Quantifying the Polygenic Contribution to Cutaneous Squamous Cell Carcinoma Risk.

TitleQuantifying the Polygenic Contribution to Cutaneous Squamous Cell Carcinoma Risk.
Publication TypeJournal Article
Year of Publication2018
AuthorsSordillo, JE, Kraft, P, Wu, AChen, Asgari, MM
JournalJ Invest Dermatol
Volume138
Issue7
Pagination1507-1510
Date Published2018 07
ISSN1523-1747
KeywordsCarcinoma, Squamous Cell, Female, Genetic Loci, Genetic Predisposition to Disease, Genome-Wide Association Study, Humans, Linear Models, Logistic Models, Male, Models, Biological, Polymorphism, Single Nucleotide, Risk Assessment, Risk Factors, Sex Factors, Skin Neoplasms
Abstract

Genetic factors play an important role in cutaneous squamous cell carcinoma risk. Genome-wide association studies have identified 21 single nucleotide polymorphisms associated with cutaneous squamous cell carcinoma risk. Yet no studies have attempted to quantify the contribution of heritability to cutaneous squamous cell carcinoma risk by calculating the population attributable risk using a combination of all discovered genetic variants. Using an additive multi-locus linear logistic model, we determined the cumulative association of these 21 genetic regions to cutaneous squamous cell carcinoma population attributable risk. We computed a multi-locus population attributable risk of 62%, suggesting that if the effects of all the risk alleles were removed from a population, the cutaneous squamous cell carcinoma risk would drop by 62%. Using stratified analysis, we also examined the impact of sex on polygenic risk score, and found that men have an increased relative risk throughout the spectrum of the polygenic risk score. Quantifying the impact of genetic predisposition on the proportion of cancer cases can guide future research decisions and public health policy planning.

DOI10.1016/j.jid.2018.01.031
Alternate JournalJ. Invest. Dermatol.
PubMed ID29452120
PubMed Central IDPMC6019610
Grant ListR01 CA166672 / CA / NCI NIH HHS / United States
R35 CA197449 / CA / NCI NIH HHS / United States
U01 HG009088 / HG / NHGRI NIH HHS / United States