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Associations of pigmentary and naevus phenotype with melanoma risk in two populations with comparable ancestry but contrasting levels of ambient sun exposure.
Cust, A E; Drummond, M; Bishop, D T; Azizi, L; Schmid, H; Jenkins, M A; Hopper, J L; Armstrong, B K; Aitken, J F; Kefford, R F; Giles, G G; Demenais, F; Goldstein, A M; Barrett, J H; Kanetsky, P A; Elder, D E; Mann, G J; Newton-Bishop, J A.
Afiliação
  • Cust AE; Cancer Epidemiology and Prevention Research, Sydney School of Public Health, The University of Sydney, Sydney, Australia.
  • Drummond M; Melanoma Institute Australia, The University of Sydney, Sydney, Australia.
  • Bishop DT; Cancer Epidemiology and Prevention Research, Sydney School of Public Health, The University of Sydney, Sydney, Australia.
  • Azizi L; Melanoma Institute Australia, The University of Sydney, Sydney, Australia.
  • Schmid H; Section of Epidemiology and Biostatistics, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK.
  • Jenkins MA; School of Mathematics and Statistics, The University of Sydney, Sydney, Australia.
  • Hopper JL; Centre for Cancer Research, Westmead Institute for Medical Research, The University of Sydney, Sydney, Australia.
  • Armstrong BK; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, Australia.
  • Aitken JF; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, Australia.
  • Kefford RF; Cancer Epidemiology and Prevention Research, Sydney School of Public Health, The University of Sydney, Sydney, Australia.
  • Giles GG; Viertel Centre for Research in Cancer Control, Cancer Council Queensland, Brisbane, Australia.
  • Demenais F; Melanoma Institute Australia, The University of Sydney, Sydney, Australia.
  • Goldstein AM; Macquarie University Health Sciences Centre, Macquarie University, Sydney, Australia.
  • Barrett JH; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Melbourne, Australia.
  • Kanetsky PA; Cancer Epidemiology Centre, Cancer Council Victoria, Melbourne, Australia.
  • Elder DE; Genetic Variation and Human Diseases Unit, UMR-946, INSERM, Université Paris Diderot, Université Sorbonne Paris Cité, Paris, France.
  • Mann GJ; Human Genetics Program, Division of Cancer Epidemiology and Genetics, National Cancer Institute, Bethesda, MD, USA.
  • Newton-Bishop JA; Section of Epidemiology and Biostatistics, Leeds Institute of Cancer and Pathology, University of Leeds, Leeds, UK.
J Eur Acad Dermatol Venereol ; 33(10): 1874-1885, 2019 Oct.
Article em En | MEDLINE | ID: mdl-31087403
ABSTRACT

BACKGROUND:

People at high risk of developing melanoma are usually identified by pigmentary and naevus phenotypes.

OBJECTIVE:

We examined whether associations of these phenotypes with melanoma risk differed by ambient sun exposure or participant characteristics in two population-based, case-control studies with comparable ancestry but different ambient sun exposure.

METHODS:

Data were analysed from 616 cases and 496 controls from the Australian Melanoma Family Study and 2012 cases and 504 controls from the Leeds (UK) case-control study. Questionnaire, interview and dermatological skin examination data were collected using the same measurement protocols. Relative risks were estimated as odds ratios using unconditional logistic regression, adjusted for potential confounders.

RESULTS:

Hair and skin colour were the strongest pigmentary phenotype risk factors. All associations of pigmentary phenotype with melanoma risk were similar across countries. The median number of clinically assessed naevi was approximately three times higher in Australia than Leeds, but the relative risks for melanoma associated with each additional common or dysplastic naevus were higher for Leeds than Australia, especially for naevi on the upper and lower limbs. Higher naevus counts on the head and neck were associated with a stronger relative risk for melanoma for women than men. The two countries had similar relative risks for melanoma based on self-reported naevus density categories, but personal perceptions of naevus number differed by country. There was no consistent evidence of interactions between phenotypes on risk.

CONCLUSIONS:

Classifying people at high risk of melanoma based on their number of naevi should ideally take into account their country of residence, type of counts (clinical or self-reported), body site on which the naevus counts are measured and sex. The presence of naevi may be a stronger indicator of a genetic predisposition in the UK than in Australia based on less opportunity for sun exposure to influence naevus development.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Luz Solar / Pigmentação da Pele / Exposição Ambiental / Melanoma / Nevo Pigmentado Tipo de estudo: Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa / Oceania Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Cutâneas / Luz Solar / Pigmentação da Pele / Exposição Ambiental / Melanoma / Nevo Pigmentado Tipo de estudo: Etiology_studies / Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Aged / Female / Humans / Male / Middle aged País/Região como assunto: Europa / Oceania Idioma: En Ano de publicação: 2019 Tipo de documento: Article