Gut microbiota and acylcarnitine metabolites connect the beneficial association between equol and adiposity in adults: a prospective cohort study

被引:12
作者
Wu, Yan-yan [1 ]
Gou, Wanglong [2 ]
Yan, Yan [1 ]
Liu, Chun-ying [1 ]
Yang, Yingdi [1 ]
Chen, Danyu [1 ]
Xie, Keliang [1 ]
Jiang, Zengliang [2 ]
Fu, Yuanqing [2 ]
Zhu, Hui-lian [3 ]
Zheng, Ju-Sheng [2 ]
Chen, Yu-ming [1 ]
机构
[1] Sun Yat Sen Univ, Sch Publ Hlth, Dept Epidemiol, Guangdong Prov Key Lab Food Nutr & Hlth, Guangzhou, Peoples R China
[2] Westlake Univ, Sch Life Sci, Key Lab Growth Regulat & Translat Res Zhejiang Pr, Hangzhou, Peoples R China
[3] Sun Yat Sen Univ, Sch Publ Hlth, Dept Nutr, Guangdong Prov Key Lab Food Nutr & Hlth, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
equol; gut microbiota; acylcarnitine; obesity; prospective study; PLASMA ACYLCARNITINES; O-DESMETHYLANGOLENSIN; SOY ISOFLAVONES; OBESITY; JAPANESE; PHARMACOKINETICS; OVERWEIGHT; PRODUCERS; DAIDZEIN; VALUES;
D O I
10.1093/ajcn/nqac252
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: Many studies have investigated the effects of soy isoflavones on weight control, but few have focused on the role of equol, a gut-derived metabolite of daidzein with greater bioavailability than other soy isoflavones. Objectives: This study examined the association of equol production with obesity and explored the mediating roles of equol-related gut microbiota and microbial carnitine metabolites. Methods: This 6.6-y prospective study included 2958 Chinese adults (2011 females and 947 males) aged 60.6 +/- 6.0 y (mean +/- SD) at baseline. Urinary equol and isoflavones were measured using HPLC-tandem MS. BMI, percentage fat mass (%FM), and serum triglycerides (TGs) were assessed every 3 y. Metagenomics sequencing and assessment of carnitine metabolites in feces were performed in a subsample of 897 participants. Results: Urinary equol, but not daidzein and genistein, was independently and inversely associated with the obesity-related indicators of BMI, %FM, and a biomarker (TGs). Equol producers (EPs) had lower odds of adiposity conditions and a reduced risk of 6.6-y obesity progression than non-EPs among total participants. Gut microbial analyses indicated that EPs had higher microbiome species richness (P = 3.42 x 10(-5)) and significantly different beta-diversity of gut microbiota compared with the non-EP group (P = 0.001), with 20 of 162 species differing significantly. EPs (compared with non-EPs) had higher abundances of Alistipes senegalensis and Coprococcus catus but lower abundances of Ruminococcus gnavus (false discovery rate <0.05). Among the 7 determined fecal acylcarnitine metabolites, palmitoylcarnitine, oleylcarnitine 18:1, and stearylcarnitine were inversely associated with EPs but positively correlated with obesity conditions and progression. Path analyses indicated that the beneficial association between equol and obesity might be mediated by gut microbiota and decreased production of 3 acylcarnitines in feces. Conclusions: This study suggests a beneficial association between equol and obesity, mediated by the gut microbiome and acylcarnitines, in adults.
引用
收藏
页码:1831 / 1841
页数:11
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