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首页> 外文期刊>Journal of Nutrition >Apolipoprotein A5 Polymorphisms Interact with Total Dietary Fat Intake in Association with Markers of Metabolic Syndrome in Puerto Rican Older Adults
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Apolipoprotein A5 Polymorphisms Interact with Total Dietary Fat Intake in Association with Markers of Metabolic Syndrome in Puerto Rican Older Adults

机译:载脂蛋白A5多态性与波多黎各老年人的代谢综合征标志物相关的总膳食脂肪摄入量

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摘要

APOA5 -1131T > C and S19W single nucleotide polymorphisms (SNP) have been consistently associated with plasma lipid concentration and metabolic syndrome (MetS), alone and in modulation by dietary factors. Puerto Ricans have a high prevalence of metabolic conditions and high minor allele frequency for these SNP, suggesting a possible role in disease for this population. We aimed to determine the association of APOA5 -1131T > C and S19W with plasma lipids and markers of MetS, alone and in interaction with total fat intake, as a percent of total energy intake, in Puerto Ricans. Anthropometric and demographic data, FFQ, and blood samples were collected at baseline from participants in the Boston Puerto Rican Health Study (n = 802, 45–75 y). APOA5 S19W was associated with plasma HDL cholesterol (HDL-C) (P = 0.044); minor allele carriers had lower HDL-C [1.12 ± 0.03 (mean ± SE)] than those with the common variant (1.18 ± 0.01 mmol/L), even after adjustment for plasma triglycerides (TG) (P = 0.012). Neither polymorphism was associated with TG or other lipids. Interaction of the -1131T > C SNP with total fat energy intake was observed for plasma TG (P = 0.032) and total cholesterol (P = 0.034). APOA5 S19W interacted with total fat intake in association with systolic (P = 0.002) and diastolic (P = 0.007) blood pressure. Neither SNP was associated with MetS in the overall analysis or after stratifying by total energy intake as fat. In conclusion, Puerto Ricans present a distinctive lipid profile in association with APOA5 polymorphisms. Dietary fat intake seems to modulate these associations. The results contribute to the understanding of health disparities in this population.
机译:APOA5 -1131T> C和S19W单核苷酸多态性 (SNP)一直与血浆脂质浓度 和代谢综合征(MetS)保持独立相关,并通过饮食 因素。波多黎各人的这些SNP的代谢状况患病率很高,而次要等位基因的频率也很高,这表明该人群在疾病中可能起着 的作用。我们旨在确定 APOA5 -1131T> C和S19W与血浆 脂质和MetS标记物的关系,单独和与总 脂肪相互作用摄入量占波多黎各人能量摄入总量的百分比。 在基线时从波士顿波多黎各的参与者中收集了人体测量学和人口统计学数据,FFQ和血液样本 > Rican健康研究(n = 802,45–75 y)。 APOA5 S19W与血浆HDL胆固醇(HDL-C)相关(P = 0.044); 较小等位基因携带者的HDL-C较低[1.12±0.03(平均值 ±SE)],即使在调整血浆甘油三酸酯 (TG)之后,仍比具有常见变体(1.18± 0.01 mmol / L)的那些(P = 0.012 )。两种多态性均与TG 或其他脂质无关。血浆TG(P = 0.032)和总胆固醇(P = 0.034)观察到-1131T> C SNP与总 脂肪能量摄入的相互作用。 APOA5 S19W与总的 脂肪摄入量以及收缩压(P = 0.002)和舒张压 (P = 0.007)相关。在总体分析中或在以总能量 摄入的脂肪进行分层后,SNP均未与 MetS相关。总之,波多黎各人呈现出与APOA5多态性相关的独特 脂质谱。饮食中的 脂肪摄入似乎可以调节这些关联。结果 有助于理解此 人口中的健康差异。

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  • 来源
    《Journal of Nutrition》 |2009年第12期|2301-2308|共8页
  • 作者单位

    Jean Mayer USDA Human Nutrition Research Center on Aging and|Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA 02111 and;

    Department of Biostatistics, School of Public Health, Boston University, Boston, MA 02118;

    Jean Mayer USDA Human Nutrition Research Center on Aging and|Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA 02111 and;

    Jean Mayer USDA Human Nutrition Research Center on Aging and|Friedman School of Nutrition Science and Policy, Tufts University, Boston, MA 02111 and;

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