Metabolism and Nutrition Research Group, Louvain Drug Research Institute, Walloon Excellence in Life Sciences and Biotechnology (WELBIO), UCLouvain, Université Catholique de Louvain, Av. E. Mounier, 73 B1.73.11, 1200 Brussels, Belgium.
Quebec Heart and Lung Institute Research Centre, Université Laval, Quebec City, QC G1V 0A6, Canada.
Cells. 2021 Jan 5;10(1):71. doi: 10.3390/cells10010071.
The global obesity epidemic continues to rise worldwide. In this context, unraveling new interconnections between biological systems involved in obesity etiology is highly relevant. Dysregulation of the endocannabinoidome (eCBome) is associated with metabolic complications in obesity. This study aims at deciphering new associations between circulating endogenous bioactive lipids belonging to the eCBome and metabolic parameters in a population of overweight or obese individuals with metabolic syndrome. To this aim, we combined different multivariate exploratory analysis methods: canonical correlation analysis and principal component analysis, revealed associations between eCBome subsets, and metabolic parameters such as leptin, lipopolysaccharide-binding protein, and non-esterified fatty acids (NEFA). Subsequent construction of predictive regression models according to the linear combination of selected endocannabinoids demonstrates good prediction performance for NEFA. Descriptive approaches reveal the importance of specific circulating endocannabinoids and key related congeners to explain variance in the metabolic parameters in our cohort. Analysis of quartiles confirmed that these bioactive lipids were significantly higher in individuals characterized by important levels for aforementioned metabolic variables. In conclusion, by proposing a methodology for the exploration of large-scale data, our study offers additional evidence of the existence of an interplay between eCBome related-entities and metabolic parameters known to be altered in obesity.
全球肥胖症患病率持续在全球范围内上升。在这种背景下,揭示肥胖病因学中涉及的生物系统之间的新联系具有重要意义。内源性大麻素系统的失调与肥胖症的代谢并发症有关。本研究旨在阐明肥胖合并代谢综合征人群中循环内源性生物活性脂质与代谢参数之间的新关联。为此,我们结合了不同的多元探索性分析方法:典型相关分析和主成分分析,揭示了内源性大麻素系统亚群与代谢参数(如瘦素、脂多糖结合蛋白和非酯化脂肪酸 (NEFA))之间的关联。根据选定的内源性大麻素的线性组合构建预测回归模型,表明对 NEFA 具有良好的预测性能。描述性方法揭示了特定循环内源性大麻素及其关键相关同系物对解释我们队列中代谢参数变化的重要性。四分位数分析证实,这些生物活性脂质在上述代谢变量水平重要的个体中显著升高。总之,通过提出一种探索大规模数据的方法,本研究为内源性大麻素系统相关实体与肥胖症中已知改变的代谢参数之间存在相互作用提供了额外证据。