循环脂联素水平的遗传变异调节减肥饮食对食欲的影响

Wenjie Ma, Tao Huang, Y. Heianza, Tiange Wang, Dianjianyi Sun, J. Tong, D. Williamson, G. Bray, F. Sacks, L. Qi
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引用次数: 16

摘要

联素在调节食欲和食物摄入方面起着关键作用。目的探讨脂联素水平遗传风险评分(GRS)与不同常量营养素摄入的减肥饮食对食欲和脂联素水平长期变化的相互作用。设计、环境和参与者:GRS是根据692名超重成人的5种脂联素相关变异来计算的,这些超重成人来自为期2年的使用新型饮食策略预防超重试验。反复测量血浆脂联素水平和食欲相关特征,包括渴望、饱腹感、预期摄入量和饥饿感。结果:在调整了年龄、性别、种族、基线体重指数和基线各自结果值后,膳食脂肪与脂联素GRS在基线至6个月的食欲评分和预期消费变化方面显示名义上显著的相互作用(相互作用P分别= 0.014和0.017)。在高脂饮食的参与者中,低脂联素水平的GRS与更大程度的食欲下降(P < 0.001)和预期消费(P = 0.008)相关,而在低脂饮食组中没有观察到显著的关联。此外,观察到GRS和膳食脂肪在6个月的脂联素水平变化之间存在显著的相互作用(相互作用P = 0.021)。较低的GRS与低脂组中脂联素的增加有关(P = 0.02),但与高脂组中脂联素的变化无关(P = 0.31)。结论不同循环脂联素基因结构的个体对不同脂肪摄入量的减肥饮食在食欲和脂联素水平上的反应可能存在差异。
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Genetic Variations of Circulating Adiponectin Levels Modulate Changes in Appetite in Response to Weight-Loss Diets
Context Adiponectin plays key roles in regulating appetite and food intake. Objective To investigate interactions between the genetic risk score (GRS) for adiponectin levels and weight-loss diets varying in macronutrient intake on long-term changes in appetite and adiponectin levels. Design, Setting, and Participants A GRS was calculated based on 5 adiponectin-associated variants in 692 overweight adults from the 2-year Preventing Overweight Using Novel Dietary Strategies trial. Main Outcome Measures Repeated measurements of plasma adiponectin levels and appetite-related traits, including cravings, fullness, prospective consumption, and hunger. Results Dietary fat showed nominally significant interactions with the adiponectin GRS on changes in appetite score and prospective consumption from baseline to 6 months (P for interaction = 0.014 and 0.017, respectively) after adjusting for age, sex, ethnicity, baseline body mass index, and baseline respective outcome values. The GRS for lower adiponectin levels was associated with a greater decrease in appetite (P < 0.001) and prospective consumption (P = 0.008) among participants consuming a high-fat diet, whereas no significant associations were observed in the low-fat group. Additionally, a significant interaction was observed between the GRS and dietary fat on 6-month changes in adiponectin levels (P for interaction = 0.021). The lower GRS was associated with a greater increase in adiponectin in the low-fat group (P = 0.02), but it was not associated with adiponectin changes in the high-fat group (P = 0.31). Conclusions Our findings suggest that individuals with varying genetic architecture of circulating adiponectin may respond divergently in appetite and adiponectin levels to weight-loss diets varying in fat intake.
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