# Tic disorders and allergic diseases: mechanistic links and the impact of allergy management – a narrative review

**Authors:** Lili Li, Wandong Hu, Ying Ren, Huan Zhang, Shushu Zhu, Tao Zhong, Hongwei Zhang

PMC · DOI: 10.3389/falgy.2026.1769483 · Frontiers in Allergy · 2026-02-12

## TL;DR

This review explores how allergic diseases like asthma and eczema may be linked to tic disorders in children, suggesting immune and stress-related factors could influence tics.

## Contribution

The paper proposes that allergic conditions affect tics through peripheral immune signaling and symptom burden, rather than direct central allergic mechanisms.

## Key findings

- Allergic diseases are more common in children with tic disorders than in controls.
- Peripheral inflammation and histamine may influence brain circuits related to tics.
- Allergy management can reduce tic severity in some cases, but certain treatments may worsen tics.

## Abstract

Tic disorders are childhood-onset neuropsychiatric conditions that frequently co-occur with allergic diseases, including asthma, allergic rhinitis, and atopic dermatitis. This narrative review maps the current clinical and mechanistic evidence linking allergic conditions to tic disorders and evaluates whether allergy focused interventions may modify tic severity. Across multiple epidemiological studies, allergic diseases are reported more often in children with tic disorders than in controls. However, direct clinical evidence supporting a canonical “central allergic response” within the brain (e.g., IgE-driven allergic effector mechanisms in the CNS) in primary tic disorders remains limited. The available literature instead more strongly supports indirect, peripheral, brain directed pathways. Peripheral inflammatory mediators may modulate the neurovascular unit and glial reactivity, thereby influencing cortico-striato-thalamo-cortical circuit excitability. Histamine, acting as both an immune mediator and a neuromodulator, may further intersect with dopaminergic signalling relevant to tic expression. In parallel, allergy related symptom burden, particularly sleep disruption and psychological stress, may contribute to tic exacerbation. Observational studies suggest that controlling allergic symptoms can be associated with reduced tic severity in some individuals, although certain anti allergic agents have been reported to coincide with tic worsening in selected cases. Overall, current findings support a model in which allergic conditions influence tic disorders primarily via immune signalling and symptom burden rather than through a direct central allergic mechanism. Allergy assessment and management may be considered in selected patients, but mechanistic studies and controlled trials are needed to clarify causality and guide evidence-based care.

## Linked entities

- **Diseases:** asthma (MONDO:0004979), allergic rhinitis (MONDO:0011786), atopic dermatitis (MONDO:0004980)

## Full-text entities

- **Genes:** OCLN (occludin) [NCBI Gene 100506658] {aka BLCPMG, PPP1R115, PTORCH1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, IGHE (immunoglobulin heavy constant epsilon) [NCBI Gene 3497] {aka IgE}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, GALNS (galactosamine (N-acetyl)-6-sulfatase) [NCBI Gene 2588] {aka GALNAC6S, GAS, GalN6S, MPS4A}, TH (tyrosine hydroxylase) [NCBI Gene 7054] {aka DYT14, DYT5b, TYH}, CDH26 (cadherin 26) [NCBI Gene 60437] {aka VR20}, CAMK2G (calcium/calmodulin dependent protein kinase II gamma) [NCBI Gene 818] {aka CAMK, CAMK-II, CAMKG, MRD59}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, IL25 (interleukin 25) [NCBI Gene 64806] {aka IL17E}, NFKB1 (nuclear factor kappa B subunit 1) [NCBI Gene 4790] {aka CVID12, EBP-1, KBF1, NF-kB, NF-kB1, NF-kappa-B1}, CDHR3 (cadherin related family member 3) [NCBI Gene 222256] {aka CDH28}, HDC (histidine decarboxylase) [NCBI Gene 3067], CLDN5 (claudin 5) [NCBI Gene 7122] {aka AWAL, BEC1, CPETRL1, TMDVCF, TMVCF}, IL33 (interleukin 33) [NCBI Gene 90865] {aka C9orf26, DVS27, IL1F11, NF-HEV, NFEHEV}, DRD2 (dopamine receptor D2) [NCBI Gene 1813] {aka D2DR, D2R}, IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL1RN (interleukin 1 receptor antagonist) [NCBI Gene 3557] {aka CRMO2, DIRA, ICIL-1RA, IL-1RN, IL-1ra, IL-1ra3}, IL2 (interleukin 2) [NCBI Gene 3558] {aka IL-2, TCGF, lymphokine}, GSK3B (glycogen synthase kinase 3 beta) [NCBI Gene 2932], IL13 (interleukin 13) [NCBI Gene 3596] {aka IL-13, P600}, CD4 (CD4 molecule) [NCBI Gene 920] {aka CD4mut, IMD79, Leu-3, OKT4D, T4}, IL5 (interleukin 5) [NCBI Gene 3567] {aka EDF, IL-5, TRF}, TSLP (thymic stromal lymphopoietin) [NCBI Gene 85480], IL4 (interleukin 4) [NCBI Gene 3565] {aka BCGF-1, BCGF1, BSF-1, BSF1, IL-4}, TJP1 (tight junction protein 1) [NCBI Gene 7082] {aka ZO-1}, CDH1 (cadherin 1) [NCBI Gene 999] {aka Arc-1, BCDS1, CD324, CDHE, ECAD, LCAM}, HRH3 (histamine receptor H3) [NCBI Gene 11255] {aka GPCR97, HH3R}, SHH (sonic hedgehog signaling molecule) [NCBI Gene 6469] {aka HHG1, HLP3, HPE3, MCOPCB5, SMMCI, ShhNC}
- **Diseases:** sleep (MESH:D012893), conduct disorders (MESH:D019955), allergic inflammation (MESH:D007249), TD (MESH:D013981), anxiety (MESH:D001007), neuroinflammation (MESH:D000090862), asthma (MESH:D001249), behavioural disorders (MESH:D001523), allergic symptom (MESH:D063926), learning impairments (MESH:D007859), fatigue (MESH:D005221), Group A beta-haemolytic streptococcal infection (MESH:D013290), neurobehavioural disorders (MESH:D009358), anxiety disorders (MESH:D001008), genetic abnormalities (MESH:D030342), conjunctivitis (MESH:D003231), epithelial injury (MESH:D009375), ADHD (MESH:D001289), Allergic rhinitis (MESH:D065631), neuropsychiatric comorbidities (MESH:C000631768), infection (MESH:D007239), TS (MESH:D005879), Allergic diseases (MESH:D004342), OCD (MESH:D009771), involuntary motor and/or vocal tics (MESH:D020323), atopic dermatitis (MESH:D003876), immune dysregulation (OMIM:614878)
- **Chemicals:** benralizumab (MESH:C571386), Histamine (MESH:D006632), NO2 (MESH:D009585), thromboxane A2 (MESH:D013928), reslizumab (MESH:C515492), glutamate (MESH:D018698), GABA (MESH:D005680), montelukast (MESH:C093875), fluticasone propionate (MESH:D000068298), O3 (MESH:D010126), Ca2+ (-), hydroxyzine (MESH:D006919), mepolizumab (MESH:C434107), omalizumab (MESH:D000069444), budesonide (MESH:D019819), dupilumab (MESH:C582203), dopamine (MESH:D004298)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

79 references — full list in the complete paper: https://tomesphere.com/paper/PMC12935891/full.md

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Source: https://tomesphere.com/paper/PMC12935891