Volume 148, Issue 3 pp. 413-415

IRF4 polymorphism rs872071 and risk of Hodgkin lymphoma

Peter Broderick

Peter Broderick

Section of Cancer Genetics, Institute of Cancer Research

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David Cunningham

David Cunningham

Section of Medicine, Royal Marsden Hospitals NHS Trust

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Jayaram Vijayakrishnan

Jayaram Vijayakrishnan

Section of Cancer Genetics, Institute of Cancer Research

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Rosie Cooke

Rosie Cooke

Section of Epidemiology, Institute of Cancer Research, Sutton, Surrey, UK

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Alan Ashworth

Alan Ashworth

The Breakthrough Breast Cancer Research Centre, London, UK

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Anthony Swerdlow

Anthony Swerdlow

Section of Epidemiology, Institute of Cancer Research, Sutton, Surrey, UK

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Richard Houlston

Richard Houlston

Section of Cancer Genetics, Institute of Cancer Research

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First published: 11 January 2010
Citations: 17
Richard S. Houlston, Section of Cancer Genetics, Institute of Cancer Research, Brookes Lawley Building, Sutton, Surrey SM2 5NG, UK.
E-mail: [email protected]

Summary

The reciprocal familial risk between chronic lymphocytic leukaemia (CLL) and Hodgkin lymphoma (HL) suggests genetic variants with pleiotropic effects may influence the risk of both CLL and HL. We have recently shown that the IRF4 variant rs872071 influences CLL risk. To examine if rs872071 genotype is associated with HL risk we genotyped two case-control series (totalling, 529 and 2192, respectively). This analysis provides evidence that IRF4 rs872071 influences HL risk; Odds Ratio = 1·21 (95% confidence interval: 1·05–1·39, P =0·009) and highlights the importance of inherited variation in B-cell developmental genes in the development of HL.

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