsThree hundred seventy-one participants were analyzed of whom 274 were HBeAg-positive (74%). Younger participants were more likely be HBeAg-positive with higher HBV DNA levels. If local laboratory ULN ALT levels were used, 35% were assigned the immune tolerant phenotype, but if updated ULN were applied, only 12% could be so defined, and the remaining 82% would be considered to have chronic hepatitis B. Among HBeAg-negative participants, only 21 (22%) were defined as inactive carriers and 14 (14%) as HBeAg-negative chronic hepatitis B; the majority (61%) had abnormal ALT and low levels of HBV DNA, thus having an indeterminant phenotype. Increasing age was associated with smaller proportions of HBeAg-positive infection.

conclusionsAmong children with chronic HBV infection living in North America, the immune tolerant phenotype is uncommon and HBeAg positivity decreases with age.

Indexed as

AdolescentAlanine TransaminaseCanadaChildCohort StudiesFemaleHepatitis B, ChronicHepatitis B e AntigensHepatitis B virusHumansMalePhenotypeUnited StatesAlanine TransaminaseHepatitis B e Antigens

Identifiers

PMID31436702
PMCPMC6814562

What OpenQuestion 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 OpenQuestion graph.