Unique Biomarker Characteristics in Gestational Diabetes Mellitus Identified by LC-MS-Based Metabolic Profiling

被引:8
|
作者
Meng, Xingjun [1 ,2 ]
Zhu, Bo [1 ,2 ]
Liu, Yan [3 ]
Fang, Lei [1 ,2 ]
Yin, Binbin [1 ,2 ]
Sun, Yanni [1 ,2 ]
Ma, Mengni [1 ,2 ]
Huang, Yuli [4 ]
Zhu, Yuning [1 ,2 ]
Zhang, Yunlong [5 ]
机构
[1] Zhejiang Univ, Womens Hosp, Sch Med, Dept Clin Lab, Hangzhou 310006, Peoples R China
[2] Zhejiang Univ, Inst Lab Med, Hangzhou 310006, Peoples R China
[3] Jinan Univ, Sch Tradit Chinese Med, Guangzhou 510632, Peoples R China
[4] Southern Med Univ, Shunde Hosp, Peoples Hosp Shunde Foshan 1, Dept Cardiol, Foshan 528300, Peoples R China
[5] Guangzhou Med Univ, Sch Basic Med Sci, Key Lab Neurosci, Guangzhou 511436, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
CARDIOVASCULAR-DISEASE; ARACHIDONIC-ACID; DOCOSAHEXAENOIC ACIDS; SERUM METABOLITES; INCREASED RISK; FATTY-ACIDS; PREGNANCY; WOMEN; ASSOCIATION; OUTCOMES;
D O I
10.1155/2021/6689414
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background. Gestational diabetes mellitus (GDM) is a type of glucose intolerance disorder that first occurs during women's pregnancy. The main diagnostic method for GDM is based on the midpregnancy oral glucose tolerance test. The rise of metabolomics has expanded the opportunity to better identify early diagnostic biomarkers and explore possible pathogenesis. Methods. We collected blood serum from 34 GDM patients and 34 normal controls for a LC-MS-based metabolomics study. Results. 184 metabolites were increased and 86 metabolites were decreased in the positive ion mode, and 65 metabolites were increased and 71 were decreased in the negative ion mode. Also, it was found that the unsaturated fatty acid metabolism was disordered in GDM. Ten metabolites with the most significant differences were selected for follow-up studies. Since the diagnostic specificity and sensitivity of a single differential metabolite are not definitive, we combined these metabolites to prepare a ROC curve. We found a set of metabolite combination with the highest sensitivity and specificity, which included eicosapentaenoic acid, docosahexaenoic acid, docosapentaenoic acid, arachidonic acid, citric acid, alpha-ketoglutaric acid, and genistein. The area under the curves (AUC) value of those metabolites was 0.984 between the GDM and control group. Conclusions. Our results provide a direction for the mechanism of GDM research and demonstrate the feasibility of developing a diagnostic test that can distinguish between GDM and normal controls clearly. Our findings were helpful to develop novel biomarkers for precision or personalized diagnosis for GDM. In addition, we provide a critical insight into the pathological and biological mechanisms for GDM.
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页数:15
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