Autoimmune disorders and risk of non-Hodgkin lymphoma subtypes: a pooled analysis within the InterLymph Consortium

Karin E. Smedby(Karolinska University Hospital), Claire M. Vajdic(UNSW Sydney), Michael O. Falster(UNSW Sydney), Eric A. Engels(National Institutes of Health), Otoniel Martı́nez-Maza(University of California, Los Angeles), Jennifer Turner(St Vincent's Hospital Sydney), Henrik Hjalgrim(Statens Serum Institut), Paolo Vineis(Imperial College London), Adele Seniori Costantini(Regione Toscana), Paige M. Bracci(University of California, San Francisco), Elizabeth A. Holly(University of California, San Francisco), Eleanor V. Willett(University of York), John J. Spinelli(BC Cancer Agency), Carlo La Vecchia(University of Milan), Tongzhang Zheng(Yale University), Nikolaus Becker(German Cancer Research Center), Sílvia de Sanjosé(Institut Català d'Oncologia), Brian C.‐H. Chiu(Northwestern University), Luigino Dal Maso(Centro di Riferimento Oncologico), Pierluigi Cocco(University of Cagliari), Marc Maynadié(Biotherapy of Genetic Diseases, Inflammatory Disorders and Cancers), Lenka Foretová(Masaryk Memorial Cancer Institute), Anthony Staines(Dublin City University), Paul Brennan(Centre international de recherche sur le cancer), Scott Davis(University of Washington), Richard K. Severson(Wayne State University), James R. Cerhan(Mayo Clinic), Elizabeth C. Breen(University of California, Los Angeles), Brenda M. Birmann(Brigham and Women's Hospital), Andrew E. Grulich(UNSW Sydney), Wendy Cozen(University of Southern California)
Blood
February 8, 2008
Cited by 619Open Access
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Abstract

Some autoimmune disorders are increasingly recognized as risk factors for non-Hodgkin lymphoma (NHL) overall, but large-scale systematic assessments of risk of NHL subtypes are lacking. We performed a pooled analysis of self-reported autoimmune conditions and risk of NHL and subtypes, including 29 423 participants in 12 case-control studies. We computed pooled odds ratios (OR) and 95% confidence intervals (CI) in a joint fixed-effects model. Sjögren syndrome was associated with a 6.5-fold increased risk of NHL, a 1000-fold increased risk of parotid gland marginal zone lymphoma (OR = 996; 95% CI, 216-4596), and with diffuse large B-cell and follicular lymphomas. Systemic lupus erythematosus was associated with a 2.7-fold increased risk of NHL and with diffuse large B-cell and marginal zone lymphomas. Hemolytic anemia was associated with diffuse large B-cell NHL. T-cell NHL risk was increased for patients with celiac disease and psoriasis. Results for rheumatoid arthritis were heterogeneous between studies. Inflammatory bowel disorders, type 1 diabetes, sarcoidosis, pernicious anemia, and multiple sclerosis were not associated with risk of NHL or subtypes. Thus, specific autoimmune disorders are associated with NHL risk beyond the development of rare NHL subtypes in affected organs. The pattern of associations with NHL subtypes may harbor clues to lymphomagenesis.


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