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Sci Rep ; 14(1): 7854, 2024 04 03.
Article in English | MEDLINE | ID: mdl-38570581

ABSTRACT

The relationship between body mass index (BMI) and melanoma and other skin cancers remains unclear. The objective of this study was to employ the Mendelian randomization (MR) approach to evaluate the effects of genetically predicted childhood adiposity on the risk of developing skin cancer later in life. Two-sample MR analyses were conducted using summary data from genome-wide association study (GWAS) meta-analyses of childhood BMI, melanoma, cutaneous squamous cell carcinoma (cSCC), and basal cell carcinoma (BCC). We used the inverse-variance-weighted (IVW) methods to obtain a pooled estimate across all genetic variants for childhood BMI. We performed multiple sensitivity analyses to evaluate the potential influence of various assumptions on our findings. We found no evidence that genetically predicted childhood BMI was associated with risks of developing melanoma, cSCC, or BCC in adulthood (OR, 95% CI: melanoma: 1.02 (0.93-1.13), cSCC 0.94 (0.79-1.11), BCC 0.97 (0.84-1.12)). Our findings do not support the conclusions from observational studies that childhood BMI is associated with increased risks of melanoma, cSCC, or BCC in adulthood. Intervening on childhood adiposity will not reduce the risk of common skin cancers later in life.


Subject(s)
Carcinoma, Basal Cell , Carcinoma, Squamous Cell , Melanoma , Pediatric Obesity , Skin Neoplasms , Humans , Child , Skin Neoplasms/epidemiology , Skin Neoplasms/genetics , Skin Neoplasms/complications , Melanoma/etiology , Melanoma/genetics , Carcinoma, Squamous Cell/pathology , Pediatric Obesity/complications , Pediatric Obesity/genetics , Genome-Wide Association Study , Carcinoma, Basal Cell/epidemiology , Carcinoma, Basal Cell/genetics , Body Mass Index , Mendelian Randomization Analysis , Genetic Predisposition to Disease , Polymorphism, Single Nucleotide
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