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Am J Kidney Dis ; 45(4): 702-7, 2005 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-15806473

RESUMO

BACKGROUND: To date, the relationship between vascular access (VA) failure and plasma total homocysteine level has been investigated only in mixed dialysis populations (ie, patients with a native arteriovenous [AV] fistula or arterial graft), whereas almost no data exist for hemodialysis patients with a native AV fistula. METHODS: In this prospective cohort study, we examined the relationship between plasma total homocysteine level and the methylenetetrahydrofolate reductase (MTHFR) gene and VA-related incident morbidity in a cohort of 205 hemodialysis patients, all with a native AV fistula. RESULTS: During follow-up, 78 patients experienced 1 or more VA thrombotic episodes. Patients with incident VA thrombosis had a significantly greater plasma total homocysteine level compared with patients without this event (P = 0.046). In Kaplan-Meier survival analysis, the hazard ratio for VA thrombosis increased in parallel with homocysteine level, such that patients in the third homocysteine level tertile had a relative risk for this outcome 1.72 times (95% CI, 1.21 to 2.24) greater than in those in the first tertile (log-rank test, 6.81; P = 0.009). In a multiple Cox regression model, plasma total homocysteine level was confirmed to be an independent predictor of AV fistula outcome. Plasma total homocysteine level was significantly greater (P < 0.001) in patients with the TT genotype of the MTHFR gene than in those with the CT or CC genotype. CONCLUSION: VA thrombosis in dialysis patients is associated with hyperhomocysteinemia. Intervention studies are needed to clarify whether decreasing plasma homocysteine concentrations may prevent VA failure in hemodialysis patients.


Assuntos
Derivação Arteriovenosa Cirúrgica/efeitos adversos , Hiper-Homocisteinemia/complicações , Diálise Renal , Trombofilia/etiologia , Trombose/epidemiologia , Adulto , Idoso , Substituição de Aminoácidos , Estudos de Coortes , Comorbidade , Nefropatias Diabéticas/complicações , Nefropatias Diabéticas/terapia , Suscetibilidade a Doenças , Feminino , Seguimentos , Genótipo , Humanos , Hiper-Homocisteinemia/enzimologia , Hiper-Homocisteinemia/genética , Incidência , Falência Renal Crônica/complicações , Falência Renal Crônica/terapia , Tábuas de Vida , Masculino , Metilenotetra-Hidrofolato Redutase (NADPH2)/genética , Pessoa de Meia-Idade , Mutação de Sentido Incorreto , Mutação Puntual , Estudos Prospectivos , Recidiva , Risco , Trombofilia/enzimologia , Trombofilia/genética , Trombose/etiologia
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