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本文引用的文献

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A systems genetics approach identifies genes and pathways for type 2 diabetes in human islets.系统遗传学方法鉴定了人类胰岛中 2 型糖尿病的基因和通路。
Cell Metab. 2012 Jul 3;16(1):122-34. doi: 10.1016/j.cmet.2012.06.006.
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Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study.血浆高密度脂蛋白胆固醇与心肌梗死风险:一项孟德尔随机化研究。
Lancet. 2012 Aug 11;380(9841):572-80. doi: 10.1016/S0140-6736(12)60312-2. Epub 2012 May 17.
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Interplay between lipids and branched-chain amino acids in development of insulin resistance.脂质和支链氨基酸在胰岛素抵抗发展中的相互作用。
Cell Metab. 2012 May 2;15(5):606-14. doi: 10.1016/j.cmet.2012.01.024.
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The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis.白细胞介素-6 受体作为预防冠心病的靶点:一项孟德尔随机分析。
Lancet. 2012 Mar 31;379(9822):1214-24. doi: 10.1016/S0140-6736(12)60110-X. Epub 2012 Mar 14.
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Structural and biochemical characterization of human mitochondrial branched-chain α-ketoacid dehydrogenase phosphatase.人线粒体支链α-酮酸脱氢酶磷酸酶的结构和生化特性。
J Biol Chem. 2012 Mar 16;287(12):9178-92. doi: 10.1074/jbc.M111.314963. Epub 2012 Jan 30.
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Genome-wide association study identifies multiple loci influencing human serum metabolite levels.全基因组关联研究鉴定出多个影响人类血清代谢物水平的位点。
Nat Genet. 2012 Jan 29;44(3):269-76. doi: 10.1038/ng.1073.
7
Weight-loss diets modify glucose-dependent insulinotropic polypeptide receptor rs2287019 genotype effects on changes in body weight, fasting glucose, and insulin resistance: the Preventing Overweight Using Novel Dietary Strategies trial.减肥饮食改变葡萄糖依赖性胰岛素释放多肽受体 rs2287019 基因型对体重、空腹血糖和胰岛素抵抗变化的影响:使用新型饮食策略预防超重试验。
Am J Clin Nutr. 2012 Feb;95(2):506-13. doi: 10.3945/ajcn.111.025270. Epub 2012 Jan 11.
8
Branched-chain amino acid levels are associated with improvement in insulin resistance with weight loss.支链氨基酸水平与体重减轻引起的胰岛素抵抗改善有关。
Diabetologia. 2012 Feb;55(2):321-30. doi: 10.1007/s00125-011-2356-5. Epub 2011 Nov 8.
9
Insulin receptor substrate 1 gene variation modifies insulin resistance response to weight-loss diets in a 2-year randomized trial: the Preventing Overweight Using Novel Dietary Strategies (POUNDS LOST) trial.胰岛素受体底物 1 基因变异可改变 2 年随机试验中减肥饮食对胰岛素抵抗的反应:预防超重使用新饮食策略(POUNDS LOST)试验。
Circulation. 2011 Aug 2;124(5):563-71. doi: 10.1161/CIRCULATIONAHA.111.025767. Epub 2011 Jul 11.
10
Differential metabolic impact of gastric bypass surgery versus dietary intervention in obese diabetic subjects despite identical weight loss.尽管肥胖糖尿病患者接受胃旁路手术和饮食干预后的体重减轻相同,但胃旁路手术与饮食干预对代谢的影响存在差异。
Sci Transl Med. 2011 Apr 27;3(80):80re2. doi: 10.1126/scitranslmed.3002043.

体重减轻饮食反应中氨基酸代谢物和体重及胰岛素抵抗变化的遗传决定因素:预防超重的新型饮食策略(POUNDS LOST)试验。

Genetic determinant for amino acid metabolites and changes in body weight and insulin resistance in response to weight-loss diets: the Preventing Overweight Using Novel Dietary Strategies (POUNDS LOST) trial.

