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Starch Digestion–Related Amylase Genetic Variant Affects 2-Year Changes in Adiposity in Response to Weight-Loss Diets: The POUNDS Lost Trial

机译:淀粉消化相关的淀粉酶遗传变异影响减肥对减肥的2年性肥胖的影响:POUNDS丢失试验

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摘要

Salivary and pancreatic amylases (encoded by AMY1 and AMY2 genes, respectively) are responsible for digesting starchy foods. AMY1 and AMY2 show copy number variations that affect differences in amylase amount and activity, and AMY1 copies have been associated with adiposity. We investigated whether genetic variants determining amylase gene copies are associated with 2-year changes in adiposity among 692 overweight and obese individuals who were randomly assigned to diets varying in macronutrient content. We found that changes in body weight (BW) and waist circumference (WC) were significantly different according to the AMY1-AMY2 rs11185098 genotype. Individuals carrying the A allele (indicating higher amylase amount and activity) showed a greater reduction in BW and WC at 6, 12, 18, and 24 months than those without the A allele (P < 0.05 for all). The association was stronger for long-term changes compared with short-term changes of these outcomes. The genetic effects on these outcomes did not significantly differ across diet groups. In conclusion, the genetic variant determining starch metabolism influences the response to weight-loss dietary intervention. Overweight and obese individuals carrying the AMY1-AMY2 rs11185098 genotype associated with higher amylase activity may have greater loss of adiposity during low-calorie diet interventions.
机译:唾液和胰淀粉酶(分别由AMY1和AMY2基因编码)负责消化淀粉类食物。 AMY1和AMY2显示拷贝数变化,影响淀粉酶数量和活性的差异,并且AMY1拷贝已与肥胖相关。我们调查了确定淀粉酶基因拷贝的遗传变异是否与692名超重和肥胖个体中2年肥胖症的改变相关,这些个体被随机分配到大量营养素含量不同的饮食中。我们发现根据AMY1-AMY2 rs11185098基因型,体重(BW)和腰围(WC)的变化显着不同。携带A等位基因的个体(表明更高的淀粉酶含量和活性)在6、12、18和24个月时的BW和WC降低比没有A等位基因的个体更大(所有P均<0.05)。与这些结果的短期变化相比,长期变化的关联性更强。不同饮食组对这些结果的遗传影响没有显着差异。总之,决定淀粉代谢的遗传变异影响减肥饮食干预的反应。携带带有较高淀粉酶活性的AMY1-AMY2 rs11185098基因型的超重和肥胖个体在低热量饮食干预期间可能会导致更多的肥胖症。

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