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Platelet count, previous infection and FCGR2B genotype predict development of chronic disease in newly diagnosed idiopathic thrombocytopenia in childhood: results of a prospective study.

Authors: Bruin, M  Bierings, M  Uiterwaal, C  Revesz, T  Bode, L  Wiesman, ME  Kuijpers, T  Tamminga, R  De Haas, M 
Citation: Bruin M, etal., Br J Haematol. 2004 Dec;127(5):561-7.
Pubmed: (View Article at PubMed) PMID:15566359
DOI: Full-text: DOI:10.1111/j.1365-2141.2004.05235.x

About 25-30% of children with acute idiopathic thrombocytopenia (ITP) develop chronic disease. It is not well known which patient characteristics influence the course of the ITP. A prospective study in 60 children with newly diagnosed ITP was performed. The aim of the study was to identify patient characteristics at the onset of thrombocytopenia that predicts the progression to chronic ITP. Clinical data and blood samples were collected at several time points during the first 6 months of the disease. Variables predicting chronic disease, as calculated in a multivariate logistic regression analysis, were a platelet count >10 x 10(9)/l at the onset [odds ratio (OR) 1.1, 95% confidence interval (CI) 1.01-1.14], the absence of infection shortly before the onset of the disease (OR 4.8, CI 1.16-19.57) and FGR2B-232I/T genotype (OR 7.9, CI 0.96-65.27). The latter may point at an immune-modulating role of Fc gamma RIIb in ITP. Although only three patients had serious bleeds, 35 patients received immune-modulating treatment for low platelet counts only. Seventeen patients were treated with intravenous immunoglobulin (IVIG) and 18 patients received corticosteroids. Patient variables did not differ between these treatment groups. However, patients receiving IVIG had significantly lower risk for chronic disease.

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CRRD Object Information
CRRD ID: 11344928
Created: 2016-07-08
Species: All species
Last Modified: 2016-07-08
Status: ACTIVE



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