TY - JOUR
T1 - Risk factors for melanoma by anatomical site
T2 - an evaluation of aetiological heterogeneity
AU - Laskar, R.
AU - Ferreiro-Iglesias, A.
AU - Bishop, D. T.
AU - Iles, M. M.
AU - Kanetsky, P. A.
AU - Armstrong, B. K.
AU - Law, M. H.
AU - Goldstein, A. M.
AU - Aitken, J. F.
AU - Giles, G. G.
AU - Australian Melanoma Family Study Investigators
AU - Leeds Case–Control Study Investigators
AU - Mann, Graham J.
AU - Schmid, Helen
AU - Hopper, John L.
AU - Holland, Elizabeth
AU - Kefford, Richard F.
AU - Jenkins, Mark A.
AU - Newton Bishop, Julia A.
AU - Affleck, Paul
AU - Barrett, Jennifer H.
AU - Harrison, Jane
AU - Randerson-Moor, Juliette
AU - Harland, Mark
AU - Taylor, John C.
AU - Whittaker, Linda
AU - Kukalizch, Kairen
AU - Leake, Susan
AU - Karpavicius, Birute
AU - Haynes, Sue
AU - Mack, Tricia
AU - Chan, May
AU - Taylor, Yvonne
AU - Davies, John
AU - King, Paul
AU - Robbins, H. A.
AU - Cust, Anne E.
N1 - Copyright the Author(s) 2020. Version archived for private and non-commercial use with the permission of the author/s and according to publisher conditions. For further rights please contact the publisher.
PY - 2021/6
Y1 - 2021/6
N2 - Background: Melanoma aetiology has been proposed to have two pathways, which are determined by naevi and type of sun exposure and related to the anatomical site where melanoma develops. Objectives: We examined associations with melanoma by anatomical site for a comprehensive set of risk factors including pigmentary and naevus phenotypes, ultraviolet radiation exposure and polygenic risk. Methods: We analysed harmonized data from 2617 people with incident first invasive melanoma and 975 healthy controls recruited through two population-based case–control studies in Australia and the UK. Questionnaire data were collected by interview using a single protocol, and pathway-specific polygenic risk scores were derived from DNA samples. We estimated adjusted odds ratios using unconditional logistic regression that compared melanoma cases at each anatomical site with all controls. Results: When cases were compared with control participants, there were stronger associations for many naevi vs. no naevi for melanomas on the trunk, and upper and lower limbs than on the head and neck (P-heterogeneity < 0·001). Very fair skin (vs. olive/brown skin) was more weakly related to melanoma on the trunk than to melanomas at other sites (P-heterogeneity = 0·04). There was no significant difference by anatomical site for polygenic risk. Increased weekday sun exposure was positively associated with melanoma on the head and neck but not on other sites. Conclusions: We found evidence of aetiological heterogeneity for melanoma, supporting the dual pathway hypothesis. These findings enhance understanding of risk factors for melanoma and can guide prevention and skin examination education and practices.
AB - Background: Melanoma aetiology has been proposed to have two pathways, which are determined by naevi and type of sun exposure and related to the anatomical site where melanoma develops. Objectives: We examined associations with melanoma by anatomical site for a comprehensive set of risk factors including pigmentary and naevus phenotypes, ultraviolet radiation exposure and polygenic risk. Methods: We analysed harmonized data from 2617 people with incident first invasive melanoma and 975 healthy controls recruited through two population-based case–control studies in Australia and the UK. Questionnaire data were collected by interview using a single protocol, and pathway-specific polygenic risk scores were derived from DNA samples. We estimated adjusted odds ratios using unconditional logistic regression that compared melanoma cases at each anatomical site with all controls. Results: When cases were compared with control participants, there were stronger associations for many naevi vs. no naevi for melanomas on the trunk, and upper and lower limbs than on the head and neck (P-heterogeneity < 0·001). Very fair skin (vs. olive/brown skin) was more weakly related to melanoma on the trunk than to melanomas at other sites (P-heterogeneity = 0·04). There was no significant difference by anatomical site for polygenic risk. Increased weekday sun exposure was positively associated with melanoma on the head and neck but not on other sites. Conclusions: We found evidence of aetiological heterogeneity for melanoma, supporting the dual pathway hypothesis. These findings enhance understanding of risk factors for melanoma and can guide prevention and skin examination education and practices.
UR - http://www.scopus.com/inward/record.url?scp=85101125550&partnerID=8YFLogxK
UR - http://purl.org/au-research/grants/nhmrc/566946
UR - http://purl.org/au-research/grants/nhmrc/107359
UR - http://purl.org/au-research/grants/nhmrc/211172
UR - http://purl.org/au-research/grants/nhmrc/402761
U2 - 10.1111/bjd.19705
DO - 10.1111/bjd.19705
M3 - Article
C2 - 33270213
AN - SCOPUS:85101125550
SN - 0007-0963
VL - 184
SP - 1085
EP - 1093
JO - British Journal of Dermatology
JF - British Journal of Dermatology
IS - 6
ER -