Abstract

ObjectiveDiabetic kidney disease (DKD) leads to low high albuminuria and gradually progresses to very high albuminuria with kidney insufficiency. However, about 20–40% of DKD is normoalbuminuric DKD (NADKD), which has impaired kidney function but normal urine albumin. This study is to investigate the urine metabolomic profiles of patients with NADKD and albuminuria DKD (ADKD).MethodsIn total, 95 patients were divided into a simple diabetes mellitus group (SDM group), an ADKD group, and a NADKD group. All subjects were analyzed for urine metabolites using non-targeted metabolomics based on ultra-performance liquid chromatography – tandem mass spectrometry.ResultsThe urine metabolomic profiles of the SDM group, NADKD group, and ADKD group were significantly different, and 65 different metabolites were identified among the three groups. Metabolic pathway analysis of these differential metabolites found that the top three significantly changed metabolic pathways were linoleic acid metabolism, citrate cycle, and, arginine and proline metabolism. There are 12 metabolites enriched in these three metabolic pathways. In detail, compared with those in the SDM group, the levels of γ-linolenic acid in the ADKD group were increased significantly, while the levels of succinic acid, cis-aconitic acid, citric acid, L-proline, L-erythro-4-hydroxyglutamate, N-methylhydantoin, N-carbamoylputrescine, spermidine, and 5-aminopentanoic acid were reduced significantly; compared with those in the NADKD group, the levels of linoleic acid, γ-linolenic acid, and L-malic acid in the ADKD group were increased significantly (P < 0.05), while the levels of L-proline, L-erythro-4-hydroxyglutamate, N-carbamoylputrescine, and spermidine were significantly reduced (P < 0.05). However, there were no significant difference between the SDM group and NADKD group (P > 0.05).ConclusionThe urine metabolomic profiles between the NADKD group and the ADKD group are significantly different. Specifically, these two groups have distinct levels of linoleic acid, γ-linolenic acid, L-malic acid, L-proline, L-erythro-4-hydroxyglutamate, N-carbamoylputrescine, and spermidine.

Highlights

  • Diabetic kidney disease (DKD) is the most common microvascular complication in patients with diabetes mellitus (DM)

  • There was no significant difference in sex and C1q among SDM, normoalbuminuric DKD (NADKD), and albuminuria DKD (ADKD) (P > 0.05)

  • Pairwise comparison analysis showed that compared with the SDM group, the age and cystatin C (CysC) of the NADKD group increased while estimated glomerular filtration rate (eGFR) decreased (P < 0.05)

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Summary

Introduction

Diabetic kidney disease (DKD) is the most common microvascular complication in patients with diabetes mellitus (DM). Recent studies (Pichaiwong et al, 2019; Viswanathan et al, 2019) have shown that many patients with DM have kidney glomerular filtration dysfunction after kidney injury, they have normal albuminuria. This is called normoalbuminuric DKD (NADKD) (Gohda et al, 2018). Some studies speculate that the occurrence of NADKD may be related to genetic factors, estrogen levels, and kidney injury patterns in patients with NADKD (Chen et al, 2017; Silva et al, 2017; Yamanouchi et al, 2019). Prospective studies exploring the pathogenesis of NADKD at the metabolomics level are limited

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