Mennen L I, Sapinho D, Ito H, Galan P, Hercberg S, Scalbert A
U557 Inserm, U1125 Inra, Cnam, Paris 13/CRNH I-d-F, 74 rue Marcel Cachin, Bobigny, France.
Eur J Clin Nutr. 2008 Apr;62(4):519-25. doi: 10.1038/sj.ejcn.1602744. Epub 2007 Apr 4.
OBJECTIVE: Estimation of dietary intake of polyphenols is difficult, due to limited availability of food composition data and bias inherent to dietary assessment methods. The aim of the present study was to evaluate whether we could detect polyphenols and their metabolites in a spot urine sample in a free-living human population and whether it was related to those observed in 24-h urine samples, for potential use as a biomarkers of polyphenol intake. SUBJECTS: Four 24-h urine samples and two spot urine samples were collected from 154 participants of the SU.VI.MAX cohort (a randomized primary-prevention trial evaluating the effect of daily antioxidant supplementation on chronic diseases) in two separate studies over, respectively, a 7- and 2-day periods. Thirteen polyphenols and metabolites (chlorogenic acid (CGA), caffeic acid (CA), m-coumaric acid (mCOU), gallic acid (GA), 4-O-methylgallic acid (MeGA), quercetin (Q), isorhamnetin (MeQ), kaempferol (K), hesperetin (HESP), naringenin (NAR), phloretin (PHLOR), enterolactone (ENL) and enterodiol (END) were measured using HPLC-ESI-MS-MS. RESULTS: Correlations between the urinary excretion levels were observed. The most significant were explained by metabolic filiations (CGA/CA, CA/mCOU, GA/MeGA, Q/MeQ, NAR/PHLOR, ENL/END) or co-occurrence in a same food source (NAR/HESP). Concentrations in spot samples correlated with those in 24-h urine sample (P<0.02, except for CA and for MeQ). Intra-individual variations were smaller than inter-individual variations for all polyphenols (P<0.01) except for MeGA and for PHLOR. CONCLUSION: These results show that these polyphenols and metabolites are useful biomarkers for polyphenol intake.
目的:由于食物成分数据有限以及膳食评估方法存在固有偏差,多酚类物质的膳食摄入量估算较为困难。本研究的目的是评估在自由生活的人群中,能否从即时尿样中检测到多酚及其代谢物,以及其是否与24小时尿样中观察到的情况相关,以作为多酚摄入量的潜在生物标志物。 对象:在两项独立研究中,分别在7天和2天的时间段内,从SU.VI.MAX队列研究(一项评估每日补充抗氧化剂对慢性病影响的随机一级预防试验)的154名参与者中收集了四份24小时尿样和两份即时尿样。使用HPLC-ESI-MS-MS测定了13种多酚及其代谢物(绿原酸(CGA)、咖啡酸(CA)、间香豆酸(mCOU)、没食子酸(GA)、4-O-甲基没食子酸(MeGA)、槲皮素(Q)、异鼠李素(MeQ)、山奈酚(K)、橙皮素(HESP)、柚皮素(NAR)、根皮素(PHLOR)、肠内酯(ENL)和肠二醇(END))。 结果:观察到尿排泄水平之间的相关性。最显著的相关性由代谢关联(CGA/CA、CA/mCOU、GA/MeGA、Q/MeQ、NAR/PHLOR、ENL/END)或同一食物来源中的共存(NAR/HESP)来解释。即时尿样中的浓度与24小时尿样中的浓度相关(P<0.02,CA和MeQ除外)。除MeGA和PHLOR外,所有多酚的个体内变异均小于个体间变异(P<0.01)。 结论:这些结果表明,这些多酚及其代谢物是多酚摄入量的有用生物标志物。
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