Department of Public and Population Health Sciences, Keck School of Medicine of the University of Southern California, Los Angeles, CA, 90032, USA.
Department of Integrative Physiology, University of Colorado, Boulder, CO, USA.
Sci Rep. 2024 Mar 28;14(1):7384. doi: 10.1038/s41598-024-57751-2.
To assess cardiometabolic profiles and proteomics to identify biomarkers associated with the metabolically healthy and unhealthy obesity. Young adults (N = 156) enrolled were classified as not having obesity, metabolically healthy obesity (MHO) and metabolically unhealthy obesity (MUHO) based on NCEP ATP-III criteria. Plasma proteomics at study entry were measured using Olink Cardiometabolic Explore panel. Linear regression was used to assess associations between proteomics and obesity groups as well as cardiometabolic traits of glucose, insulin, and lipid profiles at baseline and follow-up visits. Enriched biological pathways were further identified based on the significant proteomic features. Among the baseline 95 (61%) and 61 (39%) participants classified as not having obesity and having obesity (8 MHO and 53 MUHO), respectively. Eighty of the participants were followed-up with an average 4.6 years. Forty-one proteins were associated with obesity (FDR < 0.05), 29 of which had strong associations with insulin-related traits and lipid profiles (FDR < 0.05). Inflammation, immunomodulation, extracellular matrix remodeling and endoplasmic reticulum lumen functions were enriched by 40 proteins. In this study population, obesity and MHO were associated with insulin resistance and dysregulated lipid profiles. The underlying mechanism included elevated inflammation and deteriorated extracellular matrix remodeling function.
评估心脏代谢特征和蛋白质组学,以确定与代谢健康和不健康肥胖相关的生物标志物。根据 NCEP ATP-III 标准,纳入的年轻成年人(N=156)被分为非肥胖、代谢健康肥胖(MHO)和代谢不健康肥胖(MUHO)。使用 Olink 心脏代谢探索面板测量研究开始时的血浆蛋白质组学。线性回归用于评估蛋白质组学与肥胖组之间的关联,以及基线和随访时葡萄糖、胰岛素和脂质谱的心脏代谢特征。根据显著的蛋白质组学特征进一步确定富集的生物学途径。在基线时,分别有 95 名(61%)和 61 名(39%)参与者被归类为非肥胖和肥胖(8 名 MHO 和 53 名 MUHO)。其中 80 名参与者进行了平均 4.6 年的随访。有 41 种蛋白质与肥胖相关(FDR<0.05),其中 29 种与胰岛素相关特征和脂质谱有很强的关联(FDR<0.05)。有 40 种蛋白质与炎症、免疫调节、细胞外基质重塑和内质网腔功能有关。在本研究人群中,肥胖和 MHO 与胰岛素抵抗和脂质谱失调有关。其潜在机制包括炎症升高和细胞外基质重塑功能恶化。