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1.
Exp Oncol ; 43(4): 341-345, 2021 12.
Artigo em Inglês | MEDLINE | ID: mdl-34967547

RESUMO

AIM: To investigate the association between SRA1 rs801460 and rs10463297 variants and proliferative type of benign breast disease with atypia development in Ukrainian females. MATERIALS AND METHODS: 83 individuals diagnosed with proliferative type of benign breast disease with atypia and 115 without atypia were enrolled in the study. The rs801460 and rs10463297 variants genotyping was performed using polymerase chain reaction-restriction fragment length polymorphism analysis. Hematoxylin and eosin, toluidine blue and van Gieson's picrofuchsin methods were used for sections staining. RESULTS: It was revealed that SRA1 rs801460-variant is associated with proliferative type of benign breast disease with atypia development both before and after adjustment for risk factors (age, body mass index, age of menarche, oral contraceptives intake and burdened history of breast cancer). The risk for mentioned disease in the individuals with rs801460 TT-genotype is 2.2 times higher (confidence interval 1.010-4.800; p = 0.047) than in individuals with the CC and CT genotypes. No link between SRA1 rs10463297 and proliferative type of benign breast disease with atypia occurrence in Ukrainian females was found. CONCLUSION: The present study specified that SRA1 rs801460, but not rs10463297, can be the strong genetic predictor for benign breast disease with atypia in Ukrainian females.


Assuntos
Neoplasias da Mama , Proteínas de Transporte/genética , Doença da Mama Fibrocística , Neoplasias da Mama/epidemiologia , Neoplasias da Mama/genética , Etnicidade , Feminino , Doença da Mama Fibrocística/complicações , Doença da Mama Fibrocística/epidemiologia , Genótipo , Humanos , Fatores de Risco , Ucrânia
2.
Fiziol Zh (1994) ; 63(1): 33-42, 2017.
Artigo em Ucraniano | MEDLINE | ID: mdl-29975826

RESUMO

The results of γ-glutamyl carboxylase gene rs2592551 polymorphism determining in 170 patients with ischemic atherothrombotic stroke and 124 subjects without acute cerebrovascular disease (control group) have been evaluated. Obtained results revealed that rs2592551 polymorphism was related to ischemic stroke in Ukrainian population. The risk for this disease in patients with T/T genotype was higher than in major C-allele carriers (odds ratio (OR) = 3.117; 95% confidence interval (CI) = 1.016-9.566; P = 0.047). After dividing patients into subgroups, formed by the presence of certain risk factors for atherosclerosis, similar association has been established for women and non-smokers. At the same time, the heterozygous genotype (C/T) in females had significantly protective effect against ischemic stroke development when compared to C/C and T/T genotypes (OR = 0.460; 95% CI 0.213-0.994; P = 0.048). Statistical significance of these results persisted even after adjustment for age, body mass index, smoking and hypertension.


Assuntos
Aterosclerose/genética , Isquemia Encefálica/genética , Carbono-Carbono Ligases/genética , Predisposição Genética para Doença , Polimorfismo de Nucleotídeo Único , Acidente Vascular Cerebral/genética , Adulto , Idoso , Idoso de 80 Anos ou mais , Alelos , Aterosclerose/enzimologia , Aterosclerose/patologia , Índice de Massa Corporal , Isquemia Encefálica/enzimologia , Isquemia Encefálica/patologia , Carbono-Carbono Ligases/metabolismo , Estudos de Casos e Controles , Feminino , Expressão Gênica , Frequência do Gene , Heterozigoto , Humanos , Hipertensão/fisiopatologia , Masculino , Pessoa de Meia-Idade , Fatores de Risco , Fatores Sexuais , Fumar/fisiopatologia , Acidente Vascular Cerebral/enzimologia , Acidente Vascular Cerebral/patologia , Ucrânia
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