Volume 118, Issue 5 , Pages 1126-1132, November 2006
The role of allergic rhinitis in nasal responses to sudden temperature changes
Background
Air conditioning–induced rhinitis in allergic individuals is a common epidemiologic finding, but its physiopathology is still controversial. The aim of this study was to describe and compare the effects of experimental air conditioning temperature changes on the nasal mucosa of individuals with persistent allergic rhinitis compared with a control group.
Methods
A case-control challenge study was performed in a laboratory of thermal comfort with experimental twin challenge chambers set at a 12°C difference in temperature. A group of 32 patients with persistent allergic rhinitis and a group of 16 control subjects were exposed for 30 minutes, 3 times alternately in each chamber. Nasal symptom scores were recorded and nasal samples collected before, immediately after, and 24 and 48 hours after the challenge.
Results
The rhinitis group showed a higher symptom score, epithelial shedding, percentage of eosinophils, total inflammatory cells, leukotriene C4, eosinophil cationic protein, albumin, and tryptase levels compared with controls. There was also a significant increase in symptom score, total cells recovered, percentage of eosinophils, epithelial shedding, albumin, myeloperoxidase, and soluble intercellular adhesion molecule 1 in both groups compared with baseline levels.
Conclusion
Sudden temperature changes led to a more pronounced inflammatory nasal response in the rhinitis group with the recruitment and activation of eosinophils.
Clinical implications
Persistent allergic rhinitis is a risk factor for developing sudden temperature change–related rhinitis even in the absence of allergen exposure.
Key words: Indoor air quality, environmental illness, air conditioning, inflammatory mediators
Abbreviations used: ECP, Eosinophil cationic protein, IAQ, Indoor air quality, LT, Leukotriene, PAR, Persistent allergic rhinitis, sICAM-1, Soluble intercellular adhesion molecule 1
Supported by Fundação de Amparo a Pesquisa do Estado de São Paulo, São Paulo State Research Support Foundation, Brazil, grants 03/00846-5 and 02/09082-5.Disclosure of potential conflict of interest: The authors have received grant support from São Paulo Research Support Foundation.
PII: S0091-6749(06)01392-3
doi:10.1016/j.jaci.2006.07.005
© 2006 American Academy of Allergy, Asthma and Immunology. Published by Elsevier Inc. All rights reserved.
Volume 118, Issue 5 , Pages 1126-1132, November 2006
