Evidence map›Paper›PMID 26481725›Full record

ArticleBMC gastroenterology2015

Prevalence of inflammatory bowel disease among coeliac disease patients in a Hungarian coeliac centre.

Dorottya Kocsis, Zsuzsanna Tóth, Ágnes A Csontos, Pál Miheller, Péter Pák, László Herszényi, Miklós Tóth, Zsolt Tulassay, Márk Juhász

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
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

7 citing papers in PubMed, 53 citations in OpenAlex.

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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

9 authors at 3 institutions in 1 country.

Dorottya Kocsis2nd Department of Medicine, Semmelweis University, Szentkirályi st. 46., 1088, Budapest, Hungary. kocsisdorottya1@gmail.com.
Zsuzsanna TóthPeterfy S. u. Hospital, Gastroenterology Unit, Péterfy S. st. 8-20., 1076, Budapest, Hungary. toth.zsuzsanna88@gmail.com.
Ágnes A Csontos2nd Department of Medicine, Semmelweis University, Szentkirályi st. 46., 1088, Budapest, Hungary. csontosagnesanna@gmail.com.
Pál Miheller2nd Department of Medicine, Semmelweis University, Szentkirályi st. 46., 1088, Budapest, Hungary. pmiheller@gmail.com.
Péter PákVaszary Kolos. Hospital, Gastroenterology Unit, Petőfi S. st. 26-28., 2500, Esztergom, Hungary. pakpet@t-online.hu.
László Herszényi2nd Department of Medicine, Semmelweis University, Szentkirályi st. 46., 1088, Budapest, Hungary. herszenyi.laszlo@gmail.com.
Miklós Tóth2nd Department of Medicine, Semmelweis University, Szentkirályi st. 46., 1088, Budapest, Hungary. totmik@gmail.com.
Zsolt Tulassay2nd Department of Medicine, Semmelweis University, Szentkirályi st. 46., 1088, Budapest, Hungary. tulassay.zsolt@med.semmelweis-univ.hu.
Márk Juhász2nd Department of Medicine, Semmelweis University, Szentkirályi st. 46., 1088, Budapest, Hungary. juhaszmarkdr@gmail.com.
Semmelweis University · HUBM Központi Kórház · HUPéterfy Sándor Utcai Kórház-Rendelőintézet és Baleseti Központ · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCeliac disease, Crohn disease and ulcerative colitis are inflammatory disorders of the gastrointestinal tract with some common genetic, immunological and environmental factors involved in their pathogenesis. Several research shown that patients with celiac disease have increased risk of developing inflammatory bowel disease when compared with that of the general population. The aim of this study is to determine the prevalence of inflammatory bowel disease in our celiac patient cohort over a 15-year-long study period.

methodsTo diagnose celiac disease, serological tests were used, and duodenal biopsy samples were taken to determine the degree of mucosal injury. To set up the diagnosis of inflammatory bowel disease, clinical parameters, imaging techniques, colonoscopy histology were applied. DEXA for measuring bone mineral density was performed on every patient.

resultsIn our material, 8/245 (3,2 %) coeliac disease patients presented inflammatory bowel disease (four males, mean age 37, range 22-67), 6/8 Crohn's disease, and 2/8 ulcerative colitis. In 7/8 patients the diagnosis of coeliac disease was made first and inflammatory bowel disease was identified during follow-up. The average time period during the set-up of the two diagnosis was 10,7 years. Coeliac disease serology was positive in all cases. The distribution of histology results according to Marsh classification: 1/8 M1, 2/8 M2, 3/8 M3a, 2/8 M3b. The distribution according to the Montreal classification: 4/6 Crohn's disease patients are B1, 2/6 Crohn's disease patients are B2, 2/2 ulcerative colitis patients are S2. Normal bone mineral density was detected in 2/8 case, osteopenia in 4/8 and osteoporosis in 2/8 patients.

conclusionsWithin our cohort of patients with coeliac disease, inflammatory bowel disease was significantly more common (3,2 %) than in the general population.

Indexed as

AdultAgedBone DensityCeliac DiseaseColitis, UlcerativeCrohn DiseaseFemaleHumansHungaryLongitudinal StudiesMaleMiddle AgedPrevalenceRisk FactorsSerologic TestsYoung Adult

Identifiers

PMID26481725
PMCPMC4612406
OpenAlexW2164846210

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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.