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A Iipidomics Analysis of the Relationship Between Dietary Fatty Acid Composition and Insulin Sensitivity in Young Adults

机译:年轻人饮食中脂肪酸组成与胰岛素敏感性关系的成因组学分析

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摘要

Relative to diets enriched in palmitic acid (PA), diets rich in oleic acid (OA) are associated with reduced risk of type 2 diabetes. To gain insight into mechanisms underlying these observations, we applied comprehensive lipidomic profiling to specimens collected from healthy adults enrolled in a randomized, crossover trial comparing a high-PA diet to a low-PA/high-OA (HOA) diet. Effects on insulin sensitivity (S_I) and disposition index (DI) were assessed by intravenous glucose tolerance testing, In women, but not men, S_I and DI were higher during HOA. The effect of HOA on S_I correlated positively with physical fitness upon enrollment. Principal components analysis of either fasted or fed-state metabolites identified one factor affected by diet and heavily weighted by the PA/OA ratio of serum and muscle lipids. In women, this factor correlated inversely with S_I in the fasted and fed states. Medium-chain acylcarnitines emerged as strong negative correlates of S_I, and the HOA diet was accompanied by lower serum and muscle ceramide concentrations and reductions in molecular biomarkers of inflammatory and oxidative stress. This study provides evidence that the dietary PA/OA ratio impacts diabetes risk in women.
机译:相对于富含棕榈酸(PA)的饮食,富含油酸(OA)的饮食与2型糖尿病的风险降低相关。为了深入了解这些观察结果的潜在机制,我们对从健康成年人中收集的标本进行了全面的脂质组分析,该研究是将高PA饮食与低PA /高OA(HOA)饮食进行比较的随机交叉试验。通过静脉内葡萄糖耐量试验评估对胰岛素敏感性(S_I)和处置指数(DI)的影响。在女性而非男性中,HOA期间S_I和DI较高。 HOA对S_I的影响与入选时的身体健康程度呈正相关。对禁食或进食状态代谢物的主成分分析确定了一个因素,该因素受饮食影响,并且受血清和肌肉脂质的PA / OA比重重。在女性中,该因素与禁食和进食状态下的S_I成反比。中链酰基肉碱成为S_I的强负相关,而HOA饮食则伴随着较低的血清和肌肉神经酰胺浓度,以及炎症和氧化应激的分子生物标志物减少。这项研究提供了饮食中PA / OA比例影响女性糖尿病风险的证据。

著录项

  • 来源
    《Diabetes》 |2013年第4期|1054-1063|共10页
  • 作者单位

    Department of Pediatrics, University of Vermont, Burlington, Ver-mont ,Department of Medicine, University of Vermont, Burlington, Ver-mont;

    Department of Medical Biostatistics, University of Vermont, Burlington, Vermont;

    Department of Medicine, University of Vermont, Burlington, Ver-mont;

    Stedman Nutrition and Metabolism Center, Duke University, Durham, North Carolina ,Department of Medicine, Duke University, Durham, North Carolina ,Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina;

    Stedman Nutrition and Metabolism Center, Duke University, Durham, North Carolina ,Department of Medicine, Duke University, Durham, North Carolina ,Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina;

    Stedman Nutrition and Metabolism Center, Duke University, Durham, North Carolina ,Department of Medicine, Duke University, Durham, North Carolina ,Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina;

    Department of Medicine, University of Vermont, Burlington, Ver-mont;

    Pennington Biomedical Research Center, Baton Rouge, Louisiana.;

    Department of Medicine, University of Vermont, Burlington, Ver-mont;

    Stedman Nutrition and Metabolism Center, Duke University, Durham, North Carolina ,Department of Medicine, Duke University, Durham, North Carolina ,Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina;

    Stedman Nutrition and Metabolism Center, Duke University, Durham, North Carolina ,Department of Medicine, Duke University, Durham, North Carolina ,Department of Pharmacology and Cancer Biology, Duke University, Durham, North Carolina;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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