A metabolomics-based approach for predicting stages of chronic kidney disease

•Metabolites indicative of CKD were formerly identified using a metabolomic method.•In this study, CKD-related plasma metabolites were quantified by LC/MS.•A multivariate regression equation was constructed using nine plasma metabolites.•This equation was predictive of the severity of CKD.•This may...

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Published inBiochemical and biophysical research communications Vol. 445; no. 2; pp. 412 - 416
Main Authors Kobayashi, Toshihiro, Yoshida, Tatsunari, Fujisawa, Tatsuya, Matsumura, Yuriko, Ozawa, Toshihiko, Yanai, Hiroyuki, Iwasawa, Atsuo, Kamachi, Toshiaki, Fujiwara, Kouichi, Kohno, Masahiro, Tanaka, Noriaki
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 07.03.2014
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ISSN0006-291X
1090-2104
1090-2104
DOI10.1016/j.bbrc.2014.02.021

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Summary:•Metabolites indicative of CKD were formerly identified using a metabolomic method.•In this study, CKD-related plasma metabolites were quantified by LC/MS.•A multivariate regression equation was constructed using nine plasma metabolites.•This equation was predictive of the severity of CKD.•This may be a novel method of identifying patients with early-stage CKD. Chronic kidney disease (CKD) is a major epidemiologic problem and a risk factor for cardiovascular events and cerebrovascular accidents. Because CKD shows irreversible progression, early diagnosis is desirable. Renal function can be evaluated by measuring creatinine-based estimated glomerular filtration rate (eGFR). This method, however, has low sensitivity during early phases of CKD. Cystatin C (CysC) may be a more sensitive predictor. Using a metabolomic method, we previously identified metabolites in CKD and hemodialysis patients. To develop a new index of renal hypofunction, plasma samples were collected from volunteers with and without CKD and metabolite concentrations were assayed by quantitative liquid chromatography/mass spectrometry. These results were used to construct a multivariate regression equation for an inverse of CysC-based eGFR, with eGFR and CKD stage calculated from concentrations of blood metabolites. This equation was able to predict CKD stages with 81.3% accuracy (range, 73.9–87.0% during 20 repeats). This procedure may become a novel method of identifying patients with early-stage CKD.
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ISSN:0006-291X
1090-2104
1090-2104
DOI:10.1016/j.bbrc.2014.02.021