Fernández-Navarro Tania, Salazar Nuria, Gutiérrez-Díaz Isabel, de Los Reyes-Gavilán Clara G, Gueimonde Miguel, González Sonia
Area of Physiology, Department of Functional Biology, University of Oviedo, 33006 Asturias, Spain.
Department of Microbiology and Biochemistry of Dairy Products, Instituto de Productos Lácteos de Asturias, Consejo Superior de Investigaciones Científicas (IPLA-CSIC), Paseo Río Linares s/n, Villaviciosa, 33300 Asturias, Spain.
Nutrients. 2017 May 27;9(6):551. doi: 10.3390/nu9060551.
Obesity has been related to an increased risk of multiple diseases in which oxidative stress and inflammation play a role. Gut microbiota has emerged as a mediator in this interaction, providing new mechanistic insights at the interface between fat metabolism dysregulation and obesity development. Our aim was to analyze the interrelationship among obesity, diet, oxidative stress, inflammation and the intestinal microbiota in 68 healthy adults (29.4% normal-weight). Diet was assessed through a food frequency questionnaire and converted into nutrients and dietary compounds using food composition tables. The intestinal microbiota was assessed by quantitative PCR, fecal short chain fatty acids by gas chromatography and serum biomarkers by standard protocols. Higher levels of malondialdehyde (MDA), C reactive protein (CRP), serum leptin, glucose, fat percentage and the intestinal group were found in the obese people. Cluster analysis of body mass index, fat mass, glucose, LDL/HDL ratio, leptin, MDA and CRP classified the subjects into two groups. The levels of the intestinal group were lower in the cluster and linked to a higher pro-oxidant and pro-inflammatory status, whose individuals also had lower intake of fruits, dried fruits, and fish. These results could be useful for designing strategies targeted to obesity prevention.
肥胖与多种疾病风险增加相关,氧化应激和炎症在这些疾病中起作用。肠道微生物群已成为这种相互作用的介质,在脂肪代谢失调与肥胖发展之间的界面提供了新的机制见解。我们的目的是分析68名健康成年人(29.4%体重正常)中肥胖、饮食、氧化应激、炎症和肠道微生物群之间的相互关系。通过食物频率问卷评估饮食,并使用食物成分表将其转化为营养素和膳食化合物。通过定量PCR评估肠道微生物群,通过气相色谱法评估粪便短链脂肪酸,通过标准方案评估血清生物标志物。肥胖人群中丙二醛(MDA)、C反应蛋白(CRP)、血清瘦素、葡萄糖、脂肪百分比和肠道菌群水平较高。对体重指数、脂肪量、葡萄糖、低密度脂蛋白/高密度脂蛋白比值、瘦素、MDA和CRP进行聚类分析,将受试者分为两组。肠道菌群水平在聚类中较低,且与较高的促氧化和促炎状态相关,这些个体的水果、干果和鱼类摄入量也较低。这些结果可能有助于设计针对肥胖预防的策略。