Integrated biomarker profiling of the metabolome associated with type 2 diabetes mellitus among Tibetan in China

被引:2
作者
Meng, Jinli [1 ]
Huang, Fangfang [2 ]
Shi, Jing [3 ,4 ]
Zhang, Chenghui [5 ]
Feng, Li [1 ]
Wang, Suyuan [5 ]
Li, Hengyan [1 ]
Guo, Yongyue [1 ]
Hu, Xin [1 ]
Li, Xiaomei [1 ]
He, Wanlin [1 ]
Cheng, Jian [6 ]
Wu, Yunhong [5 ]
机构
[1] Hosp Chengdu Off Peoples Govt Tibetan Autonomous R, Dept Radiol, 20 Xi Mian Qiao Heng Jie, Chengdu, Sichuan, Peoples R China
[2] Hubei Univ Chinese Med, Wuhan 430065, Peoples R China
[3] Hosp Chengdu Off Peoples Govt Tibetan Autonomous R, Dept Sci, 20 Xi Mian Qiao Heng Jie, Chengdu, Sichuan, Peoples R China
[4] Hosp Chengdu Off Peoples Govt Tibetan Autonomous R, Educ Sect, 20 Xi Mian Qiao Heng Jie, Chengdu, Sichuan, Peoples R China
[5] Hosp Chengdu Off Peoples Govt Tibetan Autonomous R, Dept Endocrinol & Metab, 20 Xi Mian Qiao Heng Jie, Chengdu, Sichuan, Peoples R China
[6] Sichuan Univ, West China Hosp, Dept Neurosurg, Chengdu, Peoples R China
关键词
Tibetan; Type 2 diabetes mellitus; Serum metabolomics; Machine learning; Biomarker; SERUM URIC-ACID; INSULIN-RESISTANCE; FASTING GLUCOSE; PLASMA-GLUCOSE; PREVALENCE; RISK; PROGRESSION; MARKERS; HEALTH;
D O I
10.1186/s13098-023-01124-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
IntroductionMetabolomic signatures of type 2 diabetes mellitus (T2DM) in Tibetan Chinese population, a group with high diabetes burden, remain largely unclear. Identifying the serum metabolite profile of Tibetan T2DM (T-T2DM) individuals may provide novel insights into early T2DM diagnosis and intervention.MethodsHence, we conducted untargeted metabolomics analysis of plasma samples from a retrospective cohort study with 100 healthy controls and 100 T-T2DM patients by using liquid chromatography-mass spectrometry.ResultsThe T-T2DM group had significant metabolic alterations that are distinct from known diabetes risk indicators, such as body mass index, fasting plasma glucose, and glycosylated hemoglobin levels. The optimal metabolite panels for predicting T-T2DM were selected using a tenfold cross-validation random forest classification model. Compared with the clinical features, the metabolite prediction model provided a better predictive value. We also analyzed the correlation of metabolites with clinical indices and found 10 metabolites that were independently predictive of T-T2DM.ConclusionBy using the metabolites identified in this study, we may provide stable and accurate biomarkers for early T-T2DM warning and diagnosis. Our study also provides a rich and open-access data resource for optimizing T-T2DM management.
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页数:12
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