Literature DB >> 22285224

Variation in oral calcitriol response in patients with stages 3-4 CKD.

Abigail B Shoben1, Gregory Levin, Ian H de Boer, Catherine Yeung, Suzanne Watnick, Ernie Ayers, Bryan Kestenbaum.   

Abstract

BACKGROUND: Oral calcitriol decreases parathyroid hormone (PTH) concentrations in patients who have chronic kidney disease (CKD); however, treatment response is highly variable. We evaluated whether patient characteristics affect the PTH response to oral calcitriol in nondialysis patients with CKD in a clinic-based setting. STUDY
DESIGN: Cohort study. SETTING & PARTICIPANTS: This study included 379 new oral calcitriol users in the Veterans' Affairs Northwest Health Network. All had stages 3-4 CKD, hyperparathyroidism, and a serum PTH measurement before and 1-6 months after initiating oral calcitriol therapy. PREDICTORS: Patient-level characteristics hypothesized to affect calcitriol response: race, body size, concurrent medications, and kidney function. OUTCOMES: Relative decrease in serum PTH concentration after starting oral calcitriol therapy. MEASUREMENTS: Data were abstracted from the Veterans' Affairs Northwest Health Network (VISN 20) Data Warehouse, which includes electronic pharmacy and laboratory records.
RESULTS: Mean estimated glomerular filtration rate was 30 mL/min/1.73 m(2) and mean initial PTH concentration was 199 pg/mL. Regular- (0.25 μg/d) and low-dose (<0.25 μg/d) oral calcitriol were associated with on average 23% and 13% relative decreases in serum PTH concentrations, respectively. After adjustment for calcitriol dosage, initial PTH concentration, and time to follow-up measurement, African American race was associated with a blunted calcitriol response (geometric mean final PTH value, 26% higher; 95% CI, 8%-47%). Serum albumin concentration <3.5 g/dL also was associated with a diminished calcitriol response (geometric mean final PTH, 19% higher; 95% CI, 6%-35%). Although numbers were small, concurrent use of benzodiazepines and nonactivated vitamin D supplements was associated with a significantly greater PTH response. LIMITATIONS: Clinic-based study is limited by the availability of PTH measurements after starting calcitriol therapy. Study of a predominantly older male population.
CONCLUSIONS: In patients with stages 3-4 CKD, African American race and low serum albumin level are associated with a diminished PTH response to oral calcitriol.
Copyright © 2012 National Kidney Foundation, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22285224      PMCID: PMC3328668          DOI: 10.1053/j.ajkd.2011.11.041

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  17 in total

1.  Intestinal and hepatic CYP3A4 catalyze hydroxylation of 1alpha,25-dihydroxyvitamin D(3): implications for drug-induced osteomalacia.

Authors:  Yang Xu; Takanori Hashizume; Margaret C Shuhart; Connie L Davis; Wendel L Nelson; Toshiyuki Sakaki; Thomas F Kalhorn; Paul B Watkins; Erin G Schuetz; Kenneth E Thummel
Journal:  Mol Pharmacol       Date:  2005-10-05       Impact factor: 4.436

Review 2.  Transport of vitamin D metabolites.

Authors:  J G Haddad
Journal:  Clin Orthop Relat Res       Date:  1979 Jul-Aug       Impact factor: 4.176

3.  Metabolic studies using recombinant escherichia coli cells producing rat mitochondrial CYP24 CYP24 can convert 1alpha,25-dihydroxyvitamin D3 to calcitroic acid.

Authors:  T Sakaki; N Sawada; Y Nonaka; Y Ohyama; K Inouye
Journal:  Eur J Biochem       Date:  1999-05

4.  A controlled trial of the early treatment of secondary hyperparathyroidism with calcitriol in hemodialysis patients.

Authors:  J A Delmez; J Kelber; K Y Norwood; K S Giles; E Slatopolsky
Journal:  Clin Nephrol       Date:  2000-10       Impact factor: 0.975

5.  Low-dose calcitriol prevents the rise in 1,84-iPTH without affecting serum calcium and phosphate in patients with moderate renal failure (prospective placebo-controlled multicentre trial).

Authors:  E Ritz; S Küster; H Schmidt-Gayk; G Stein; C Scholz; G Kraatz; A Heidland
Journal:  Nephrol Dial Transplant       Date:  1995-12       Impact factor: 5.992

6.  25-Hydroxyvitamin D transport in human plasma. Isolation and partial characterization of calcifidiol-binding protein.

Authors:  J G Haddad; J Walgate
Journal:  J Biol Chem       Date:  1976-08-25       Impact factor: 5.157

7.  Performance evaluation of automated assays for beta-CrossLaps, N-MID-Osteocalcin and intact parathyroid hormone (BIOROSE Multicenter Study).

Authors:  Heinrich Schmidt-Gayk; Eberhard Spanuth; Jochem Kötting; Reiner Bartl; Dieter Felsenberg; Johannes Pfeilschifter; Friedhelm Raue; Heinz Jürgen Roth
Journal:  Clin Chem Lab Med       Date:  2004-01       Impact factor: 3.694

8.  Low dose calcitriol versus placebo in patients with predialysis chronic renal failure.

Authors:  K P Nordal; E Dahl
Journal:  J Clin Endocrinol Metab       Date:  1988-11       Impact factor: 5.958

9.  Seasonal variation in vitamin D, vitamin D-binding protein, and dehydroepiandrosterone: risk of prostate cancer in black and white men.

Authors:  E H Corder; G D Friedman; J H Vogelman; N Orentreich
Journal:  Cancer Epidemiol Biomarkers Prev       Date:  1995-09       Impact factor: 4.254

10.  Demographic differences and trends of vitamin D insufficiency in the US population, 1988-2004.

Authors:  Adit A Ginde; Mark C Liu; Carlos A Camargo
Journal:  Arch Intern Med       Date:  2009-03-23
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.