Institute of Preventive Medicine, Copenhagen University Hospital, Centre for Health and Society, Copenhagen, Denmark.
Int J Obes (Lond). 2009 Nov;33(11):1227-34. doi: 10.1038/ijo.2009.159. Epub 2009 Aug 18.
The A risk allele of rs9939609 of the fat mass- and obesity-associated gene (FTO) increases body fat mass.
To examine whether FTO rs9939609 affects obese individuals' response to a high-fat, low-carbohydrate (CHO) (HF) or low-fat, high-CHO (LF), hypo-energetic diet and whether the effect of the FTO variant depends on dietary fat and CHO content.
In a 10-week, European, multi-centre dietary intervention study 771 obese women and men were randomized to either LF (20-25% of energy (%E) from fat, 60-65%E from CHO) or HF (40-45%E from fat, 40-45%E from CHO), hypo-energetic diet (measured resting metabolic rate multiplied by 1.3-600 kcal day(-1)). Body weight, fat mass (FM), fat-free mass (FFM), waist circumference (WC), resting energy expenditure (REE), fasting fat oxidation as % of REE (FatOx), insulin release (HOMA-beta) and a surrogate measure of insulin resistance (HOMA-IR) were measured at baseline and after the intervention. In all, 764 individuals were genotyped for FTO rs9939609.
For A-allele carriers the drop-out rate was higher on HF than LF diet (in AT, P=0.002; in AT/AA combined, P=0.003). Among those individuals completing the intervention, we found no effect of FTO rs9939609 genotype on Deltaweight, DeltaFM, DeltaFFM, DeltaWC or DeltaFatOx. However, participants with TT had a smaller reduction in REE on LF than on HF diet (75 kcal/24 h; interaction: P=0.0055). These individuals also showed the greatest reduction in HOMA-beta and HOMA-IR (interaction: P=0.0083 and P=0.047).
The FTO rs9939609 may interact with the macronutrient composition in weight loss diets in various ways; carriers of the A allele on LF diet appear to have a lower risk for drop out, and TT individuals have a smaller decrease in REE and greater decrease in HOMA-beta and HOMA-IR on LF than on HF diet.
脂肪量和肥胖相关基因(FTO)的 rs9939609 风险等位基因 A 会增加体脂肪量。
研究 FTO rs9939609 是否会影响肥胖个体对高脂肪、低碳水化合物(CHO)(HF)或低脂肪、高 CHO(LF)、低能量饮食的反应,以及 FTO 变异的影响是否取决于饮食中的脂肪和 CHO 含量。
在一项为期 10 周的欧洲多中心饮食干预研究中,771 名肥胖女性和男性被随机分配到 LF(脂肪提供 20-25%的能量(%E),CHO 提供 60-65%E)或 HF(脂肪提供 40-45%E,CHO 提供 40-45%E),低能量饮食(测量静息代谢率乘以 1.3-600 卡路里/天(-1))。在基线和干预后测量体重、体脂肪量(FM)、去脂体重(FFM)、腰围(WC)、静息能量消耗(REE)、作为 REE 的%的空腹脂肪氧化(FatOx)、胰岛素释放(HOMA-beta)和胰岛素抵抗的替代测量(HOMA-IR)。共有 764 人接受了 FTO rs9939609 基因分型。
与 HF 饮食相比,A 等位基因携带者的 HF 饮食的退出率更高(在 AT 中,P=0.002;在 AT/AA 联合中,P=0.003)。在完成干预的这些个体中,我们没有发现 FTO rs9939609 基因型对 Deltaweight、DeltaFM、DeltaFFM、DeltaWC 或 DeltaFatOx 的影响。然而,TT 参与者在 LF 饮食上的 REE 减少量小于 HF 饮食(75 卡路里/24 小时;交互作用:P=0.0055)。这些个体还显示出 HOMA-beta 和 HOMA-IR 的最大降低(交互作用:P=0.0083 和 P=0.047)。
FTO rs9939609 可能以多种方式与减肥饮食中的宏量营养素组成相互作用;LF 饮食上携带 A 等位基因的携带者似乎有更低的退出风险,而 TT 个体在 LF 饮食上的 REE 下降较小,HOMA-beta 和 HOMA-IR 下降较大。