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Polymorphisms in inflammatory cytokines and Fcgamma receptors in childhood chronic immune thrombocytopenic purpura: a pilot study.

Authors: Foster, CB  Zhu, S  Erichsen, HC  Lehrnbecher, T  Hart, ES  Choi, E  Stein, S  Smith, MW  Steinberg, SM  Imbach, P  Kuhne, T  Chanock, SJ   
Citation: Foster CB, etal., Br J Haematol. 2001 Jun;113(3):596-9.
Pubmed: (View Article at PubMed) PMID:11380443

Inflammatory cytokines and low-affinity Fcgamma receptor (FcgammaR) polymorphisms were investigated in 37 children with chronic immune thrombocytopenic purpura (cITP) and 218 controls. Genotype analysis included common variants in the regulatory regions of cytokines, TNF, LTA, IL1RN, IL1A, IL1B, IL4, IL6 and IL10, and structural variants of the low affinity FcgammaRs, FCGR2A, FCGR3A and FCGR3B. Associations were observed for TNF (P = 0.0032), LTA (P = 0.019), FCGR3A (P = 0.038) and FCGR3B (P = 0.0034). Two combinations of genotypes (TNF and FCGR3A; P = 0.0003, and LTA and FCGR3B; P = 0.011) were significantly associated with cITP. These results provide preliminary evidence that variant genotypes of FcgammaRs and cytokines contribute to cITP pathogenesis.


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RGD Object Information
RGD ID: 11040776
Created: 2016-03-15
Species: All species
Last Modified: 2016-03-15
Status: ACTIVE


RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.