Prognostic Factors Influencing the Patency of Hemodialysis Vascular Access: Literature Review and Novel Therapeutic Modality by Far Infrared Therapy

被引:46
作者
Lin, Chih-Ching [1 ,2 ]
Yang, Wu-Chang [1 ,2 ]
机构
[1] Taipei Vet Gen Hosp, Dept Med, Div Nephrol, Taipei 112, Taiwan
[2] Natl Yang Ming Univ, Sch Med, Taipei 112, Taiwan
关键词
far-infrared therapy; genotype polymorphism; heme oxygenase-1; hemodialysis; vascular access; HEME OXYGENASE-1 GENE; SMOOTH-MUSCLE-CELLS; RECOMBINANT-HUMAN-ERYTHROPOIETIN; CORONARY-ARTERY DISEASE; NITRIC-OXIDE SYNTHASE; MICROSATELLITE POLYMORPHISM; ARTERIOVENOUS-FISTULA; ANTICARDIOLIPIN ANTIBODY; PROMOTER POLYMORPHISM; ENDOTHELIAL FUNCTION;
D O I
10.1016/S1726-4901(09)70035-8
中图分类号
R5 [内科学];
学科分类号
100201 [内科学];
摘要
In Taiwan, more than 85% of patients with end-stage renal disease undergo maintenance hemodialysis (HD). The native arteriovenous fistula (AVF) accounts for a prevalence of more than 80% of the vascular access in our patients. Some mechanical factors may affect the patency of hemodialysis vascular access, such as surgical skill, puncture technique and shear stress on the vascular endothelium. Several medical factors have also been identified to be associated with vascular access prognosis in HD patients, including stasis, hypercoagulability, endothelial cell injury, medications, red cell mass and genotype polymorphisms of transforming growth factor-beta 1 and methylene tetrahydrofolate reductase. According to our previous study, AVF failure was associated with a longer dinucleotide (GT)(n) repeat (n >= 30) in the promoter of the heme oxygenase-1 (HO-1) gene, Our recent study also demonstrated that far-infrared therapy, a noninvasive and convenient therapeutic modality, can improve access flow, inflammatory status and survival of the AVF in HID patients through both its thermal and non-thermal (endothelial-improving, anti-inflammatory, anti proliferative, antioxidative) effects by upregulating NF-E2-related factor-2-dependent HO-1 expression, leading to the inhibition of expression of E-selectin, vascular cell adhesion molecule-1, and intercellular adhesion molecule-1. [J Chin Med Assoc 2009;72(3): 109-116]
引用
收藏
页码:109 / 116
页数:8
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