TY - JOUR
T1 - Antiproteinuric treatment reduces urinary loss of vitamin D-binding protein but does not affect vitamin D status in patients with chronic kidney disease
AU - Doorenbos, Carolina R. C.
AU - de Cuba, Milton M.
AU - Vogt, Liffert
AU - Kema, Ido P.
AU - van den Born, Jacob
AU - Gans, Reinold O. B.
AU - Navis, Gerjan
AU - de Borst, Martin H.
PY - 2012/1
Y1 - 2012/1
N2 - Vitamin D deficiency is common in chronic kidney disease (CKD). Increased urinary loss of vitamin D binding protein (VDBP), the main transporter of 25-hydroxyvitamin D-3 in the circulation, has been postulated to contribute to vitamin D deficiency in proteinuria. To test this hypothesis we analyzed urinary and plasma levels of VDBP, 25-hydroxyvitamin D-3 and 1,25-dihydroxyvitamin D-3 from proteinuric patients, before and after antiproteinuric interventions.We performed a post-hoc analysis of a clinical trial in CKD patients (n = 13, creatinine clearance median 60 (range 25-177) ml/min) subjected to the following study periods: washout (no antiproteinuric treatment, 4 weeks), lisinopril 40 mg QD (ACEi, 6 weeks), or indomethacin 75 mg BID (NSAID, 4 weeks) in randomized sequence. Healthy subjects screened for donation (n = 10) served as controls. Plasma and urine VDBP levels were measured by ELISA, 25-hydroxyvitamin D-3 levels by LC-MS and 1,25-dihydroxyvitamin D-3 levels by radioimmunoassay.In CKD patients urinary VDBP excretion was strongly increased (median (range) 5413 (155-211,027) mu g/24 h) as compared to healthy controls (64 (23-111) mu g/24 h, p <0.001). Both NSAID and ACEi significantly decreased urinary VDBP excretion, in proportion to proteinuria reduction. Plasma VDBP, 25-hydroxyvitamin D-3 and 1,25-dihydroxyvitamin D3 levels, however, were similar between patients and controls and not affected by antiproteinuric intervention.Urinary VDBP excretion is markedly increased in proteinuria and responds to antiproteinuric treatment. Urinary VDBP loss is not associated with plasma VDBP or vitamin D-3 levels, suggesting that urinary loss of VDBP does not affect vitamin D status. (C) 2011 Elsevier Ltd. All rights reserved.
AB - Vitamin D deficiency is common in chronic kidney disease (CKD). Increased urinary loss of vitamin D binding protein (VDBP), the main transporter of 25-hydroxyvitamin D-3 in the circulation, has been postulated to contribute to vitamin D deficiency in proteinuria. To test this hypothesis we analyzed urinary and plasma levels of VDBP, 25-hydroxyvitamin D-3 and 1,25-dihydroxyvitamin D-3 from proteinuric patients, before and after antiproteinuric interventions.We performed a post-hoc analysis of a clinical trial in CKD patients (n = 13, creatinine clearance median 60 (range 25-177) ml/min) subjected to the following study periods: washout (no antiproteinuric treatment, 4 weeks), lisinopril 40 mg QD (ACEi, 6 weeks), or indomethacin 75 mg BID (NSAID, 4 weeks) in randomized sequence. Healthy subjects screened for donation (n = 10) served as controls. Plasma and urine VDBP levels were measured by ELISA, 25-hydroxyvitamin D-3 levels by LC-MS and 1,25-dihydroxyvitamin D-3 levels by radioimmunoassay.In CKD patients urinary VDBP excretion was strongly increased (median (range) 5413 (155-211,027) mu g/24 h) as compared to healthy controls (64 (23-111) mu g/24 h, p <0.001). Both NSAID and ACEi significantly decreased urinary VDBP excretion, in proportion to proteinuria reduction. Plasma VDBP, 25-hydroxyvitamin D-3 and 1,25-dihydroxyvitamin D3 levels, however, were similar between patients and controls and not affected by antiproteinuric intervention.Urinary VDBP excretion is markedly increased in proteinuria and responds to antiproteinuric treatment. Urinary VDBP loss is not associated with plasma VDBP or vitamin D-3 levels, suggesting that urinary loss of VDBP does not affect vitamin D status. (C) 2011 Elsevier Ltd. All rights reserved.
KW - Vitamin D binding protein
KW - Vitamin D-3
KW - Proteinuria
KW - RAAS blockade
KW - D METABOLISM
KW - RENOPROTECTION
U2 - 10.1016/j.jsbmb.2011.09.002
DO - 10.1016/j.jsbmb.2011.09.002
M3 - Article
SN - 0960-0760
VL - 128
SP - 56
EP - 61
JO - Journal of steroid biochemistry and molecular biology
JF - Journal of steroid biochemistry and molecular biology
IS - 1-2
ER -