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The fat mass and obesity-associated ( FTO) rs9939609 A allele has been associated with obesity and dietary energy intakes in healthy children but its relation to metabolic complications in SGA-treated children is not known. Objectives
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Results: A meta-analysis of 10 studies (comprising 6951 participants) that reported the results of additive genetic models showed that individuals with the FTO TA genotype and AA genotype (those with the obesity-predisposing A allele) had .18-kg (95% CI: −0.09-, .45-kg; P = 0.19; NS) and .44-kg (95% CI: 0.09-, .79-kg; P = 0.015) greater weig.
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OBJECTIVE—To examine the longitudinal association of fat mass-and obesity-associated (FTO) variant with obesity, circulating adipokine levels, and FTO expression in various materials from human and mouse. RESEARCH DESIGN AND METHODS—We genotyped rs9939609 in 2,287 men and 3,520 women from two prospective cohorts.Plasma adiponectin and leptin were measured in a subset of diabetic men (n.
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The FTO A/T polymorphism (rs9939609) has been strongly associated with body mass-related traits in nonathletic populations, but rarely with elite athletic performance. The aim of the study was to investigate the association between the A/T polymorphism and athlete status in elite swimmers.
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The purpose of this study was to assess the connection between FTO rs9939609 (A/T) polymorphism and food preference. The study included 77 participants, 36 of whom were obese and had a low-calorie intake, and 41 non-obese participants with a high-calorie intake. Using a food frequency questionnaire (FFQ), the researchers calculated sweet and fatty food propensity scores. Genomic DNA was.
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Fat mass and obesity-associated protein also known as alpha-ketoglutarate-dependent dioxygenase FTO is an enzyme that in humans is encoded by the FTO gene located on chromosome 16. As one homolog in the AlkB family proteins, it is the first mRNA demethylase that has been identified. [5]
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However, when participants were stratified into higher and lower FTO methylation groups, the AA genotype possesses a 2.04-fold increased obesity risk in comparison to TT genotype (95%CI, 1.07-3.89.
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Background: Children with rs9939609 FTO variant alleles (homozygous = AA and heterozygous = AT) are predisposed to greater adiposity than are those with 2 wild-type alleles (TT). Objective: Because FTO is highly expressed in hypothalamic regions that are important for appetite, FTO genotype may affect energy balance by influencing eating behavior.
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The lower levels of HDL were observed in AT/AA genotypes compared to the TT wild type genotype of FTO rs9939609 polymorphism (P = 0.004). Adjustments of age, BMI, and physical activity did not change the results. However, the significant association between FTO genotype and the HDL level was disappeared after further adjustments for dietary intake.
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Despite no evidence of any epistasis, we then went on to perform genotype combination analysis for rs9939609 and rs1544410, which showed that the FTO "AA" and VDR "CC" genotype combination and the FTO "TT" and VDR "CT" combination gave the highest and lowest mean BMI respectively (AA:CC-TT:CT; p = 0.016). This supports the fact.
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FTO gene variants have been associated with obesity phenotypes in sedentary and obese populations, but rarely with skeletal muscle and elite athlete phenotypes. In 1089 participants, comprising 530 elite rugby athletes and 559 non-athletes, DNA was collected and genotyped for the FTO rs9939609 variant using real-time PCR. In a subgroup of non-resistance trained individuals (NT; n = 120), we.
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It has been found that food cravings declined with age, but this age effect was different across variants of FTO rs9939609, while TT homozygotes showed the typical age-related decline in food cravings, as well as no such decline among A-carriers. 31 Besides, the FTO genotype have effect on the relationship between age and emotional eating, with.
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have been noted in several ethnic groups [22-27], includ-ing our previous report that FTO rs9939609 TT genotype was associated with obesity and preference for a high-fat diet in adult individuals from Jakarta [28]. Expression of the FTO gene also afects various parts of the brain that regulate energy balance and appetite [3, 29, 30].
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This gene is a nuclear protein of the AlkB related non-haem iron and 2-oxoglutarate-dependent oxygenase superfamily but the exact physiological function of this gene is not known. Other non-heme iron enzymes function to reverse alkylated DNA and RNA damage by oxidative demethylation.
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Women carrying the risk allele (TA or AA) of the FTO -rs9939609 genetic variant had a 1.16 kg/m 2 higher BMI over the follow-up period than those carrying the wild-type genotype (TT), even when.
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All data were normally distributed according to the Shapiro-Wilk normality test. Regarding FTO rs9939609 genotype, about half of the participants were heterozygote (n = 98), about 30% of them were TT wild type (n = 60), and about 20% of them were AA homozygote (n = 38).The genotype distribution of the study population was in Hardy-Weinberg equilibrium.