KMID : 1102220230420050591
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Kidney Research and Clinical Practice 2023 Volume.42 No. 5 p.591 ~ p.605
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Serum and urine metabolomic biomarkers for predicting prognosis in patients with immunoglobulin A nephropathy
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Jeon You-Hyun
Lee Su-Jin Kim Da-Woon Kim Suhk-Mann Bae Sun-Sik Han Mi-Yeun Seong Eun-Young Song Sang-Heon
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Abstract
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Background : Immunoglobulin A nephropathy (IgAN) is the most prevalent form of glomerulonephritis worldwide. Prediction of disease progression in IgAN can help to provide individualized treatment based on accurate risk stratification.
Methods : We performed proton nuclear magnetic resonance-based metabolomics analyses of serum and urine samples from healthy controls, non-progressor (NP), and progressor (P) groups to identify metabolic profiles of IgAN disease progression. Metabolites that were significantly different between the NP and P groups were selected for pathway analysis. Subsequently, we analyzed multivariate area under the receiver operating characteristic (ROC) curves to evaluate the predictive power of metabolites associated with IgAN progression.
Results : We observed several distinct metabolic fingerprints of the P group involving the following metabolic pathways: glycolipid metabolism; valine, leucine, and isoleucine biosynthesis; aminoacyl-transfer RNA biosynthesis; glycine, serine, and threonine metabolism; and glyoxylate and dicarboxylate metabolism. In multivariate ROC analyses, the combinations of serum glycerol, threonine, and proteinuria (area under the curve [AUC], 0.923; 95% confidence interval [CI], 0.667-1.000) and of urinary leucine, valine, and proteinuria (AUC, 0.912; 95% CI, 0.667-1.000) showed the highest discriminatory ability to predict IgAN disease progression.
Conclusion : This study identified serum and urine metabolites profiles that can aid in the identification of progressive IgAN and proposed perturbed metabolic pathways associated with the identified metabolites.
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KEYWORD
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Disease progression, IgA nephropathy, Metabolic networks and pathways, Metabolomics
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