Differential sex‐association between PCSK1 polymorphisms and obesity risk in Portuguese children

Abstract

AbstractObjectivesThe proprotein convertase subtilisin/Kexin type 1 gene (PCSK1) is implicated in hypothalamic appetite control. Several studies have addressed the relationship between PCSK1 polymorphisms and obesity, although conflicting results were observed. We tested the potential association of four PCSK1 variants with the risk of overweight/obesity and related variables in Portuguese children.MethodsThis is a case–control study, where four PCSK1 variants, rs6230 (c.−101T>C), rs6232 (p.N221D), rs6235 (p.S690T), and rs3811942 (c.*265T>C), were analyzed in Portuguese children (aged 5–13 years‐old). Anthropometric measures were objectively collected and used to provide weight‐for‐age, height‐for‐age, and body mass index (BMI) for age. The indices generated were compared to standard reference values of WHO to obtain the corresponding Z‐scores.ResultsLogistic regression, in the dominant model, revealed no significant associations between the four individual PCSK1 variants and the risk of overweight/obesity in the total population. However, stratifying the sample by sex, a marginally significant association was found between the rs6235 minor C‐allele and increased overweight/obesity in boys (n = 345) (OR 1.55 [1.01–2.38] p = .044), but not in girls (n = 340) (OR 0.73 [0.46–1.14] p = .169). Consistently, boys with genotype GG presented lower BMI Z‐score (0.62) when compared to those with the genotypes GC + CC (1.04). Testing for different effects in males versus females, a significant interaction was found between the rs6235 polymorphism and sex for BMI Z‐score (p = .025).ConclusionsResults of this study suggest for a sex‐differentiated association between PCSK1 rs6235 and overweight/ obesity in Portuguese children.