Unique plasma metabolomic signature of osteonecrosis of the femoral head

被引:29
作者
Liu, Xiaolin [1 ]
Li, Qing [1 ]
Sheng, Jiagen [1 ,2 ]
Hu, Bin [1 ]
Zhu, Zhenzhong [2 ]
Zhou, Shumin [1 ]
Yin, Junhui [1 ]
Gong, Qiang [1 ]
Wang, Yang [1 ]
Zhang, Changqing [1 ,2 ]
机构
[1] Shanghai Jiao Tong Univ, Inst Microsurg Extrem, Shanghai Peoples Hosp 6, 600 Yishan Rd, Shanghai 200233, Peoples R China
[2] Shanghai Jiao Tong Univ, Dept Orthoped Surg, Shanghai Peoples Hosp 6, 600 Yishan Rd, Shanghai 200233, Peoples R China
基金
中国国家自然科学基金;
关键词
metabolomics; osteonecrosis; femoral head; metabolism; pathway; DEHYDROEPIANDROSTERONE-SULFATE; OXIDATIVE STRESS; NONTRAUMATIC NECROSIS; DISEASE; RISK; MECHANISMS; APOPTOSIS; LIQUID; MODEL;
D O I
10.1002/jor.23129
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Metabolomic analysis was performed to determine the metabolomic signature of osteonecrosis of the femoral head (ONFH), and to investigate the underlying relationship between the metabolomic signature and the pathogenesis of ONFH. Plasma samples were collected from 30 ONFH patients and 30 normal subjects. The global metabolomic profile was obtained through a combination of high-throughput liquid- and gas-chromatography-based mass spectrometry analyses. All statistical analyses were conducted using the R software. The results showed clear differences in the metabolomic signature between the plasma of ONFH patients compared with normal subjects. Among the 354 identified metabolites, the expression of 123 metabolites were significantly changed in ONFH patients compared with normal subjects (p<0.05, q<0.10). Bioinformatics analysis revealed that these abnormal metabolites were mainly involved in lipid-, glutathione-, nucleotide-, and energy-associated pathways, which might be related to enhanced inflammation, oxidative stress, and energy deficiency due to ONFH. This study provides the first metabolomic analysis of ONFH, and identifies a previously unrecognized metabolic signature in ONFH plasma. The results offer new insights into the pathological mechanisms of ONFH through its influence on metabolic pathways, providing the requisite framework for identifying biomarkers or novel targets for therapeutic intervention. (c) 2015 Orthopaedic Research Society. Published by Wiley Periodicals, Inc. J Orthop Res 34:1158-1167, 2016.
引用
收藏
页码:1158 / 1167
页数:10
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