Evidence map›Paper›PMID 24756015›Full record

ArticleAnnals of hepatology

Association between serum IgE level and adverse clinical endpoints in primary sclerosing cholangitis.

James H Tabibian, Felicity Enders, Mohamad H Imam, Gururaj Kolar, Keith D Lindor, Jayant A Talwalkar

Open access · hybridAbstract read
In one paragraph

Article in Annals of hepatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. The Role of Inflammation in Cholestatic Liver Injury.Journal of inflammation research · 2023
    Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Primary sclerosing cholangitis: A review and update.Liver research (Beijing, China) · 2017
    Article
  8. Article
  9. Endoscopic management of benign biliary strictures.World journal of gastrointestinal endoscopy · 2015
    Review
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

6 authors at 3 institutions in 1 country.

James H TabibianDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA; Center for Clinical and Translational Sciences, Mayo Graduate School, Rochester, MN, USA.
Felicity EndersDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, MN, USA.
Mohamad H ImamDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
Gururaj KolarDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
Keith D LindorExecutive Vice Provost, Health Solutions, Arizona State University, USA.
Jayant A TalwalkarDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
Mayo Clinic in Arizona · USArizona State University · USMayo Clinic · US

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
MULTIDISCRIPLINARY TRAINING IN DIGESTIVE DISEASEST32DK007198 · NIDDK · MAYO CLINIC ROCHESTER · PI Harmeet Malhi · 1986 to 2026
$8.9M
NCATS NIH HHS UL1TR000135NIDDK NIH HHS T32 DK007198NIDDK NIH HHS T32DK007198
6 · The paper itself

Abstract

introductionPrimary sclerosing cholangitis (PSC) is an idiopathic hepatobiliary disorder associated with an increased risk for cholangiocarcinoma (CCA) and a median survival time of 12 years. Reliable predictors of CCA and other major adverse events in PSC are currently lacking. Recently, serum IgE was found to be associated with CCA in a Japanese cohort of PSC patients. Our aim in this study was to determine whether IgE levels predict time to CCA, liver transplantation, or death in a Western (USA-based) cohort of PSC patients. MATERIAL AND

methodsThirty-eight patients with PSC and IgE levels were identified and categorized into low or high IgE groups based on the sample median. Groups were compared with respect to clinical characteristics and adverse endpoint-free survival, and the association between IgE and endpoints was assessed with multivariate proportional-hazards models.

resultsThe median sample age at PSC diagnosis was 41 years, and median serum IgE level was 47.6 kU/L. Low and high IgE groups differed significantly only with respect to IgG subclasses, which were higher among the latter (p < 0.05). There were no significant differences in composite endpoint-free (p = 0.83) or CCA-free survival (p = 0.20). In multivariate analyses, only Mayo PSC risk score and MELD score were significant predictors of endpoint-free survival (p < 0.05).

conclusionsSerum IgE level is associated with several IgG subclass levels but not time to CCA, liver transplantation, or death among PSC patients in a USA-based cohort. While Mayo PSC risk score and MELD score can predict these outcomes, more specific predictors of CCA are needed.

Indexed as

Bile Ducts, IntrahepaticLiver TransplantationAdultBile Duct NeoplasmsCholangiocarcinomaCholangitis, SclerosingCohort StudiesDisease-Free SurvivalDisease ProgressionEnd Stage Liver DiseaseFemaleHumansImmunoglobulin EMaleMiddle AgedMultivariate AnalysisImmunoglobulin E

Identifiers

PMID24756015
PMCPMC4215553
OpenAlexW2187326794

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.