Lipids in Health and Disease (Oct 2023)

Ceramide d18:1/24:1 as a potential biomarker to differentiate obesity subtypes with unfavorable health outcomes

  • Baowen Yu,
  • Moran Hu,
  • Wanzi Jiang,
  • Yizhe Ma,
  • Jingya Ye,
  • Qinyi Wu,
  • Wen Guo,
  • Yan Sun,
  • Min Zhou,
  • Yiwen Xu,
  • Zhoulu Wu,
  • Yiwen Wang,
  • Sin Man Lam,
  • Guanghou Shui,
  • Jingyu Gu,
  • John Zhong Li,
  • Zhenzhen Fu,
  • Yingyun Gong,
  • Hongwen Zhou

DOI
https://doi.org/10.1186/s12944-023-01921-0
Journal volume & issue
Vol. 22, no. 1
pp. 1 – 12

Abstract

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Abstract Background 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. Methods 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). Results 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. Conclusions 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. Trial registration 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.

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