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1.
Nephrol Dial Transplant ; 17(5): 865-70, 2002 May.
Article in English | MEDLINE | ID: mdl-11981075

ABSTRACT

BACKGROUND: In a recent uncontrolled retrospective report we suggested that the long-term supplementation of high-dose, i.v. folinic acid combined with high-dose i.v. pyridoxine was highly effective in correcting plasma total homocysteine (tHcy) concentrations in haemodialysis patients. To confirm these findings, we conducted a randomized, controlled trial aimed at evaluating whether i.v. or oral folinic acid provided improved tHcy-lowering efficacy in haemodialysis patients compared with oral folic acid. METHODS: In a 6-month prospective, randomized, controlled trial, 60 chronic haemodialysis patients, matched for age, gender, dialysis duration, and average screening pre-treatment-fasting tHcy levels, were given either 50 mg/week of i.v. calcium folinate (group 1), 50 mg/week of oral calcium folinate (group 2), or 45 mg/week oral folic acid (group 3). All 60 patients also received 750 mg/week of i.v. vitamin B6 and 3 mg/week of oral vitamin B12. RESULTS: Fasting tHcy decreased significantly and to a similar extent in the three groups after 2 months of treatment and remained stable at 4 and 6 months (16.6+/-3.5, 18.3+/-4, and 19.1+/-3.1, in groups 1, 2, and 3, respectively, P=NS). Mean percentage reduction at 6 months was also similar in the three treatment groups (46, 43, and 42% in groups 1, 2, and 3, respectively, P=NS). CONCLUSIONS: These findings show that the tHcy-lowering effects of high-dose i.v. folinic acid, oral folinic acid, or oral folic acid were comparable, suggesting that the hyperhomocysteinaemia observed in haemodialysis patients is not due to abnormal folate metabolism. Furthermore, they are compatible with the view that other abnormalities are also involved in the impaired clearance of homocysteine in uraemic patients.


Subject(s)
Folic Acid/therapeutic use , Hematinics/therapeutic use , Hyperhomocysteinemia/drug therapy , Leucovorin/therapeutic use , Renal Dialysis , Vitamin B 12/therapeutic use , Vitamin B 6/therapeutic use , Administration, Oral , Aged , Dose-Response Relationship, Drug , Drug Therapy, Combination , Female , Folic Acid/administration & dosage , Hematinics/administration & dosage , Humans , Hyperhomocysteinemia/etiology , Injections, Intravenous , Leucovorin/administration & dosage , Male , Middle Aged , Prospective Studies , Renal Dialysis/adverse effects , Time Factors , Vitamin B 12/administration & dosage , Vitamin B 6/administration & dosage
2.
Transplantation ; 73(4): 663-5, 2002 Feb 27.
Article in English | MEDLINE | ID: mdl-11889451

ABSTRACT

BACKGROUND: We conducted a prospective, uncontrolled, open study to assess the relationship between homocysteine (tHcy) and oxidative stress in chronic, stable, renal transplant recipients (RTR). METHODS: Included in the study were 17 chronic, stable RTR. All the patients received folic acid (5 mg/day). tHcy and total antioxidant capacity (TAOC) were measured before and at the end of the study period. RESULTS: Mean tHcy concentration was 26+/-10 micromol/L. tHcy significantly decreased during the study period (26+/-10 vs. 18+/-7 micromol/L; P<0.001). There was a significant inverse relationship between TAOC and tHcy (r= -0.33; P=0.01). TAOC significantly increased during the study period (1.49+/-0.23-1.78+/-0.6; P<0.001). There was an inverse relationship between the variation in tHcy and the variation in TAOC (r= -0.44; P=0.01). CONCLUSION: Our results demonstrate that hyperhomocysteinemia contributed to increased oxidative stress in RTR. tHcy-lowering treatment with folic acid may lower oxidative stress.


Subject(s)
Antioxidants/therapeutic use , Folic Acid/therapeutic use , Hyperhomocysteinemia/drug therapy , Kidney Transplantation/physiology , Oxidative Stress/drug effects , Postoperative Complications/drug therapy , Adult , Fasting , Female , Folic Acid/blood , Homocysteine/blood , Humans , Male , Time Factors
3.
Ann Thorac Surg ; 74(6): 2156-60; discussion 2160, 2002 Dec.
Article in English | MEDLINE | ID: mdl-12643410

ABSTRACT

BACKGROUND: Cardiac troponin I (CTnI) has been shown to be a marker of myocardial injury. The aim of this prospective, randomized study was to compare intermittent antegrade warm cardioplegia with tepid blood cardioplegia in patients undergoing first elective coronary artery bypass graft, using CTnI release as the criterion for evaluating the adequacy of myocardial protection. METHODS: Seventy patients were randomly assigned to one of two cardioplegia groups. CTnI concentrations were measured in serial venous blood samples drawn immediately before cardiopulmonary bypass and after aortic unclamping at 6, 9, 12, and 24 hours. Analysis of covariance with repeated measures was performed to test the effect of the type of cardioplegia and time on CTnI concentration. RESULTS: The total amount of CTnI released (8.23 +/- 20.5 microg in the warm group and 3.19 +/- 2.4 microg in the tepid group) was not statistically different (p = 0.23). The CTnI concentration did not differ for any sample in either of the two groups when adjusted on ejection fraction and the number of preoperative myocardial infarctions (p = 0.06). No patient in the tepid group versus 4 patients in the warm group showed CTnI evidence of perioperative myocardial infarction (p = 0.12). CONCLUSIONS: Our study showed no preference for warm or tepid cardioplegia in terms of myocardial protection, either for clinical or biological data.


Subject(s)
Heart Arrest, Induced/methods , Aged , Electrocardiography , Female , Humans , Male , Prospective Studies , Temperature , Troponin I/blood
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