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本文引用的文献

1
Validation of a semiquantitative food frequency questionnaire for estimation of intakes of energy, fats and cholesterol among Singaporeans.一份用于评估新加坡人能量、脂肪和胆固醇摄入量的半定量食物频率问卷的验证
Asia Pac J Clin Nutr. 2000 Dec;9(4):282-8. doi: 10.1046/j.1440-6047.2000.00187.x.
2
Relationships between circulating metabolic intermediates and insulin action in overweight to obese, inactive men and women.超重至肥胖、缺乏运动的男性和女性体内循环代谢中间产物与胰岛素作用之间的关系。
Diabetes Care. 2009 Sep;32(9):1678-83. doi: 10.2337/dc08-2075. Epub 2009 Jun 5.
3
Is there a clear threshold for fasting plasma glucose that differentiates between those with and without neuropathy and chronic kidney disease?: the Singapore Prospective Study Program.是否存在一个明确的空腹血糖阈值来区分有无神经病变和慢性肾病的患者?:新加坡前瞻性研究项目
Am J Epidemiol. 2009 Jun 15;169(12):1454-62. doi: 10.1093/aje/kwp076. Epub 2009 Apr 30.
4
Physical inactivity and obesity underlie the insulin resistance of aging.缺乏身体活动和肥胖是衰老导致胰岛素抵抗的根本原因。
Diabetes Care. 2009 Aug;32(8):1547-9. doi: 10.2337/dc09-0267. Epub 2009 Apr 28.
5
High heritability of metabolomic profiles in families burdened with premature cardiovascular disease.患有早发性心血管疾病的家族中代谢组学特征的高遗传性。
Mol Syst Biol. 2009;5:258. doi: 10.1038/msb.2009.11. Epub 2009 Apr 7.
6
A branched-chain amino acid-related metabolic signature that differentiates obese and lean humans and contributes to insulin resistance.一种与支链氨基酸相关的代谢特征,可区分肥胖和消瘦人群,并导致胰岛素抵抗。
Cell Metab. 2009 Apr;9(4):311-26. doi: 10.1016/j.cmet.2009.02.002.
7
Insulin sensitivity: modulation by nutrients and inflammation.胰岛素敏感性:受营养物质和炎症的调节
J Clin Invest. 2008 Sep;118(9):2992-3002. doi: 10.1172/JCI34260.
8
Whole-body skeletal muscle mass is not related to glucose tolerance or insulin sensitivity in overweight and obese men and women.在超重和肥胖的男性及女性中,全身骨骼肌质量与葡萄糖耐量或胰岛素敏感性无关。
Appl Physiol Nutr Metab. 2008 Aug;33(4):769-74. doi: 10.1139/H08-060.
9
Genetic networks of liver metabolism revealed by integration of metabolic and transcriptional profiling.通过整合代谢和转录谱揭示的肝脏代谢遗传网络
PLoS Genet. 2008 Mar 14;4(3):e1000034. doi: 10.1371/journal.pgen.1000034.
10
Mechanisms of disease:Molecular and metabolic mechanisms of insulin resistance and beta-cell failure in type 2 diabetes.疾病机制:2型糖尿病中胰岛素抵抗和β细胞功能衰竭的分子与代谢机制
Nat Rev Mol Cell Biol. 2008 Mar;9(3):193-205. doi: 10.1038/nrm2327.

胰岛素抵抗与中国和亚洲印度男性蛋白质代谢改变的代谢特征有关。

Insulin resistance is associated with a metabolic profile of altered protein metabolism in Chinese and Asian-Indian men.

机构信息

Department of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Republic of Singapore.

出版信息

Diabetologia. 2010 Apr;53(4):757-67. doi: 10.1007/s00125-009-1637-8. Epub 2010 Jan 15.

DOI:10.1007/s00125-009-1637-8
PMID:20076942
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3753085/
Abstract

AIMS/HYPOTHESIS: Insulin resistance (IR) is associated with obesity, but can also develop in individuals with normal body weight. We employed comprehensive profiling methods to identify metabolic events associated with IR, while controlling for obesity.

METHODS

We selected 263 non-obese (BMI approximately 24 kg/m2) Asian-Indian and Chinese men from a large cross-sectional study carried out in Singapore. Individuals taking medication for diabetes or hyperlipidaemia were excluded. Participants were separated into lower and upper tertiles of IR based on HOMA indices of < or =1.06 or > or =1.93, respectively. MS-based metabolic profiling of acylcarnitines, amino acids and organic acids was combined with hormonal and cytokine profiling in all participants.

RESULTS

After controlling for BMI, commonly accepted risk factors for IR, including circulating fatty acids and inflammatory cytokines, did not discriminate the upper and lower quartiles of insulin sensitivity in either Asian- Indian or Chinese men. Instead, IR was correlated with increased levels of alanine, proline, valine, leucine/isoleucine, phenylalanine, tyrosine, glutamate/glutamine and ornithine, and a cluster of branched-chain and related amino acids identified by principal components analysis. These changes were not due to increased protein intake by individuals in the upper quartile of IR. Increased abdominal adiposity and leptin, and decreased adiponectin and IGF-binding protein 1 were also correlated with IR.

CONCLUSIONS/INTERPRETATION: These findings demonstrate that perturbations in amino acid homeostasis, but not inflammatory markers or NEFAs, are associated with IR in individuals of relatively low body mass.

摘要

目的/假设:胰岛素抵抗(IR)与肥胖有关,但也可发生在体重正常的个体中。我们采用综合分析方法来鉴定与 IR 相关的代谢事件,同时控制肥胖因素。

方法

我们从新加坡进行的一项大型横断面研究中选择了 263 名非肥胖(BMI 约为 24kg/m2)的亚裔印度人和中国人。排除了服用治疗糖尿病或高脂血症药物的个体。根据 HOMA 指数(<或=1.06 或>或=1.93),将参与者分为胰岛素敏感性低(IR)和高(IR)两个三分位组。对所有参与者进行基于 MS 的酰基肉碱、氨基酸和有机酸代谢谱分析,并结合激素和细胞因子谱分析。

结果

在控制 BMI 后,包括循环脂肪酸和炎症细胞因子在内的公认的 IR 危险因素并不能区分亚裔印度人和中国人中胰岛素敏感性的高(IR)和低(IR)四分位数。相反,IR 与丙氨酸、脯氨酸、缬氨酸、亮氨酸/异亮氨酸、苯丙氨酸、酪氨酸、谷氨酸/谷氨酰胺和鸟氨酸水平升高相关,主成分分析鉴定的支链氨基酸和相关氨基酸簇也与 IR 相关。这些变化不是由于 IR 四分位数较高的个体蛋白质摄入增加所致。增加的腹部肥胖和瘦素,以及减少的脂联素和 IGF 结合蛋白 1 也与 IR 相关。

结论/解释:这些发现表明,在体重相对较低的个体中,氨基酸稳态的紊乱,而不是炎症标志物或非酯化脂肪酸,与 IR 相关。