The effect of atopy, childhood crowding, and other immune-related factors on non-Hodgkin lymphoma risk

被引:33
作者
Cozen, W.
Cerhan, J. R.
Martinez-Maza, O.
Ward, M. H.
Linet, M.
Colt, J. S.
Davis, S.
Severson, R. K.
Hartge, P.
Bernstein, L.
机构
[1] Univ So Calif, Keck Sch Med, Norris Comprehens Canc Ctr, Dept Prevent Med, Los Angeles, CA 90089 USA
[2] Univ So Calif, Keck Sch Med, Dept Pathol, Los Angeles, CA 90089 USA
[3] Mayo Clin, Coll Med, Dept Hlth Sci Res, Rochester, MN USA
[4] Univ Calif Los Angeles, David Geffen Sch Med, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90024 USA
[5] Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90024 USA
[6] NCI, Dept Hlth & Human Serv, Div Canc Epidemiol & Genet, Bethesda, MD 20892 USA
[7] Univ Washington, Fred Hutchinson Canc Res Ctr, Seattle, WA 98195 USA
[8] Wayne State Univ, Karmanos Canc Inst, Dept Family Med, Detroit, MI 48202 USA
关键词
non-Hodgkin lymphoma; sibship size; birth order; allergy; atopy; childhood exposures; immune response;
D O I
10.1007/s10552-007-9025-5
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective Since adult immune responsiveness is influenced by early childhood exposures, we examined the role of family size, history of atopic disease, and other childhood immune-related exposures in a multi-center case-control study of NHL. Methods Interviews were completed with 1,321 cases ascertained from population-based cancer registries in Seattle, Detroit, Los Angeles and Iowa, and with 1,057 frequency-matched controls, selected by random-digit dialing and from the Medicare files database. Multivariable logistic regression was used to estimate risk. Results A history of any allergy (excluding drug allergies), decreased risk of all NHL (Odds Ratio [OR] = 0.7, 95% Confidence Interval [CI] = 0.6-1.0), diffuse large B-cell lymphoma [DLBCL] (OR = 0.6, 95% CI = 0.4-0.9), and follicular NHL (OR = 0.7, 95 CI = 0.5, 1.0). A similar effect was observed for hay fever. A history of eczema was associated with an increased risk of follicular lymphoma (OR = 1.9, 95% CI = 1.1-3.4), but not DLBCL (OR = 1.1, 95% CI = 0.6-2.0). Asthma did not affect risk. Youngest compared to oldest siblings had a 90% increased risk of DLBCL (95% CI = 1.2-3.1; p for trend with increasing birth order = 0.006), but not follicular lymphoma (OR = 1.1, 95% CI = 0.6-1.8). Conclusions We infer that some childhood and immune-related factors may alter NHL risk.
引用
收藏
页码:821 / 831
页数:11
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