Berkowitz Loni, Salazar Cristian, Ryff Carol D, Coe Christopher L, Rigotti Attilio
Center of Molecular Nutrition and Chronic Diseases, Department of Nutrition, Diabetes and Metabolism, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, Chile.
Institute on Aging, University of Wisconsin-Madison, Madison, WI, United States.
Front Cardiovasc Med. 2022 Dec 12;9:1092331. doi: 10.3389/fcvm.2022.1092331. eCollection 2022.
Sphingolipids are components of cell membrane structure, but also circulate in serum and are essential mediators of many cellular functions. While ceramides have been proposed previously as a useful biomarker for cardiometabolic disease, the involvement of other sphingolipids is still controversial. The aim of this study was to investigate the cross-sectional association between blood sphingolipidomic profiles and metabolic syndrome (MetS) as well as other atherosclerotic risk factors in a large population-based study in the U.S.
Clinical data and serum sphingolipidomic profiling from 2,063 subjects who participated in the biomarker project of the Midlife in the United States (MIDUS) study were used.
Consistent with previous reports, we found a positive association between most ceramide levels and obesity, atherogenic dyslipidemia, impaired glucose metabolism, and MetS prevalence. In contrast, most simple β-glycosphingolipids (i.e., hexosylceramides and lactosylceramides) were inversely associated with dysmetabolic biomarkers. However, this latter sphingolipid class showed a positive link with inflammatory and vascular damage-associated biomarkers in subjects with MetS. Through metabolic network analysis, we found that the relationship between ceramides and simple β-glycosphingolipids differed significantly not only according to MetS status, but also with respect to the participants' C-reactive protein levels.
Our findings suggest that a comprehensive sphingolipid profile is more informative about MetS than ceramides alone, and it may reveal new insights into the pathophysiology and further diabetic vs. cardiovascular risk in patients with MetS.
鞘脂是细胞膜结构的组成成分,也在血清中循环,是许多细胞功能的重要介质。虽然此前已提出神经酰胺可作为心脏代谢疾病的有用生物标志物,但其他鞘脂的作用仍存在争议。本研究的目的是在美国一项基于人群的大型研究中,调查血液鞘脂组学谱与代谢综合征(MetS)以及其他动脉粥样硬化危险因素之间的横断面关联。
使用了参与美国中年(MIDUS)研究生物标志物项目的2063名受试者的临床数据和血清鞘脂组学分析结果。
与先前的报告一致,我们发现大多数神经酰胺水平与肥胖、致动脉粥样硬化血脂异常、糖代谢受损和MetS患病率之间呈正相关。相比之下,大多数简单的β-糖鞘脂(即己糖神经酰胺和乳糖神经酰胺)与代谢紊乱生物标志物呈负相关。然而,在后一类鞘脂中,在患有MetS的受试者中,其与炎症和血管损伤相关生物标志物呈正相关。通过代谢网络分析,我们发现神经酰胺和简单β-糖鞘脂之间的关系不仅根据MetS状态有显著差异,而且与参与者的C反应蛋白水平有关。
我们的研究结果表明,综合鞘脂谱比单独的神经酰胺更能提供有关MetS的信息,并且可能揭示MetS患者病理生理学以及进一步的糖尿病与心血管风险方面的新见解。