ReviewJournal of community hospital internal medicine perspectives2026
From Villi to Alveoli: Lung Involvement in Celiac Disease - A Narrative Review.
Review in Journal of community hospital internal medicine perspectives, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Background: Celiac disease (CD) is a chronic, immune-mediated enteropathy triggered by gluten that affects about 1% of the population and may present with extraintestinal manifestations. Pulmonary complications are considered rare and are poorly characterized. Lane-Hamilton syndrome is the best described lung manifestation, but data suggests a broader spectrum of respiratory involvement. Methods: We performed a narrative review with structured search strategy of PubMed and Embase (January 1, 1970-December 1, 2025) using the terms Results: Pulmonary involvement in CD appears to represent one of its extraintestinal manifestations, alongside hematologic, dermatologic, neurologic, hepatic, and skeletal. LHS is well defined: several systematic reviews identified dozens of pediatric and adult cases. Increased risk of pneumonia (especially pneumococcal) is demonstrated in observational studies and described in systematic reviews. Moreover, CD has been associated with interstitial lung disease, bronchiectasis, asthma, chronic obstructive pulmonary disease, and chronic cough. Conclusions: Pulmonary involvement in CD is uncommon but clinically important. For hospital internists, a bidirectional approach is suggested: to screen for CD in selected pulmonary presentations, and to systematically assess respiratory symptoms in patients with CD.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.