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Individual serum saturated fatty acids and markers of chronic subclinical inflammation: the Insulin Resistance Atherosclerosis Study

机译:个体血清饱和脂肪酸和慢性亚临床炎症标志物:胰岛素抵抗性动脉粥样硬化研究

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摘要

Recent evidence has documented distinct effects of individual saturated FAs (SFAs) on cardiometabolic outcomes, with potential protective effects from odd- and very long-chain SFAs (VLSFAs). Cross-sectional and prospective associations of individual serum SFAs (12:0, 14:0, 15:0, 16:0, 18:0, 20:0, 22:0, and total SFA) with proinflammatory biomarkers and adiponectin were investigated in 555 adults from the IRAS. Principal component analysis (PCA) of proinflammatory markers yielded three clusters: principal component (PC) 1: fibrinogen, white cell count, C-reactive protein; PC 2: plasminogen activator inhibitor-1 (PAI-1), TNF-α, IL-18; PC 3: IL-6 and IL-8. Cross-sectional analyses on proinflammatory PCs and adiponectin, and prospective analyses on 5 year PAI-1 and fibrinogen concentrations were conducted with multiple regression. Total SFA and 16:0 were positively associated with PC 1 and PC 2, and negatively associated with adiponectin. The 14:0 was positively associated with PC 1 and negatively associated with adiponectin. In contrast, 15:0, 20:0, and 22:0 were negatively associated with PC 2, and 20:0 and 22:0 were positively associated with adiponectin. The 18:0 was negatively associated with PC 3. Prospectively, 15:0, 18:0, 20:0, and 22:0 were negatively associated with 5 year PAI-1 concentrations. The results demonstrate that individual SFAs have distinct roles in subclinical inflammation, highlighting the unique metabolic impacts of individual SFAs.
机译:最近的证据表明,单个饱和脂肪酸(SFA)对心脏代谢的影响显着,具有奇数和超长链SFA(VLSFA)的潜在保护作用。研究了个体血清SFA(12:0、14:0、15:0、16:0、18:0、20:0、22:0和总SFA)与促炎性生物标志物和脂联素的横断面和前瞻性关联来自IRAS的555名成年人。促炎标记物的主成分分析(PCA)产生三个聚类:主成分(PC)1:纤维蛋白原,白细胞计数,C反应蛋白; PC 2:纤溶酶原激活物抑制剂-1(PAI-1),TNF-α,IL-18; PC 3:IL-6和IL-8。进行多元回归分析,对促炎性PCs和脂联素进行横断面分析,并对5年PAI-1和纤维蛋白原浓度进行前瞻性分析。总SFA和16:0与PC 1和PC 2正相关,与脂连蛋白负相关。 14:0与PC 1正相关,与脂连蛋白负相关。相反,15:0、20:0和22:0与PC 2呈负相关,而20:0和22:0与脂联素呈正相关。 18:0与PC 3呈负相关。预期15:0、18:0、20:0和22:0与5年PAI-1浓度呈负相关。结果表明,单个SFA在亚临床炎症中具有独特的作用,突出了单个SFA的独特代谢影响。

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