Riboflavin is a determinant of total homocysteine plasma concentrations in end-stage renal disease patients

被引:30
|
作者
Skoupy, S
Födinger, M
Veitl, M
Perschl, A
Puttinger, H
Röhrer, C
Schindler, K
Vychytil, A
Hörl, WH
Sunder-Plassmann, G
机构
[1] Univ Vienna, Dept Med 3, Div Nephrol & Dialysis, A-1090 Vienna, Austria
[2] Univ Vienna, Dept Lab Med, Div Endocrinol & Metab, A-1090 Vienna, Austria
来源
关键词
D O I
10.1097/01.ASN.0000013299.11876.F6
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The effect of thiamine (vitamin B-1) or riboflavin (vitamin B-2) availability on fasting total homocysteine (tHcy) plasma levels in end-stage renal disease patients is unknown. A cross-sectional study was performed in a population of non-vitamin supplemented patients maintained on continuous ambulatory peritoneal dialysis. Red blood cell availability of thiamine (alpha-ETK) and of riboflavin (alpha-EGR), along with other predictors of tHcy plasma levels, was considered in the analysis. There was a linear association of alpha-EGR with tHcy plasma concentrations (P = 0.009), which was not observed for alpha-ETK. Among red blood cell vitamins, alpha-EGR was the only predictor of tHcy levels (P = 0.035), whereas alpha-ETK, red blood cell pyridoxal-5-phosphate supply (alpha-EGOT) and red blood cell folate levels had no effect, The risk for having a high tHcy plasma levels within the fourth quartile (plasma tHcy >38.3 mumol/L) was increased by an alpha-EGR > median (odds ratio, 4.706, 95% confidence interval, 1.124 to 19.704; P = 0.026). By way of contrast, alpha-ETK had no effect in these analyses. Independent predictors of tHcy plasma levels were serum albumin, alpha-EGR, red blood cell folate, and certain MTHFR genotypes. A logistic regression analysis showed that the MTHFR genotype is a predictor for having a tHey plasma concentration within the fourth quartile. In summary, riboflavin availability, as measured by alpha-EGR, is a determinant of fasting tHcy plasma levels in peritoneal dialysis patients. This finding may have implications for tHcy lowering therapy in individuals with end-stage renal disease.
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页码:1331 / 1337
页数:7
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