机构信息

Department of Nutrition, Harvard School of Public Health, 665 Huntington Ave, Boston, MA 02115, USA.

出版信息

Circulation. 2013 Mar 26;127(12):1283-9. doi: 10.1161/CIRCULATIONAHA.112.000586. Epub 2013 Feb 27.

DOI:10.1161/CIRCULATIONAHA.112.000586
PMID:23446828
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3860590/
Abstract

BACKGROUND

Circulating branched-chain amino acids and aromatic amino acids were recently related to insulin resistance and diabetes mellitus in prospective cohorts. We tested the effects of a genetic determinant of branched-chain amino acid/aromatic amino acid ratio on changes in body weight and insulin resistance in a 2-year diet intervention trial.

METHODS AND RESULTS

We genotyped the branched-chain amino acid/aromatic amino acid ratio-associated variant rs1440581 near the PPM1K gene in 734 overweight or obese adults who were assigned to 1 of 4 diets varying in macronutrient content. At 6 months, dietary fat significantly modified genetic effects on changes in weight, fasting insulin, and homeostasis model assessment of insulin resistance (HOMA-IR) after adjustment for the confounders (all P for interaction ≤0.006). Further adjustment for weight change did not appreciably change the interactions for fasting insulin and HOMA-IR. In the high-fat diet group, the C allele was related to less weight loss and smaller decreases in serum insulin and HOMA-IR (all P ≤ 0.02 in an additive pattern), whereas an opposite genotype effect on changes in insulin and HOMA-IR was observed in the low-fat diet group (P=0.02 and P=0.04, respectively). At 2 years, the gene-diet interactions remained significant for weight loss (P=0.008) but became null for changes in serum insulin and HOMA-IR resulting from weight regain.

CONCLUSIONS

Individuals carrying the C allele of the branched-chain amino acid/aromatic amino acid ratio-associated variant rs1440581 may benefit less in weight loss and improvement of insulin sensitivity than those without this allele when undertaking an energy-restricted high-fat diet.

CLINICAL TRIAL REGISTRATION

URL: http://www.clinicaltrials.gov. Unique identifier: NCT00072995.

摘要

背景

循环支链氨基酸和芳香族氨基酸最近与前瞻性队列中的胰岛素抵抗和糖尿病有关。我们在为期 2 年的饮食干预试验中,测试了支链氨基酸/芳香族氨基酸比值的遗传决定因素对体重变化和胰岛素抵抗的影响。

方法和结果

我们在 734 名超重或肥胖成年人中对 PPM1K 基因附近与支链氨基酸/芳香族氨基酸比值相关的 rs1440581 基因进行了基因分型,这些成年人被分配到 4 种不同宏量营养素含量的饮食之一。6 个月时,在调整混杂因素后,饮食脂肪显著改变了遗传对体重变化、空腹胰岛素和稳态模型评估的胰岛素抵抗(HOMA-IR)的影响(所有交互作用 P 值均≤0.006)。进一步调整体重变化并没有显著改变空腹胰岛素和 HOMA-IR 的相互作用。在高脂肪饮食组中,C 等位基因与体重减轻较少、血清胰岛素和 HOMA-IR 降低幅度较小有关(在加性模式下,所有 P 值均≤0.02),而在低脂肪饮食组中观察到相反的基因型对胰岛素和 HOMA-IR 变化的影响(P=0.02 和 P=0.04)。2 年后,体重减轻的基因-饮食相互作用仍然显著(P=0.008),但由于体重恢复导致血清胰岛素和 HOMA-IR 的变化,这种相互作用变为无效。

结论

当进行能量限制的高脂肪饮食时,携带与支链氨基酸/芳香族氨基酸比值相关的 rs1440581 基因 C 等位基因的个体在体重减轻和改善胰岛素敏感性方面可能不如没有该等位基因的个体获益大。

临床试验注册

网址:http://www.clinicaltrials.gov。唯一标识符:NCT00072995。