Differentiation of type 2 diabetes mellitus with different complications by proteomic analysis of plasma low abundance proteins

被引:11
|
作者
Yeh S.-H. [1 ]
Chang W.-C. [2 ]
Chuang H. [3 ]
Huang H.-C. [4 ]
Liu R.-T. [5 ]
Yang K.D. [6 ,7 ]
机构
[1] MacKay Medical College, Institute of Long-term Care, New Taipei City, Sanzhi District
[2] Chang Gung Memorial Hospital-Kaohsiung Medical Center, Department of Medical Research, Kaohsiung
[3] Kaohsiung Chang Gung Memorial Hospital, Proteomic Core Laboratory, Department of Medical Research, Kaohsiung
[4] Kaohsiung Chang Gung Memorial Hospital, Department of Medical Research, Kaohsiung
[5] Chang Gung Memorial Hospital-Kaohsiung Medical Center, Chang Gung University, Division of Endocrinology and Metabolism, Kaohsiung
[6] MacKay Memorial Hospital, Department of Research and Development, Taipei 104, New Taipei City
[7] MacKay Medical College, Department of Medicine, New Taipei City
关键词
Albuminuria; Low abundance proteins; Nephropathy; Plasma proteome; Retinopathy; Type; 2; diabetes;
D O I
10.1186/s40200-016-0246-6
中图分类号
学科分类号
摘要
Background: Few biomarkers of type 2 diabetes mellitus (T2DM) are replicable in the differentiation of T2DM with different complications. We aimed to identify proteomic biomarkers among T2DM patients with nephropathy or retinopathy. Methods: Plasma low abundance proteins were enriched by depletion of 14 high abundance proteins using an affinity removal system, and subjected to nanoflow liquid chromatography electrospray ionization (nano LC-ESI) mass spectrometry after a gel electrophoresis with in-gel digestion. The plasma differential proteomes between normal adults and diabetic patients were validated by another cohort of 149 T2DM patients. Results: A total of 826 proteins in plasma were consistently identified from 8 plasma samples of normal adults, and 817 proteins were consistently identified in 8 plasma samples of T2DM patients. Using the MetaCore analysis, low abundance proteins in plasma between normal adults and T2DM patients were significantly different in 5 functional pathways. Moreover, plasma prolactin-induced protein (PIP), thrombospondin-2 (THBS2), L1 cell adhesion molecule (L1CAM) and neutrophil gelatinase-associated lipocalin (NGAL) levels were higher in T2DM patients. Further, PIP, THBS2 and NGAL were significantly higher in T2DM patients with nephropathy (albuminuria) but not in those with retinopathy, while L1CAM levels were higher in T2DM patients with retinopathy. Conclusions: This study identified that higher PIP, THBS2 and/or NGAL levels were significantly associated with nephropathy of T2DM, and higher L1CAM but normal PIP, THBS2 or NGAL was significantly associated with retinopathy of T2DM. © 2016 Yeh et al.
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