Mineral metabolism and arterial functions in end-stage renal disease:: Potential role of 25-hydroxyvitamin D deficiency
Mineral metabolism and arterial functions in end-stage renal disease:: Potential role of 25-hydroxyvitamin D deficiency
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DOI:
10.1681/asn.2006060573
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发表时间:
2007-02-01
影响因子:
13.6
通讯作者:
Metivier, Fabien
中科院分区:
文献类型:
--
作者:
London, Gerard M.;Guerin, Alain P.;Metivier, Fabien
In ESRD, arterial function is abnormal, characterized by decreased capacitive function (arterial stiffening) and reduced conduit function, shown by diminished flow-mediated dilation (FMD). The pathophysiology of these abnormalities is not clear, and this cross-sectional study analyzed possible relationships among arterial alterations and cardiovascular risk factors, including mineral metabolism parameters, such as serum parathormone, and vitamin D "nutritional" and "hormonal" status by measuring serum 25-hydroxyvitamin D [25(OH)D-3] and 1,25-dihydroxyvitamin D-3 [1,25(OH)(2)D-3] levels. Aortic stiffness (pulse wave velocity), brachial artery (BA) distensibility (echotracking; n = 42), BA FMD (hand-warming; n = 37), and arterial calcification scores (echography and plain x-rays) were measured in 52 stable and uncomplicated patients who were on hemodialysis. 25(OH)D-3 and 1,25(OH)(2)D-3 serum levels were low and weakly correlated (r = 0.365, P < 0.05). After adjustment for BP and age, multivariate analyses indicated that 25(OH)D-3 and 1,25(OH)(2)D-3 were negatively correlated with aortic pulse wave velocity (P < 0.001) and positively correlated with BA distensibility (P < 0.01) and FMD (P < 0.001). Arterial calcification scores were not independently associated with 25(OH)D-3 and 1,25(OH)(2)D, serum concentrations. These results suggest that nutritional vitamin D deficiency and low 1,25(OH)(2)D-3 could be associated with arteriosclerosis and endothelial dysfunction in patients who have ESRD and are on hemodialysis.