The PORtromb Project: prothrombin G20210A mutation and venous thromboembolism in young people

• Type: Article in International Scientific Journal
• Date: 2002

Authors

Mansilha A. (Author) FMUP; araujo, f (Author) Other; Sampaio, S (Author) Other; Ribeiro, LMC (Author) Other; Braga, A (Author) Other

Journal

The Journal is awaiting validation by the Administrative Services.

Title: CARDIOVASCULAR SURGERY

Vol. 10

Pages: 45-48

ISSN: 0967-2109

Indexing

ISI Web of Knowledge - 7 Citations

Scopus - 7 Citations

Other information

Authenticus ID: P-000-QCG

DOI: 10.1016/s0967-2109(00)00150-2

Abstract (EN): Recently a new identified genetic variant in the 3'-untranslated region of the prothrombin gene (G20210A allele) associated with increased plasma prothrombin levels has been linked to an increased risk of venous thromboembolism (VTE). To determine the importance of this G20210A allele as a causative risk factor for WE in the general population, we analysed the data of an epidemiologic investigation on thrombophilia in young people, the Oporto Thrombophilia Study (PORtromb). Forty cases (mean,age: 27 yr old) with a first episode of WE under 40 yr old, and 100 healthy subjects, were evaluated. Heterozygosity for the G20210A allele was present in 12.5% of WE cases and in 5% of controls, indicating a possible marginal increase of WE risk in carriers of the allele (odds ratio: 2.71: 95% CI 0.74-9.95).

Language: English

Type (Professor's evaluation): Scientific

No. of pages: 4