The association of genotype polymorphisms with vascular access patency in hemodialysis patients. Issue 1 (May 2019)
- Record Type:
- Journal Article
- Title:
- The association of genotype polymorphisms with vascular access patency in hemodialysis patients. Issue 1 (May 2019)
- Main Title:
- The association of genotype polymorphisms with vascular access patency in hemodialysis patients
- Authors:
- Chen, Chun-Fan
Lin, Chih-Ching - Abstract:
- Some hemodialysis patients suffer from repeat dysfunction of dialysis vascular access and need procedures of angioplasty, thrombectomy, and even temporary catheter use. Why these patients are vulnerable to vascular access dysfunction and how to improve its patency are imperative to be discovered. Traditional risk factors for vascular access function had been widely investigated but could not fully explain this question. Several genotype polymorphisms were demonstrated to increase the incidence of cardiovascular disease and might also be linked to higher risk of vascular access dysfunction. As the major causes of arteriovenous access thrombosis are hypercoagulable status and arteriovenous access stenosis, the investigated genes mainly focus on the mediators of the coagulation cascade, inflammatory process, and endothelial dysfunction. The reported polymorphisms of genes significantly associated with arteriovenous access dysfunction included genes encoding methylene tetrahydrofolate reductase, coagulation factors, heme oxygenase-1, matrix metalloproteinase, transforming growth factor-β1, tumor necrosis factor-α, vascular endothelial growth factor-A, renin-angiotensin-aldosterone system, and protein methyl transferase. However, further prospective study is indispensable to elucidate the association between the genotype polymorphisms and the outcome of vascular access. More and more therapeutic options that focus on genotype polymorphisms may generate a great benefit to theSome hemodialysis patients suffer from repeat dysfunction of dialysis vascular access and need procedures of angioplasty, thrombectomy, and even temporary catheter use. Why these patients are vulnerable to vascular access dysfunction and how to improve its patency are imperative to be discovered. Traditional risk factors for vascular access function had been widely investigated but could not fully explain this question. Several genotype polymorphisms were demonstrated to increase the incidence of cardiovascular disease and might also be linked to higher risk of vascular access dysfunction. As the major causes of arteriovenous access thrombosis are hypercoagulable status and arteriovenous access stenosis, the investigated genes mainly focus on the mediators of the coagulation cascade, inflammatory process, and endothelial dysfunction. The reported polymorphisms of genes significantly associated with arteriovenous access dysfunction included genes encoding methylene tetrahydrofolate reductase, coagulation factors, heme oxygenase-1, matrix metalloproteinase, transforming growth factor-β1, tumor necrosis factor-α, vascular endothelial growth factor-A, renin-angiotensin-aldosterone system, and protein methyl transferase. However, further prospective study is indispensable to elucidate the association between the genotype polymorphisms and the outcome of vascular access. More and more therapeutic options that focus on genotype polymorphisms may generate a great benefit to the patency of vascular access of uremic patients. … (more)
- Is Part Of:
- Journal of vascular access. Volume 20:Issue 1(2019)Supplement
- Journal:
- Journal of vascular access
- Issue:
- Volume 20:Issue 1(2019)Supplement
- Issue Display:
- Volume 20, Issue 1 (2019)
- Year:
- 2019
- Volume:
- 20
- Issue:
- 1
- Issue Sort Value:
- 2019-0020-0001-0000
- Page Start:
- 24
- Page End:
- 30
- Publication Date:
- 2019-05
- Subjects:
- Genotype polymorphism -- single nucleotide polymorphism -- arteriovenous fistula -- arteriovenous graft -- hemodialysis
Arterial catheterization -- Periodicals
Intravenous catheterization -- Periodicals
612.13 - Journal URLs:
- http://journals.sagepub.com/home/jva ↗
http://www.uk.sagepub.com/home.nav ↗ - DOI:
- 10.1177/1129729818758556 ↗
- Languages:
- English
- ISSNs:
- 1129-7298
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 10686.xml