American Diabetes Association
DC211520_Suppliments.pdf (1.57 MB)

Circulating Palmitoyl Sphingomyelin Is Associated With Cardiovascular Disease in Individuals With Type 2 Diabetes: Findings From the China Da Qing Diabetes Study

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posted on 2022-02-01, 20:09 authored by Yanyan Chen, Hongmei Jia, Xin Qian, Jinping Wang, Meng Yu, Qiuhong Gong, Yali An, Hui Li, Sidong Li, Na Shi, Zhongmei Zou, Guangwei Li
OBJECTIVE To investigate the association of potential cardiovascular disease (CVD) biomarkers in patients with type 2 diabetes.


We enrolled 120 participants (aged 61.5–69.5 years) with type 2 diabetes and 60 (aged 62.5-73.5 years) with normal glucose tolerance in the discovery group from the original Da Qing Diabetes Study. Their diabetes status was confirmed in 1986; then, the participants were followed over 23 years to collect CVD outcome data. Untargeted and targeted metabolomics analyses based on UPLC-MS/MS were used to identify potential markers. Multivariable regression analysis was used to evaluate the association between metabolites and CVD outcomes. An independent group of 335 patients (aged 67.0–77.0 years) with diabetes was used for biomarker validation.

RESULTS In the discovery group, untargeted metabolomics analysis found 16 lipids and fatty acids metabolites associated with CVD risk in patients with diabetes, with palmitoyl sphingomyelin (PSM) having the strongest association. Plasma PSM concentrations were significantly higher in cases of diabetes with CVD than without (41.68 ± 10.47 vs. 9.69 ± 1.47 μg/mL; P < 0.0001). The odds ratio (OR) of CVD for 1 µg/mL PSM change was 1.19 (95% confidence interval [CI] 1.13–1.25) after adjustment of clinical confounders. The validation study confirmed that PSM was significantly associated with increased CVD risk in diabetes (OR, 1.22; 95% CI, 1.16–1.30).

CONCLUSIONS Changes in lipid and fatty acid content were significantly associated with CVD risk in the diabetic Chinese population. PSM is a potential biomarker of increased CVD risk in diabetes.


This study was funded by the Chinese Academy of Medical Sciences, Novo Nordisk Union Diabetes Research Talent Fund (UTF). This work was part of the China Da Qing Diabetes Study Follow-Up Study, which was supported by CDC/WHO Cooperative Agreement (U58/CCU424123-01-02), the China-Japan Friendship Hospital, Da Qing First Hospital and the Chinese Academy of Medical Sciences Innovation Fund for Medical Sciences (CIFMS) (2020-I2M-2-006).


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