4.0 Article

Autoimmune disease in individuals and close family members and susceptibility to non-Hodgkin's lymphoma

Journal

ARTHRITIS AND RHEUMATISM
Volume 58, Issue 3, Pages 657-666

Publisher

WILEY-LISS
DOI: 10.1002/art.23267

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Funding

  1. Intramural NIH HHS Funding Source: Medline
  2. NCI NIH HHS [N02-CP-01309] Funding Source: Medline

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Objective. Rheumatoid arthritis (RA), systemic lupus erythematosus (SLE), and Sjogren's syndrome have been consistently associated with an increased risk of non-Hodgkin's lymphoma (NHL). This study was initiated to evaluate the risks of NHL associated with a personal or family history of a wide range of autoimmune diseases. Methods. A population-based case-control study was conducted that included 24,728 NHL patients in Denmark (years 1977-1997) and Sweden (years 19641998) and 55,632 controls. Using univariate logistic and hierarchical regression models, we determined odds ratios (ORs) of NHL associated with a personal history of hospital-diagnosed autoimmune conditions. Risks of NHL associated with a family history of the same autoimmune conditions were assessed. by similar regression analyses that included 25,941 NHL patients and 58,551 controls. Results. A personal history of systemic autoimmune diseases (RA, SLE, Sjogren's syndrome, systemic sclerosis) was clearly linked with NHL risk, both for individual conditions (hierarchical odds ratios [ORh] ranged from 1.6 to 5.4) and as a group (ORh 2.64 [95% confidence interval (95% CI) 1.72-4.07]). In contrast a family history of systemic autoimmune diseases was modestly and nonsignificantly associated with NHL (ORh 1.31 [95% CI 0.85-2.03]). An increased risk of NHL was found for a personal history of 5 nonsystemic autoimmune conditions (autoimmune hemolytic anemia, Hashimoto thyroiditis, Crohn's disease, psoriasis, and sarcoidosis) (ORh ranged from 1.5 to 2.6) of 27 conditions examined. Conclusion. Overall, our results demonstrate a strong relationship of personal history of systemic autoimmune diseases with NHL risk and suggest that shared susceptibility may explain a very small fraction of this increase, at best. Positive associations were found for a personal history of some, though far from all, nonsystemic autoimmune conditions.

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