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Lupus-related single nucleotide polymorphisms and risk of diffuse large B-cell lymphoma
S. Bernatsky, HA. Velásquez García, JJ. Spinelli, P. Gaffney, KE. Smedby, R. Ramsey-Goldman, SS. Wang, HO. Adami, D. Albanes, E. Angelucci, SM. Ansell, YW. Asmann, N. Becker, Y. Benavente, SI. Berndt, KA. Bertrand, BM. Birmann, H. Boeing, P....
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články
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Directory of Open Access Journals
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- Publikační typ
- časopisecké články MeSH
Objective: Determinants of the increased risk of diffuse large B-cell lymphoma (DLBCL) in SLE are unclear. Using data from a recent lymphoma genome-wide association study (GWAS), we assessed whether certain lupus-related single nucleotide polymorphisms (SNPs) were also associated with DLBCL. Methods: GWAS data on European Caucasians from the International Lymphoma Epidemiology Consortium (InterLymph) provided a total of 3857 DLBCL cases and 7666 general-population controls. Data were pooled in a random-effects meta-analysis. Results: Among the 28 SLE-related SNPs investigated, the two most convincingly associated with risk of DLBCL included the CD40 SLE risk allele rs4810485 on chromosome 20q13 (OR per risk allele=1.09, 95% CI 1.02 to 1.16, p=0.0134), and the HLA SLE risk allele rs1270942 on chromosome 6p21.33 (OR per risk allele=1.17, 95% CI 1.01 to 1.36, p=0.0362). Of additional possible interest were rs2205960 and rs12537284. The rs2205960 SNP, related to a cytokine of the tumour necrosis factor superfamily TNFSF4, was associated with an OR per risk allele of 1.07, 95% CI 1.00 to 1.16, p=0.0549. The OR for the rs12537284 (chromosome 7q32, IRF5 gene) risk allele was 1.08, 95% CI 0.99 to 1.18, p=0.0765. Conclusions: These data suggest several plausible genetic links between DLBCL and SLE.
Center for Chronic Immunodeficiency University Medical Center Freiburg Freiburg Germany
Centre for Big Data Research in Health University of New South Wales Sydney Australia
Centre Heni Becquerel Université de Rouen Rouen France
Chronic Disease Prevention Unit National Institute for Health and Welfare Helsinki Finland
Danish Cancer Society Research Center Copenhagen Denmark
Department of Biomedical Science University of Cagliari Monserrato Italy
Department of Biostatistics Yale School of Public Health New Haven USA
Department of Computational Biology St Jude Children's Research Hospital Memphis Tennessee USA
Department of Environmental Health Sciences Yale School of Public Health New Haven USA
Department of Epidemiology Brown School of Public Health Providence USA
Department of Epidemiology German Institute for Human Nutrition Potsdam Germany
Department of Epidemiology Harvard T H Chan School of Public Health Boston USA
Department of Epidemiology University of North Carolina at Chapel Hill Chapel Hill USA
Department of Family Medicine and Public Health Sciences Wayne State University Detroit USA
Department of Health Sciences Research Mayo Clinic Rochester USA
Department of Health Sciences University of York York UK
Department of Hematology Centre Léon Bérard Lyon France
Department of Hematology Hospices Civils de Lyon Pierre benite Cedex France
Department of Immunology Genetics and Pathology Uppsala University Uppsala Sweden
Department of Internal Medicine Carver College of Medicine The University of Iowa Iowa City USA
Department of Medicine Mayo Clinic Rochester USA
Department of Medicine Memorial Sloan Kettering Cancer Center New York USA
Department of Population Health New York University School of Medicine New York USA
Department of Public Health Clinical and Molecular Medicine University of Cagliari Monserrato Italy
Departments of Laboratory Medicine and Pathology Memorial Sloan Kettering Cancer Center New York USA
Division of Cancer Epidemiology and Genetics National Cancer Institute Bethesda USA
Division of Cancer Epidemiology German Cancer Research Center Heidelberg Germany
Division of Cancer Etiology Department of Population Sciences Beckman Research Institute Duarte USA
Division of Endocrinology Diabetes and Metabolism The Ohio State University Columbus USA
Division of Hematology Department of Medicine Mayo Clinic Rochester USA
Division of Public Health Sciences Fred Hutchinson Cancer Research Center Seattle USA
Division of Rheumatology Immunology and Allergy Brigham and Women's Hospital Boston USA
Division of Rheumatology University of Calgary Calgary Canada
Epidemiology Research Program American Cancer Society Atlanta USA
Faculty of Medicine and Health Sciences Macquarie University Sydney Australia
Feinberg School of Medicine Northwestern University Chicago USA
Genetic Epidemiology Laboratory Department of Pathology University of Melbourne Melbourne Australia
Genome Sciences Centre BC Cancer Agency Vancouver Canada
Hematology Unit Ospedale Oncologico di Riferimento Regionale 'A Businco' Cagliari Italy
Human Genetics Foundation Turin Italy
INSERM U1052 Cancer Research Center of Lyon Centre Léon Bérard Lyon France
Institute for Risk Assessment Sciences Utrecht University Utrecht The Netherlands
International Agency for Research on Cancer Lyon France
Lymphoid Malignancies Unit Henri Mondor Hospital and University Paris Est Créteil France
MRC PHE Centre for Environment and Health School of Public Health Imperial College London London UK
Ontario Health Study Toronto Canada
School of Nursing and Human Sciences Dublin City University Dublin Ireland
Slone Epidemiology Center Boston University Boston USA
Sydney School of Public Health The University of Sydney Sydney Australia
The Tisch Cancer Institute Icahn School of Medicine at Mount Sinai New York USA
Citace poskytuje Crossref.org
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- $a Bernatsky, Sasha $u Division of Clinical Epidemiology, Research Institute of the McGill University Health Centre, Montreal, Canada.
