We read with interest the letter by Boulon et al.
1
The proposed association between prothrombin G20210A and thromboangiitis obliterans is very interesting. Prior studies have suggested that prothrombin G20210A interacts with other cardiovascular risk factors (especially smoking) to increase the risk of vascular events,2
and this interaction could further explain the association of prothrombin G20210A and thromboangiitis obliterans seen by Bérard et al. and Avcu et al.3
, 4
The literature search conducted in our systematic review did not identify the study by Bérard et al.3
, 5
; had the study been included there would have been no changes in the association of lower extremity peripheral arterial disease (PAD) prothrombin G20210A (pooled random effect odds ratio 1.68 [95% confidence interval 0.94–3.00]; I2 52.1%; p = .08). Furthermore, the addition of the study by Bérard et al. does not modify the association between prothrombin G20210A and critical limb ischemia secondary to PAD (even in the absence of positive cases).3
Finally, we agree that well-designed prospective cohort studies are needed to evaluate the role of prothrombin G20210A in the progression and outcome of patients with PAD.References
- Re: Prothrombin G20210A mutation and lower extremity peripheral arterial disease. A systematic review and meta-analysis.Eur J Vasc Endovasc Surg. 2015;
- Interaction of coagulation defects and cardiovascular risk factors: increased risk of myocardial infarction associated with factor V Leiden or prothrombin 20210A.Circulation. 1998; 97: 1037-1041
- Novel risk factors for premature peripheral arterial occlusive disease in non-diabetic patients: a case-control study.PLoS One. 2013; 8: e37882
- The role of prothrombotic mutations in patients with Buerger's disease.Thromb Res. 2000; 100: 143-147
- Prothrombin G20210A mutation and lower extremity peripheral arterial disease: a systematic review and meta-analysis.Eur J Vasc Endovasc Surg. 2015; 50: 232-240
Article info
Publication history
Published online: September 22, 2015
Identification
Copyright
© 2015 European Society for Vascular Surgery. Published by Elsevier Inc.
User license
Elsevier user license | How you can reuse
Elsevier's open access license policy

Elsevier user license
Permitted
For non-commercial purposes:
- Read, print & download
- Text & data mine
- Translate the article
Not Permitted
- Reuse portions or extracts from the article in other works
- Redistribute or republish the final article
- Sell or re-use for commercial purposes
Elsevier's open access license policy
ScienceDirect
Access this article on ScienceDirectLinked Article
- Re: ‘Prothrombin G20210 Mutation and Lower Extremity Peripheral Arterial Disease: A Systematic Review and Meta-analysis’European Journal of Vascular and Endovascular SurgeryVol. 50Issue 6
- PreviewVasquez et al.1 showed that prothrombin G20210 mutation is significantly elevated in patients with peripheral occlusive arterial disease (POAD) suffering from critical limb ischemia (CLI) but not in the others. Interestingly, this mutation has been reported to be more prevalent in patients with Buerger's disease.2,3 Avcu et al.2 found an increased frequency of the G20210 mutation in Buerger's disease (OR 7.98, 2.45–25.13). Buerger's disease is characterized by diffuse arterial thrombosis and a severe clinical picture, most often at the CLI stage.
- Full-Text
- Preview
Related Articles
Comments
Commenting Guidelines
To submit a comment for a journal article, please use the space above and note the following:
- We will review submitted comments as soon as possible, striving for within two business days.
- This forum is intended for constructive dialogue. Comments that are commercial or promotional in nature, pertain to specific medical cases, are not relevant to the article for which they have been submitted, or are otherwise inappropriate will not be posted.
- We require that commenters identify themselves with names and affiliations.
- Comments must be in compliance with our Terms & Conditions.
- Comments are not peer-reviewed.