Department of Endocrinology, the First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, China.
Lipids Health Dis. 2023 Oct 4;22(1):166. doi: 10.1186/s12944-023-01921-0.
The criteria for metabolically healthy obesity (MHO) and metabolically unhealthy obesity (MUO) remain controversial. This research aimed to identify a potential biomarker to differentiate the subtypes of obesity.
The study conducted a lipidomic evaluation of ceramide in the serum of 77 Chinese adults who had undergone hyperinsulinemic-euglycemic clamps. These adults were divided into three groups according to the clinical data: normal weight control group (N = 21), MHO (N = 20), and MUO (N = 36).
The serum Cer d18:1/24:1 level in the MHO group was lower than that in the MUO group. As the Cer d18:1/24:1 level increased, insulin sensitivity decreased, and the unfavorable parameters increased in parallel. Multivariate logistic regression analysis revealed that serum Cer d18:1/24:1 levels were independently correlated with MUO in obesity. Individuals with higher levels of Cer d18:1/24:1 also had an elevated risk of cardiovascular disease. Most ceramide subtype levels increased in obesity compared to normal-weight individuals, but the levels of serum Cer d18:0/18:0 and Cer d18:1/16:0 decreased in obesity.
The relationships between ceramide subtypes and metabolic profiles might be heterogeneous in populations with different body weights. Cer d18:1/24:1 could be a biomarker that can be used to differentiate MUO from MHO, and to better predict who will develop unfavorable health outcomes among obese individuals.
The First Affiliated Hospital of Nanjing Medical University's Institutional Review Board authorized this study protocol, and all participants provided written informed consent (2014-SR-003) prior to study entry.
代谢健康肥胖(MHO)和代谢不健康肥胖(MUO)的标准仍存在争议。本研究旨在寻找一种潜在的生物标志物来区分肥胖的亚型。
本研究对 77 名接受高胰岛素正葡萄糖钳夹术的中国成年人的血清神经酰胺进行了脂质组学评估。根据临床数据,这些成年人分为三组:正常体重对照组(N=21)、MHO(N=20)和 MUO(N=36)。
MHO 组血清 Cer d18:1/24:1 水平低于 MUO 组。随着 Cer d18:1/24:1 水平的升高,胰岛素敏感性降低,不利参数平行升高。多变量 logistic 回归分析显示,血清 Cer d18:1/24:1 水平与肥胖中的 MUO 独立相关。Cer d18:1/24:1 水平较高的个体患心血管疾病的风险也较高。与正常体重个体相比,大多数神经酰胺亚型水平在肥胖中升高,但血清 Cer d18:0/18:0 和 Cer d18:1/16:0 水平在肥胖中降低。
在体重不同的人群中,神经酰胺亚型与代谢谱之间的关系可能存在异质性。Cer d18:1/24:1 可能是一种生物标志物,可用于区分 MUO 与 MHO,并更好地预测肥胖个体中哪些人会出现不利的健康结果。
南京医科大学第一附属医院机构审查委员会授权了这项研究方案,所有参与者在研究入组前均签署了书面知情同意书(2014-SR-003)。