Evidence map›Paper›PMID 29522202›Full record

ArticleInflammatory bowel diseases2018

Natural History of Established and De Novo Inflammatory Bowel Disease After Liver Transplantation for Primary Sclerosing Cholangitis.

Mohamad A Mouchli, Siddharth Singh, Lisa Boardman, David H Bruining, Amy L Lightner, Charles B Rosen, Julie K Heimbach, Bashar Hasan, John J Poterucha, Kymberly D Watt and 3 more

Open access · bronzeAbstract readVideo-Audio Media
In one paragraph

Article in Inflammatory bowel diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
  2. Review
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  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
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  11. The microbiota and the gut-liver axis in primary sclerosing cholangitis.Nature reviews. Gastroenterology & hepatology · 2023
    Review
  12. Article
  13. Secondary causes of inflammatory bowel diseases.World journal of gastroenterology · 2020
    Review
  14. Review
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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

13 authors at 3 institutions in 1 country.

Mohamad A MouchliDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Siddharth SinghDivision of Gastroenterology, Department of Internal Medicine, UCSD, La Jolla, California.
Lisa BoardmanDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
David H BruiningDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Amy L LightnerDivision of Colon and Rectal Surgery, Mayo Clinic, Rochester, Minnesota.
Charles B RosenDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Julie K HeimbachWilliam J. von Liebig Center for Transplantation and Clinical Regeneration, Mayo Clinic, Rochester, Minnesota.
Bashar HasanDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
John J PoteruchaDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Kymberly D WattDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Sunanda V KaneDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Laura E RaffalsDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Edward V LoftusDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Mayo Clinic · USWinnMed · USUniversity of California, San Diego · US

Funding

PILOT AND FEASIBILTY PROGRAMP30DK084567 · NIDDK · MAYO CLINIC ROCHESTER · PI GREGORY J. GORES · 2009 to 2026
$22.2M
San Diego Biomedical Informatics Education & Research (SABER)T15LM011271 · NLM · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SHAMIM NEMATI · 2012 to 2026
$9.7M
Time lapse to cancer: defining transition from polyp to colorectal cancer (PQ14)R01CA170357 · NCI · MAYO CLINIC ROCHESTER · PI BOARDMAN, LISA ALLYN · 2012 to 2016
$2.5M
NCI NIH HHS R01 CA170357NIDDK NIH HHS P30 DK084567NLM NIH HHS T15 LM011271
6 · The paper itself

Abstract

Background: The course of inflammatory bowel disease (IBD) after liver transplantation (LT) for primary sclerosing cholangitis (PSC) is poorly understood. We describe the natural history of established IBD after LT (including risk of disease progression, colectomy, and neoplasia) and de novo IBD. Methods: In a retrospective cohort, we identified all patients with PSC who underwent LT for advanced PSC at Mayo Clinic, Rochester, Minnesota. Risk factors were identified using multivariate Cox proportional hazard analysis. Results: Three hundred seventy-three patients were identified (mean age, 47.5 ± 11.7 years; 64.9% male). Over a median (range) of 10 (5.5-17.1) years, 151 patients with PSC-IBD with an intact colon at the time of LT were studied. Post-LT, despite transplant-related immunosuppression, 56/151 (37.1%) required escalation of therapy, whereas 87 had a stable course (57.6%) and 8 patients (5.3%) improved. The 1-, 5-, and 10-year risks of progression of IBD were 4.0%, 18.5%, and 25.5%, respectively. On multivariate analysis, tacrolimus-based immunosuppression post-LT were associated with unfavorable course, and azathioprine use after LT was associated with improved course post-LT. Of 84 patients with no evidence of IBD at the time of LT, 22 (26.2%) developed de novo IBD post-LT. The 1-, 5-, and 10-year cumulative incidences of de novo IBD were 5.5%, 20.0%, and 25.4%, respectively. On univariate analysis, mycophenolate mofetil use after LT was associated with increased risk of de novo IBD, but azathioprine use after LT seemed to be protective. Conclusions: The 10-year cumulative probability of IBD flare requiring escalation of therapy after LT for PSC was 25.5%, despite immunosuppression for LT. The 10-year cumulative risk of de novo IBD after LT for PSC was 25.4%. Transplant-related immunosuppression may modify the risk of de novo IBD, with an increased risk with mycophenolate and a decreased risk with azathioprine. 10.1093/ibd/izx096_video1izx096.video15746673864001.

Indexed as

AdultAgedCholangitis, SclerosingFemaleHumansImmunosuppressive AgentsIncidenceInflammatory Bowel DiseasesLiver TransplantationMaleMiddle AgedMinnesotaMultivariate AnalysisRetrospective StudiesRisk FactorsTime FactorsImmunosuppressive Agents

Identifiers

PMID29522202
PMCPMC6085995
OpenAlexW2790142597

What OpenQuestion holds

Textmetadata
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.