The association of host and genetic melanoma risk factors with Breslow thickness in the Western Australian Melanoma Health Study

G. Cadby, S. V. Ward, J. M. Cole, E. K. Moses, M. Millward, L. J. Palmer

    Research output: Contribution to journalArticlepeer-review

    8 Scopus citations

    Abstract

    Background Breslow thickness is the most important predictor of survival in localized malignant melanoma. A number of melanoma risk factors have been shown to be associated with Breslow thickness; however, the role of genetic loci has been little investigated to date. Objectives To investigate the association of known melanoma susceptibility genetic loci with Breslow thickness. Methods Participants were 800 individuals from the Western Australian Melanoma Health Study who completed a questionnaire and provided a DNA sample. Genetic association analyses between single-nucleotide polymorphisms (SNPs) from 15 candidate melanoma susceptibility genes and Breslow thickness were performed, controlling for relevant covariates. Results Older age at diagnosis and absence of naevi were associated with increased Breslow thickness. Following adjustment for multiple testing, no SNPs were significantly associated with Breslow thickness. Conclusions Associations observed between Breslow thickness and age and naevi reinforce current knowledge. Some evidence of shared genetic determinants between melanoma risk and Breslow thickness was found. Further studies are required to confirm this finding. What's already known about this topic? Breslow thickness is the single most important predictor of survival in localized malignant melanoma. Breslow thickness and melanoma susceptibility share common host risk factors. What does this study add? Breslow thickness was associated with age and presence of naevi. There may be some evidence of shared genetic determinants between Breslow thickness and melanoma susceptibility.

    Original languageEnglish (US)
    Pages (from-to)851-857
    Number of pages7
    JournalBritish Journal of Dermatology
    Volume170
    Issue number4
    DOIs
    StatePublished - 2014

    ASJC Scopus subject areas

    • Dermatology

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