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ACE/DD genotype is associated with hemostasis balance disturbances reflecting hypercoagulability and endothelial dysfunction in patients with untreated hypertension

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dc.contributor.author Makris, TK en
dc.contributor.author Stavroulakis, GA en
dc.contributor.author Dafni, UG en
dc.contributor.author Gialeraki, AE en
dc.contributor.author Krespi, PG en
dc.contributor.author Hatzizacharias, AN en
dc.contributor.author Tsoukala, CG en
dc.contributor.author Vythoulkas, JS en
dc.contributor.author Kyriakidis, MK en
dc.date.accessioned 2014-03-01T01:49:45Z
dc.date.available 2014-03-01T01:49:45Z
dc.date.issued 2000 en
dc.identifier.issn 0002-8703 en
dc.identifier.uri https://dspace.lib.ntua.gr/xmlui/handle/123456789/25903
dc.subject.classification Cardiac & Cardiovascular Systems en
dc.subject.other ANGIOTENSIN-CONVERTING ENZYME en
dc.subject.other PLASMINOGEN-ACTIVATOR INHIBITOR-1 en
dc.subject.other CORONARY-ARTERY DISEASE en
dc.subject.other ISCHEMIC-HEART-DISEASE en
dc.subject.other GENE POLYMORPHISM en
dc.subject.other MYOCARDIAL-INFARCTION en
dc.subject.other BORDERLINE HYPERTENSION en
dc.subject.other FIBRINOLYTIC BALANCE en
dc.subject.other CELL DAMAGE en
dc.subject.other RISK en
dc.title ACE/DD genotype is associated with hemostasis balance disturbances reflecting hypercoagulability and endothelial dysfunction in patients with untreated hypertension en
heal.type journalArticle en
heal.language English en
heal.publicationDate 2000 en
heal.abstract Background Angiotensin-converting enzyme (ACE) gene polymorphism has been associated with an increased incidence of myocardial infarction. Recent studies have investigated a potential influence of ACE gene polymorphism on fibrinolysis or endothelial function. It has been previously established that essential hypertension is accompanied by endothelial dysfunction and fibrinolytic balance disorders. The aim of our study was to study the relation between ACE gene polymorphism and fibrinolytic/hemostatic factors as well as endothelial cell damage markers in patients with hypertension. Methods The following parameters were evaluated in 104 patients with previously untreated hypertension: plasminogen activator inhibitor-1 (PAI-1), tissue plasminogen activator (IPA) antigen, fibrinogen, D-dimer, and von Willebrand factor (vWF). The genotype of the ACE gene was also determined (by the polymerase chain reaction method), and patients were characterized according to the observed alleles as deletion/deletion IDD), insertion/insertion till, or insertion/deletion (ID). Results Those with DD genotype tn = 42) had significantly higher plasma levels of PAI-I antigen (P = .012), IPA antigen (P = .0001), fibrinogen (P = .0002), D-dimer (P = .0001) and VWF (P = .0004) compared with ID (n = 30) or II (n = 32) genotypes. The ACE gene genotypes appeared to be significant predictors for plasma PAI-1 antigen, tPA antigen, fibrinogen, D-dimer, and VWF even after adjustment for age, sex, body mass index, triglyceride and cholesterol levels, and blood pressure. Conclusions Our findings suggest that the ACE/DD genotype is associated with hemostasis balance disturbances reflecting hypercoagulability and endothelial damage in patients with untreated hypertension. en
heal.publisher MOSBY, INC en
heal.journalName AMERICAN HEART JOURNAL en
dc.identifier.isi ISI:000165075200010 en
dc.identifier.volume 140 en
dc.identifier.issue 5 en
dc.identifier.spage 760 en
dc.identifier.epage 765 en


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