Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
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PMID
15947871
TITLE
An analysis of risk factors for cutaneous melanoma by anatomical site (Australia).
ABSTRACT
OBJECTIVE NlmCategory: OBJECTIVE
Emerging evidence suggests that melanomas arising on the head and neck that are not lentigo maligna melanomas have different associations with phenotypic and environmental risk factors than those on the trunk and other sites. We sought to test this hypothesis in a population-based study in Queensland, Australia.
METHODS NlmCategory: METHODS
Emerging evidence suggests that melanomas arising on the head and neck that are not lentigo maligna melanomas have different associations with phenotypic and environmental risk factors than those on the trunk and other sites. We sought to test this hypothesis in a population-based study in Queensland, Australia. Risk factor data were collected from 2360 participants with incident cutaneous melanoma diagnosed 1982--1990, including 167 participants with lentigo maligna melanoma. For each risk factor, polytomous logistic regression analysis, using the trunk as a reference category, was used to estimate the odds ratio and 95% confidence interval for cutaneous melanomas by anatomical site.
RESULTS NlmCategory: RESULTS
Emerging evidence suggests that melanomas arising on the head and neck that are not lentigo maligna melanomas have different associations with phenotypic and environmental risk factors than those on the trunk and other sites. We sought to test this hypothesis in a population-based study in Queensland, Australia. Risk factor data were collected from 2360 participants with incident cutaneous melanoma diagnosed 1982--1990, including 167 participants with lentigo maligna melanoma. For each risk factor, polytomous logistic regression analysis, using the trunk as a reference category, was used to estimate the odds ratio and 95% confidence interval for cutaneous melanomas by anatomical site. Participants with melanomas of the head and neck were significantly older than those with melanomas of the trunk (males 52.7 versus 49.7 years; females 47.8 versus 40.5 years). Compared with patients with truncal melanomas, those of the head and neck were less likely to have many nevi (OR 0.41, 95% CI 0.13--1.31), although this did not reach statistical significance. Among females, melanomas of the lower limb were negatively associated with a past history of non-melanoma skin cancer (OR 0.41, 95% CI 0.23-0.74).
CONCLUSIONS NlmCategory: CONCLUSIONS
Emerging evidence suggests that melanomas arising on the head and neck that are not lentigo maligna melanomas have different associations with phenotypic and environmental risk factors than those on the trunk and other sites. We sought to test this hypothesis in a population-based study in Queensland, Australia. Risk factor data were collected from 2360 participants with incident cutaneous melanoma diagnosed 1982--1990, including 167 participants with lentigo maligna melanoma. For each risk factor, polytomous logistic regression analysis, using the trunk as a reference category, was used to estimate the odds ratio and 95% confidence interval for cutaneous melanomas by anatomical site. Participants with melanomas of the head and neck were significantly older than those with melanomas of the trunk (males 52.7 versus 49.7 years; females 47.8 versus 40.5 years). Compared with patients with truncal melanomas, those of the head and neck were less likely to have many nevi (OR 0.41, 95% CI 0.13--1.31), although this did not reach statistical significance. Among females, melanomas of the lower limb were negatively associated with a past history of non-melanoma skin cancer (OR 0.41, 95% CI 0.23-0.74). We have observed heterogeneity for melanoma risk by anatomical site, lending weight to the hypothesis that cutaneous melanomas may develop through multiple causal pathways.
DATE PUBLISHED
2005 Apr
HISTORY
PUBSTATUS PUBSTATUSDATE
received 2004/03/02
accepted 2004/05/05
pubmed 2005/06/11 09:00
medline 2005/10/15 09:00
entrez 2005/06/11 09:00
AUTHORS
NAME COLLECTIVENAME LASTNAME FORENAME INITIALS AFFILIATION AFFILIATIONINFO
Siskind V Siskind Victor V Division of Population Studies and Human Genetics, Queensland Institute of Medical Research, Brisbane, QLD, Australia.
Whiteman DC Whiteman David C DC
Aitken JF Aitken Joanne F JF
Martin NG Martin Nicholas G NG
Green AC Green Adèle C AC
INVESTIGATORS
JOURNAL
VOLUME: 16
ISSUE: 3
TITLE: Cancer causes & control : CCC
ISOABBREVIATION: Cancer Causes Control
YEAR: 2005
MONTH: Apr
DAY:
MEDLINEDATE:
SEASON:
CITEDMEDIUM: Print
ISSN: 0957-5243
ISSNTYPE: Print
MEDLINE JOURNAL
MEDLINETA: Cancer Causes Control
COUNTRY: Netherlands
ISSNLINKING: 0957-5243
NLMUNIQUEID: 9100846
PUBLICATION TYPE
PUBLICATIONTYPE TEXT
Journal Article
COMMENTS AND CORRECTIONS
GRANTS
GENERAL NOTE
KEYWORDS
MESH HEADINGS
DESCRIPTORNAME QUALIFIERNAME
Adult
Age Factors
Australia epidemiology
Environment epidemiology
Female epidemiology
Humans epidemiology
Male epidemiology
Melanoma etiology
Middle Aged etiology
Odds Ratio etiology
Phenotype etiology
Regression Analysis etiology
Risk Factors etiology
Sex Factors etiology
Skin Neoplasms etiology
SUPPLEMENTARY MESH
GENE SYMBOLS
CHEMICALS
OTHER ID's