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- $a Lupus-related single nucleotide polymorphisms and risk of diffuse large B-cell lymphoma / $c S. Bernatsky, HA. Velásquez García, JJ. Spinelli, P. Gaffney, KE. Smedby, R. Ramsey-Goldman, SS. Wang, HO. Adami, D. Albanes, E. Angelucci, SM. Ansell, YW. Asmann, N. Becker, Y. Benavente, SI. Berndt, KA. Bertrand, BM. Birmann, H. Boeing, P. Boffetta, PM. Bracci, P. Brennan, AR. Brooks-Wilson, JR. Cerhan, SJ. Chanock, J. Clavel, L. Conde, KH. Cotenbader, DG. Cox, W. Cozen, S. Crouch, AJ. De Roos, S. de Sanjose, S. Di Lollo, WR. Diver, A. Dogan, L. Foretova, H. Ghesquières, GG. Giles, B. Glimelius, TM. Habermann, C. Haioun, P. Hartge, H. Hjalgrim, TR. Holford, EA. Holly, RD. Jackson, R. Kaaks, E. Kane, RS. Kelly, RJ. Klein, P. Kraft, A. Kricker, Q. Lan, C. Lawrence, M. Liebow, T. Lightfoot, BK. Link, M. Maynadie, J. McKay, M. Melbye, TJ. Molina, A. Monnereau, LM. Morton, A. Nieters, KE. North, AJ. Novak, K. Offit, MP. Purdue, M. Rais, J. Riby, E. Roman, N. Rothman, G. Salles, G. Severi, RK. Severson, CF. Skibola, SL. Slager, A. Smith, MT. Smith, MC. Southey, A. Staines, LR. Teras, CA. Thompson, H. Tilly, LF. Tinker, A. Tjonneland, J. Turner, CM. Vajdic, RCH. Vermeulen, J. Vijai, P. Vineis, J. Virtamo, Z. Wang, S. Weinstein, TE. Witzig, A. Zelenetz, A. Zeleniuch-Jacquotte, Y. Zhang, T. Zheng, M. Zucca, AE. Clarke,
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- $a Objective: Determinants of the increased risk of diffuse large B-cell lymphoma (DLBCL) in SLE are unclear. Using data from a recent lymphoma genome-wide association study (GWAS), we assessed whether certain lupus-related single nucleotide polymorphisms (SNPs) were also associated with DLBCL. Methods: GWAS data on European Caucasians from the International Lymphoma Epidemiology Consortium (InterLymph) provided a total of 3857 DLBCL cases and 7666 general-population controls. Data were pooled in a random-effects meta-analysis. Results: Among the 28 SLE-related SNPs investigated, the two most convincingly associated with risk of DLBCL included the CD40 SLE risk allele rs4810485 on chromosome 20q13 (OR per risk allele=1.09, 95% CI 1.02 to 1.16, p=0.0134), and the HLA SLE risk allele rs1270942 on chromosome 6p21.33 (OR per risk allele=1.17, 95% CI 1.01 to 1.36, p=0.0362). Of additional possible interest were rs2205960 and rs12537284. The rs2205960 SNP, related to a cytokine of the tumour necrosis factor superfamily TNFSF4, was associated with an OR per risk allele of 1.07, 95% CI 1.00 to 1.16, p=0.0549. The OR for the rs12537284 (chromosome 7q32, IRF5 gene) risk allele was 1.08, 95% CI 0.99 to 1.18, p=0.0765. Conclusions: These data suggest several plausible genetic links between DLBCL and SLE.
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