Cortés-Martín Adrián, Iglesias-Aguirre Carlos E, Meoro Amparo, Selma María Victoria, Espín Juan Carlos
Laboratory of Food & Health, Research Group on Quality, Safety, and Bioactivity of Plant Foods, CEBAS-CSIC, Campus de Espinardo, 30100 Murcia, Spain.
Service of Endocrinology, Reina Sofía University Hospital, Avda. Intendente Jorge Palacios s/n, 30003 Murcia, Spain.
Microorganisms. 2020 Mar 15;8(3):416. doi: 10.3390/microorganisms8030416.
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 ( = 69) vs. MetS patients ( = 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.
肠道微生物群(GM)作为对抗多种疾病的新靶点已受到关注,这些疾病包括代谢综合征(MetS),这是一种具有多种因素(糖尿病、肥胖、血脂异常、高血压等)的病理状况,会增加心血管疾病(CVD)风险。然而,与肥胖相关的代谢功能障碍相关的特征性分类学特征的存在仍存在争议。为了研究CVD危险因素和(或)其相关药物治疗对MetS患者GM组成和功能的影响,我们比较了肥胖个体(n = 69)与MetS患者(n = 50)的GM,以及患者内部根据其治疗情况的GM。我们还探讨了药物、GM、临床变量、内毒素血症和短链脂肪酸之间的关联。MetS患者常用的多种药物治疗阻碍了药物与GM谱之间的准确关联。我们的结果突出了MetS患者分类学特征的异质性,这主要取决于CVD危险因素。高血压和(或)其相关药物是塑造GM的主要因素,变形菌门中产生脂多糖的微生物群数量过多。在精准医学的背景下,我们的结果强调,针对GM来预防和(或)治疗MetS时,应根据MetS患者的CVD危险因素和相关药物,更个体化地考虑这些患者。