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 inAmerican journal of industrial medicine Vol. 45; no. 2; pp. 186 - 193
Main Authors Mas, S., Casterad, X., Laso, N., Lafuente, M.J., Panades, R., Calleja, A., Hernandez, S., Turuguet, D., Deulofeu, R., Ballesta, A., Ascaso, C., Lafuente, A.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.02.2004
Wiley-Liss
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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.
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