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Article

Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke

  • Authors:
    • Hyun-Kyung Park
    • Myung-Chun Kim
    • Sung-Min Kim
    • Dae Jean Jo
  • View Affiliations / Copyright

    Affiliations: Department of Emergency Medicine, School of Medicine, Kyung Hee University Hospital at Gangdong, Seoul, Republic of Korea, Department of Neurosurgery, School of Medicine, Kyung Hee University Hospital at Gangdong, Seoul, Republic of Korea
  • Pages: 343-349
    |
    Published online on: November 1, 2012
       https://doi.org/10.3892/etm.2012.790
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Abstract

The renin-angiotensin system has an important role in the pathogenesis of stroke. We investigated whether two missense single nucleotide polymorphisms (SNPs; rs4762, Thr207Met, T207M; and rs699, Met268Thr, M268T) of angiotensinogen (AGT; serpin peptidase inhibitor, clade A, member 8) are associated with the development and clinical phenotypes of ischemic stroke (IS) and intracerebral hemorrhage (ICH). We analyzed 197 stroke patients (120 IS and 77 ICH) and 301 control subjects. The patients were classified into subgroups in accordance to the scores of the National Institutes of Health Stroke Survey (NIHSS, <6 and ≥6) and Modified Barthel Index (MBI, <60 and ≥60). Multiple logistic regression models were used to analyze the genotype and allele distributions of each SNP. One of the missense SNPs, rs4762 (T207M) was associated with the development of ICH (P=0.038 in log-additive model and P=0.021 in allele distributions). The T allele frequency of T207M was higher in the ICH group (16.2%) compared with the control group (9.6%). The TC haplotype frequency differed significantly between the ICH and control groups (P=0.014). With regard to clinical features, T207M correlated with the NIHSS scores of the ICH patients (P=0.039 in codominant1, P=0.015 in dominant, P=0.011 in overdominant and P=0.039 in log-additive models). However, the two missense SNPs, rs4762 and rs699, were not associated with IS and its clinical features, including NIHSS and MBI scores. These data suggest that a missense SNP (rs4762, T207M) of the AGT gene may be associated with the development of ICH and contribute to the neurological functional levels of ICH patients.
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Copy and paste a formatted citation
Spandidos Publications style
Park H, Kim M, Kim S and Jo D: Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke. Exp Ther Med 5: 343-349, 2013.
APA
Park, H., Kim, M., Kim, S., & Jo, D. (2013). Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke. Experimental and Therapeutic Medicine, 5, 343-349. https://doi.org/10.3892/etm.2012.790
MLA
Park, H., Kim, M., Kim, S., Jo, D."Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke". Experimental and Therapeutic Medicine 5.1 (2013): 343-349.
Chicago
Park, H., Kim, M., Kim, S., Jo, D."Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke". Experimental and Therapeutic Medicine 5, no. 1 (2013): 343-349. https://doi.org/10.3892/etm.2012.790
Copy and paste a formatted citation
x
Spandidos Publications style
Park H, Kim M, Kim S and Jo D: Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke. Exp Ther Med 5: 343-349, 2013.
APA
Park, H., Kim, M., Kim, S., & Jo, D. (2013). Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke. Experimental and Therapeutic Medicine, 5, 343-349. https://doi.org/10.3892/etm.2012.790
MLA
Park, H., Kim, M., Kim, S., Jo, D."Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke". Experimental and Therapeutic Medicine 5.1 (2013): 343-349.
Chicago
Park, H., Kim, M., Kim, S., Jo, D."Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke". Experimental and Therapeutic Medicine 5, no. 1 (2013): 343-349. https://doi.org/10.3892/etm.2012.790
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