Could GSD type i expand the spectrum of disorders with elevated plasma chitotriosidase activity?

Journal of Pediatric Endocrinology and Metabolism

Volumn 26, Issue 11-12, 2013, Pages 1149-1152

  Tümer, Leyla ^a   Kasapkara, Çigdem Seher ^a   Biberoglu, Gürsel ^a   Ezgü, Fatih ^a   Hasanoglu, Alev ^a  

^a GAZI UNIVERSITY   (Turkey)

Author keywords

Chitotriosidase activity; Glycogen storage disease type I

Indexed keywords

CHITOTRIOSIDASE;

ADOLESCENT; ADULT; ARTICLE; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DIFFERENTIAL DIAGNOSIS; ENZYME ACTIVITY; ENZYME BLOOD LEVEL; FEMALE; GLYCOGEN STORAGE DISEASE TYPE 1; HEPATOMEGALY; HUMAN; HUMAN TISSUE; LIVER BIOPSY; MALE; PRESCHOOL CHILD; SCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; CHILD, PRESCHOOL; FEMALE; GLYCOGEN STORAGE DISEASE TYPE I; HEXOSAMINIDASES; HUMANS; INFANT; MALE; YOUNG ADULT;

EID: 84888085489     PISSN: 0334018X     EISSN: 21910251     Source Type: Journal    
DOI: 10.1515/jpem-2013-0066     Document Type: Article

References (17)

1. Froissart R, Piraud M, Boudjemline AM, Vianey-Saban C, Petit F, et al. Glucose-6-phosphatase deficiency. Orphanet J Rare Dis 2011;6:27. doi: 10.1186/1750-1172-6-27.
2. Yildiz BS, Barutcuoglu B, Alihanoglu YI, Alkan MB, Bilgin M, et al. Serum Chitotriosidase Activity in Acute Coronary Syndrome. J Atheroscler Thromb 2013;20:134-41.
3. Orchard PJ, Lund T, Miller W, Rothman SM, Raymond G, et al. Chitotriosidase as a biomarker of cerebral adrenoleukodystrophy. J Neuroinflamm. 2011;8:144. doi: 10.1186/1742-2094-8-144.
4. Hollak CE, van Weely S, van Oers MH, Aerts JM. Marked elevation of plasma chitotriosidase activity. A novel hallmark of Gaucher disease. J Clin Invest 1994;93:1288-92.
5. Boot RG, Verhoek M, de Fost M, Hollak CE, Maas M, et al. Marked elevation of the chemokine CCL18/PARC in Gaucher disease: a novel surrogate marker for assessing therapeutic intervention. Blood 2004;103:33-9.
6. Imrie J, Wraith JE. Isolated splenomegaly as the presenting feature of Niemann-Pick disease type C. Arch Dis Child 2001;84:427-9.
7. Tasci C, Tapan S, Ozkaya S, Demirer E, Deniz O, et al. Efficacy of serum chitotriosidase activity in early treatment of patients with active tuberculosis and a negative sputum smear. Ther Clin Risk Manag 2012;8: 369-72.
8. Cakir G, Gumus S, Ucar E, Kaya H, Tozkoparan E, et al. Serum chitotriosidase activity in pulmonary tuberculosis: response to treatment and correlations with clinical parameters. Ann Lab Med 2012;32:184-9.
9. Vandevenne M, Campisi V, Freichels A, Gillard C, Gaspard G, et al. Comparative functional analysis of the human macrophage chitotriosidase. Protein Sci 2011;20:1451-63. doi: 10.1002/pro.676.
10. Bussink AP, Speijer D, Aerts JM, Boot RG. Evolution of mammalian chitinase(-like) members of family 18 glycosyl hydrolases. Genetics 2007;177:959-70.
11. Labadaridis I, Dimitriou E, Theodorakis M, Kafalidis G, Velegraki A, et al. Chitotriosidase in neonates with fungal and bacterial infections.Arch Dis Child Fetal Neonatal Ed 2005;90:F531-2.
12. Artieda M, Cenarro A, Gañán A, Jericó I, Gonzalvo C, et al. Serum chitotriosidase activity is increased in subjects with atherosclerosis disease. Arterioscler Thromb Vasc Biol 2003;23:1645-52.
13. van Eijk M, van Roomen CP, Renkema GH, Bussink AP, Andrews L, et al. Characterization of human phagocyte-derived chitotriosidase, a component of innate immunity. Int Immunol 2005;17:1505-12.
14. Renkema GH, Boot RG, Au FL, Donker-Koopman WE, Strijland A, et al. Chitotriosidase, a chitinase, and the 39-kDa human cartilage glycoprotein, a chitin-binding lectin, are homologues of family 18 glycosyl hydrolases secreted by human macrophages. Eur J Biochem 1998;251:504-9.
15. Renkema GH, Boot RG, Muijsers AO, Donker-Koopman WE, Aerts JM. Purification and characterization of human chitotriosidase, a novel member of the chitinase family of proteins. J Biol Chem 1995;270:2198-202.
16. Bargagli E, Maggiorelli C, Rottoli P. Human chitotriosidase: a potential new marker of sarcoidosis severity. Respiration 2008;76:234-8.
17. Guo Y, He W, Boer AM, Wevers RA, de Bruijn AM, et al. Elevated plasma chitotriosidase activity in various lysosomal storage disorders. J Inherit Metab Dis 1995;18:717-22.