Serum YKL-40 Levels and Chitotriosidase Activity in Patients with Beta-Thalassemia Major

被引:7
作者
Musumeci, Maria [1 ]
Caruso, Vincenzo [2 ]
Medulla, Emilia [2 ]
Torrisi, Venerando [3 ]
Migale, Roberta [4 ]
Angeletti, Silvia [1 ]
Musumeci, Salvatore [5 ,6 ]
机构
[1] Univ Rome, Dept Lab Med & Microbiol, Ctr Integrated Res, I-00128 Rome, Italy
[2] Ctr Microcitemia, I-95123 Catania, Italy
[3] IRMA, I-95024 Acireale, Catania, Italy
[4] Univ London Imperial Coll Sci Technol & Med, Inst Reprod & Dev Biol, Parturit Res Grp, Dept Surg & Canc, London W12 0NN, England
[5] Univ Catania, Dept Chem Sci, I-95125 Catania, Italy
[6] CNR, Inst Biomol Chem, I-95125 Catania, Italy
关键词
RHEUMATOID-ARTHRITIS; HEPATITIS-C; MARKER; FIBROSIS; EXPRESSION; BIOMARKER; PROTEIN; CHI3L1; GENE; MACROPHAGES;
D O I
10.1155/2014/965971
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background. YKL-40 association with human disease has been the object of many years of investigation. beta-thalassemia patients are affected by hepatic siderosis, which determines a fibrotic process and tissue remodelling. Chitotriosidase has been found to be increased in thalassemic patients returning to normal in patients submitted to bone marrow transplantation. YKL-40 is associated with macrophage activation in liver and in other tissues. The aim of the study was to analyse the level of serum YKL-40 and plasma chitotriosidase activity of patients with beta-thalassemia to assess whether their expression correlates with liver disease and degree of liver siderosis. Methods. Expression of YKL-40 and chitotriosidase as a marker of inflammation in 69 thalassemic patients were evaluated. We sought to investigate whether these two chitinases could be considered as a significant biomarker to evaluate therapy effectiveness. Results. Surprisingly we found normal value of YKL-40. We, also, analysed chitotriosidase activity in the same patients that was slightly increased as a consequence of macrophage activation. Conclusions. These data would suggest a good treatment for these patients.
引用
收藏
页数:6
相关论文
共 33 条
[1]   Plasma chitotriosidase activity in acute Plasmodium falciparum malaria [J].
Barone, R ;
Simporé, J ;
Malaguarnera, L ;
Pignatelli, S ;
Musumeci, S .
CLINICA CHIMICA ACTA, 2003, 331 (1-2) :79-85
[2]   Plasma chitotriosidase activity in patients with β-thalassemia [J].
Barone, R ;
Di Gregorio, F ;
Romeo, MA ;
Schilirò, G ;
Pavone, L .
BLOOD CELLS MOLECULES AND DISEASES, 1999, 25 (01) :1-8
[3]   Plasma chitotriosidase activity in β-thalassemia major:: a comparative study between Sicilian and Sardinian patients [J].
Barone, R ;
Bertrand, G ;
Simporò, J ;
Malaguarnera, M ;
Musumeci, S .
CLINICA CHIMICA ACTA, 2001, 306 (1-2) :91-96
[4]   Strong induction of members of the chitinase family of proteins in atherosclerosis - Chitotriosidase and human cartilage gp-39 expressed in lesion macrophages [J].
Boot, RG ;
van Achterberg, TAE ;
van Aken, BE ;
Renkema, GH ;
Jacobs, MJHM ;
Aerts, JMFG ;
de Vries, CJM .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (03) :687-694
[5]  
Borgna-Pignatti C, 2011, EXPERT REV HEMATOL, V4, P353, DOI [10.1586/ehm.11.29, 10.1586/EHM.11.29]
[6]   A chitinase-like protein in the lung and circulation of patients with severe asthma [J].
Chupp, Geoffrey L. ;
Lee, Chun Geun ;
Jarjour, Nizar ;
Shim, Yun Michael ;
Holm, Carole T. ;
He, Susan ;
Dziura, James D. ;
Reed, Jennifer ;
Coyle, Anthony J. ;
Kiener, Peter ;
Cullen, Mark ;
Grandsaigne, Martine ;
Dombret, Marie-Christine ;
Aubier, Michel ;
Pretolani, Marina ;
Elias, Jack A. .
NEW ENGLAND JOURNAL OF MEDICINE, 2007, 357 (20) :2016-2027
[7]  
Cianciulli Paolo, 2008, Pediatr Endocrinol Rev, V6 Suppl 1, P208
[8]   YKL-40 (cartilage gp-39) induces proliferative events in cultured chondrocytes and synoviocytes and increases glycosaminoglycan synthesis in chondrocytes [J].
De Ceuninck, F ;
Gaufillier, S ;
Bonnaud, A ;
Sabatini, M ;
Lesur, C ;
Pastoureau, P .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 285 (04) :926-931
[9]   Elevated plasma chitotriosidase activity in various lysosomal storage disorders [J].
Guo, YF ;
He, W ;
Boer, AM ;
Wevers, RA ;
deBruijn, AM ;
Groener, JEMM ;
Hollak, CEM ;
Aerts, JMFG ;
Galjaard, H ;
vanDiggelen, OP .
JOURNAL OF INHERITED METABOLIC DISEASE, 1995, 18 (06) :717-722
[10]   MARKED ELEVATION OF PLASMA CHITOTRIOSIDASE ACTIVITY - A NOVEL HALLMARK OF GAUCHER DISEASE [J].
HOLLAK, CEM ;
VANWEELY, S ;
VANOERS, MHJ ;
AERTS, JMFG .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 93 (03) :1288-1292