Evidence map›Paper›PMID 31560892›Full record

ArticleGastroenterology2020

Community-Based Study of Celiac Disease Autoimmunity Progression in Adults.

Rok Seon Choung, Shahryar Khaleghi, Amanda K Cartee, Eric V Marietta, Joseph J Larson, Katherine S King, Otto Savolainen, Alastair B Ross, S Vincent Rajkumar, Michael J Camilleri and 2 more

Open access · greenAbstract read
In one paragraph

Article in Gastroenterology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

13 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Review
  4. Can diet change the natural history of gastrointestinal diseases?JGH open : an open access journal of gastroenterology and hepatology · 2024
    Review
  5. Review
  6. Population level screening for celiac disease: is now the time?Current opinion in gastroenterology · 2023
    Review
  7. Celiac Disease in the Elderly.Current treatment options in gastroenterology · 2022
    Article
  8. Review
  9. Article
  10. The global burden of coeliac disease: opportunities and challenges.Nature reviews. Gastroenterology & hepatology · 2022
    Review
  11. Article
  12. Article
  13. 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

12 authors at 4 institutions in 3 countries.

Rok Seon ChoungDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Shahryar KhaleghiDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Amanda K CarteeDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Eric V MariettaDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Joseph J LarsonDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota.
Katherine S KingDivision of Biomedical Statistics and Informatics, Mayo Clinic, Rochester, Minnesota.
Otto SavolainenDepartment of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden.
Alastair B RossDepartment of Biology and Biological Engineering, Chalmers University of Technology, Gothenburg, Sweden; Proteins and Metabolites Team, AgResearch, Lincoln, New Zealand.
S Vincent RajkumarDivision of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota.
Michael J CamilleriDepartment of Dermatology and Laboratory Medicine and Pathology, Mayo Clinic, Rochester, Minnesota.
Alberto Rubio-TapiaDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota.
Joseph A MurrayDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, Minnesota. Electronic address: murray.joseph@mayo.edu.
Mayo Clinic · USWinnMed · USAgResearch · NZChalmers University of Technology · SE

Funding

Rochester Epidemiology ProjectR01AG034676 · NIA · MAYO CLINIC ROCHESTER · PI ROCCA, WALTER A, ST SAUVER, JENNIFER LYNN · 2010 to 2019
$9.5M
EPIDEMIOLOGY OF CELIAC DISEASE--A POPULATION BASED STUDYR01DK057892 · NIDDK · MAYO CLINIC ROCHESTER · PI MURRAY, JOSEPH A · 2000 to 2010
$3.9M
Interdisciplinary Infrastructure for Aging Research: Rochester Epidemiology ProjectR33AG058738 · NIA · MAYO CLINIC ROCHESTER · PI LEBRASSEUR, NATHAN K, OLSON, JANET E · 2020 to 2022
$2.4M
NIA NIH HHS R01 AG034676NIA NIH HHS R33 AG058738NIDDK NIH HHS R01 DK057892
6 · The paper itself

Abstract

BACKGROUND &

aimsCeliac disease can develop at any age, but outcomes of adults with positive results from serologic tests for tissue transglutaminase antibodies (tTGA) without endoscopic determination of celiac disease (called celiac autoimmunity) have not been thoroughly evaluated. We investigated the proportion of adults with celiac autoimmunity at a community medical center and their progression to celiac disease.

methodsWe analyzed waste blood samples from a community clinic from 15,551 adults for tTGA and, if titer results were above 2 U/mL, for endomysial antibody. The blood samples had been collected at 2 time points (median interval, 8.8 years) from 2006 through 2017. We collected data from the clinic on diagnoses of celiac disease based on duodenal biopsy analysis.

resultsOf the serum samples collected at the first time point, 15,398 had negative results for tTGA, and 153 had positive results for tTGA (>4 U/mL). Based on medical records, 6 individuals received a diagnosis of celiac disease, for a cumulative incidence of celiac disease diagnosis of 0.06% (95% confidence interval, 0.01-0.11). Forty-nine (0.32%) individuals with a negative result from the first serologic test for tTGA had a positive result from the second test. Among the 153 adults who were tTGA positive at the first time point, 31 (20%) had a subsequent diagnosis of celiac disease, 81 (53%) remained positive for tTGA without a clinical diagnosis of celiac disease, and 41 (27%) had negative test results for tTGA at the second time point. Higher initial tTGA titers, female sex, and a history of hypothyroidism and autoimmune disease were associated with increased risks of subsequent diagnosis of celiac disease. Interestingly, adults whose first blood sample had a positive test result but second blood sample had a negative result for tTGA were older, had lower-than-average initial tTGA titer results, and had a higher mean body mass index than adults whose blood samples were positive for tTGA at both time points and adults later diagnosed with celiac disease.

conclusionsIn an analysis of serum samples collected from a community clinic an average of 8.8 years apart, we found that fewer than 1% of adults with negative results from an initial test for tTGA have a positive result on a second test. Of adults with positive results from the test for tTGA, only 20% are later diagnosed with celiac disease; the remaining individuals maintain persistent increases in tTGA without diagnoses of celiac disease or have negative results from second tests.

Indexed as

AutoimmunityAdultAutoantibodiesBiopsyCeliac DiseaseCommunity Health CentersDisease ProgressionFemaleFollow-Up StudiesGTP-Binding ProteinsHumansIncidenceMaleMiddle AgedMinnesotaProspective StudiesAutoantibodiesGTP-Binding ProteinsProtein Glutamine gamma Glutamyltransferase 2TransglutaminasesDe Novo DiseaseEpidemiologyPreclinical PhaseSerology

Identifiers

PMID31560892
PMCPMC7065356
OpenAlexW2975135783

What OpenQuestion holds

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Registered trials

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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.