Abstract | OBJECTIVES: 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.
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Authors | Christine Bobin-Dubigeon, Armelle Lefrançois, Jean-Marc Classe, Marie-Pierre Joalland, Jean-Marie Bard |
Journal | Clinical biochemistry
(Clin Biochem)
Vol. 48
Issue 16-17
Pg. 1181-3
(Nov 2015)
ISSN: 1873-2933 [Electronic] United States |
PMID | 26188919
(Publication Type: Journal Article)
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Copyright | Copyright © 2015 The Canadian Society of Clinical Chemists. Published by Elsevier Inc. All rights reserved. |
Chemical References |
- Biomarkers, Tumor
- Lipoproteins, HDL
- Lipoproteins, LDL
- Serum Amyloid A Protein
- oxidized low density lipoprotein
- Carboxylic Ester Hydrolases
- arylesterase
- Aryldialkylphosphatase
- PON1 protein, human
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Topics |
- Aryldialkylphosphatase
(metabolism)
- Biomarkers, Tumor
(blood)
- Breast Neoplasms
(blood, diagnosis, metabolism)
- Carboxylic Ester Hydrolases
(metabolism)
- Female
- Humans
- Hydrolysis
- Inflammation
(blood, diagnosis, metabolism)
- Lipoproteins, HDL
(blood)
- Lipoproteins, LDL
(blood)
- Neoplasm Recurrence, Local
(blood, diagnosis, metabolism)
- Oxidative Stress
(physiology)
- Serum Amyloid A Protein
(metabolism)
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