Quantitative proteomics analysis of vitreous body from type 2 diabetic patients with proliferative diabetic retinopathy

• Published in: BMC ophthalmology Vol. 18; no. 1; p. 151
• Main Authors: Li, Jianqing, Lu, Qianyi, Lu, Peirong
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 26.06.2018; BioMed Central; BMC
• Subjects: Apolipoproteins; Bioinformatics; Cardiovascular disease; Care and treatment; Complications and side effects; Diabetes; Diabetes mellitus; Diabetic retinopathy; Mass spectrometry; Mass spectroscopy; Ophthalmology; Pathogenesis; Principal components analysis; Proliferative diabetic retinopathy; Proteins; Proteomics; Quantitative proteomics; Retina; Retinopathy; Risk factors; Scientific imaging; Software; United States > US; Proliferative diabetic retinopathy; Bioinformatics; Quantitative proteomics
• ISSN: 1471-2415; 1471-2415
• DOI: 10.1186/s12886-018-0821-3

To compare the abundance of vitreous proteins between the patients with proliferative diabetic retinopathy (PDR) and idiopathic macular hole (IMH). In this study, we performed mass spectrometry-based label-free quantitative proteomics analysis of vitreous samples from type 2 diabetic patients with PDR (n = 9) and IMH subjects (n = 9) and identified the abundance of 610 proteins. Out of 610 proteins, 64 proteins (Group A) were unique to PDR patients, while 212 proteins (Group B) could be identified in IMH vitreous only. Among the other 334 proteins that could be detected in both PDR and IMH eyes, 62 proteins differed significantly (p < 0.05, fold change > 2), which included 52 proteins (Group C) and 10 proteins (Group D) over- and under-expressed in PDR vitreous compared with the control. All proteins in these four groups were counted as significant proteins in our study. We identified and quantified 610 proteins in total, which included 338 significant proteins in our study. Protein distribution analysis demonstrated a clear separation of protein expression in PDR and IMH. The protein function analysis illustrated that immunity and transport related proteins might be associated with PDR.