Concentration of hydroxyproline in blood: A biological marker in occupational exposure to asbestos and its relationship with PiZ and PiS polymorphism in the alpha-1 antitrypsin gene
Background Hydroxyproline (OHP) is one of the most abundant amino acids in collagen and, in general, it provides a good measure of overall collagen catabolism. Methods Asbestos workers suffering from asbestosis (cases n = 85); asbestos exposed workers without asbestosis (exposed controls, EC, n = 86...
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Published in | American journal of industrial medicine Vol. 45; no. 2; pp. 186 - 193 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken
Wiley Subscription Services, Inc., A Wiley Company
01.02.2004
Wiley-Liss |
Subjects | |
Online Access | Get full text |
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Summary: | Background
Hydroxyproline (OHP) is one of the most abundant amino acids in collagen and, in general, it provides a good measure of overall collagen catabolism.
Methods
Asbestos workers suffering from asbestosis (cases n = 85); asbestos exposed workers without asbestosis (exposed controls, EC, n = 86), and non‐exposed population (non‐exposed controls, NEC, n = 122) were studied. The concentration of free OHP in whole blood was measured following the Pico‐Tag procedure.
Results
Concentration of OHP in blood was significantly different in the three groups studied (P < 0.001), being higher in cases (19.8 ± 14.7 μmol/L) than in EC (16 ± 12.4) and NEC (13.5 ± 6.7). When all individuals were grouped and stratified by the Pi*S and Pi*Z polymorphisms in the alpha‐1‐antitrypsin gene, the highest OHP levels were detected in the Pi*S homozygotes, one of the asbestosis‐at risk‐genotypes (Pi*S homozygotes, x = 24.5 ± 11.7; Pi*S heterozygotes, x = 16.6 ± 10.0; wild type, wt, x = 15.9 ± 11.8).
Conclusions
Blood OHP concentration could be used for monitoring human exposure to asbestos, either as a marker for occupational monitoring or as an additional clinical parameter in diagnostic exploration of asbestosis. Am. J. Ind. Med. 45:186–193, 2004. © 2004 Wiley‐Liss, Inc. |
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Bibliography: | istex:A9500C763BBF65F8268337BC5022144C62E00854 ark:/67375/WNG-N579P9X1-6 ArticleID:AJIM10350 Mutua General Foundation Colegio de Farmaceuticos de Barcelona (to XC) Institution at which the work was performed: Department of Pharmacology, School of Medicine, IDIBAPS, University of Barcelona, C/Casanova 143, 08036 Barcelona, Spain. ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0271-3586 1097-0274 |
DOI: | 10.1002/ajim.10350 |