TY - JOUR
T1 - Serum metabolic signatures of fulminant type 1 diabetes
AU - Jia, Weiping
AU - Jia, Wei
AU - Lu, Jingyi
AU - Zhou, Jian
AU - Bao, Yuqian
AU - Chen, Tianlu
AU - Zhang, Yinan
AU - Zhao, Aihua
AU - Qiu, Yunping
AU - Xie, Guoxiang
AU - Wang, Congrong
PY - 2012/9/7
Y1 - 2012/9/7
N2 - Fulminant type 1 diabetes (FT1DM) is a relatively new clinical entity featured by acute destruction of pancreatic beta cells. Clinical consequences of FT1DM could be fatal when timely medications are not provided, suggesting the particular importance of rapid and accurate diagnosis. Here we report a serum metabonomics study of FT1DM patients, together with healthy control subjects (NC), type 2 diabetes (T2DM), classic type 1 diabetes (T1DM), and diabetic ketoacidosis (DKA) patients, with the aim of discovering metabolic markers associated with FT1DM. A total of 79 subjects were enrolled (22 NC, 22 T1DM, 22 T2DM, 8 DKA and 5 FT1DM) and the serum metabolic profiling of fasting blood samples was performed using gas chromatography time-of-flight mass spectrometry (GC-TOFMS) coupled with multivariate and univariate statistical analyses. Serum metabolites differentially expressed in FT1DM relative to NC, or to T2DM, T1DM and DKA were identified. Three metabolite markers, 5-oxoproline, glutamate, and homocysteine, were significantly altered among FT1DM, T2DM, T1DM, and DKA. In addition, the three metabolite markers, 5-oxoproline, glutamate, and homocysteine, presented similar patterns of distribution across groups. The results showed that the metabolic signatures of FT1DM identified in this study could be of potential clinical significance for the accurate diagnosis of FT1DM.
AB - Fulminant type 1 diabetes (FT1DM) is a relatively new clinical entity featured by acute destruction of pancreatic beta cells. Clinical consequences of FT1DM could be fatal when timely medications are not provided, suggesting the particular importance of rapid and accurate diagnosis. Here we report a serum metabonomics study of FT1DM patients, together with healthy control subjects (NC), type 2 diabetes (T2DM), classic type 1 diabetes (T1DM), and diabetic ketoacidosis (DKA) patients, with the aim of discovering metabolic markers associated with FT1DM. A total of 79 subjects were enrolled (22 NC, 22 T1DM, 22 T2DM, 8 DKA and 5 FT1DM) and the serum metabolic profiling of fasting blood samples was performed using gas chromatography time-of-flight mass spectrometry (GC-TOFMS) coupled with multivariate and univariate statistical analyses. Serum metabolites differentially expressed in FT1DM relative to NC, or to T2DM, T1DM and DKA were identified. Three metabolite markers, 5-oxoproline, glutamate, and homocysteine, were significantly altered among FT1DM, T2DM, T1DM, and DKA. In addition, the three metabolite markers, 5-oxoproline, glutamate, and homocysteine, presented similar patterns of distribution across groups. The results showed that the metabolic signatures of FT1DM identified in this study could be of potential clinical significance for the accurate diagnosis of FT1DM.
KW - FT1DM
KW - biomarker
KW - fulminant type 1 diabetes
KW - metabolomics
KW - metabonomics
KW - serum
UR - http://www.scopus.com/inward/record.url?scp=84866133036&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84866133036&partnerID=8YFLogxK
U2 - 10.1021/pr300523x
DO - 10.1021/pr300523x
M3 - Article
C2 - 22894710
AN - SCOPUS:84866133036
SN - 1535-3893
VL - 11
SP - 4705
EP - 4711
JO - Journal of Proteome Research
JF - Journal of Proteome Research
IS - 9
ER -