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脂肪酸作为体内脂质过氧化的决定因素:来自东芬兰高血压和非高血压人群的 EFFGE 研究。

Fatty acids as determinants of in-vivo lipid peroxidation: the EFFGE study in Eastern Finnish hypertensive and non-hypertensive subjects.

机构信息

The Research Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Finland.

出版信息

Ann Med. 2013 Sep;45(5-6):455-64. doi: 10.3109/07853890.2013.809915. Epub 2013 Jul 3.

Abstract

BACKGROUND

The degree of fatty acid (FA) unsaturation as a determinant of lipid peroxidation has been inadequately studied.

METHODS

We examined associations of plasma free F2α-isoprostanes (F2-IsoPs), an indicator of in-vivo lipid peroxidation, with the levels/intake of FAs, adjusted for the risk factors of cardiovascular disease (CVD) in 1211 Finnish men and women, of whom 50% were hypertensive, aged 59.3 ± 8.3 years, mean ± SD.

RESULTS

Elevated age- and sex-adjusted plasma free levels of omega-6 and omega-3 polyunsaturated Fas (PUFAs), saturated FAs (SFAs), and the PUFA/SFA and the omega-6/omega-3 PUFA ratios were all associated with decreased F2-IsoPs. High dietary SFA intake was associated with elevated F2-IsoP concentrations. In a multivariable regression (with clinical, nutritional, and behavioral CVD risk factors), female gender, body mass index (BMI), serum apolipoprotein A1, and NT-proBNP (natriuretic peptide) were positively associated with the F2-IsoPs, whereas the dietary PUFA/SFA ratio, plasma β-carotene, the omega-6/omega-3 PUFA ratio, and protein intake showed inverse associations.

CONCLUSIONS

We propose that elevated lipid peroxidation is associated with several risk factors of CVD, such as a low PUFA/SFA ratio, whereas the FA precursors of lipid peroxidation, i.e. omega-3 and omega-6 PUFAs are associated with attenuated F2-IsoP levels. These findings provide mechanistic support for earlier observations linking PUFA to improved cardiovascular health.

摘要

背景

脂肪酸(FA)饱和度作为脂质过氧化的决定因素,其研究还不够充分。

方法

我们研究了血浆游离 F2α-异前列腺素(F2-IsoPs)与 FA 水平/摄入的相关性,F2-IsoPs 是体内脂质过氧化的一个指标,在 1211 名芬兰男女中进行了心血管疾病(CVD)危险因素的调整,其中 50%为高血压,年龄 59.3±8.3 岁,平均值±标准差。

结果

年龄和性别调整后的血浆游离 ω-6 和 ω-3 多不饱和脂肪酸(PUFA)、饱和脂肪酸(SFA)以及 PUFA/SFA 和 ω-6/ω-3 PUFA 比值升高,与 F2-IsoPs 降低相关。高膳食 SFA 摄入与 F2-IsoP 浓度升高相关。在多变量回归(包含临床、营养和行为性 CVD 危险因素)中,女性性别、体重指数(BMI)、血清载脂蛋白 A1 和 NT-proBNP(脑钠肽)与 F2-IsoPs 呈正相关,而膳食 PUFA/SFA 比值、血浆 β-胡萝卜素、ω-6/ω-3 PUFA 比值和蛋白质摄入与 F2-IsoPs 呈负相关。

结论

我们提出,脂质过氧化升高与 CVD 的几个危险因素相关,如 PUFA/SFA 比值较低,而脂质过氧化的 FA 前体,即 ω-3 和 ω-6 PUFA 与 F2-IsoP 水平降低相关。这些发现为以前将 PUFA 与改善心血管健康联系起来的观察结果提供了机制支持。

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