4.6 Article

NMR-Based Metabolomics in Differential Diagnosis of Chronic Kidney Disease (CKD) Subtypes

期刊

METABOLITES
卷 12, 期 6, 页码 -

出版社

MDPI
DOI: 10.3390/metabo12060490

关键词

CKD; urine; metabolomics; NMR spectroscopy; glomerulonephritis; IgA; membranous; eGFR

资金

  1. Operational Program 'Competitiveness, Entrepreneurship and Innovation' [MIS 5002550, MIS 5002636, NSRF 2014-2020]
  2. European Union (European Regional Development Fund)
  3. EU [CT-2011-285950]
  4. NIHR Imperial Biomedical Research Centre (BRC)

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This study analyzed the urine metabolomics of Chronic Kidney Disease (CKD) patients and found specific metabolic patterns for chronic glomerulonephritis, but not for diabetic nephropathy and hypertensive nephrosclerosis.
Chronic Kidney Disease (CKD) is considered as a major public health problem as it can lead to end-stage kidney failure, which requires replacement therapy. A prompt and accurate diagnosis, along with the appropriate treatment, can delay CKD's progression, significantly. Herein, we sought to determine whether CKD etiology can be reflected in urine metabolomics during its early stage. This is achieved through the analysis of the urine metabolic fingerprint from 108 CKD patients by means of Nuclear Magnetic Resonance (NMR) spectroscopy metabolomic analysis. We report the first NMR-metabolomics data regarding the three most common etiologies of CKD: Chronic Glomerulonephritis (IgA and Membranous Nephropathy), Diabetic Nephropathy (DN) and Hypertensive Nephrosclerosis (HN). Analysis aided a moderate glomerulonephritis clustering, providing characterization of the metabolic fluctuations between the CKD subtypes and control disease. The urine metabolome of IgA Nephropathy reveals a specific metabolism, reflecting its different etiology or origin and is useful for determining the origin of the disease. In contrast, urine metabolomes from DN and HN patients did not reveal any indicative metabolic pattern, which is consistent with their fused clinical phenotype. These findings may contribute to improving diagnostics and prognostic approaches for CKD, as well as improving our understanding of its pathology.

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