Evidence map›Paper›PMID 22859356›Full record

ArticleThe Journal of rheumatology2012

Increased risk of systemic lupus erythematosus in 29,000 patients with biopsy-verified celiac disease.

Jonas F Ludvigsson, Alberto Rubio-Tapia, Vaidehi Chowdhary, Joseph A Murray, Julia F Simard

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of rheumatology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

24 citing papers in PubMed, 1 synthesis or guideline pooled it, 66 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Article
  4. Coeliac disease: complications and comorbidities.Nature reviews. Gastroenterology & hepatology · 2025
    Review
  5. Review
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  7. Review
  8. Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Prevalence of celiac disease in Iranian patients with rheumatologic disorders.Gastroenterology and hepatology from bed to bench · 2018
    Article
  17. Article
  18. Article
  19. Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Jonas F LudvigssonClinical Epidemiology Unit, Department of Medicine, Karolinska University Hospital and Karolinska Institutet, Stockholm, Sweden. jonasludvigsson@yahoo.com
Alberto Rubio-Tapia
Vaidehi Chowdhary
Joseph A Murray
Julia F Simard
Karolinska Institutet · SEÖrebro University Hospital · SE

Funding

EPIDEMIOLOGY OF CELIAC DISEASE--A POPULATION BASED STUDYR01DK057892 · NIDDK · MAYO CLINIC ROCHESTER · PI MURRAY, JOSEPH A · 2000 to 2010
$3.9M
A HLA Mouse Model for Gluten Sensitivity and EnteropathyR01DK071003 · NIDDK · MAYO CLINIC ROCHESTER · PI MURRAY, JOSEPH A · 2006 to 2009
$1.1M
Role of HLA-DR3 in Pathogenesis of Systemic Lupus Erythematosus (SLE)K23AR057815 · NIAMS · MAYO CLINIC ROCHESTER · PI CHOWDHARY, VAIDEHI RADHAKRISHNA · 2010 to 2014
$642k
A HLA Mouse Model for Gluten Sensitivity and EnteropathyR56DK071003 · NIDDK · MAYO CLINIC ROCHESTER · PI MURRAY, JOSEPH A · 2010 to 2010
$394k
NIAMS NIH HHS K23 AR057815NIAMS NIH HHS K23 AR057815-01A1NIDDK NIH HHS DK057892NIDDK NIH HHS DK071003NIDDK NIH HHS R01 DK057892NIDDK NIH HHS R01 DK071003NIDDK NIH HHS R56 DK071003
6 · The paper itself

Abstract

objectiveTo investigate a possible association between celiac disease (CD) and systemic lupus erythematosus (SLE). Case series have indicated a possible association, but population-based studies are lacking.

methodsWe compared the risk of SLE in 29,048 individuals with biopsy-verified CD (villous atrophy, Marsh 3) from Sweden's 28 pathology departments with that in 144,352 matched individuals from the general population identified through the Swedish Total Population Register. SLE was defined as having at least 2 records of SLE in the Swedish Patient Register. We used Cox regression to estimate hazard ratios (HR) for SLE.

resultsDuring followup, 54 individuals with CD had an incident SLE. This corresponded to an HR of 3.49 (95% CI 2.48-4.90), with an absolute risk of 17/100,000 person-years and an excess risk of 12/100,000. Beyond 5 years of followup, the HR for SLE was 2.54 (95% CI 1.57-4.10). While SLE was predominantly female, we found similar risk estimates in men and women. When we restricted our outcome to individuals who also had a dispensation for a medication used in SLE, the HR was 2.43 (95% CI 1.22-4.87). The HR for having 2 records of SLE diagnoses, out of which at least 1 had occurred in a department of rheumatology, nephrology/dialysis, internal medicine, or pediatrics, was 2.87 (95% CI 1.97-4.17).

conclusionIndividuals with CD were at a 3-fold increased risk of SLE compared to the general population. Although this excess risk remained more than 5 years after CD diagnosis, absolute risks were low.

Indexed as

AdultCeliac DiseaseComorbidityFemaleHumansIncidenceLupus Erythematosus, SystemicMaleMiddle AgedPrevalenceRegistriesRiskSweden

Identifiers

PMID22859356
PMCPMC3463642
OpenAlexW2098882577

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.