Evidence map›Paper›PMID 27527747›Full record

ArticleThe American journal of gastroenterology2016

A Cross-Sectional Study of the Prevalence of Gastrointestinal Symptoms and Pathology in Patients With Common Variable Immunodeficiency.

Silje F Jørgensen, Henrik M Reims, Didrik Frydenlund, Kristian Holm, Vemund Paulsen, Annika E Michelsen, Kristin K Jørgensen, Liv T Osnes, Jorunn Bratlie, Tor J Eide and 13 more

Abstract read
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In one paragraph

Article in The American journal of gastroenterology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 60 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed, 1 pooled it
5.4field-weighted citation impact, top 4% 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

60 citing papers in PubMed, 1 synthesis or guideline pooled it, 118 citations in OpenAlex.

  1. Pooled it
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  8. Chronic persistent Norovirus in the immune-compromised host.Current opinion in infectious diseases · 2025
    Review
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  12. Gastrointestinal Tract Findings in Patients with Primary Immunodeficiency: A Single-Center 6-Year Experience.The Turkish journal of gastroenterology : the official journal of Turkish Society of Gastroenterology · 2025
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 4 institutions in 1 country.

Silje F JørgensenResearch Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Henrik M ReimsDepartment of Pathology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Didrik FrydenlundDepartment of Pathology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Kristian HolmResearch Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Vemund PaulsenDepartment of Transplantation Medicine, Section of Gastroenterology, Oslo University Hospital Rikshospitalet, Oslo, Norway.
Annika E MichelsenResearch Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Kristin K JørgensenNorwegian PSC Research Center, Oslo University Hospital Rikshospitalet, Oslo, Norway.
Liv T OsnesDepartment of Immunology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Jorunn BratlieResearch Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Tor J EideDepartment of Pathology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Christen P DahlResearch Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Ellen HolterDepartment of Microbiology, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Rune R TronstadDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Kurt HanevikDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Hans-Richard BrattbakkDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Fatemeh KavehMedical Genetics Department, Oslo University Hospital, Ullevål, Oslo, Norway.
Torunn FiskerstrandDepartment of Clinical Science, University of Bergen, Bergen, Norway.
Anne-Marte B KranInstitute of Clinical Medicine, University of Oslo, Oslo, Norway.
Thor UelandResearch Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Tom H KarlsenResearch Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Pål AukrustResearch Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Knut E A LundinDepartment of Transplantation Medicine, Section of Gastroenterology, Oslo University Hospital Rikshospitalet, Oslo, Norway.
Børre FevangResearch Institute of Internal Medicine, Oslo University Hospital, Rikshospitalet, Oslo, Norway.
Oslo University Hospital · NOUniversity of Bergen · NOUniversity of Oslo · NOUiT The Arctic University of Norway · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe objective of this study was to study the prevalence of gastrointestinal (GI) symptoms and histopathology in patients with common variable immunodeficiency (CVID) as well as linking the findings to GI infections and markers of systemic immune activation.

methodsIn this cross-sectional study, we addressed GI symptoms in 103 patients and GI histopathological findings in 53 patients who underwent upper and lower endoscopic examination. The most frequent histopathological findings were linked to GI symptoms, B-cell phenotype, and markers of systemic immune activation (soluble (s)CD14, sCD25, and sCD163). Microarray analysis compared "celiac-like disease" in CVID to celiac disease. Screening for selected bacterial and viral infections in fecal samples and gut mucosal biopsies was performed.

resultsThe main findings of this study were as follows: most common GI symptoms were bloating (34%), pain (30%), and diarrhea (26%). The most frequent histopathological findings were increased intraepithelial lymphocytes in the descending part of the duodenum, i.e., "celiac-like disease" (46% of patients), decreased numbers of plasma cells in GI tract mucosa (62%), and lymphoid hyperplasia (38%), none of which were associated with GI symptoms. Reduced plasma cells in GI mucosa were associated with B-cell phenotypic characteristics of CVID, and increased serum levels of sCD14 (P=0.025), sCD25 (P=0.01), and sCD163 (P=0.04). Microarray analyses distinguished between CVID patients with "celiac-like disease" and celiac disease. Positive tests for bacterial and viral infections were scarce both in fecal samples and gut mucosal biopsies, including PCR test for norovirus in biopsy specimens (0 positive tests).

conclusionsIn conclusion, GI pathology is common in CVID, but does not necessarily cause symptoms. However, reduced plasma cells in GI mucosa were linked to systemic immune activation, "celiac-like disease" in CVID and true celiac disease appear to be different disease entities, as assessed by gene expression, and infections (including norovirus) are rarely a cause of the CVID enteropathy.

Indexed as

Abdominal PainAdultAgedAged, 80 and overB-LymphocytesCeliac DiseaseColonoscopyCommon Variable ImmunodeficiencyConstipationCross-Sectional StudiesDiarrheaDuodenumEndoscopy, Digestive SystemEsophageal MucosaFemaleGastric Mucosa

Identifiers

PMID27527747
OpenAlexW2512804017

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.