Detection and Characterization of a Biochemical Signature Associated with Diabetic Nephropathy Using Near-infrared Spectroscopy on Tissue Sections

被引:24
作者
De Bruyne, Sander [1 ]
Van Dorpe, Jo [2 ]
Himpe, Jonas [1 ]
Van Biesen, Wim [3 ]
Delanghe, Sigurd [3 ]
Speeckaert, Marijn M. [3 ,4 ]
Delanghe, Joris R. [1 ]
机构
[1] Univ Ghent, Dept Clin Chem Microbiol & Immunol, B-9000 Ghent, Belgium
[2] Ghent Univ Hosp, Dept Pathol, B-9000 Ghent, Belgium
[3] Ghent Univ Hosp, Dept Internal Med, Nephrol Div, B-9000 Ghent, Belgium
[4] Res Fdn Flanders, B-1000 Brussels, Belgium
关键词
near-infrared spectroscopy; diabetic nephropathy; post-translational modifications; renal tissue; KIDNEY-DISEASE; PROTEIN; CARBAMYLATION; GLYCATION;
D O I
10.3390/jcm8071022
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
Histological evaluation of renal biopsies is currently the gold standard for acquiring important diagnostic and prognostic information in diabetic nephropathy (DN) patients. Nevertheless, there is an unmet clinical need for new biomarkers that allow earlier diagnosis and risk stratification. As biochemical changes in tissues must precede any symptomatic or morphological expression of a disease, we explored the potential of near-infrared (NIR) spectroscopy in the detection of a biochemical signature associated with DN. Kidney tissue sections were investigated using NIR spectroscopy, followed by principal component analysis and soft independent modelling of class analogy. A biochemical signature indicative of DN was detected, which enabled perfect discrimination between tissue sections with normal histological findings (n = 27) and sections obtained from DN patients (n = 26). Some spectral changes related to carbamoylation and glycation reactions appeared to be similar to the ones obtained in patients with DN. In addition, treatment with the deglycating enzyme fructosamine-3-kinase resulted in partial to pronounced restorations of the spectral pattern. Significant relationships were found between spectral features and laboratory parameters indicative of glycemic and uremic load, such as hemoglobin A1c, urea, creatinine, estimated glomerular filtration rate, and proteinuria. The presented method could be a useful tool to complement histopathological analysis in order to prevent or delay further disease progression, especially in the setting of post-transplant surveillance kidney biopsies.
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页数:12
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