Lipid metabolites as potential diagnostic and prognostic biomarkers for acute community acquired pneumonia

被引:48
|
作者
To, Kelvin K. W. [1 ,2 ,3 ,4 ]
Lee, Kim-Chung [4 ]
Wong, Samson S. Y. [1 ,2 ,3 ,4 ]
Sze, Kong-Hung [4 ]
Ke, Yi-Hong [4 ]
Lui, Yin-Ming [4 ]
Tang, Bone S. F. [5 ]
Li, Iris W. S. [4 ]
Lau, Susanna K. P. [1 ,2 ,3 ,4 ]
Hung, Ivan F. N. [1 ,2 ,3 ,6 ]
Law, Chun-Yiu [7 ]
Lam, Ching-Wan [7 ]
Yuen, Kwok-Yung [1 ,2 ,3 ,4 ]
机构
[1] Univ Hong Kong, State Key Lab Emerging Infect Dis, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, Carol Yu Ctr Infect, Hong Kong, Hong Kong, Peoples R China
[3] Univ Hong Kong, Res Ctr Infect & Immunol, Hong Kong, Hong Kong, Peoples R China
[4] Univ Hong Kong, Dept Microbiol, Hong Kong, Hong Kong, Peoples R China
[5] Hong Kong Sanat Hosp, Dept Pathol, Hong Kong, Hong Kong, Peoples R China
[6] Univ Hong Kong, Dept Med, Hong Kong, Hong Kong, Peoples R China
[7] Univ Hong Kong, Dept Pathol, Hong Kong, Hong Kong, Peoples R China
关键词
Biomarkers; Glycolipids; Phospholipids; Pneumonia; Sphingolipids; ACUTE LUNG INJURY; RESPIRATORY SYNDROME CORONAVIRUS; LYSOPHOSPHATIDYLCHOLINE; LYSOPHOSPHATIDYLETHANOLAMINE; SPHINGOLIPIDS; METABOLOMICS; INFLAMMATION; SURFACTANT; MANAGEMENT; MEDIATORS;
D O I
10.1016/j.diagmicrobio.2016.03.012
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Early diagnosis of acute community-acquired pneumonia (CAP) is important in patient triage and treatment decisions. To identify biomarkers that distinguish patients with CAP from non-CAP controls, we conducted an untargeted global metabolome analysis for plasma samples from 142 patients with CAP (CAP cases) and 97 without CAP (non-CAP controls). Thirteen lipid metabolites could discriminate between CAP cases and non-CAP controls with area-under-the-receiver-operating-characteristic curve of >0.8 (P <= 10(-9)). The levels of glycosphingolipids, sphingomyelins, lysophosphatidylcholines and L-palmitoylcamitine were higher, while the levels of lysophosphatidylethanolamines were lower in the CAP cases than those in non-CAP controls. All 13 metabolites could distinguish CAP cases from the non-infection, extrapulmonary infection and non-CAP respiratory tract infection subgroups. The levels of trihexosylceramide (d18:1/16:0) were higher, while the levels of lysophosphatidylethanolamines were lower, in the fatal than those of non-fatal CAP cases. Our findings suggest that lipid metabolites are potential diagnostic and prognostic biomarkers for CAP. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:249 / 254
页数:6
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