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Published Online First: 15 August 2007. doi:10.1136/oem.2007.033548
Occupational and Environmental Medicine 2008;65:132-140
Copyright © 2008 by the BMJ Publishing Group Ltd.

ORIGINAL ARTICLES

Plasma polychlorobiphenyl and organochlorine pesticide level and risk of major lymphoma subtypes

P Cocco1, P Brennan2, A Ibba1, S de Sanjosé Llongueras3, M Maynadié4, A Nieters5, N Becker5, M G Ennas6, M G Tocco1, P Boffetta2

1 Department of Public Health, Occupational Health Section, University of Cagliari, Cagliari, Italy
2 International Agency for Research on Cancer, Lyon, France
3 Catalan Institute of Oncology, Barcelona, Spain
4 Registre des Hémopathies Malignes de Côte d’Or, Dijon, France
5 Division of Cancer Epidemiology, German Cancer Research Center, Heidelberg, Germany
6 Department of Cytomorphology, University of Cagliari, Cagliari, Italy

Professor Pierluigi Cocco, Department of Public Health, Occupational Health Section, Asse Didattico - Policlinico Universitario, SS 554, Km 4,500, 09042 Monserrato (Cagliari), Italy; coccop{at}pacs.unica.it

Background: There is conflicting epidemiological evidence concerning an increase in risk of non-Hodgkin’s lymphoma (NHL) associated with elevated blood levels of persistent organochlorine (OC) pesticides and polychlorobiphenyls (PCBs).

Methods: We measured the concentration of 17 OC pesticides, including hexachlorobenzene (HCB), four lindane isomers ({alpha}-, β-, {gamma}- and {delta}-hexachlorocyclohexane (HCH)), two chlordane species (heptachlor and oxy-chlordane), four cyclodiene insecticides (aldrin, dieldrin, endrin and mirex), six dichloro-diphenyl-trichloroethane (DDT) isomers and nine PCB congeners (PCBs 28, 52, 101, 118, 138, 153, 170, 180 and 194) in plasma samples of 377 subjects, including 174 NHL cases and 203 controls from France, Germany and Spain. The risk of NHL and its major subtypes associated with increasing blood levels of OC pesticides and PCBs was calculated using unconditional logistic regression.

Results: Risk of NHL, diffuse large B cell lymphoma (DLBCL) and chronic lymphatic leukaemia (CLL) did not increase with plasma levels of HCB, β-HCH, p,p'-dichloro-diphenyl-dichloroethylene (DDE), or total and individual PCBs or their functional groups, in the overall study population. Substantial heterogeneity in DLBCL risk associated with immunotoxic PCBs (p = 0.03) existed between the Spanish subgroup (odds ratio (OR) for immunotoxic PCB plasma level above the median vs below the median was 0.7, 95% CI 0.3 to 1.6) and the French and German subgroups combined (OR 3.2, 95% CI 0.9 to 11.5).

Conclusion: We did not find evidence of an association between NHL risk and plasma level of OC pesticides and PCBs.


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