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Scientific article
Open access
English

Prothrombin G20210A mutation and lower extremity peripheral arterial disease: a systematic review and meta-analysis

Published inEuropean journal of vascular and endovascular surgery, vol. 50, no. 2, p. 232-240
Publication date2015
Abstract

Despite being an important risk factor for venous thromboembolism, the role of the prothrombin G20210A mutation in patients with arterial disease remains unclear. The aim of this review was to evaluate the association of prothrombin G20210A and lower extremity peripheral arterial disease (PAD).

Keywords
  • Chi-Square Distribution
  • Critical Illness
  • Gene Frequency
  • Genetic Predisposition to Disease
  • Humans
  • Ischemia/diagnosis/genetics
  • Lower Extremity/blood supply
  • Mutation
  • Odds Ratio
  • Peripheral Arterial Disease/diagnosis/genetics
  • Phenotype
  • Prothrombin/genetics
  • Risk Assessment
  • Risk Factors
  • Thrombophilia/blood/complications/diagnosis/genetics
Citation (ISO format)
VAZQUEZ, F et al. Prothrombin G20210A mutation and lower extremity peripheral arterial disease: a systematic review and meta-analysis. In: European journal of vascular and endovascular surgery, 2015, vol. 50, n° 2, p. 232–240. doi: 10.1016/j.ejvs.2015.04.033
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Article (Published version)
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Identifiers
ISSN of the journal1078-5884
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Technical informations

Creation17/11/2015 15:09:00
First validation17/11/2015 15:09:00
Update time15/03/2023 00:04:34
Status update15/03/2023 00:04:33
Last indexation02/05/2024 17:14:11
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