Evidence map›Paper›PMID 32655231›Full record

ArticleJournal of clinical and experimental hepatology

Celiac Disease and Portal Hypertension: A Causal Association or Just a Coincidence?

Amit Tanwar, Gaurav K Gupta, Virender Chauhan, Deepak Sharma, Mukesh K Jain, Hemendra Bhardwaj, Ashok Jhajharia, Sandeep Nijhawan

Open access · greenAbstract read
In one paragraph

Article in Journal of clinical and experimental hepatology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 36% 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

4 citing papers in PubMed, 11 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

8 authors at 1 institution in 1 country.

Amit TanwarDepartment of Gastroenterology, SMS Medical College and Hospital, Jaipur, India.
Gaurav K GuptaDepartment of Gastroenterology, SMS Medical College and Hospital, Jaipur, India.
Virender ChauhanDepartment of Gastroenterology, SMS Medical College and Hospital, Jaipur, India.
Deepak SharmaDepartment of Gastroenterology, SMS Medical College and Hospital, Jaipur, India.
Mukesh K JainDepartment of Gastroenterology, SMS Medical College and Hospital, Jaipur, India.
Hemendra BhardwajDepartment of Gastroenterology, SMS Medical College and Hospital, Jaipur, India.
Ashok JhajhariaDepartment of Gastroenterology, SMS Medical College and Hospital, Jaipur, India.
Sandeep NijhawanDepartment of Gastroenterology, SMS Medical College and Hospital, Jaipur, India.
Sawai ManSingh Medical College and Hospital · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionCeliac disease (CD) has been linked to portal hypertension (PHT) of varied etiology, but the causality association has never been proved. We aim to study the prevalence of CD in patients of PHT of different etiology.

methodsA prospective observational study was conducted from June 2017 to December 2018 involving all the cases of PHT of varied etiology. Consecutive patients of PHT with chronic liver disease (CLD) of defined etiology like ethanol, viral hepatitis (B or C), Budd-Chiari syndrome (BCS), autoimmune-related cirrhosis, and cryptogenic CLD (cCLD) (group A) and those with noncirrhotic PHT (NCPHT), which included noncirrhotic portal fibrosis (NCPF) and extrahepatic portal vein obstruction (EHPVO) (group B), were screened for CD by IgA anti-tTG antibody followed by duodenal biopsy in serology-positive patients.

resultsOut of a total of 464 patients, group A constituted 382 patients, CLD related to ethanol (155), cCLD (147), hepatitis B (42), hepatitis C (21), autoimmune (10), and BCS (7), whereas 82 patients were in group B with NCPF (64) and EHPVO (18). Total 29 patients were diagnosed with CD in both groups, 17 in group A (4.5%) and 12 in group B (14.6%). In group A, 13 patients with cCLD, two with HBV-related CLD, one with BCS, and one with autoimmune-related CLD were concomitantly diagnosed as CD. In group B, CD was diagnosed in 12 patients of NCPF (11) and EHPVO (1). Liver histology showed chronic hepatitis in two patients and was normal in three patients.

conclusionCD is common in PHT of different etiology, especially in cCLD, NCPH and autoimmune hepatitis; however, the etiological basis for this association is still to be defined. The likelihood of CD is higher in liver disease than the general population, and these patients should be screened for CD.

Indexed as

AIH, autoimmune hepatitisANA, anti-nuclear antibodyAnti LKM, anti-liver kidney microsome antibodyASMA, anti-smooth muscle antibodyBCS, Budd–Chiari syndromec CLD, cryptogenic chronic liver diseaseCD, celiac diseaseceliac diseasechronic liver diseaseCLD, chronic liver diseaseEHPVO, extrahepatic portal vein obstructionHBs Ag, hepatitis B surface antigenHBV, hepatitis B virusHLA, human leukocyte antigenIg G, immunoglobulin GNCIPH, noncirrhotic idiopathic portal hypertensionNCPF, noncirrhotic portal fibrosisNCPH, noncirrhotic portal hypertensionnoncirrhotic portal hypertensionPHT, portal hypertensionportal hypertensiontTG antibody, tissue transglutaminase antibody

Identifiers

PMID32655231
PMCPMC7335706
OpenAlexW2990102608

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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.