Plasma signature metabolites of dietary fat intake characterize associations with prevalent metabolic syndrome

IF 6.9 Q1 FOOD SCIENCE & TECHNOLOGY Food frontiers Pub Date : 2024-10-16 DOI:10.1002/fft2.505
Xuzhi Wan, Hongbo Shi, Wei Jia, Li Zhu, Yimei Tian, Denghui Meng, Anli Wang, Yaoran Li, Xiaohui Liu, Haoyu Li, Lange Zhang, Pan Zhuang, Yu Zhang, Jingjing Jiao
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Abstract

The metabolic response to dietary fat intake and its relation with metabolic syndrome (MetS) remains unclear. Here, we identified dietary fat related signature metabolites and characterized their associations with MetS prevalence. We enrolled 236 participants from the Precision Nutrition and Food Safety for Dietary Prevention of Chronic Disease study in China. Nontargeted metabolomics was conducted to investigate plasma metabolome. The signature metabolites in relation to dietary fat intake were assessed using elastic net regression with a 10-fold cross-validation. We identified multi-metabolite profiles comprising of 28, 19, 23, 31, and 25 metabolites, which were robustly correlated with dietary intake of saturated fatty acids, monounsaturated fatty acids, polyunsaturated fatty acids (PUFAs), n − 3 PUFAs, and n − 6 PUFAs, respectively (r = .47–.54; p < .001). After adjustment for potential risk factors, metabolic signatures of PUFAs and n − 3 PUFAs were inversely associated with 31% and 48% lower MetS prevalence, respectively. Dietary intake of n − 3 and n − 6 PUFAs ameliorates key metabolites involved in the glyoxylate and dicarboxylate metabolism, arginine biosynthesis, and tricarboxylic acid cycle. Our findings revealed plasma metabolic signatures characterizing dietary fat intake and supported the beneficial role of PUFAs especially n − 3 PUFAs in MetS prevention.

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膳食脂肪摄入的血浆特征代谢物与普遍代谢综合征的相关性
膳食脂肪摄入的代谢反应及其与代谢综合征(MetS)的关系尚不清楚。在这里,我们确定了与膳食脂肪相关的特征代谢物,并描述了它们与MetS患病率的关系。我们招募了236名来自中国精准营养和食品安全饮食预防慢性病研究的参与者。采用非靶向代谢组学研究血浆代谢组学。与膳食脂肪摄入相关的标志性代谢物采用弹性净回归和10倍交叉验证进行评估。我们确定了包括28、19、23、31和25种代谢物的多代谢物谱,这些代谢物分别与饮食中饱和脂肪酸、单不饱和脂肪酸、多不饱和脂肪酸(PUFAs)、n - 3 PUFAs和n - 6 PUFAs的摄入量密切相关(r = 0.47 - 0.54;p & lt;措施)。在对潜在危险因素进行调整后,PUFAs和n - 3 PUFAs的代谢特征分别与31%和48%的MetS患病率降低呈负相关。饮食中摄入n - 3和n - 6 PUFAs可改善参与乙醛酸和二羧酸代谢、精氨酸生物合成和三羧酸循环的关键代谢产物。我们的研究结果揭示了表征膳食脂肪摄入的血浆代谢特征,并支持PUFAs特别是n - 3 PUFAs在MetS预防中的有益作用。
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CiteScore
10.50
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0
审稿时长
10 weeks
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