PMID- 28924539 OWN - NLM STAT- PubMed-not-MEDLINE LR - 20201001 IS - 1311-0160 (Print) IS - 2199-5761 (Electronic) IS - 1311-0160 (Linking) VI - 20 IP - 1 DP - 2017 Jun 30 TI - Genetic Polymorphisms of Hemostatic Factors and Thrombotic Risk in Non BCR-ABL Myeloproliferative Neoplasms: A Pilot Study. PG - 35-42 LID - 10.1515/bjmg-2017-0005 [doi] AB - The most important complications of Philadelphianegagive (non BCR-ABL) myeloproliferative neoplasms (MPNs) are vascular events. Our aim was to evaluate the effects of single nucleotide polymorphisms (SNPs), platelet glycoproteins (GPs) (Ia/IIa, Ibalpha, IIb/IIIa and VI), von Willebrand factor (vWF), coagulation factor VII (FVII), beta-fibrinogen, and the risk of thrombosis in patients with non BCR-ABL MPNs at the Lithuanian University of Health Sciences. Kaunas, Lithuania. Genotyping was done for 108 patients. The TT genotype of the GP Ia/IIa c.807C>T polymorphism was more frequently found in the group of MPN patients with arterial thrombosis compared to MPN patients who were thrombosis-free [26.5 vs. 11.5%, p = 0.049; odds ratio (OR) 2.68; 95% confidence interval (95% CI) 1.01-7.38]. The CT genotype of the beta-fibrinogen c.-148C>T polymorphism occurred more frequently in MPN patients with arterial, and total thrombosis compared to the wild or homozygous genotype (57.7 vs. 40.0 vs. 12.5%; p = 0.027), (64.7 vs. 44.4 vs. 25%; p = 0.032), respectively. The carrier state for the c.-323P10 variant of FVII SNP (summation of P10/10 and P0/10) was more frequent in MPN patients with thrombosis compared to the wild-type genotype carriers (71.4 vs. 43.4%; p = 0.049; OR 3.26; 95% CI 1.01-11.31). The coexistence of heterozygous beta-fibrinogen c.-148C>T and FVII c.-323P0/10 SNP, increased the risk of arterial thrombosis (21.1 vs. 3.7%, p = 0.008; OR 6.93; 95% CI 1.38-34.80). The TT genotype of GP Ia/IIa c.807C>T, the CT genotype of beta-fibrinogen c.-148C>T and FVII c.-323P0/10 SNP could be associated with risk of thrombosis in MPN patients. FAU - Dambrauskiene, R AU - Dambrauskiene R AD - Department of Oncology and Hematology, Institute of Oncology, Lithuanian University of Health Sciences, Kaunas, Lithuania. FAU - Gerbutavicius, R AU - Gerbutavicius R AD - Department of Oncology and Hematology, Institute of Oncology, Lithuanian University of Health Sciences, Kaunas, Lithuania. FAU - Ugenskiene, R AU - Ugenskiene R AD - Lithuanian University of Health Sciences, Institute of Oncology, Oncology Research Laboratory, Kaunas, Lithuania. FAU - Jankauskaite, R AU - Jankauskaite R AD - Lithuanian University of Health Sciences, Institute of Oncology, Oncology Research Laboratory, Kaunas, Lithuania. FAU - Savukaityte, A AU - Savukaityte A AD - Lithuanian University of Health Sciences, Institute of Oncology, Oncology Research Laboratory, Kaunas, Lithuania. FAU - Simoliuniene, R AU - Simoliuniene R AD - Department of Physics, Mathematics and Biophysics, Lithuanian University of Health Sciences, Kaunas, Lithuania. FAU - Rudzianskiene, M AU - Rudzianskiene M AD - Department of Oncology and Hematology, Institute of Oncology, Lithuanian University of Health Sciences, Kaunas, Lithuania. FAU - Gerbutaviciene, R AU - Gerbutaviciene R AD - Department of Drug Technology and Social Pharmacy, Faculty of Pharmacy, Lithuanian University of Health Sciences, Kaunas, Lithuania. FAU - Juozaityte, E AU - Juozaityte E AD - Department of Oncology and Hematology, Institute of Oncology, Lithuanian University of Health Sciences, Kaunas, Lithuania. LA - eng PT - Journal Article DEP - 20170630 PL - Poland TA - Balkan J Med Genet JT - Balkan journal of medical genetics : BJMG JID - 9806959 PMC - PMC5596820 OTO - NOTNLM OT - Genetic polymorphism OT - Myeloproliferative neoplasia OT - Thrombosis EDAT- 2017/09/20 06:00 MHDA- 2017/09/20 06:01 PMCR- 2017/06/30 CRDT- 2017/09/20 06:00 PHST- 2017/09/20 06:00 [entrez] PHST- 2017/09/20 06:00 [pubmed] PHST- 2017/09/20 06:01 [medline] PHST- 2017/06/30 00:00 [pmc-release] AID - bjmg-2017-0005 [pii] AID - 10.1515/bjmg-2017-0005 [doi] PST - epublish SO - Balkan J Med Genet. 2017 Jun 30;20(1):35-42. doi: 10.1515/bjmg-2017-0005. eCollection 2017 Jun 30.