Evidence map›Paper›PMID 41331827›Full record

ArticleGut pathogens2025

Nasopharyngeal viral infection as a source of elevated fecal calprotectin: a diagnostic pitfall in intestinal inflammation.

Chun-Ting Chen, Annemiek A van der Eijk, Jolanda J C Voermans, Hanneke J van Vuuren, Maikel P Peppelenbosch, Vincent T Janmaat

Abstract read
In one paragraph

Article in Gut pathogens, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

6 authors.

Chun-Ting ChenDepartment of Gastroenterology and Hepatology, Erasmus MC-University Medical Center Rotterdam, PO Box 2040, Rotterdam, NL-3000 CA, The Netherlands.
Annemiek A van der EijkDepartment of Viroscience, Erasmus MC-University Medical Center Rotterdam, PO Box 2040, Rotterdam, NL-3000 CA, The Netherlands.ORCID http://orcid.org/0000-0002-8918-5536
Jolanda J C VoermansDepartment of Viroscience, Erasmus MC-University Medical Center Rotterdam, PO Box 2040, Rotterdam, NL-3000 CA, The Netherlands.ORCID http://orcid.org/0000-0002-5607-7395
Hanneke J van VuurenDepartment of Gastroenterology and Hepatology, Erasmus MC-University Medical Center Rotterdam, PO Box 2040, Rotterdam, NL-3000 CA, The Netherlands.
Maikel P PeppelenboschDepartment of Gastroenterology and Hepatology, Erasmus MC-University Medical Center Rotterdam, PO Box 2040, Rotterdam, NL-3000 CA, The Netherlands. m.peppelenbosch@erasmusmc.nl.ORCID http://orcid.org/0000-0001-9112-6028
Vincent T JanmaatDepartment of Gastroenterology and Hepatology, Erasmus MC-University Medical Center Rotterdam, PO Box 2040, Rotterdam, NL-3000 CA, The Netherlands. v.janmaat@erasmusmc.nl.ORCID http://orcid.org/0000-0002-8279-1816

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fecal calprotectin is widely used as a non-invasive biomarker for intestinal inflammation, particularly in inflammatory bowel disease (IBD), the most common clinical context for its use, where misinterpretation can lead to unnecessary invasive procedures or inappropriate therapy escalation. However, its specificity has been questioned due to elevated levels observed in non-intestinal conditions. Here, we investigated whether nasopharyngeal viral infections contribute to elevated fecal calprotectin, thereby confounding its diagnostic interpretation. Bioinformatic analysis revealed high constitutive expression of calprotectin subunits (S100A8/A9) in squamous epithelia of the upper aerodigestive tract compared with distal gut mucosa. To assess gastrointestinal stability of epithelial-derived calprotectin, healthy volunteers ingested porcine calprotectin, which was subsequently detected in feces, demonstrating resistance to intestinal degradation. In a retrospective cohort, patients with non-SARS-CoV-2 respiratory viral infections displayed significantly higher fecal calprotectin levels than SARS-CoV-2 patients (447 µg/g vs. 82 µg/g, p < 0.001), despite limited gastrointestinal involvement. Nasopharyngeal calprotectin levels did not differ significantly between viral etiologies, but in COVID-19 patients, fecal calprotectin positively correlated with nasopharyngeal calprotectin (R = 0.43, p = 0.008) and viral load (R = 0.13, p = 0.026). These findings suggest that calprotectin released from proximal epithelial tissues during viral infection can persist through the gastrointestinal tract and influence fecal calprotectin levels, underscoring the importance of contextual interpretation of this biomarker and the value of incorporating virological assessment into diagnostic workflows.

Indexed as

Biomarker specificityDiagnostic pitfallFecal calprotectinInflammatory bowel diseaseNasopharyngeal infectionSARS-CoV-2

Identifiers

PMID41331827
PMCPMC12673681

What Socratic holds

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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 Socratic graph.