| Literature DB >> 33466285 |
Clara Depommier1, Nicolas Flamand2, Rudy Pelicaen1, Dominique Maiter3,4, Jean-Paul Thissen3,4, Audrey Loumaye3,4, Michel P Hermans3,4, Amandine Everard1, Nathalie M Delzenne1, Vincenzo Di Marzo2,5,6, Patrice D Cani1.
Abstract
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.Entities:
Keywords: LBP; NEFA; endocannabinoidome; endocannabinoids; human; leptin; metabolic syndrome; multivariate analysis; obesity
Year: 2021 PMID: 33466285 PMCID: PMC7824762 DOI: 10.3390/cells10010071
Source DB: PubMed Journal: Cells ISSN: 2073-4409 Impact factor: 6.600