There is No Distinctive Gut Microbiota Signature in the Metabolic Syndrome: Contribution of Cardiovascular Disease Risk Factors and Associated Medication

被引:19
作者
Cortes-Martin, Adrian [1 ]
Iglesias-Aguirre, Carlos E. [1 ]
Meoro, Amparo [2 ]
Victoria Selma, Maria [1 ]
Carlos Espin, Juan [1 ]
机构
[1] CEBAS CSIC, Lab Food & Hlth, Res Grp Qual Safety & Bioact Plant Foods, Campus Espinardo, Murcia 30100, Spain
[2] Reina Sofia Univ Hosp, Serv Endocrinol, Avda Intendente Jorge Palacios S-N, Murcia 30003, Spain
关键词
Gut microbiota; metabolic syndrome; obesity; cardiovascular risk; drug treatment; diabetes; dyslipidemia; hypertension; precision medicine; CHAIN FATTY-ACIDS; OBESITY; RECOMMENDATIONS; MANAGEMENT;
D O I
10.3390/microorganisms8030416
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The gut microbiota (GM) has attracted attention as a new target to combat several diseases, including metabolic syndrome (MetS), a pathological condition with many factors (diabetes, obesity, dyslipidemia, hypertension, etc.) that increase cardiovascular disease (CVD) risk. However, the existence of a characteristic taxonomic signature associated with obesity-related metabolic dysfunctions is under debate. To investigate the contribution of the CVD risk factors and(or) their associated drug treatments in the composition and functionality of GM in MetS patients, we compared the GM of obese individuals (n = 69) vs. MetS patients (n = 50), as well as within patients, depending on their treatments. We also explored associations between medication, GM, clinical variables, endotoxemia, and short-chain fatty acids. Poly-drug treatments, conventional in MetS patients, prevented the accurate association between medication and GM profiles. Our results highlight the heterogeneity of taxonomic signatures in MetS patients, which mainly depend on the CVD risk factors. Hypertension and(or) its associated medication was the primary trait involved in the shaping of GM, with an overabundance of lipopolysaccharide-producing microbial groups from the Proteobacteria phylum. In the context of precision medicine, our results highlight that targeting GM to prevent and(or) treat MetS should consider MetS patients more individually, according to their CVD risk factors and associated medication.
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页数:18
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