Literature DB >> 29460634

Serum Metabolomics Study of Gliclazide-Modified-Release-Treated Type 2 Diabetes Mellitus Patients Using a Gas Chromatography-Mass Spectrometry Method.

Yang Zhou1,2, Cheng Hu3,4, Xinjie Zhao1,2, Ping Luo1,2, Jingyi Lu3, Qing Li3, Miao Chen3, Dandan Yan3, Xin Lu1,2, Hongwei Kong1,2, Weiping Jia3, Guowang Xu1,2.   

Abstract

Sulfonylureas are one of the commonly used drugs in type 2 diabetes mellitus (T2DM) but with considerable incidence of monotherapy failure. However, the mechanism of patients' drug response is unclear, and suitability evaluation biomarkers are in urgent need for precision medicine. In this study, a pseudotargeted gas chromatography-mass spectrometry method was employed to investigate the serum metabolic profiling of 66 significant responders and 24 nonsignificant responders at baseline and 16 weeks after gliclazide modified-release (MR) monotherapy. Clinical improvements in blood glucose level and insulin sensitivity were closely associated with the alterations of TCA cycle, ketone body metabolism, lipid oxidation, branched-chain amino acid catabolism, and gut flora metabolism. The different baseline metabolic profiling observed in the two groups implied that patients with lower dyslipidemia level may be more suitable for sulfonylurea therapy. The biomarker panel consisting of HbA1c, 5,8,11,14,17-eicosapentaenoic acid, methyl 8,11,14-eicosatrienoate, and methyl hexadecanoate shows a very good prediction ability for the suitability of gliclazide treatment, and it may be meaningful in personalized medicine of T2DM patients by sulfonylurea therapy.

Entities:  

Keywords:  biomarker; gas chromatography−mass spectrometry; gliclazide modified release; metabolomics; sulfonylureas; type 2 diabetes mellitus

Mesh:

Substances:

Year:  2018        PMID: 29460634     DOI: 10.1021/acs.jproteome.7b00866

Source DB:  PubMed          Journal:  J Proteome Res        ISSN: 1535-3893            Impact factor:   4.466


  3 in total

1.  Development of a plasma pseudotargeted metabolomics method based on ultra-high-performance liquid chromatography-mass spectrometry.

Authors:  Fujian Zheng; Xinjie Zhao; Zhongda Zeng; Lichao Wang; Wangjie Lv; Qingqing Wang; Guowang Xu
Journal:  Nat Protoc       Date:  2020-06-24       Impact factor: 13.491

2.  Biomarkers of Metabolomics in Inflammatory Bowel Disease and Damp-Heat Syndrome: A Preliminary Study.

Authors:  Xingxing Wu; Kexin Liu; Qi Wu; Mao Wang; Xuelian Chen; Yuge Li; Lin Qian; Changyin Li; Guoliang Dai; Qide Zhang; Genglin Mu; Jing Wu; Zhaowei Shan
Journal:  Evid Based Complement Alternat Med       Date:  2022-07-01       Impact factor: 2.650

3.  A multi-omics investigation of the molecular characteristics and classification of six metabolic syndrome relevant diseases.

Authors:  Di Chen; Xinjie Zhao; Zhigang Sui; Huan Niu; Luonan Chen; Cheng Hu; Qiuhui Xuan; Xuhong Hou; Rong Zhang; Lina Zhou; Yanli Li; Huiming Yuan; Yukui Zhang; Jiarui Wu; Lihua Zhang; Ren'an Wu; Hai-Long Piao; Guowang Xu; Weiping Jia
Journal:  Theranostics       Date:  2020-01-12       Impact factor: 11.556

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.