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Genes (Basel) ; 14(2)2023 02 12.
Artigo em Inglês | MEDLINE | ID: mdl-36833398

RESUMO

Coronary artery disease (CAD) is a common and fatal cardiovascular disease. Among known CAD risk factors, miRNA polymorphisms, such as Has-miR-143 (rs41291957 C>G) and Has-miR-146a (rs2910164 G>A), have emerged as important genetic markers of CAD. Despite many genetic association studies in multiple populations, no study assessing the association between CAD risk and SNPs of miR-143 and miR-146 was documented in the Japanese people. Therefore, using the TaqMan SNP assay, we investigated two SNP genotypes in 151 subjects with forensic autopsy-proven CAD. After pathological observation, we used ImageJ software to assess the degree of coronary artery atresia. Moreover, the genotypes and miRNA content of the two groups of samples with atresia <10% and >10% were analyzed. The results showed that the CC genotype of rs2910164 was more frequent in patients with CAD than in controls, which was associated with the risk of CAD in the study population. However, Has-miR-143 rs41291957 genotype did not show a clear correlation with the risk of CAD.


Assuntos
Doença da Artéria Coronariana , MicroRNAs , Humanos , Doença da Artéria Coronariana/genética , Predisposição Genética para Doença , Povo Asiático , Estudos de Casos e Controles , MicroRNAs/genética , Polimorfismo de Nucleotídeo Único
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