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Impact of atopy on risk of glioma: a Mendelian randomisation study.
Disney-Hogg, Linden; Cornish, Alex J; Sud, Amit; Law, Philip J; Kinnersley, Ben; Jacobs, Daniel I; Ostrom, Quinn T; Labreche, Karim; Eckel-Passow, Jeanette E; Armstrong, Georgina N; Claus, Elizabeth B; Il'yasova, Dora; Schildkraut, Joellen; Barnholtz-Sloan, Jill S; Olson, Sara H; Bernstein, Jonine L; Lai, Rose K; Schoemaker, Minouk J; Simon, Matthias; Hoffmann, Per; Nöthen, Markus M; Jöckel, Karl-Heinz; Chanock, Stephen; Rajaraman, Preetha; Johansen, Christoffer; Jenkins, Robert B; Melin, Beatrice S; Wrensch, Margaret R; Sanson, Marc; Bondy, Melissa L; Houlston, Richard S.
Affiliation
  • Disney-Hogg L; Division of Genetics and Epidemiology, The Institute of Cancer Research, 15 Cotswold Road, London, SM2 5NG, UK.
  • Cornish AJ; Division of Genetics and Epidemiology, The Institute of Cancer Research, 15 Cotswold Road, London, SM2 5NG, UK.
  • Sud A; Division of Genetics and Epidemiology, The Institute of Cancer Research, 15 Cotswold Road, London, SM2 5NG, UK.
  • Law PJ; Division of Genetics and Epidemiology, The Institute of Cancer Research, 15 Cotswold Road, London, SM2 5NG, UK.
  • Kinnersley B; Division of Genetics and Epidemiology, The Institute of Cancer Research, 15 Cotswold Road, London, SM2 5NG, UK.
  • Jacobs DI; Department of Medicine, Section of Epidemiology and Population Sciences, Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
  • Ostrom QT; Case Comprehensive Cancer Center, School of Medicine, Case Western Reserve University, Cleveland, OH, USA.
  • Labreche K; Division of Genetics and Epidemiology, The Institute of Cancer Research, 15 Cotswold Road, London, SM2 5NG, UK.
  • Eckel-Passow JE; Division of Biomedical Statistics and Informatics, Mayo Clinic College of Medicine, Rochester, MN, USA.
  • Armstrong GN; Department of Medicine, Section of Epidemiology and Population Sciences, Dan L. Duncan Comprehensive Cancer Center, Baylor College of Medicine, Houston, TX, USA.
  • Claus EB; School of Public Health, Yale University, New Haven, CT, USA.
  • Il'yasova D; Department of Neurosurgery, Brigham and Women's Hospital, Boston, MA, USA.
  • Schildkraut J; Department of Epidemiology and Biostatistics, School of Public Health, Georgia State University, Atlanta, GA, USA.
  • Barnholtz-Sloan JS; Duke Cancer Institute, Duke University Medical Center, Durham, NC, USA.
  • Olson SH; Cancer Control and Prevention Program, Department of Community and Family Medicine, Duke University Medical Center, Durham, NC, USA.
  • Bernstein JL; Duke Cancer Institute, Duke University Medical Center, Durham, NC, USA.
  • Lai RK; Cancer Control and Prevention Program, Department of Community and Family Medicine, Duke University Medical Center, Durham, NC, USA.
  • Schoemaker MJ; Case Comprehensive Cancer Center, School of Medicine, Case Western Reserve University, Cleveland, OH, USA.
  • Simon M; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Hoffmann P; Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY, USA.
  • Nöthen MM; Departments of Neurology and Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, CA, USA.
  • Jöckel KH; Division of Genetics and Epidemiology, The Institute of Cancer Research, 15 Cotswold Road, London, SM2 5NG, UK.
  • Chanock S; Department of Neurosurgery, University of Bonn Medical Center, Sigmund-Freud Str. 25, 53105, Bonn, Germany.
  • Rajaraman P; Human Genomics Research Group, Department of Biomedicine, University of Basel, Basel, Switzerland.
  • Johansen C; Department of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany.
  • Jenkins RB; Department of Genomics, Life & Brain Center, University of Bonn, Bonn, Germany.
  • Melin BS; Institute of Human Genetics, University of Bonn School of Medicine & University Hospital Bonn, Bonn, Germany.
  • Wrensch MR; Institute for Medical Informatics, Biometry and Epidemiology, University Hospital Essen, University of Duisburg-Essen, Essen, Germany.
  • Sanson M; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, USA.
  • Bondy ML; Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, USA.
  • Houlston RS; Institute of Cancer Epidemiology, Danish Cancer Society, Copenhagen, Denmark.
BMC Med ; 16(1): 42, 2018 03 15.
Article in En | MEDLINE | ID: mdl-29540232
ABSTRACT

BACKGROUND:

An inverse relationship between allergies with glioma risk has been reported in several but not all epidemiological observational studies. We performed an analysis of genetic variants associated with atopy to assess the relationship with glioma risk using Mendelian randomisation (MR), an approach unaffected by biases from temporal variability and reverse causation that might have affected earlier investigations.

METHODS:

Two-sample MR was undertaken using genome-wide association study data. We used single nucleotide polymorphisms (SNPs) associated with atopic dermatitis, asthma and hay fever, IgE levels, and self-reported allergy as instrumental variables. We calculated MR estimates for the odds ratio (OR) for each risk factor with glioma using SNP-glioma estimates from 12,488 cases and 18,169 controls, using inverse-variance weighting (IVW), maximum likelihood estimation (MLE), weighted median estimate (WME) and mode-based estimate (MBE) methods. Violation of MR assumptions due to directional pleiotropy were sought using MR-Egger regression and HEIDI-outlier analysis.

RESULTS:

Under IVW, MLE, WME and MBE methods, associations between glioma risk with asthma and hay fever, self-reported allergy and IgE levels were non-significant. An inverse relationship between atopic dermatitis and glioma risk was found by IVW (OR 0.96, 95% confidence interval (CI) 0.93-1.00, P = 0.041) and MLE (OR 0.96, 95% CI 0.94-0.99, P = 0.003), but not by WME (OR 0.96, 95% CI 0.91-1.01, P = 0.114) or MBE (OR 0.97, 95% CI 0.92-1.02, P = 0.194).

CONCLUSIONS:

Our investigation does not provide strong evidence for relationship between atopy and the risk of developing glioma, but findings do not preclude a small effect in relation to atopic dermatitis. Our analysis also serves to illustrate the value of using several MR methods to derive robust conclusions.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genome-Wide Association Study / Mendelian Randomization Analysis / Glioma Type of study: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Limits: Humans Language: En Journal: BMC Med Journal subject: MEDICINA Year: 2018 Document type: Article Affiliation country: Reino Unido

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Genome-Wide Association Study / Mendelian Randomization Analysis / Glioma Type of study: Clinical_trials / Etiology_studies / Observational_studies / Risk_factors_studies Limits: Humans Language: En Journal: BMC Med Journal subject: MEDICINA Year: 2018 Document type: Article Affiliation country: Reino Unido