Relationships between gut microbiota, plasma metabolites, and metabolic syndrome traits in the METSIM cohort

被引:259
作者
Org, Elin [1 ,2 ]
Blum, Yuna [1 ]
Kasela, Silva [2 ,3 ]
Mehrabian, Margarete [1 ]
Kuusisto, Johanna [4 ,5 ]
Kangas, Antti J. [6 ,7 ]
Soininen, Pasi [6 ,7 ,8 ]
Wang, Zeneng [9 ]
Ala-Korpela, Mika [6 ,7 ,8 ,10 ,11 ]
Hazen, Stanley L. [9 ]
Laakso, Markku [4 ,5 ]
Lusis, Aldons J. [1 ,12 ,13 ]
机构
[1] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90095 USA
[2] Univ Tartu, Estonian Genome Ctr, EE-51010 Tartu, Estonia
[3] Univ Tartu, Inst Mol & Cell Biol, EE-51010 Tartu, Estonia
[4] Univ Eastern Finland, Inst Clin Med, Internal Med, Kuopio, Finland
[5] Kuopio Univ Hosp, Kuopio, Finland
[6] Univ Oulu, Computat Med, Fac Med, Oulu, Finland
[7] Bioctr Oulu, Oulu, Finland
[8] Univ Eastern Finland, Sch Pharm, NMR Metabol Lab, Kuopio, Finland
[9] Cleveland Clin, Dept Cellular & Mol Med, Cleveland, OH 44195 USA
[10] Univ Bristol, Sch Social & Community Med, Computat Med, Bristol, Avon, England
[11] Univ Bristol, MRC, Integrat Epidemiol Unit, Bristol, Avon, England
[12] Univ Calif Los Angeles, Dept Human Genet, Los Angeles, CA 90095 USA
[13] Univ Calif Los Angeles, Dept Microbiol Immunol & Mol Genet, Los Angeles, CA 90095 USA
基金
美国国家卫生研究院; 英国医学研究理事会;
关键词
Host-microbiota interactions; TMAO; Metabolic traits; Serum metabolites; Type; 2; diabetes; INSULIN SENSITIVITY; L-CARNITINE; HIGH-FAT; RISK; POPULATION; DIET; PHOSPHATIDYLCHOLINE; ENTEROTYPES; DIVERSITY; REVEALS;
D O I
10.1186/s13059-017-1194-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: The gut microbiome is a complex and metabolically active community that directly influences host phenotypes. In this study, we profile gut microbiota using 16S rRNA gene sequencing in 531 well-phenotyped Finnish men from the Metabolic Syndrome In Men (METSIM) study. Results: We investigate gut microbiota relationships with a variety of factors that have an impact on the development of metabolic and cardiovascular traits. We identify novel associations between gut microbiota and fasting serum levels of a number of metabolites, including fatty acids, amino acids, lipids, and glucose. In particular, we detect associations with fasting plasma trimethylamine N-oxide (TMAO) levels, a gut microbiota-dependent metabolite associated with coronary artery disease and stroke. We further investigate the gut microbiota composition and microbiota-metabolite relationships in subjects with different body mass index and individuals with normal or altered oral glucose tolerance. Finally, we perform microbiota co-occurrence network analysis, which shows that certain metabolites strongly correlate with microbial community structure and that some of these correlations are specific for the pre-diabetic state. Conclusions: Our study identifies novel relationships between the composition of the gut microbiota and circulating metabolites and provides a resource for future studies to understand host-gut microbiota relationships.
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收藏
页数:14
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