Source:http://linkedlifedata.com/resource/pubmed/id/17287628
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2007-2-8
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pubmed:abstractText |
A common factor V gene haplotype, the FVR2 haplotype (FVHR2), has been associated with a reduced cofactor activity in activated protein C-mediated activated factor VIII inactivation. Our aim was to investigate the role of FVHR2 as a possible determinant of factor VIII levels in a population study. A total of 516 individuals (401 men, 115 women; mean age 58.4 +/- 10.8 years) were enrolled within the frame of a regional cardiovascular survey, characterized for factor VIII coagulant activity (FVIII:c) and factor V coagulant activity (FV:c) levels, and genotyped for factor V polymorphisms. In men without signs of overt inflammation, FVHR2 carriers had higher levels of FVIII:c than noncarriers (154 IU/dl, 95% confidence interval = 143-166 versus 142 IU/dl, 95% confidence interval = 138-147; P = 0.045) and were more represented in individuals with high (> or = 150 IU/dl) FVIII:c levels (21.2 versus 10.8%; odds ratio = 2.27, 95% confidence interval = 1.17-4.39 after adjustment for age, blood group and high-sensitivity C-reactive protein levels). In conclusion, this clinical report suggests the common FVHR2 as a possible independent determinant of FVIII:c levels. The report concomitantly addresses the relationship between factor V and factor VIII levels and supports the hypothesis of a mild prothrombotic role of FVHR2 by means of increased factor VIII levels.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0957-5235
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
18
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
125-9
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:17287628-Aged,
pubmed-meshheading:17287628-Blood Coagulation,
pubmed-meshheading:17287628-Data Collection,
pubmed-meshheading:17287628-Factor V,
pubmed-meshheading:17287628-Factor VIII,
pubmed-meshheading:17287628-Female,
pubmed-meshheading:17287628-Genotype,
pubmed-meshheading:17287628-Haplotypes,
pubmed-meshheading:17287628-Heterozygote,
pubmed-meshheading:17287628-Humans,
pubmed-meshheading:17287628-Male,
pubmed-meshheading:17287628-Middle Aged,
pubmed-meshheading:17287628-Molecular Epidemiology,
pubmed-meshheading:17287628-Polymorphism, Genetic,
pubmed-meshheading:17287628-Thrombophilia
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pubmed:year |
2007
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pubmed:articleTitle |
Increased factor VIII coagulant activity levels in male carriers of the factor V R2 polymorphism.
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pubmed:affiliation |
Department of Clinical and Experimental Medicine, University of Verona, Italy. trentinik@jumpy.it
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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