Literature DB >> 16137900

Elevated plasma chemokine CCL18/PARC in beta-thalassemia.

E Dimitriou1, M Verhoek, S Altun, F Karabatsos, M Moraitou, J Youssef, R Boot, J Sarafidou, M Karagiorga, H Aerts, H Michelakakis.   

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.

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Year:  2005        PMID: 16137900     DOI: 10.1016/j.bcmd.2005.07.006

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  3 in total

1.  Hyperferritinemia and iron overload in type 1 Gaucher disease.

Authors:  Philip Stein; Hannah Yu; Dhanpat Jain; Pramod K Mistry
Journal:  Am J Hematol       Date:  2010-07       Impact factor: 10.047

Review 2.  Management of non-neuronopathic Gaucher disease with special reference to pregnancy, splenectomy, bisphosphonate therapy, use of biomarkers and bone disease monitoring.

Authors:  T M Cox; J M F G Aerts; N Belmatoug; M D Cappellini; S vom Dahl; J Goldblatt; G A Grabowski; C E M Hollak; P Hwu; M Maas; A M Martins; P K Mistry; G M Pastores; A Tylki-Szymanska; J Yee; N Weinreb
Journal:  J Inherit Metab Dis       Date:  2008-05-23       Impact factor: 4.982

3.  Plasma proteome profiling combined with clinical and genetic features reveals the pathophysiological characteristics of β-thalassemia.

Authors:  Na Li; Peng An; Jifeng Wang; Tingting Zhang; Xiaoqing Qing; Bowen Wu; Lang Sun; Xiang Ding; Lili Niu; Zhensheng Xie; Mengmeng Zhang; Xiaojing Guo; Xiulan Chen; Tanxi Cai; Jianming Luo; Fudi Wang; Fuquan Yang
Journal:  iScience       Date:  2022-03-16
  3 in total

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