Folate supplementation fails to affect vascular function and carotid artery intima media thickness in cyclosporin A-treated renal transplant recipients
Contribuinte(s) |
K.M. Koch |
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Data(s) |
01/01/2006
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Resumo |
Background: Cyclosporin A (CsA)-treated renal transplant recipients (RTR) exhibit relative hyperhomocystinemia and vascular dysfunction. Folate supplementation lowers homocysteine and has been shown to improve vascular function in healthy subjects and patients with coronary artery disease. The aim of this study was to assess the effects of 3 months of folate supplementation (5 mg/day) on vascular function and structure in RTR. Methods: A double-blind, placebo-controlled crossover study was conducted in 10 CsA-treated RTR. Vascular structure was measured as carotid artery intima media thickness (IMT) and function was assessed as changes in brachial artery diameter during reactive hyperemia (RE) and in response to glyceryl trinitrate (GTN). Function data were analyzed as absolute and percent change from baseline and area under the diameter/time curve. Blood samples were collected before and after supplementation and analyzed for total plasma homocysteine, folate, vitamin B-12 and asymmetric dimethyl arginine (ADMA) in addition to regular measures of hemoglobin, hematocrit, mean corpuscular volume (MCV) and serum creatinine. Results: Folate supplementation significantly increased plasma folate by 687% (p < 0.005) and decreased homocysteine by 37% (p < 0.05) with no changes (p > 0.05) in vitamin B 12 or ADMA. There were no significant (p > 0.05) changes in vascular structure or function during the placebo or the folate supplementation phases; IMT; placebo pre mean +/- SD, 0.52 +/- 0.12, post 0.50 +/- 0.11; folate pre 0.55 +/- 0.17, post 0.49 +/- 10.20 mm 5% change in brachial artery diameter (RH, placebo pre 10 +/- 8, post 6 +/- 5; folate pre 9 +/- 7, post 7 +/- 5; GTN, placebo pre 18 +/- 10, post 17 +/- 9, folate pre 16 +/- 9, post-supplementation 18 +/- 8). Conclusion: Three months of folate supplementation decreases plasma homocysteine but has no effect on endothelial function or carotid artery IMT in RTR. |
Identificador | |
Idioma(s) |
eng |
Publicador |
Dustri-Verlag Dr Karl Feistle |
Palavras-Chave | #Asymmetric Dimethylarginine #Brachial Artery Reactivity (bar) #Carotid Artery Intima Media Thickness (imt) #Folate #Homocysteine #Renal Transplant Recipients (rtr) #Vascular Function #Urology & Nephrology #Improves Endothelial Function #Folic-acid Supplementation #Homocysteine Levels #Hemodialysis-patients #Plasma Homocysteine #Hyperhomocysteinaemic Subjects #No Change #Disease #Therapy #C1 #321012 Nephrology and Urology #321003 Cardiology (incl. Cardiovascular Diseases) #730115 Urogenital system and disorders #730106 Cardiovascular system and diseases |
Tipo |
Journal Article |