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Association of the Angptl3 Gene Polymorphisms and Haplotypes With Cardiovascular Diseases in Birjand Longitudinal Aging Study (Blas) Publisher



Poursalehi F1, 2 ; Aghasizadeh M1, 2, 6 ; Ghorbanzadeh S1, 2 ; Heydari F1, 2 ; Kazemi T2, 3 ; Sharifi F4 ; Moodi M5 ; Fakrzadeh H4 ; Mirimoghaddam E2
Authors
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Authors Affiliations
  1. 1. Student Research Committee, Department of Molecular Medicine, Faculty of Medicine, BUMS, Birjand, Iran
  2. 2. Department of Molecular Medicine, Cardiovascular Diseases Research Center, Faculty of Medicine, Razi Hospital, Birjand University of Medical Sciences (BUMS), Birjand, Iran
  3. 3. Razi Clinical Research Development Unit (RCRDU), Faculty of Medicine, BUMS, Birjand, Iran
  4. 4. Elderly Health Research Center, Endocrinology and Metabolism Population Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  5. 5. Department of Education and Health Promotion, Social Determinants of Health Research Center, School of Health, BUMS, Birjand, Iran
  6. 6. International UNESCO Center for Health-Related Basic Sciences and Human Nutrition, Mashhad University of Medical Sciences, Mashhad, Iran

Source: Egyptian Journal of Medical Human Genetics Published:2022


Abstract

Subject: Cardiovascular disease is now well established as an interaction between genetic and environmental components. Newly identified single nucleotide polymorphisms of angiopoietin-like 3 (ANGPTL3) influence lipid concentrations and risk of coronary artery disease. The current study aimed to determine the association between ANGPTL3 gene variants with incident CVDs in elderly population of the Birjand longitudinal aging study (BLAS). Method: Totally, 360 individuals were recruited in baseline of BLAS including 128 patients with CVD and 153 control subjects. DNA extraction of samples and genotyping were performed by Tetra-ARMS PCR (amplification refractory mutation system polymerase chain reaction). The association between three polymorphisms of ANGPTL3 gene (rs1748195, rs11207997, and rs10789117 variants) with CVD and its risk factors were evaluated using multivariate analysis. Results: Univariate and multiple analyses showed that individuals carrying the GG genotype of rs1748195 and those carrying the TT genotype of rs11207997 directly increased the risk of CVD. CC genotype of rs1748195 and rs11207997 polymorphisms had a significant negative relationship with the disease. In addition, the findings of this study indicate a significant difference in LDL, HDL, cholesterol levels between different genotypes of the rs1748195 and rs10789117 in the healthy group. Individuals with haplotypes CAC, CCC and CCT showed a significant positive relationship with CVD, CVA, AMI and CHD. As well as haplotype was associated with a 1.7-fold increase in risk of CVA, AMI, and CHD. Conclusion: We found that polymorphism of ANGPTL3 gene might support to identify individuals with a cardiometabolic and genetic disorders susceptibility. Three haplotypes CAC, CCC and CCT associated with CVD, CVA, AMI and CHD were reported. © 2022, The Author(s).