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Relationship between polymorphisms of tumor necrosis factor alpha gene and primary myelodysplastic syndromes / 中华血液学杂志
Chinese Journal of Hematology ; (12): 873-876, 2013.
Article Dans Chinois | WPRIM | ID: wpr-272097
ABSTRACT
<p><b>OBJECTIVE</b>To investigate the association of single nucleus polymorphisms(SNP)of tumor necrosis factor alpha (TNF-α) gene (-308 G>A and -238 G>A genotypes) with susceptibility to primary myelodysplastic syndromes (MDS).</p><p><b>METHODS</b>Two SNPs (TNF-α-308 G>A,TNF-α-238 G>A) of TNF-α gene were detected by Taqman probes in 341 MDS patients and 365 unrelated-healthy controls.</p><p><b>RESULTS</b>Compared to healthy controls, the frequency of TNF-α-308 AA+AG genotype and A allele increased (18% vs 10%, P=0.015, 9% vs 5%, P=0.021, respectively) in refractory cytopenia with multilineage dysplasia (RCMD) patients. There was no correlation of TNF-α-308 G>A genotype and allele frequency between MDS and controls. No difference in the genotype and allele frequency of TNF-α-238 G>A were found between controls and MDS or the subtypes of MDS (P>0.05). We did not find any linkage between plasma level of TNF-α and TNF-α-308 G>A or TNF-α-238 G>A genotype. Statistic differences were observed between platelet count[58(1-611)×10⁹/L vs 90(7-352)×10⁹/L]and bone marrow blasts in MDS patients carrying TNF-α-308 G>A GG and AA+AG genotype (P=0.024, 0.019, respectively).</p><p><b>CONCLUSION</b>TNF-α-308 G>A polymorphism was correlated with susceptibility to MDS-RCMD.</p>
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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Sang / Syndromes myélodysplasiques / Études cas-témoins / Facteur de nécrose tumorale alpha / Prédisposition génétique à une maladie / Polymorphisme de nucléotide simple / Fréquence d&apos;allèle / Génétique / Génotype Type d'étude: Étude observationnelle / Facteurs de risque Limites du sujet: Humains langue: Chinois Texte intégral: Chinese Journal of Hematology Année: 2013 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Sang / Syndromes myélodysplasiques / Études cas-témoins / Facteur de nécrose tumorale alpha / Prédisposition génétique à une maladie / Polymorphisme de nucléotide simple / Fréquence d&apos;allèle / Génétique / Génotype Type d'étude: Étude observationnelle / Facteurs de risque Limites du sujet: Humains langue: Chinois Texte intégral: Chinese Journal of Hematology Année: 2013 Type: Article