Epstein-Barr virus-associated Hodgkin's disease: Epidemiologic characteristics in international data

Sally L. Glaser(Cancer Prevention Institute of California), Ruby J. Lin(Cancer Prevention Institute of California), Susan L. Stewart(Cancer Prevention Institute of California), Richard F. Ambinder(Johns Hopkins University), Ruth F. Jarrett(MRC University of Glasgow Centre for Virus Research), Pierre Brousset(Hôpitaux Universitaires Paris-Ouest), Gorm Pallesen(Aarhus University), Margaret L. Gulley(The University of Texas Health Science Center at San Antonio), Gulfaraz Khan(Tufts University), Jane O'Grady(Oxford Health NHS Foundation Trust), Michael Hummel(Freie Universität Berlin), María Victoria Preciado(Hospital General de Niños Ricardo Gutierrez), Hans Knecht(University of Massachusetts Chan Medical School), John K. C. Chan(Queen Elizabeth Hospital), Alexander Claviez(Christian-Albrechts-Universität zu Kiel)
International Journal of Cancer
February 7, 1997
Cited by 499Open Access
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Abstract

Hodgkin's disease (HD) has long been suspected to have an infectious precursor, and indirect evidence has implicated Epstein-Barr virus (EBV), a ubiquitous herpesvirus, as a causal agent. Recent molecular studies using EBER in situ hybridization or latency membrane protein-I (LMP-I) immunohistochemistry have identified EBV latent infection in up to 50% of HD tumors. However, the epidemiologic features of these cases have not been examined in detail. To explore the epidemiology of EBV-positive HD so as to understand the role of EBV in HD etiology more clearly, this project accumulated patient data from 14 studies that had applied these EBV assays to HD tumors. With information on age at diagnosis, sex, ethnicity, histologic subtype, country of residence, clinical stage and EBV tumor status from 1,546 HD patients, we examined risk for EBV-positive disease using logistic regression. Forty percent of subjects had EBV-positive tumors, and EBV prevalence varied significantly across groups defined by the study variables. Odds ratios (OR) for EBV-associated HD were significantly elevated for Hispanics vs. whites (OR = 4.1), mixed cellularity vs. nodular sclerosis histologic subtypes (OR = 7.3, 13.4, 4.9 for ages 0-14, 15-49, 50+ years), children from economically less-developed vs. more-developed regions and young adult males vs. females (OR = 2.5). These findings suggest that age, sex, ethnicity and the physiologic effects of poverty may represent biologic modifiers of the EBV association and confirm that this association is strongly but variably linked to histologic subtype. The data augment biologic evidence that EBV is actively involved in HD pathogenesis in some cases but describe epidemiologic complexity in this process.


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