Maqoud Fatima, Calabrese Francesco Maria, Celano Giuseppe, Mallardi Domenica, Goscilo Francesco, D'Attoma Benedetta, Ignazzi Antonia, Linsalata Michele, Bitetto Gabriele, Di Chito Martina, Pesole Pasqua Letizia, Diciolla Arianna, Apa Carmen Aurora, De Pergola Giovanni, Giannelli Gianluigi, De Angelis Maria, Russo Francesco
Functional Gastrointestinal Disorders Research Group, National Institute of Gastroenterology IRCCS "Saverio de Bellis", Castellana Grotte, 70013 Bari, Italy.
Department of Soil, Plant and Food Science, University of Bari Aldo Moro, 70126 Bari, Italy.
Nutrients. 2024 Dec 28;17(1):72. doi: 10.3390/nu17010072.
This study explores the link between body mass index (BMI), intestinal permeability, and associated changes in anthropometric and impedance parameters, lipid profiles, inflammatory markers, fecal metabolites, and gut microbiota taxa composition in participants having excessive body mass.
A cohort of 58 obese individuals with comparable diet, age, and height was divided into three groups based on a priori clustering analyses that fit with BMI class ranges: Group I (25-29.9), Group II (30-39.9), and Group III (>40). Anthropometric and clinical parameters were assessed, including plasma C-reactive protein and cytokine profiles as inflammation markers. Intestinal permeability was measured using a multisaccharide assay, with fecal/serum zonulin and serum claudin-5 and claudin-15 levels. Fecal microbiota composition and metabolomic profiles were analyzed using a phylogenetic microarray and GC-MS techniques.
The statistical analyses of the clinical parameters were based on the full sample set, whereas a subset composed of 37 randomized patients was inspected for the GC/MS metabolite profiling of fecal specimens. An increase in potentially pro-inflammatory bacterial genera (e.g., , , ) and a reduction in beneficial genera (e.g., , Clostridia UCG-014, ) were measured. The gas chromatography/mass spectrometry analysis of urine samples evidenced a statistically significant increase in m-cymen-8-ol, 1,3,5-Undecatriene, (E, Z) and a decreased concentration of p-cresol, carvone, p-cresol, and nonane.
Together, these data demonstrated how an increased BMI led to significant changes in inflammatory markers, intestinal barrier metabolites, glucose metabolism, endocrine indicators, and fecal metabolomic profiles that can indicate a different metabolite production from gut microbiota. Our findings suggest that targeting intestinal permeability may offer a therapeutic approach to prevent and manage obesity and related metabolic complications, reinforcing the link between gut barrier function and obesity.
本研究探讨体重指数(BMI)、肠道通透性以及超重参与者人体测量和阻抗参数、血脂谱、炎症标志物、粪便代谢物和肠道微生物群分类组成的相关变化之间的联系。
根据符合BMI分类范围的先验聚类分析,将58名饮食、年龄和身高相近的肥胖个体分为三组:第一组(25 - 29.9)、第二组(30 - 39.9)和第三组(>40)。评估人体测量和临床参数,包括作为炎症标志物的血浆C反应蛋白和细胞因子谱。使用多糖测定法测量肠道通透性,检测粪便/血清连蛋白和血清闭合蛋白-5及闭合蛋白-15水平。使用系统发育微阵列和气相色谱-质谱技术分析粪便微生物群组成和代谢组学谱。
临床参数的统计分析基于完整样本集,而对由37名随机患者组成的子集进行粪便标本的气相色谱/质谱代谢物谱分析。检测到潜在促炎细菌属(如, , )增加,有益菌属(如,梭菌属UCG - 014, )减少。尿液样本的气相色谱/质谱分析表明,间伞花烃-8-醇、1,3,5-十一碳三烯(E,Z)有统计学显著增加,对甲酚、香芹酮、对甲酚和壬烷浓度降低。
这些数据共同表明,BMI升高如何导致炎症标志物、肠道屏障代谢物、葡萄糖代谢、内分泌指标和粪便代谢组学谱发生显著变化,这些变化可能表明肠道微生物群产生了不同的代谢物。我们的研究结果表明,针对肠道通透性可能提供一种预防和管理肥胖及相关代谢并发症的治疗方法,加强了肠道屏障功能与肥胖之间的联系。