Association between Glioma and History of Allergies, Asthma, and Eczema: A Case-Control Study with Three Groups of Controls

  1. Dora Il'yasova1,2,
  2. Bridget McCarthy5,
  3. Jennifer Marcello1,2,
  4. Joellen M. Schildkraut1,
  5. Patricia G. Moorman1,
  6. Bhuma Krishnamachari5,
  7. Francis Ali-Osman2,3,
  8. Darell D. Bigner2,4 and
  9. Faith Davis5
  1. 1Duke Comprehensive Cancer Center, 2Preston Robert Tisch Brain Tumor Center at Duke, Departments of 3Surgery, and 4Pathology and Pediatric Brain Tumor Foundation Institute at Duke, Duke University Medical Center, Durham, North Carolina; and 5Division of Epidemiology and Biostatistics, University of Illinois at Chicago, Chicago, Illinois
  1. Requests for reprints:
    Dora Il'yasova, PhD, Assistant Professor, Cancer Control and Prevention Program/Department of Community and Family Medicine, Duke University Medical Center, 2424 Erwin Road, Hock Building, Ste 602, Box 2949, Durham, NC 27710. Phone: 919-668-6531; Fax: 919-681-4785. E-mail: dora.ilyasova{at}duke.edu

Abstract

Because glioma etiology is largely unknown, the inverse association of glioma risk with atopic conditions is promising and deserves close scrutiny. We examined the association between a history of allergies, asthma, and eczema, and glioma risk using sibling, friend, and clinic-based controls. This analysis included 388 incident glioma cases and 80 sibling, 191 friend, and 177 clinic-based controls. Each subject's medical history was assessed via a Web-based or telephone survey. Odds ratios (OR) and their 95% confidence intervals (CI) for the associations with allergies, asthma, eczema, and the overall number of these conditions were calculated from conditional (for sibling and friend controls) and unconditional (for clinic-based controls) logistic models. Allergies were consistently inversely associated with the glioma: ORs were 0.53 (95% CI, 0.15-1.84), 0.54 (95% CI, 0.28-1.07), and 0.34 (95% CI, 0.23-0.50) with sibling, friend, and clinic-based controls, respectively. Asthma showed an inverse association only in the comparison with sibling controls (OR, 0.43; 95% CI, 0.19-1.00). Eczema showed an inverse association only in the comparison with friend controls (OR, 0.42; 95% CI, 0.15-1.18). The overall number of these conditions (ordinal score 0, 1, 2, 3) was inversely associated with glioma: The risk decreased 31% to 45% with each addition of an atopic condition. These estimates were the most stable when different control groups were considered. Comparing the prevalence of these conditions in the three control groups with published data, we note that clinic-based controls generally better approximate the prevalence data for population-based groups. These controls seem to present a reasonable choice for clinic-centered case-control studies. (Cancer Epidemiol Biomarkers Prev 2009;18(4):1232–8)

Footnotes

  • Grant support: NIH Specialized Programs of Research Excellence grant 5P50 CA108786-4.

    • Accepted February 19, 2009.
    • Received October 21, 2008.
    • Revision received January 16, 2009.
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