Melanoma risk prediction using a multilocus genetic risk score in the Women's Health Initiative cohort

• Published in: Journal of the American Academy of Dermatology 2018-07, Vol.79 (1), p.36-41.e10
• Main Authors: Cho, Hyunje G., Ransohoff, Katherine J., Yang, Lingyao, Hedlin, Haley, Assimes, Themistocles, Han, Jiali, Stefanick, Marcia, Tang, Jean Y., Sarin, Kavita Y.
• Format: Article
• Language: English
• Subjects: Age Distribution; Aged; Cohort Studies; Databases, Factual; Female; Genetic Predisposition to Disease - epidemiology; genetic risk score; Genome-Wide Association Study; Humans; Logistic Models; melanoma; Melanoma - epidemiology; Melanoma - genetics; Melanoma - pathology; Middle Aged; Polymorphism, Single Nucleotide; postmenopausal; Postmenopause; Predictive Value of Tests; Prevalence; Prognosis; Proportional Hazards Models; Risk Assessment; single-nucleotide polymorphism; Skin Neoplasms - epidemiology; Skin Neoplasms - genetics; Skin Neoplasms - pathology; United States - epidemiology; women; Women's Health; Women's Health Initiative
• ISSN: 0190-9622; 1097-6787
• DOI: 10.1016/j.jaad.2018.02.052

Single-nucleotide polymorphisms (SNPs) associated with melanoma have been identified though genome-wide association studies. However, the combined impact of these SNPs on melanoma development remains unclear, particularly in postmenopausal women who carry a lower melanoma risk. We examine the contribution of a combined polygenic risk score on melanoma development in postmenopausal women. Genetic risk scores were calculated using 21 genome-wide association study–significant SNPs. Their combined effect on melanoma development was evaluated in 19,102 postmenopausal white women in the clinical trial and observational study arms of the Women's Health Initiative dataset. Compared to the tertile of weighted genetic risk score with the lowest genetic risk, the women in the tertile with the highest genetic risk were 1.9 times more likely to develop melanoma (95% confidence interval 1.50-2.42). The incremental change in c-index from adding genetic risk scores to age were 0.075 (95% confidence interval 0.041-0.109) for incident melanoma. Limitations include a lack of information on nevi count, Fitzpatrick skin type, family history of melanoma, and potential reporting and selection bias in the Women's Health Initiative cohort. Higher genetic risk is associated with increased melanoma prevalence and incidence in postmenopausal women, but current genetic information may have a limited role in risk prediction when phenotypic information is available.