Donate Help Contact The AHA Sign In Home
American Heart Association
Arteriosclerosis, Thrombosis, and Vascular Biology
Search: search_blue_button Advanced Search
Arteriosclerosis, Thrombosis, and Vascular Biology. 2003;23:1645-1652
Published online before print July 31, 2003, doi: 10.1161/01.ATV.0000089329.09061.07
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
23/9/1645    most recent
01.ATV.0000089329.09061.07v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Artieda, M.
Right arrow Articles by Civeira, F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Artieda, M.
Right arrow Articles by Civeira, F.
Related Collections
Right arrow ACE/Angiotension receptors
Right arrow CT and MRI
(Arteriosclerosis, Thrombosis, and Vascular Biology. 2003;23:1645.)
© 2003 American Heart Association, Inc.


Atherosclerosis and Lipoproteins

Serum Chitotriosidase Activity Is Increased in Subjects With Atherosclerosis Disease

Marta Artieda; Ana Cenarro; Alberto Gañán; Ivonne Jericó; Carmen Gonzalvo; Juan M. Casado; Isabel Vitoria; José Puzo; Miguel Pocoví; Fernando Civeira

From Laboratorio de Investigación Molecular (M.A., A.C., C.G., F.C.), Servicio de Cardiología (J.M.C.), and Servicio de Medicina Interna (I.V., F.C.), Hospital Universitario Miguel Servet, Zaragoza; Departamento de Bioquímica y Biología Molecular y Celular (A.G., M.P.), Universidad de Zaragoza; Servicio de Neurología (I.J.), Hospital Clínico Universitario Lozano Blesa, Zaragoza; and Servicio de Bioquímica (J.P.), Hospital San Jorge, Huesca, Spain.

Correspondence to Marta Artieda, Laboratorio de Investigación Molecular, Hospital Universitario Miguel Servet, Isabel la Católica, 1-3, 50009 Zaragoza, Spain. E-mail martieda{at}hmservet.insalud.es

Objective— This study was undertaken to analyze the relation between serum activity of chitotriosidase enzyme, a protein synthesized exclusively by activated macrophages, and atherosclerotic lesion extent in subjects with atherothrombotic stroke (ATS) and in subjects with ischemic heart disease (IHD).

Methods and Results— We assayed the serum chitotriosidase activity and a common chitotriosidase gene polymorphism that causes deficiency in chitotriosidase activity in 3 Spanish populations, ATS (n=153), IHD (n=124), and control (n=148) subjects. Statistical differences were found in serum chitotriosidase activity between ATS (88.1±4.6 nmol/mL · h, P<0.0001) and IHD subjects (79.0±6.3, P=0.002) versus control group (70.9±5.2). These observed differences were not attributable to a distinct allelic or genotype distribution. The extension of the atherosclerotic lesion in carotids of ATS subjects was measured by duplex sonography. Chitotriosidase activities were 66.9±9.6, 88.7±8.3, and 107.7±11.8 for subjects with carotid stenosis <=30%, 31% to 60%, and >60%, respectively. Statistical differences were observed between subjects with major and intermediate stenosis grade compared with subjects with minor stenosis, P=0.005 and P=0.016, respectively.

Conclusions— Serum chitotriosidase activity is significantly increased in individuals suffering from atherosclerosis disease and is related to the severity of the atherosclerotic lesion, suggesting a possible role as atherosclerotic extent marker.


Key Words: chitotriosidase • macrophage • atherothrombotic stroke • ischemic heart disease • atherosclerosis




This article has been cited by other articles:


Home page
BioinformaticsHome page
F. Pappalardo, S. Musumeci, and S. Motta
Modeling immune system control of atherogenesis
Bioinformatics, August 1, 2008; 24(15): 1715 - 1721.
[Abstract] [Full Text] [PDF]


Home page
Mult SclerHome page
S Sotgiu, R Barone, G Arru, M L Fois, M Pugliatti, A Sanna, G Rosati, and S Musumeci
Intrathecal chitotriosidase and the outcome of multiple sclerosis
Multiple Sclerosis, September 1, 2006; 12(5): 551 - 557.
[Abstract] [PDF]


Home page
GutHome page
L Malaguarnera, M Di Rosa, A M Zambito, N dell'Ombra, F Nicoletti, and M Malaguarnera
Chitotriosidase gene expression in Kupffer cells from patients with non-alcoholic fatty liver disease
Gut, September 1, 2006; 55(9): 1313 - 1320.
[Abstract] [Full Text] [PDF]


Home page
J. Physiol.Home page
L. Anderson
Candidate-based proteomics in the search for biomarkers of cardiovascular disease
J. Physiol., February 15, 2005; 563(1): 23 - 60.
[Abstract] [Full Text] [PDF]


Home page
Mol. Cell. ProteomicsHome page
E. M. Fach, L.-A. Garulacan, J. Gao, Q. Xiao, S. M. Storm, Y. P. Dubaquie, S. A. Hefta, and G. J. Opiteck
In Vitro Biomarker Discovery for Atherosclerosis by Proteomics
Mol. Cell. Proteomics, December 1, 2004; 3(12): 1200 - 1210.
[Abstract] [Full Text] [PDF]