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肠型可能驱动与饮食相关的心血管代谢危险因素。

Enterotype May Drive the Dietary-Associated Cardiometabolic Risk Factors.

作者信息

de Moraes Ana C F, Fernandes Gabriel R, da Silva Isis T, Almeida-Pititto Bianca, Gomes Everton P, Pereira Alexandre da Costa, Ferreira Sandra R G

机构信息

Department of Epidemiology, School of Public Health, University of São Paulo São Paulo, Brazil.

René Rachou Research Center, Oswaldo Cruz Foundation Belo Horizonte, Brazil.

出版信息

Front Cell Infect Microbiol. 2017 Feb 23;7:47. doi: 10.3389/fcimb.2017.00047. eCollection 2017.

DOI:10.3389/fcimb.2017.00047
PMID:28280715
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5322172/
Abstract

Analyses of typical bacterial clusters in humans named enterotypes may facilitate understanding the host differences in the cardiometabolic profile. It stills unknown whether the three previously described enterotypes were present in populations living below the equator. We examined how the identification of enterotypes could be useful to explain the dietary associations with cardiometabolic risk factors in Brazilian subjects. In this cross-sectional study, a convenience sample of 268 adults (54.2% women) reported their dietary habits and had clinical and biological samples collected. In this study, we analyzed biochemical data and metagenomics of fecal microbiota (16SrRNA sequencing, V4 region). Continuous variables were compared using ANOVA, and categorical variables using chi-square test. Vsearch clustered the operational taxonomic units, and Silva Database provided the taxonomic signatures. Spearman coefficient was used to verify the correlation between bacteria abundances within each enterotype. One hundred subjects were classified as omnivore, 102 lacto-ovo-vegetarians, and 66 strict vegetarians. We found the same structure as the three previously described enterotypes: 111 participants were assigned to , 55 to , and 102 to enterotype. The cluster contained higher amount of strict vegetarians individuals than the other enterotypes (40.0 vs. 20.7 and 20.6, = 0.04). Subjects in this enterotype had a similar anthropometric profile but a lower mean LDL-c concentration than the enterotype (96 ± 23 vs. 109 ± 32 mg/dL, = 0.04). We observed significant correlations between bacterial abundances and cardiometabolic risk factors, but coefficients differed depending on the enterotype. In enterotype, (r BMI = -0.33, = 0.03, and r HDL-c = 0.33, = 0.04), (r 2h glucose = -0.35, = 0.02), (r BMI = -0.36, = 0.02 and r waist = -0.36, = 0.02), and (r insulin = -0.35, = 0.02) abundances were associated to better cardiometabolic profile. The three enterotypes previously described are present in Brazilians, supporting that those bacterial clusters are not population-specific. Diet-independent lower LDL-c levels in subjects from than in other enterotypes suggest that a protective bacterial cluster in the former should be driving this association. Enterotypes seem to be useful to understand the impact of daily diet exposure on cardiometabolic risk factors. Prospective studies are needed to confirm their utility for predicting phenotypes in humans.

摘要

对人类中名为肠型的典型细菌群落进行分析,可能有助于理解宿主在心脏代谢特征方面的差异。目前仍不清楚先前描述的三种肠型是否存在于赤道以南地区的人群中。我们研究了肠型的识别如何有助于解释巴西受试者饮食与心脏代谢风险因素之间的关联。在这项横断面研究中,选取了268名成年人(54.2%为女性)的便利样本,他们报告了自己的饮食习惯,并采集了临床和生物样本。在本研究中,我们分析了粪便微生物群的生化数据和宏基因组学(16SrRNA测序,V4区域)。连续变量使用方差分析进行比较,分类变量使用卡方检验。Vsearch对操作分类单元进行聚类,Silva数据库提供分类特征。使用斯皮尔曼系数来验证每种肠型内细菌丰度之间的相关性。100名受试者被归类为杂食者,102名是蛋奶素食者,66名是严格素食者。我们发现了与先前描述的三种肠型相同的结构:111名参与者被分配到肠型1,55名到肠型2,102名到肠型3。肠型3中严格素食者个体的数量高于其他肠型(40.0%对20.7%和20.6%,P = 0.04)。该肠型的受试者具有相似的人体测量特征,但平均低密度脂蛋白胆固醇(LDL-c)浓度低于肠型1(96±23对109±32mg/dL,P = 0.04)。我们观察到细菌丰度与心脏代谢风险因素之间存在显著相关性,但系数因肠型而异。在肠型3中,拟杆菌属(r体重指数=-0.33,P = 0.03,r高密度脂蛋白胆固醇=0.33,P = 0.04)、双歧杆菌属(r餐后2小时血糖=-0.35,P = 0.02)、普雷沃氏菌属(r体重指数=-0.36,P = 0.02和r腰围=-0.36,P = 0.02)以及罗氏菌属(r胰岛素=-0.35,P = 0.02)的丰度与更好的心脏代谢特征相关。先前描述的三种肠型存在于巴西人中,这支持了这些细菌群落并非特定于某一人群。肠型3受试者中与饮食无关的较低LDL-c水平表明,前者中一种具有保护作用的细菌群落驱动了这种关联。肠型似乎有助于理解日常饮食暴露对心脏代谢风险因素的影响。需要进行前瞻性研究来证实它们在预测人类表型方面的效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a0d/5322172/3604a40907ea/fcimb-07-00047-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a0d/5322172/b96ce2336bbb/fcimb-07-00047-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a0d/5322172/d195ee1b9bc5/fcimb-07-00047-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a0d/5322172/3604a40907ea/fcimb-07-00047-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a0d/5322172/b96ce2336bbb/fcimb-07-00047-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a0d/5322172/d195ee1b9bc5/fcimb-07-00047-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a0d/5322172/3604a40907ea/fcimb-07-00047-g0003.jpg

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