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Clinics ; 68(1): 5-9, Jan. 2013. ilus, tab
Article in English | LILACS | ID: lil-665911

ABSTRACT

OBJECTIVE: The JAK2 46/1 haplotype has recently been described as a major contributing factor to the development of myeloproliferative neoplasm, whether positive or negative forthe JAK2 V617F mutation. The G allele, identified by a single-nucleotide polymorphism known as JAK2 rs10974944, is part of the JAK2 46/1 haplotype. The aim of this study was to verify the association between the presence of the G allele and the development of BCR-ABL-negative chronic myeloproliferative neoplasms in our population. METHODS: Blood and oral mucosa swab samples were obtained from 56 patients of two local Brazilian hospitals who had previously been diagnosed with BCR-ABL-negative chronic myeloproliferative neoplasms. Blood samples from 90 local blood donors were used as controls. The presence of the G allele was assessed using a PCR-RFLP assay after extracting DNA from the samples. RESULTS: The presence of the G allele was strongly associated with the presence of BCR-ABL-negative chronic myeloproliferative neoplasms (p = 0.0001; OR = 2.674; 95% CI = 1.630-4.385) in the studied population. CONCLUSION: In agreement with previous reports, the JAK2 46/1 haplotype, represented in this study by the presence of the G allele, is an important predisposing factor in the oncogenetic development of these neoplasms in our population.


Subject(s)
Aged , Aged, 80 and over , Female , Humans , Male , Middle Aged , Young Adult , Haplotypes/genetics , /genetics , Myeloproliferative Disorders/genetics , Brazil , Chi-Square Distribution , Chronic Disease , Fusion Proteins, bcr-abl/genetics , Gene Frequency , Mutation/genetics , Polymerase Chain Reaction , Polymorphism, Restriction Fragment Length/genetics , Sex Distribution
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