# Atopy and Other Sensitivities in Non-Celiac Wheat Sensitivity: Is There an Associated Hypersensitivity Background?

**Authors:** Aurelio Seidita, Pasquale Mansueto, Mirco Pistone, Maurizio Soresi, Diana Di Liberto, Marianna Lauricella, Lydia Giannitrapani, Giovanni Pratelli, Giuseppe Mazzarella, Alessandra Camarca, Francesco Maurano, Giuseppe Mogavero, Antonio Carroccio

PMC · DOI: 10.3390/nu18040609 · Nutrients · 2026-02-12

## TL;DR

The study finds that people with non-celiac wheat sensitivity are more likely to have allergies and other food sensitivities compared to those with celiac disease or IBS.

## Contribution

The study identifies atopic diseases and multiple food sensitivities as potential markers for non-celiac wheat sensitivity.

## Key findings

- NCWS patients had higher atopic disease prevalence than celiac and IBS/FD patients.
- Multiple food sensitivities and milk intolerance were more common in NCWS patients.
- Atopic disease and food sensitivities are associated with NCWS diagnosis in regression analysis.

## Abstract

Background: A hypersensitivity reaction has been hypothesized as one of the possible pathophysiological mechanisms involved in non-celiac wheat sensitivity (NCWS). Some studies have reported a high frequency of atopic diseases in NCWS patients. Objectives: This study aimed (A) to define the presence and features of atopic diseases and other hypersensitivities in NCWS patients and (B) to search for possible allergic features which could address a NCWS diagnosis. Methods: Clinical, laboratory and histological data from NCWS patients before the start of a wheat-free diet were retrospectively analyzed and compared to control subjects with celiac disease (CeD) or irritable bowel syndrome/functional dyspepsia (IBS/FD). Results: Atopic disease prevalence was higher in the NCWS patients (32.8%) than in those with CeD (19.3%) and IBS/FD (21.5%) (p = 0.001 for both). Similarly, NCWS subjects reported a higher frequency of multiple food sensitivities (MFSs) (39.8%) and self-reported milk intolerance (SRMI) (65.9%) compared to the control groups (p < 0.001 for both). On multiple logistic regression analysis, a coexistent atopic disease (OR 1.481), MFS (OR 3.882) and SRMI (OR 2.259) proved to be variables associated with the NCWS diagnosis. Conclusions: NCWS subjects have a higher frequency of atopic disease, MFS and SRMI when compared to both CeD and IBS/FD patients. All these conditions could be considered as an expression of an underlying hypersensitivity milieu characterizing NCWS and might be of support in the differential diagnosis between NCWS and functional gastrointestinal disorders, if inserted into a broader diagnostic panel.

## Linked entities

- **Diseases:** celiac disease (MONDO:0005130), irritable bowel syndrome (MONDO:0005052)

## Full-text entities

- **Genes:** AGXT (alanine--glyoxylate aminotransferase) [NCBI Gene 189] {aka AGT, AGT1, AGXT1, PH1, SPAT, SPT}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, TLR4 (toll like receptor 4) [NCBI Gene 7099] {aka ARMD10, CD284, TLR-4, TOLL}, HLA-A (major histocompatibility complex, class I, A) [NCBI Gene 3105] {aka HLAA}, HP (haptoglobin) [NCBI Gene 3240] {aka HP2ALPHA2, HPA1S}, TGM2 (transglutaminase 2) [NCBI Gene 7052] {aka G(h), TG(C), TGC, hTG2, tTG}
- **Diseases:** Lactose intolerance (MESH:D007787), conjunctivitis (MESH:D003231), MFSs (MESH:D000073923), malabsorption (MESH:D008286), atopic conditions (MESH:C566404), WA (MESH:D021182), inflammatory (MESH:D007249), gastrointestinal and/or extraintestinal symptoms (MESH:D012817), disease (MESH:D004194), injury to (MESH:D014947), IgA deficit (MESH:D017098), anemia (MESH:D000740), food allergies (MESH:D005512), allergic asthma (MESH:D001249), intolerances (MESH:D005633), weight loss (MESH:D015431), abdominal pain (MESH:D015746), FD (MESH:D000795), CMPA (MESH:D016269), IBS (MESH:D053560), gastrointestinal disorders (MESH:D005767), allergic rhinitis (MESH:D065631), MFS (MESH:D008382), ACD (MESH:C535474), Hypersensitivity (MESH:D004342), Atopic disease (MESH:D006969), Allergic conjunctivitis (MESH:D003233), Atopy (MESH:C564133), Dermatitis (MESH:D003872), Contact Dermatitis (MESH:D003877), inflammatory bowel diseases (MESH:D015212), mucosal damage (MESH:D052016), duodenal villous atrophy (MESH:C564019), autoimmune diseases (MESH:D001327), rhinitis (MESH:D012220), IBS (MESH:D043183), CeD (MESH:D002446), atopic dermatitis (MESH:D003876), IP impairment (MESH:D007410), dyspepsia (MESH:D004415), atopic march (MESH:D015775), enteropathy (MESH:C538273)
- **Chemicals:** Oligosaccharides (MESH:D009844), IP (-), Ni (MESH:D009532), lactose (MESH:D007785), Disaccharides (MESH:D004187)
- **Species:** Olea europaea (common olive, species) [taxon 4146], Homo sapiens (human, species) [taxon 9606], Felis catus (cat, species) [taxon 9685], Parietaria officinalis (species) [taxon 13187], Canis lupus familiaris (dog, subspecies) [taxon 9615], Salsola kali (common saltwort, species) [taxon 151250], Bos taurus (bovine, species) [taxon 9913], Alternaria sect. Alternaria (section) [taxon 2499237], Aspergillus (genus) [taxon 5052], Artemisia vulgaris (common mugwort, species) [taxon 4220]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12943107/full.md

## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12943107/full.md

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Source: https://tomesphere.com/paper/PMC12943107