A polymorphism in AGT and AGTR1 gene is associated with lead-related high blood pressure
DC Field | Value | Language |
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dc.contributor.author | Kim, Hyung-Ki | - |
dc.contributor.author | Lee, Hwayoung | - |
dc.contributor.author | Kwon, Jun-Tack | - |
dc.contributor.author | Kim, Hak-Jae | - |
dc.date.accessioned | 2021-08-11T19:24:49Z | - |
dc.date.available | 2021-08-11T19:24:49Z | - |
dc.date.issued | 2015-12 | - |
dc.identifier.issn | 1470-3203 | - |
dc.identifier.issn | 1752-8976 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/10076 | - |
dc.description.abstract | We investigated the association of polymorphisms in two renin-angiotensin system-related genes, expressed as angiotensinogen (AGT) and angiotensin II type 1 receptor (AGTR1), with blood lead levels and lead-related blood pressure in lead-exposed male workers in Korea. A cross-sectional study involving 808 lead-exposed male workers in Korea was conducted using a restriction fragment length polymorphism-based strategy to differentiate the various genotypes of polymorphisms in the AGT and AGTR1 genes. The association of clinical characteristics with genotypes as modifiers was estimated after adjustment for age, smoking status, drinking status, body mass index and job duration of each subject. Genotype and allele frequencies of the M235T polymorphism in AGT were associated with lead-related high blood pressure status. Moreover, blood lead levels were associated with allele frequencies of the AGT M235T polymorphism. These results suggested that the M/M genotype and M allele of AGT are risk factors for lead-related high blood pressure. | - |
dc.format.extent | 8 | - |
dc.language | 영어 | - |
dc.language.iso | ENG | - |
dc.publisher | SAGE Publications | - |
dc.title | A polymorphism in AGT and AGTR1 gene is associated with lead-related high blood pressure | - |
dc.type | Article | - |
dc.publisher.location | 영국 | - |
dc.identifier.doi | 10.1177/1470320313516174 | - |
dc.identifier.scopusid | 2-s2.0-84952941574 | - |
dc.identifier.wosid | 000367626500003 | - |
dc.identifier.bibliographicCitation | JRAAS - Journal of the Renin-Angiotensin-Aldosterone System, v.16, no.4, pp 712 - 719 | - |
dc.citation.title | JRAAS - Journal of the Renin-Angiotensin-Aldosterone System | - |
dc.citation.volume | 16 | - |
dc.citation.number | 4 | - |
dc.citation.startPage | 712 | - |
dc.citation.endPage | 719 | - |
dc.type.docType | Article | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Cardiovascular System & Cardiology | - |
dc.relation.journalWebOfScienceCategory | Peripheral Vascular Disease | - |
dc.subject.keywordPlus | II TYPE-1 RECEPTOR | - |
dc.subject.keywordPlus | ANGIOTENSIN-CONVERTING ENZYME | - |
dc.subject.keywordPlus | HUMAN ESSENTIAL-HYPERTENSION | - |
dc.subject.keywordPlus | LEFT-VENTRICULAR MASS | - |
dc.subject.keywordPlus | RISK-FACTOR | - |
dc.subject.keywordPlus | EXPOSURE | - |
dc.subject.keywordPlus | WORKERS | - |
dc.subject.keywordPlus | SYSTEM | - |
dc.subject.keywordPlus | ABSORPTION | - |
dc.subject.keywordPlus | INFARCTION | - |
dc.subject.keywordAuthor | Angiotensin II type I receptor | - |
dc.subject.keywordAuthor | angiotensinogen | - |
dc.subject.keywordAuthor | hypertension | - |
dc.subject.keywordAuthor | lead | - |
dc.subject.keywordAuthor | polymorphism | - |
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