Scientific article
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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)
accessLevelPublic
Identifiers
Journal ISSN1078-5884
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233downloads

Technical informations

Creation11/17/2015 3:09:00 PM
First validation11/17/2015 3:09:00 PM
Update time02/03/2025 11:30:53 AM
Status update02/03/2025 11:30:53 AM
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