Department of Clinical Sciences, Lund University, Malmö, Sweden.
J Clin Endocrinol Metab. 2018 Apr 1;103(4):1491-1501. doi: 10.1210/jc.2017-02114.
Emerging evidence has related the gut microbiome and circulating metabolites to human obesity. Gut microbiota is responsible for several metabolic functions, and altered plasma metabolome might reflect differences in the gut microbiome.
To identify a plasma metabolite profile associated with body mass index (BMI) in a general population and investigate whether such metabolite profile is associated with distinct composition of the gut microbiota.
Targeted profiling of 48 plasma metabolites was performed in a population of 920 Swedish adults (mean age, 39 years; 53% women) from the ongoing Malmö Offspring Study using targeted liquid chromatography-mass spectrometry. Gut microbiota was analyzed by sequencing the 16S ribosomal RNA gene (V1-V3 region) in fecal samples of 674 study participants.
BMI was associated with 19 metabolites (P < 0.001 for all), of which glutamate provided the strongest direct association (P = 5.2e-53). By orthogonal partial least squares regression, a metabolite principal component predictive of BMI was constructed (PCBMI). In addition to glutamate, PCBMI was dominated by branched-chain amino acids (BCAAs) and related metabolites. Four gut microbiota genera (Blautia, Dorea, Ruminococcus, and SHA-98) were associated with both BMI and PCBMI (P < 8.0e-4 for all). When simultaneously regressing PCBMI and metabolite-associated gut bacteria against BMI, only PCBMI remained statistically significant.
We discovered associations between four gut microbiota genera (Blautia, Dorea, Ruminococcus, and SHA-98) and BMI-predictive plasma metabolites, including glutamate and BCAAs. Thus, these metabolites could be mediators between gut microbiota and obesity, pointing to potential future opportunities for targeting the gut microbiota in prevention of obesity.
越来越多的证据表明肠道微生物组和循环代谢物与人类肥胖有关。肠道微生物群负责多种代谢功能,而改变的血浆代谢组可能反映了肠道微生物群的差异。
在一般人群中确定与体重指数(BMI)相关的血浆代谢物谱,并研究这种代谢物谱是否与肠道微生物群的不同组成有关。
使用靶向液相色谱-质谱法对来自正在进行的马尔默后代研究的 920 名瑞典成年人(平均年龄 39 岁,53%为女性)的 48 种血浆代谢物进行靶向分析。通过对 674 名研究参与者的粪便样本进行 16S 核糖体 RNA 基因(V1-V3 区)测序,分析肠道微生物群。
BMI 与 19 种代谢物相关(所有 P < 0.001),其中谷氨酸提供了最强的直接关联(P = 5.2e-53)。通过正交偏最小二乘回归,构建了一个可预测 BMI 的代谢物主成分(PCBMI)。除了谷氨酸,PCBMI 还主要由支链氨基酸(BCAAs)和相关代谢物组成。有 4 种肠道微生物属(Blautia、Dorea、Ruminococcus 和 SHA-98)与 BMI 和 PCBMI 均相关(所有 P < 8.0e-4)。当同时将 PCBMI 和与代谢物相关的肠道细菌回归到 BMI 时,只有 PCBMI 仍然具有统计学意义。
我们发现了四种肠道微生物属(Blautia、Dorea、Ruminococcus 和 SHA-98)与 BMI 预测性血浆代谢物之间的关联,包括谷氨酸和 BCAAs。因此,这些代谢物可能是肠道微生物群和肥胖之间的中介物,为靶向肠道微生物群预防肥胖提供了潜在的未来机会。