4.4 Article

Allergies, genetic polymorphisms of Th2 interleukins, and childhood acute lymphoblastic leukemia: The ESTELLE study

期刊

PEDIATRIC BLOOD & CANCER
卷 69, 期 3, 页码 -

出版社

WILEY
DOI: 10.1002/pbc.29402

关键词

etiology; allergy; case-control studies; childhood leukemia; cytokines; epidemiology; gene-environment interaction; gene-gene interaction; genetics; lymphoblastic leukemia

资金

  1. Institut National Du Cancer
  2. Ligue Nationale Contre le Cancer
  3. Association Enfants et Sante
  4. Institut National de la Sante et de la Recherche Medicale
  5. Canceropole Ile de France
  6. Agence Nationale de la Recherche [ANR-10-COHO-0009]
  7. Universite Libanaise
  8. Fondation ARC pour la Recherche sur le Cancer [PDF20190508759]
  9. Agence Nationale de Securite Sanitaire de l'Alimentation, de l'Environnement et du Travail [2013/1/24]
  10. INCa-DHOS
  11. Agence Nationale de la Recherche (ANR) [ANR-10-COHO-0009] Funding Source: Agence Nationale de la Recherche (ANR)

向作者/读者索取更多资源

A negative association between a history of allergy and childhood acute lymphoblastic leukemia (ALL) was found, with a significant inverse association with allergic rhinitis or sinusitis. Genetic polymorphisms in IL4 and IL4R may interact with allergic symptoms, indicating a potential modification of the association between allergies and childhood ALL.
Context A negative association between a history of allergy and childhood acute lymphoblastic leukemia (ALL) has been reported in previous studies, but remains debated. This work aimed to investigate this association accounting for genetic polymorphisms of the Th2 pathway cytokines (IL4, IL10, IL13, and IL4R). Methods Analyses were based on the French case-control study ESTELLE (2010-2011). The complete sample included 629 ALL cases and 1421 population-based controls frequency-matched on age and gender. The child's medical history was collected through standardized maternal interview. Biological samples were collected, and genotyping data were available for 411 cases and 704 controls of European origin. Odds ratios (OR) were estimated using unconditional regression models adjusted for potential confounders. Results In the complete sample, a significant inverse association was observed between ALL and reported history of allergic rhinitis or sinusitis (OR = 0.65 [0.42-0.98]; P = 0.04), but there was no obvious association with allergies overall. There was an interaction between genetic polymorphisms in IL4 and IL4R (P-interaction = 0.003), as well as a gene-environment interaction between IL4R-rs1801275 and a reported history of asthma (IOR = 0.23; P-int = 0.008) and eczema (IOR = 0.47; P-int = 0.06). We observed no interaction with the candidate polymorphisms in IL4 and IL13. Conclusion These results suggest that the association between allergic symptoms and childhood ALL could be modified by IL4R-rs1801275, and that this variant could also interact with a functional variant in IL4 gene. Although they warrant confirmation, these results could help understand the pathological mechanisms under the reported inverse association between allergy and childhood ALL.

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