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

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...

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Autores principales: PARK, HYUN-KYUNG, KIM, MYUNG-CHUN, KIM, SUNG-MIN, JO, DAE JEAN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524280/
https://www.ncbi.nlm.nih.gov/pubmed/23251296
http://dx.doi.org/10.3892/etm.2012.790
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author PARK, HYUN-KYUNG
KIM, MYUNG-CHUN
KIM, SUNG-MIN
JO, DAE JEAN
author_facet PARK, HYUN-KYUNG
KIM, MYUNG-CHUN
KIM, SUNG-MIN
JO, DAE JEAN
author_sort PARK, HYUN-KYUNG
collection PubMed
description 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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spelling pubmed-35242802012-12-18 Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke PARK, HYUN-KYUNG KIM, MYUNG-CHUN KIM, SUNG-MIN JO, DAE JEAN Exp Ther Med Articles 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. D.A. Spandidos 2013-01 2012-01-11 /pmc/articles/PMC3524280/ /pubmed/23251296 http://dx.doi.org/10.3892/etm.2012.790 Text en Copyright © 2013, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
PARK, HYUN-KYUNG
KIM, MYUNG-CHUN
KIM, SUNG-MIN
JO, DAE JEAN
Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke
title Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke
title_full Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke
title_fullStr Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke
title_full_unstemmed Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke
title_short Assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke
title_sort assessment of two missense polymorphisms (rs4762 and rs699) of the angiotensinogen gene and stroke
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3524280/
https://www.ncbi.nlm.nih.gov/pubmed/23251296
http://dx.doi.org/10.3892/etm.2012.790
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