Four novel polymorphisms were identified in the fibrinogen gene cluster. Three of them were localized in the promoter regions of the Aa-chain (a 128 C/G, a 58 G/A) or the g-chain (g 239 A/G) gene, while the remaining one was identified in intron 9 of the g-chain gene (g 7792 C/T). Genotype distributions for these polymorphisms were analyzed in 200 healthy Italian individuals and were in Hardy–Weinberg equilibrium. Since high levels of plasma fibrinogen have been associated with an increased risk of cardiovascular disease and genetic variations have been evaluated as thrombotic risk predictors, we analyzed their role in determining the plasma levels of this protein. Owing to the low frequency of the rare allele of a 128 C/G and g 239 A/G polymorphisms, association with plasma fibrinogen levels was investigated for only a 58 G/A and g 7792 C/T. We also investigated in the same population two previously identified polymorphisms in the fibrinogen gene cluster (a TaqI and b 455 G/A)chosen for their widely studied association with plasma fibrinogen levels. In the multivariate linear regression analysis, no statistically significant association with plasma fibrinogen levels was found

Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein / M. Menegatti, R. Asselta, S. Duga, M. Malcovati, P. Bucciarelli, P.M. Mannucci, M.L. Tenchini. - In: THROMBOSIS RESEARCH. - ISSN 0049-3848. - 103:4(2001), pp. 299-307.

Identification of four novel polymorphisms in the Aα and γ fibrinogen genes and analysis of association with plasma levels of the protein

M. Menegatti
Primo
;
R. Asselta
Secondo
;
S. Duga;M. Malcovati;P. Bucciarelli;P.M. Mannucci
Penultimo
;
M.L. Tenchini
Ultimo
2001

Abstract

Four novel polymorphisms were identified in the fibrinogen gene cluster. Three of them were localized in the promoter regions of the Aa-chain (a 128 C/G, a 58 G/A) or the g-chain (g 239 A/G) gene, while the remaining one was identified in intron 9 of the g-chain gene (g 7792 C/T). Genotype distributions for these polymorphisms were analyzed in 200 healthy Italian individuals and were in Hardy–Weinberg equilibrium. Since high levels of plasma fibrinogen have been associated with an increased risk of cardiovascular disease and genetic variations have been evaluated as thrombotic risk predictors, we analyzed their role in determining the plasma levels of this protein. Owing to the low frequency of the rare allele of a 128 C/G and g 239 A/G polymorphisms, association with plasma fibrinogen levels was investigated for only a 58 G/A and g 7792 C/T. We also investigated in the same population two previously identified polymorphisms in the fibrinogen gene cluster (a TaqI and b 455 G/A)chosen for their widely studied association with plasma fibrinogen levels. In the multivariate linear regression analysis, no statistically significant association with plasma fibrinogen levels was found
Cardiovascular disease; DNA polymorphism; Fibrinogen; Fibrinogen gene cluster; Vascular risk marker
Settore BIO/11 - Biologia Molecolare
Settore MED/09 - Medicina Interna
Settore BIO/13 - Biologia Applicata
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/53682
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