Evidence map›Paper›PMID 23644957›Full record

ArticleThe American journal of gastroenterology2013

Villous atrophy and negative celiac serology: a diagnostic and therapeutic dilemma.

Marisa DeGaetani, Christina A Tennyson, Benjamin Lebwohl, Suzanne K Lewis, Hussein Abu Daya, Carolina Arguelles-Grande, Govind Bhagat, Peter H R Green

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Article in The American journal of gastroenterology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 83 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
83citing papers in PubMed, 1 pooled it
16.3field-weighted citation impact, top 1% 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

83 citing papers in PubMed, 1 synthesis or guideline pooled it, 206 citations in OpenAlex.

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23 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 1 institution in 1 country.

Marisa DeGaetaniCeliac Disease Center, Columbia University College of Physicians and Surgeons, Columbia University Medical Center, New York, NY 10032, USA.
Christina A Tennyson
Benjamin Lebwohl
Suzanne K Lewis
Hussein Abu Daya
Carolina Arguelles-Grande
Govind Bhagat
Peter H R Green
Columbia University Irving Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesPatients with villous atrophy (VA) and negative celiac disease (CD) serologies pose a diagnostic and therapeutic dilemma. When a definitive etiology for VA is not determined, patients are characterized as having unclassified sprue (US), the optimal management of which is unknown.

methodsWe studied adult patients with VA on biopsy and negative celiac serologies, evaluated at our tertiary referral center over a 10-year period. Testing for HLA DQ2/8 alleles, antienterocyte antibodies, giardia stool antigen, bacterial overgrowth, total serum immunoglobulins, and HIV was noted. Treatment, response, and repeat-biopsy findings were recorded.

resultsThe most common diagnoses of the 72 patients were seronegative CD, medication-related villous atrophy, and US. Of those with US, the majority reported symptomatic improvement with immunosuppressive therapy. Some patients initially labeled as unclassified were found to have VA associated with olmesartan use.

conclusionsThe role of medications in the development of VA and the optimal dose and length of immunosuppression for patients with US should be investigated further.

Indexed as

AdultAgedAged, 80 and overAngiotensin II Type 1 Receptor BlockersAtrophyAutoantibodiesBiopsyCeliac DiseaseDatabases, FactualDuodenumFemaleHLA-DQ AntigensHumansImidazolesImmunoglobulinsImmunosuppressive AgentsAngiotensin II Type 1 Receptor BlockersAutoantibodiesHLA-DQ2 antigenHLA-DQ AntigensImidazolesImmunoglobulinsImmunosuppressive AgentsolmesartanTetrazoles

Identifiers

PMID23644957
OpenAlexW1985335710

What OpenQuestion holds

Textmetadata
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.