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基于广泛靶向代谢组学的研究鉴定糖尿病肾病的潜在血清代谢生物标志物

Identification of Potential Serum Metabolic Biomarkers of Diabetic Kidney Disease: A Widely Targeted Metabolomics Study.

机构信息

Diabetes Center and Department of Endocrinology, The Second Affiliated Hospital and Yuying Children's Hospital of Wenzhou Medical University, No. 109 West Xueyuan Road, Wenzhou, China.

Center on Clinical Research, School of Ophthalmology & Optometry, Wenzhou Medical University, Wenzhou, China.

出版信息

J Diabetes Res. 2020 Mar 2;2020:3049098. doi: 10.1155/2020/3049098. eCollection 2020.

Abstract

UNLABELLED

Diabetic kidney disease is a leading cause of chronic kidney disease and end-stage renal disease across the world. Early identification of DKD is vitally important for the effective prevention and control of it. However, the available indicators are doubtful in the early diagnosis of DKD. This study is aimed at determining novel sensitive and specific biomarkers to distinguish DKD from their counterparts effectively based on the widely targeted metabolomics approach. This case-control study involved 44 T2DM patients. Among them, 24 participants with DKD were defined as the cases and another 20 without DKD were defined as the controls. The ultraperformance liquid chromatography-electrospray ionization-tandem mass spectrometry system was applied for the assessment of the serum metabolic profiles. Comprehensive analysis of metabolomics characteristics was conducted to detect the candidate metabolic biomarkers and assess their capability and feasibility.

RESULT

A total of 11 differential metabolites, including Hexadecanoic Acid (C16:0), Linolelaidic Acid (C18:2N6T), Linoleic Acid (C18:2N6C), Trans-4-Hydroxy-L-Proline, 6-Aminocaproic Acid, L-Dihydroorotic Acid, 6-Methylmercaptopurine, Piperidine, Azoxystrobin Acid, Lysopc 20:4, and Cuminaldehyde, were determined as the potential biomarkers for the DKD early identification, based on the multivariable generalized linear regression model and receiver operating characteristic analysis.

CONCLUSION

Serum metabolites might act as sensitive and specific biomarkers for DKD early detection. Further longitudinal studies are needed to confirm our findings.

摘要

目的

本研究旨在基于广泛靶向的代谢组学方法,确定新的敏感和特异生物标志物,有效区分 DKD 与其对照。

方法

本病例对照研究纳入 44 例 T2DM 患者。其中,24 例 DKD 患者为病例组,20 例无 DKD 患者为对照组。采用超高效液相色谱-电喷雾电离-串联质谱系统评估血清代谢谱。进行代谢组学特征的综合分析,以检测候选代谢生物标志物,并评估其能力和可行性。

结果

基于多变量广义线性回归模型和受试者工作特征分析,共确定了 11 种差异代谢物,包括十六烷酸(C16:0)、亚油酸(C18:2N6T)、亚油酸(C18:2N6C)、反式-4-羟脯氨酸、6-氨基己酸、L-二羟乳清酸、6-甲基巯基嘌呤、哌啶、唑菌胺酯酸、Lysopc 20:4 和肉桂醛,可作为 DKD 早期识别的潜在生物标志物。

结论

血清代谢物可能作为 DKD 早期检测的敏感和特异生物标志物。需要进一步的纵向研究来证实我们的发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/032f/7072115/d41b02b9fbbc/JDR2020-3049098.001.jpg

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