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Horm Res Paediatr ; 84(4): 248-53, 2015.
Artículo en Inglés | MEDLINE | ID: mdl-26304632

RESUMEN

BACKGROUND/AIM: The single nucleotide polymorphisms (SNPs) rs2282978 (CDK6), rs2425019 (MMP24), rs8081612 (MAP3K3), rs2871865 (IGF1R) and rs3782415 (SOCS2) were among the SNPs most strongly associated with height in a meta-analysis of 47 genome-wide association studies (GWAS) involving 114,223 adults from six ethnic groups. The present study aimed to examine associations between these SNPs and height in Brazilian children. METHODS: Cross-sectional heights of 1,008 healthy unrelated 4.4- to 9.7-year-old children were evaluated. All genotypes were determined by allele-specific polymerase chain reactions. Height standard deviation scores (SDS) were generated for this population and regressed on allele counts. Linear regressions were performed to estimate the effect of individual SNPs or a polygenic allelic score on height. RESULTS: The T allele of rs8081612 (MAP3K3), the C allele of rs2871865 (IGF1R) and the G allele of rs2425019 (MMP24) were significantly associated with a 0.091-SDS greater height (95% CI 0.089-0.093, p = 0.001) by polygenic analysis. The mean height SDS difference between children with 2 'tall' alleles and children with 4 'tall' alleles was 0.24 SDS (95% CI 0.05-0.43, p = 0.01). The observed allelic effect is consistent with that found in previous GWAS. CONCLUSIONS: Polymorphisms in MAP3K3, MMP24 and IGF1R act additively on height in children of an admixed population. These results demonstrate the importance of these loci for children's height.


Asunto(s)
Estatura/genética , Sitios Genéticos , MAP Quinasa Quinasa Quinasa 3/genética , Metaloproteinasas de la Matriz Asociadas a la Membrana/genética , Polimorfismo de Nucleótido Simple , Receptores de Somatomedina/genética , Alelos , Brasil , Niño , Preescolar , Estudios Transversales , Femenino , Estudio de Asociación del Genoma Completo , Genotipo , Humanos , Masculino , Receptor IGF Tipo 1
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