Evidence map›Paper›PMID 25881849›Full record

ArticleMedicine2015

Gastrointestinal diagnosis of classical Whipple disease: clinical, endoscopic, and histopathologic features in 191 patients.

Ute Günther, Verena Moos, Gabriel Offenmüller, Gerrit Oelkers, Walther Heise, Annette Moter, Christoph Loddenkemper, Thomas Schneider

Open access · goldAbstract read
In one paragraph

Article in Medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 1 synthesis or guideline pooled it, 119 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Deciphering whipple's disease complexity.Clinical and experimental medicine · 2026
    Review
  4. Article
  5. Article
  6. Review
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  8. [Massive pancarditis-autopsy report].Pathologie (Heidelberg, Germany) · 2023
    Article
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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 2 institutions in 2 countries.

Ute GüntherFrom the Charité - Campus Benjamin Franklin (UG, VM, GOffenmüller, GOelkers, TS), Medical Clinic I Gastroenterology, Infectious Diseases, Rheumatology; Vivantes Auguste-Viktoria-Klinikum (UG), Klinik für Innere Medizin, Infektiologie und Gastroenterologie; Evangelisches Krankenhaus Königin Elisabeth (WH), Abteilung Innere Medizin/Gastroeneterologie, Infektiologie und Nephrologie; Deutsches Herzzentrum Berlin (AM), Biofilmzentrum; and PathoTres (CL), Berlin, Germany.
Verena Moos
Gabriel Offenmüller
Gerrit Oelkers
Walther Heise
Annette Moter
Christoph Loddenkemper
Thomas Schneider
Center for Rheumatology · USInstituto de Gastroenterología · CU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classic Whipple disease (CWD) is a systemic infection caused by Tropheryma whipplei. Different diagnostic tools have been developed over the last decades: periodic acid-Schiff (PAS) staining, T whipplei-specific polymerase chain reaction (PCR), and T whipplei-specific immunohistochemistry (IHC). Despite all these advances, CWD is still difficult to diagnose because of a variety of clinical symptoms and possibly a long time span between first unspecific symptoms and the full-blown clinical picture of the disease. Herein, we report an observational cohort study summarizing epidemiologic data, clinical manifestations, and diagnostic parameters of 191 patients with CWD collected at our institution. Gastrointestinal manifestations are the most characteristic symptoms of CWD affecting 76% of the cohort. Although the small bowel was macroscopically conspicuous in only 27% of cases, 173 (91%) patients presented with characteristic histological changes in small bowel biopsies (in 2 patients, these changes were only seen within the ileum). However, 18 patients displayed normal small bowel histology without typical PAS staining. In 9 of these patients, alternative test were positive from their duodenal specimens (ie, T whipplei-specific PCR and/or IHC). Thus, in 182 patients (95%) a diagnostic hint toward CWD was obtained from small bowel biopsies. Only 9 patients (5%) were diagnosed solely based on positive T whipplei-specific PCR and/or IHC of extraintestinal fluids (eg, cerebrospinal fluid, synovial fluid) or extraintestinal tissue (eg, lymph node, synovial tissue), respectively. Thus, despite efforts to diagnose CWD from alternative specimens, gastroscopy with duodenal biopsy and subsequent histological and molecular-biological examination is the most reliable diagnostic tool for CWD.

Indexed as

TropherymaAdultAgedAged, 80 and overCerebrospinal FluidCohort StudiesDiagnosis, DifferentialFemaleGastrointestinal DiseasesGastroscopyHematologic TestsHumansImmunohistochemistryMaleMiddle AgedPolymerase Chain Reaction

Identifiers

PMID25881849
PMCPMC4602506
OpenAlexW2322042151

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.