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基于 UPLC-QTOF/MS 的股骨头坏死的全球尿液代谢组学分析。

Global urinary metabolic profiling of the osteonecrosis of the femoral head based on UPLC-QTOF/MS.

机构信息

Department of Orthopedics, Fuling Center Hospital of Chongqing City, Chongqing, 408000, China.

Department of Orthopedics, The First Affiliated Hospital, Chongqing Medical University, Youyi Road No. 1, Chongqing, 400016, China.

出版信息

Metabolomics. 2019 Feb 20;15(3):26. doi: 10.1007/s11306-019-1491-8.

Abstract

INTRODUCTION

Osteonecrosis of the femoral head (ONFH), one of the widespread orthopedic diseases with a decrease in bloodstream to the femoral head, is frequently accompanied by cellular death, trabecula fracture, and collapse of the articular surface. The exactly pathological mechanism of ONFH remains to explore and further identify.

OBJECTIVES

The aim was to identify the global urinary metabolic profiling of ONFH and to detect biomarkers of ONFH.

METHODS

Urine samples were collected from 26 ONFH patients and 26 healthy people. Ultra-performance liquid chromatography-quadrupole time of flight tandem mass spectrometry (UPLC-QTOF/MS) in combination with multivariate statistical analysis was developed and performed to identify the global urinary metabolic profiling of ONFH.

RESULTS

The urinary metabolic profiling of ONFH group was significantly separated from the control group by multivariate statistical analysis. 33 distinctly differential metabolites were detected between the ONFH patients and healthy people. Sulfate, urea, Deoxycholic acid and PE(14:0/14:1(9Z)) were screened as the potential biomarkers of ONFH. In addition, the up/down-regulation of sulfur metabolism, cysteine and methionine metabolism, glycerophospholipid metabolism, and histidine metabolism were clearly be associated with the ONFH pathogenic progress.

CONCLUSION

Our results suggested that metabolomics could serve as a promising approach for identifying the diagnostic biomarkers and elucidating the pathological mechanism of ONFH.

摘要

简介

股骨头坏死(ONFH)是一种广泛存在的骨科疾病,其特征是股骨头血流量减少,常伴有细胞死亡、小梁骨折和关节面塌陷。ONFH 的确切病理机制仍需探索和进一步确定。

目的

旨在鉴定 ONFH 的全球尿液代谢组学特征,并检测 ONFH 的生物标志物。

方法

收集 26 例 ONFH 患者和 26 例健康人的尿液样本。采用超高效液相色谱-四极杆飞行时间串联质谱联用(UPLC-QTOF/MS)结合多元统计分析方法,对 ONFH 的全球尿液代谢组学进行鉴定。

结果

多元统计分析结果显示,ONFH 组的尿液代谢组学特征与对照组明显分离。在 ONFH 患者和健康人群之间检测到 33 种明显差异的代谢产物。硫酸盐、尿素、脱氧胆酸和 PE(14:0/14:1(9Z))被筛选为 ONFH 的潜在生物标志物。此外,硫代谢、半胱氨酸和蛋氨酸代谢、甘油磷脂代谢和组氨酸代谢的上调/下调与 ONFH 的发病机制明显相关。

结论

本研究结果表明,代谢组学可作为一种有前途的方法,用于鉴定诊断生物标志物并阐明 ONFH 的病理机制。

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