| Literature DB >> 29500663 |
Camille Pouchieu1, Chantal Raherison2,3, Clément Piel2, Lucile Migault2, Camille Carles2,4, Pascale Fabbro-Perray5,6, Hugues Loiseau7, Jean-Sébastien Guillamo8, Pierre Lebailly9,10, Isabelle Baldi2,4.
Abstract
Inverse association between allergic conditions and glioma risk has been consistently reported in epidemiological studies with little attention paid to potential environmental confounders; the association with meningioma risk is less consistent. We examined the association between allergy history and risk of glioma and meningioma in adults using data from the CERENAT (CEREbral tumors: a NATional study) multicenter case-control study carried out in 4 areas in France in 2004-2010. Participants' histories of doctor-diagnosed allergic asthma, eczema, rhinitis/hay fever and other allergic conditions were collected at onset through a detailed questionnaire delivered in a face-to-face interview. Conditional logistic regression for matched sets was adjusted for participants' educational level and mobile phone use. A total of 273 glioma cases, 218 meningioma cases and 982 matched controls selected from the local electoral rolls were analyzed. A significant inverse association was found between glioma and a history of any allergy (OR 0.52, 95% CI 0.36-0.75), with a dose-effect relationship with the number of allergic conditions reported (p-trend = 0.001) and a particularly strong association with hay fever/allergic rhinitis (OR 0.46, 95% CI 0.30-0.72). Interestingly, associations with glioma risk were more pronounced in women. For meningioma, no association was observed with overall or specific allergic conditions. Our findings confirmed the inverse association between allergic conditions and glioma risk but questioned the role of allergy in meningioma risk. Future research is needed to clarify the biological mechanism of overall allergy and allergic rhinitis on glioma and to confirm the different effect by gender.Entities:
Keywords: Allergy; Case-control study; Glioma; Meningioma; Primary central nervous system neoplasm
Mesh:
Year: 2018 PMID: 29500663 DOI: 10.1007/s11060-018-2816-6
Source DB: PubMed Journal: J Neurooncol ISSN: 0167-594X Impact factor: 4.130