Evidence map›Paper›PMID 27262844›Full record

ArticleDigestive diseases and sciences2016

Natural History of Patients Presenting with Autoimmune Hepatitis and Coincident Nonalcoholic Fatty Liver Disease.

Javier De Luca-Johnson, Kirk J Wangensteen, Joshua Hanson, Edward Krawitt, Rebecca Wilcox

Abstract read
In one paragraph

Article in Digestive diseases and sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 2 pooled it
–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

44 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Guideline
  2. Guideline
  3. Article
  4. Review
  5. Review
  6. Review
  7. Autoantibodies are associated with worse outcomes in MASLD.JHEP reports : innovation in hepatology · 2025
    Article
  8. Article
  9. Journal of translational autoimmunity · 2025
    Article
  10. Article
  11. JHEP reports : innovation in hepatology · 2025
    Review
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Javier De Luca-JohnsonDepartment of Pathology and Laboratory Medicine, University of Vermont Medical Center, 89 Beaumont Avenue, Courtyard at Given S269, Burlington, VT, 05405, USA. Javier.DeLuca-Johnson@uvmhealth.org.
Kirk J WangensteenDivision of Gastroenterology, Department of Medicine, University of Pennsylvania, 3400 Civic Center Blvd, Philadelphia, PA, 19104, USA.
Joshua HansonDepartment of Pathology, University of New Mexico, Reginald Heber Fitz Hall, Room 335, 915 Camino de Salud, Albuquerque, NM, 87131, USA.
Edward KrawittDepartment of Medicine, University of Vermont Medical Center, 111 Colchester Avenue, Fletcher 311, Burlington, VT, 05401, USA.
Rebecca WilcoxDepartment of Pathology and Laboratory Medicine, University of Vermont Medical Center, 89 Beaumont Avenue, Courtyard at Given S269, Burlington, VT, 05405, USA.

Funding

Genetic basis of liver repopulationK08DK106478 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI WANGENSTEEN, KIRK J · 2015 to 2019
$787k
NIDDK NIH HHS K08 DK106478
6 · The paper itself

Abstract

backgroundGiven the increase of nonalcoholic fatty liver disease (NAFLD) in the general population, a similar rise might be expected in autoimmune hepatitis (AIH) patients.

aimsWe sought to determine the clinical outcome of patients with coincident AIH and NAFLD.

methodsWe identified all intradepartmental AIH cases, and those meeting study criteria were placed into one of three cohorts: AIH only, AIH and simple steatosis (SS), and AIH and nonalcoholic steatohepatitis (NASH). The following outcome and clinical data were analyzed: incidence of all-cause mortality, incidence of liver-related mortality, incidence of liver-related adverse outcomes, and prevalence of cirrhosis at index biopsy.

resultsOut of a total 73 study patients, 14 % classified as AIH with SS and 16 % as AIH and NASH. Fifty percent of AIH and NASH patients had cirrhosis at index biopsy as compared to 18 % of AIH-only patients (p = 0.032). Patients with AIH and NASH had a relative risk of 7.65 (95 % CI 1.43-40.8) for liver-related mortality and 2.55 (95 % CI 0.92-7.09) for liver-related adverse outcomes, as compared to the AIH-only cohort. No significant difference in outcome measures existed in comparing (AIH only) with (AIH and SS) cohorts. DISCUSSION: Patients with coincident AIH and NASH were more likely to present with cirrhosis and more likely to develop adverse clinical outcome with decreased survival as compared to AIH-only patients. These findings suggest that simultaneous exposure confers a clinically significant increased risk, which may warrant closer follow-up and surveillance.

Indexed as

AdolescentAdultAgedBiopsyCase-Control StudiesCause of DeathChildCohort StudiesComorbidityDisease ProgressionFemaleGlucocorticoidsHepatitis, AutoimmuneHumansImmunosuppressive AgentsIncidenceGlucocorticoidsImmunosuppressive AgentsAutoimmune hepatitisDiabetes mellitusNonalcoholic fatty liver diseaseNonalcoholic steatohepatitisObesity

Identifiers

PMID27262844
PMCPMC6357773

What OpenQuestion holds

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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.