TY - JOUR
T1 - Lipidomic profiling reveals distinct differences in plasma lipid composition in healthy, prediabetic, and type 2 diabetic individuals
AU - Zhong, Huanzi
AU - Fang, Chao
AU - Fan, Yanqun
AU - Lu, Yan
AU - Wen, Bo
AU - Ren, Huahui
AU - Hou, Guixue
AU - Yang, Fangming
AU - Xie, Hailiang
AU - Jie, Zhuye
AU - Peng, Ye
AU - Ye, Zhiqiang
AU - Wu, Jiegen
AU - Zi, Jin
AU - Zhao, Guoqing
AU - Chen, Jiayu
AU - Bao, Xiao
AU - Hu, Yihe
AU - Gao, Yan
AU - Zhang, Jun
AU - Yang, Huanming
AU - Wang, Jian
AU - Madsen, Lise
AU - Kristiansen, Karsten
AU - Ni, Chuanming
AU - Li, Junhua
AU - Liu, Siqi
N1 - Publisher Copyright:
© The Author 2017. Published by Oxford University Press.
PY - 2017/7/1
Y1 - 2017/7/1
N2 - The relationship between dyslipidemia and type 2 diabetes mellitus (T2D) has been extensively reported, but the global lipid profiles, especially in the East Asia population, associated with the development of T2D remain to be characterized. Liquid chromatography coupled to tandem mass spectrometry was applied to detect the global lipidome in the fasting plasma of 293 Chinese individuals, including 114 T2D patients, 81 prediabetic subjects, and 98 individuals with normal glucose tolerance (NGT). Both qualitative and quantitative analyses revealed a gradual change in plasma lipid features with T2D patients exhibiting characteristics close to those of prediabetic individuals, whereas they differed significantly from individuals with NGT. We constructed and validated a random forest classifier with 28 lipidomic features that effectively discriminated T2D from NGT or prediabetes. Most of the selected features significantly correlated with diabetic clinical indices. Hydroxybutyrylcarnitine was positively correlated with fasting plasma glucose, 2-hour postprandial glucose, glycated hemoglobin, and insulin resistance index (HOMA-IR). Lysophosphatidylcholines such as lysophosphatidylcholine (18:0), lysophosphatidylcholine (18:1), and lysophosphatidylcholine (18:2) were all negatively correlated with HOMA-IR. The altered plasma lipidome in Chinese T2D and prediabetic subjects suggests that lipid features may play a role in the pathogenesis of T2D and that such features may provide a basis for evaluating risk and monitoring disease development.
AB - The relationship between dyslipidemia and type 2 diabetes mellitus (T2D) has been extensively reported, but the global lipid profiles, especially in the East Asia population, associated with the development of T2D remain to be characterized. Liquid chromatography coupled to tandem mass spectrometry was applied to detect the global lipidome in the fasting plasma of 293 Chinese individuals, including 114 T2D patients, 81 prediabetic subjects, and 98 individuals with normal glucose tolerance (NGT). Both qualitative and quantitative analyses revealed a gradual change in plasma lipid features with T2D patients exhibiting characteristics close to those of prediabetic individuals, whereas they differed significantly from individuals with NGT. We constructed and validated a random forest classifier with 28 lipidomic features that effectively discriminated T2D from NGT or prediabetes. Most of the selected features significantly correlated with diabetic clinical indices. Hydroxybutyrylcarnitine was positively correlated with fasting plasma glucose, 2-hour postprandial glucose, glycated hemoglobin, and insulin resistance index (HOMA-IR). Lysophosphatidylcholines such as lysophosphatidylcholine (18:0), lysophosphatidylcholine (18:1), and lysophosphatidylcholine (18:2) were all negatively correlated with HOMA-IR. The altered plasma lipidome in Chinese T2D and prediabetic subjects suggests that lipid features may play a role in the pathogenesis of T2D and that such features may provide a basis for evaluating risk and monitoring disease development.
KW - Lipidomics
KW - Plasma
KW - Prediabetes
KW - Type 2 diabetes
UR - https://www.scopus.com/pages/publications/85028430064
U2 - 10.1093/gigascience/gix036
DO - 10.1093/gigascience/gix036
M3 - 文章
C2 - 28505362
AN - SCOPUS:85028430064
SN - 2047-217X
VL - 6
JO - GigaScience
JF - GigaScience
IS - 7
M1 - gix036
ER -