A pooled analysis of three studies evaluating genetic variation in innate immunity genes and non-Hodgkin lymphoma risk
H. Dean Hosgood III
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorMark P. Purdue
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorSophia S. Wang
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Division of Etiology, Department of Population Sciences, City of Hope, Duarte, CA
Search for more papers by this authorTongzhang Zheng
Department of Epidemiology and Public Health, Yale School of Medicine, New Haven, CT
Search for more papers by this authorLindsay M. Morton
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorQing Lan
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorIdan Menashe
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorYawei Zhang
Department of Epidemiology and Public Health, Yale School of Medicine, New Haven, CT
Search for more papers by this authorJames R. Cerhan
Mayo Clinic, College of Medicine, Rochester, MN, USA
Search for more papers by this authorAndrew Grulich
National Centre in HIV Epidemiology and Clinical Research, University of New South Wales, Sydney, NSW, Australia
Search for more papers by this authorWendy Cozen
Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA
Search for more papers by this authorMeredith Yeager
Core Genotyping Facility, Advanced Technology Center, National Cancer Institute, NIH, DHHS, Gaithersburg, MD, USA
Search for more papers by this authorTheodore R. Holford
Department of Epidemiology and Public Health, Yale School of Medicine, New Haven, CT
Search for more papers by this authorClaire M. Vajdic
Prince of Wales Clinical School and Lowy Cancer Research Centre, University of New South Wales, Sydney, NSW, Australia
Search for more papers by this authorScott Davis
Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA, USA
Search for more papers by this authorBrian Leaderer
Department of Epidemiology and Public Health, Yale School of Medicine, New Haven, CT
Search for more papers by this authorAnne Kricker
School of Public Health, The University of Sydney, Sydney, NSW, Australia
Search for more papers by this authorMaryjean Schenk
Department of Family Medicine and Karmanos Cancer Institute, Wayne State University, Detroit, MI, USA
Search for more papers by this authorShelia H. Zahm
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorNilanjan Chatterjee
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorStephen J. Chanock
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorNathaniel Rothman
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorPatricia Hartge
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorBruce Armstrong
School of Public Health, The University of Sydney, Sydney, NSW, Australia
Search for more papers by this authorH. Dean Hosgood III
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorMark P. Purdue
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorSophia S. Wang
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Division of Etiology, Department of Population Sciences, City of Hope, Duarte, CA
Search for more papers by this authorTongzhang Zheng
Department of Epidemiology and Public Health, Yale School of Medicine, New Haven, CT
Search for more papers by this authorLindsay M. Morton
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorQing Lan
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorIdan Menashe
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorYawei Zhang
Department of Epidemiology and Public Health, Yale School of Medicine, New Haven, CT
Search for more papers by this authorJames R. Cerhan
Mayo Clinic, College of Medicine, Rochester, MN, USA
Search for more papers by this authorAndrew Grulich
National Centre in HIV Epidemiology and Clinical Research, University of New South Wales, Sydney, NSW, Australia
Search for more papers by this authorWendy Cozen
Norris Comprehensive Cancer Center, University of Southern California, Los Angeles, CA
Search for more papers by this authorMeredith Yeager
Core Genotyping Facility, Advanced Technology Center, National Cancer Institute, NIH, DHHS, Gaithersburg, MD, USA
Search for more papers by this authorTheodore R. Holford
Department of Epidemiology and Public Health, Yale School of Medicine, New Haven, CT
Search for more papers by this authorClaire M. Vajdic
Prince of Wales Clinical School and Lowy Cancer Research Centre, University of New South Wales, Sydney, NSW, Australia
Search for more papers by this authorScott Davis
Fred Hutchinson Cancer Research Center and University of Washington, Seattle, WA, USA
Search for more papers by this authorBrian Leaderer
Department of Epidemiology and Public Health, Yale School of Medicine, New Haven, CT
Search for more papers by this authorAnne Kricker
School of Public Health, The University of Sydney, Sydney, NSW, Australia
Search for more papers by this authorMaryjean Schenk
Department of Family Medicine and Karmanos Cancer Institute, Wayne State University, Detroit, MI, USA
Search for more papers by this authorShelia H. Zahm
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorNilanjan Chatterjee
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorStephen J. Chanock
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorNathaniel Rothman
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorPatricia Hartge
Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, DHHS, Rockville, MD
Search for more papers by this authorBruce Armstrong
School of Public Health, The University of Sydney, Sydney, NSW, Australia
Search for more papers by this authorSummary
Genetic variation in immune-related genes may play a role in the development of non-Hodgkin lymphoma (NHL). To test the hypothesis that innate immunity polymorphisms may be associated with NHL risk, we genotyped 144 tag single nucleotide polymorphisms (tagSNPs) capturing common genetic variation within 12 innate immunity gene regions in three independent population-based case-control studies (1946 cases and 1808 controls). Gene-based analyses found IL1RN to be associated with NHL risk (minP = 0·03); specifically, IL1RN rs2637988 was associated with an increased risk of NHL (per-allele odds ratio = 1·15, 95% confidence interval = 1·05–1·27; Ptrend = 0·003), which was consistent across study, subtype, and gender. FCGR2A was also associated with a decreased risk of the follicular lymphoma NHL subtype (minP = 0·03). Our findings suggest that genetic variation in IL1RN and FCGR2A may play a role in lymphomagenesis. Given that conflicting results have been reported regarding the association between IL1RN SNPs and NHL risk, a larger number of innate immunity genes with sufficient genomic coverage should be evaluated systematically across many studies.
Supporting Information
Table I. Subject characteristics, by study.
Table II. Characteristics of innate immunity tagSNPs genotyped.
Table III. Odds ratios and 95% confidence intervals for innate immunity tagSNPs and risk of NHL, adjusted for age, race, gender, and study site, by study.
Table IV. Odds ratios and 95% confidence intervals for innate immunity tagSNPs and risk of NHL subtypes, adjusted for age, race, gender, and study site.
Filename | Description |
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BJH_8518_sm_tableS1-S4.xls659 KB | Supporting info item |
BJH_8518_sm_tablelegends.doc22.5 KB | Supporting info item |
Please note: The publisher is not responsible for the content or functionality of any supporting information supplied by the authors. Any queries (other than missing content) should be directed to the corresponding author for the article.
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