Format

Send to

Choose Destination
PLoS One. 2016 Jan 4;11(1):e0145984. doi: 10.1371/journal.pone.0145984. eCollection 2016.

Gender-Dependent Association of FTO Polymorphisms with Body Mass Index in Mexicans.

Author information

1
Laboratorio de Immunogenómica y Enfermedades Metabólicas, Instituto Nacional de Medicina Genómica, Secretaría de Salud, Mexico City, Mexico.
2
Programa de Ciencias Genómicas, Universidad Autónoma de la Cd. de México, Mexico City, Mexico.
3
Hospital Regional 1° de Octubre, ISSSTE, Mexico City, Mexico.
4
Clínica de Diagnóstico Autorizado, ISSSTE, Mexico City, Mexico.
5
Hospital Regional Adolfo López Mateos, ISSSTE, Mexico City, Mexico.
6
Centro Nacional para la Salud de la Infancia y la Adolescencia, Secretaría de Salud, Mexico City, Mexico.
7
Instituto Nacional de Medicina Genómica, Secretaría de Salud, Mexico City, Mexico.
8
Instituto Nacional de Pediatría, Secretaría de Salud, Mexico City, Mexico.

Abstract

To evaluate the associations between six single-nucleotide polymorphisms (SNPs) in intron 1 of FTO and body mass index (BMI), a case-control association study of 2314 unrelated Mexican-Mestizo adult subjects was performed. The association between each SNP and BMI was tested using logistic and linear regression adjusted for age, gender, and ancestry and assuming additive, recessive, and dominant effects of the minor allele. Association analysis after BMI stratification showed that all five FTO SNPs (rs1121980, rs17817449, rs3751812, rs9930506, and rs17817449), were significantly associated with obesity class II/III under an additive model (P<0.05). Interestingly, we also documented a genetic model-dependent influence of gender on the effect of FTO variants on increased BMI. Two SNPs were specifically associated in males under a dominant model, while the remainder were associated with females under additive and recessive models (P<0.05). The SNP rs9930506 showed the highest increased in obesity risk in females (odds ratio = 4.4). Linear regression using BMI as a continuous trait also revealed differential FTO SNP contributions. Homozygous individuals for the risk alleles of rs17817449, rs3751812, and rs9930506 were on average 2.18 kg/m(2) heavier than homozygous for the wild-type alleles; rs1121980 and rs8044769 showed significant but less-strong effects on BMI (1.54 kg/m(2) and 0.9 kg/m(2), respectively). Remarkably, rs9930506 also exhibited positive interactions with age and BMI in a gender-dependent manner. Women carrying the minor allele of this variant have a significant increase in BMI by year (0.42 kg/m(2), P = 1.17 x 10(-10)). Linear regression haplotype analysis under an additive model, confirmed that the TGTGC haplotype harboring all five minor alleles, increased the BMI of carriers by 2.36 kg/m(2) (P = 1.15 x 10(-5)). Our data suggest that FTO SNPs make differential contributions to obesity risk and support the hypothesis that gender differences in the mechanisms involving these variants may contribute to disease development.

PMID:
26726774
PMCID:
PMC4703196
DOI:
10.1371/journal.pone.0145984
[Indexed for MEDLINE]
Free PMC Article

Supplemental Content

Full text links

Icon for Public Library of Science Icon for PubMed Central
Loading ...
Support Center