Paired measurement of serum amyloid A (SAA) and paraoxonase 1 (PON1) as useful markers in breast cancer recurrence

被引:14
作者
Bobin-Dubigeon, Christine [1 ,2 ]
Lefrancois, Annelle [1 ]
Classe, Jean-Marc [3 ]
Joalland, Marie-Pierre [1 ]
Bard, Jean-Marie [1 ,2 ]
机构
[1] Inst Cancerol Ouest Biopathol, F-44805 St Herblain, France
[2] Univ Nantes, CNRS, IUML, MMS,EA 2160,Met Mol Sante,FR3473, F-44035 Nantes, France
[3] Inst Cancerol Ouest Oncol Chirurg, F-44805 St Herblain, France
关键词
Paraoxonase; SAA; Inflammation; Breast cancer;
D O I
10.1016/j.clinbiochem.2015.07.020
中图分类号
R446 [实验室诊断]; R-33 [实验医学、医学实验];
学科分类号
1001 ;
摘要
Objectives: Paraoxonase 1 (PON1) and serum amyloid A (SAA) are carried by HDL. In case of inflammation, SAA and PON1 tend to change in opposite direction. In this study we determined if inflammation leads to altered BONI activity using three different substrate hydrolysis rates, paraoxonase (PON), arylesterase (ARE) and lactonase (LAC) in breast cancer recurrence. Design and methods: 49 patients with a recurrence of breast cancer were analyzed for SAA, CRP, lipids, oxidized LDL, PON, ARE and LAC. Distribution of PON1 activities across the quartiles of CRP and SAA were compared by the Kruskal Wallis test. Non-parametric estimates of the survivor function were computed with Kaplan-Meier method. The association of SAA and ARE with short term death was assessed by logistic regression models. Results: HDL and ARE decrease significantly across the quartiles of CRP. No significant differences were observed across SAA quartiles. The survival time was significantly related to the level of SAA (log rank: p < 0.001) as well as the level of ARE (log rank: p = 0.039). SAA and ARE were independently related to survival time below one year. Conclusions: PON1 does not seem to be directly affected by SAA, for any of the tested substrates, PON, ARE and LAC. The combined measurement of SAA and ARE could be a useful tool in this clinical situation, since they are independently related to short term death. (C) 2015 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:1181 / 1183
页数:3
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