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β地中海贫血患者血浆趋化因子CCL18/PARC水平升高。

Elevated plasma chemokine CCL18/PARC in beta-thalassemia.

作者信息

Dimitriou E, Verhoek M, Altun S, Karabatsos F, Moraitou M, Youssef J, Boot R, Sarafidou J, Karagiorga M, Aerts H, Michelakakis H

机构信息

Department of Enzymology and Cellular Function, Institute of Child Health, "The Aghia Sophia" Children's Hospital, 11527 Athens, Greece.

出版信息

Blood Cells Mol Dis. 2005 Nov-Dec;35(3):328-31. doi: 10.1016/j.bcmd.2005.07.006. Epub 2005 Aug 31.

Abstract

Plasma CCL18/PARC, a member of the CC chemokine family, has been found to be several ten-fold increased in symptomatic Gaucher type I patients. Elevated plasma chitotriosidase levels are a well-known abnormality in Gaucher patients, however, its diagnostic use is limited by the frequent genetic deficiency in the protein. Like the situation in Gaucher disease, lipids accumulate in macrophages of patients suffering from beta-thalassemia, and, in both conditions, increased chitotriosidase levels occur. We here report that plasma CCL18/PARC is also significantly increased in patients with beta-thalassemia major (range 76.8-4977.8, median=650.8 ng/ml, n=36 and control range 10-72, median=33 ng/ml n=36 respectively, P<0.001). The CCL18/PARC levels are lower than in Gaucher patients (range 174.8-10798.7, median 2538.2 ng/ml, n=28, P<0.001). In our cohort of beta-thalassemic patients, CCL18/PARC showed a significant negative correlation to iron chelation therapy and a significant positive correlation to ferritin and chitotriosidase levels, the latter only in the patients with the wild type genotype for the enzyme. Our study demonstrates that beta-thalassemic patients have increased CCL18/PARC levels that could be of value in monitoring iron overload and compliance to therapy.

摘要

血浆CCL18/PARC是CC趋化因子家族的一员,已发现其在有症状的I型戈谢病患者中升高了几十倍。血浆壳三糖苷酶水平升高是戈谢病患者众所周知的异常情况,然而,其诊断用途因该蛋白常见的基因缺陷而受到限制。与戈谢病的情况一样,β地中海贫血患者的巨噬细胞中也会积累脂质,并且在这两种情况下,壳三糖苷酶水平都会升高。我们在此报告,重型β地中海贫血患者的血浆CCL18/PARC也显著升高(范围76.8 - 4977.8,中位数 = 650.8 ng/ml,n = 36;对照组范围10 - 72,中位数 = 33 ng/ml,n = 36,P < 0.001)。CCL18/PARC水平低于戈谢病患者(范围174.8 - 10798.7,中位数2538.2 ng/ml,n = 28,P < 0.001)。在我们的β地中海贫血患者队列中,CCL18/PARC与铁螯合疗法呈显著负相关,与铁蛋白和壳三糖苷酶水平呈显著正相关,后者仅在该酶野生型基因型的患者中存在。我们的研究表明,β地中海贫血患者的CCL18/PARC水平升高,这可能对监测铁过载和治疗依从性有价值。

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