TET2 rs1548483 SNP Associating with Susceptibility to Molecularly Annotated Polycythemia Vera and Primary Myelofibrosis

Background: The complexity of myeloproliferative neoplasms (MPNs) cannot be characterized by acquired somatic mutations alone. Individual genetic background is thought to contribute to the development of MPNs. The aim of our study was to assess the association between the TET2 rs1548483 single nucle...

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Veröffentlicht in:Journal of personalized medicine 2020-12, Vol.10 (4), p.259
Hauptverfasser: Lighezan, Diana L., Bojan, Anca S., Iancu, Mihaela, Pop, Raluca M., Gligor-Popa, Ștefana, Tripon, Florin, Cosma, Adriana S., Tomuleasa, Ciprian, Dima, Delia, Zdrenghea, Mihnea, Fetica, Bogdan, Ioniță, Ioana, Gaál, Ildikó O., Vișan, Simona, Mirea, Andreea-Manuela, Popp, Radu A., Florea, Mira, Araniciu, Cătălin, Petrescu, Lucian, Pop, Ioan V., Bănescu, Claudia, Trifa, Adrian P.
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Sprache:eng
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Zusammenfassung:Background: The complexity of myeloproliferative neoplasms (MPNs) cannot be characterized by acquired somatic mutations alone. Individual genetic background is thought to contribute to the development of MPNs. The aim of our study was to assess the association between the TET2 rs1548483 single nucleotide polymorphism (SNP) and the susceptibility to polycythemia vera (PV), essential thrombocythemia (ET), primary myelofibrosis (PMF) or chronic myeloid leukemia (CML). Methods: We evaluated the TET2 rs1548483 SNP through real-time PCR in 1601 MPN patients out of which 431 with PV, 688 with TE, 233 with PMF, 249 with CML and 197 controls. We included only patients with a molecularly proven driver mutation, such as JAK2 V617F, CALR or BCR-ABL1. Results: Significant association between TET2 rs154843 variant allele and JAK2 V617F-positive PV and PMF (OR = 1.70; 95% CI: 1.01–2.91; p-value = 0.046, and OR = 2.04; 95% CI: 1.10–3.77; p-value = 0.024, respectively), and type 2 CALR-positive PMF (OR = 2.98; 95% CI: 1.12–7.93; p-value = 0.035) was noted. Conclusions: The TET2 rs1548483 SNP is associated with the susceptibility to molecularly annotated PV and PMF.
ISSN:2075-4426
2075-4426
DOI:10.3390/jpm10040259