Paricalcitol does not improve glucose metabolism in patients with stage 3-4 chronic kidney disease

被引:39
作者
de Boer, Ian H. [1 ,2 ,3 ]
Sachs, Michael [1 ,2 ]
Hoofnagle, Andrew N. [4 ]
Utzschneider, Kristina M. [5 ,6 ]
Kahn, Steven E. [5 ,6 ]
Kestenbaum, Bryan [1 ,2 ,3 ]
Himmelfarb, Jonathan [1 ,2 ]
机构
[1] Univ Washington, Dept Med, Div Nephrol, Seattle, WA 98104 USA
[2] Univ Washington, Dept Med, Kidney Res Inst, Seattle, WA 98104 USA
[3] Univ Washington, Dept Epidemiol, Seattle, WA 98104 USA
[4] Univ Washington, Dept Lab Med, Seattle, WA 98104 USA
[5] VA Puget Sound Hlth Care Syst, Dept Med, Div Metab Endocrinol & Nutr, Seattle, WA USA
[6] Univ Washington, Seattle, WA 98104 USA
基金
美国国家卫生研究院;
关键词
chronic kidney disease; clinical trial; insulin resistance; metabolism; vitamin D; FIBROBLAST GROWTH FACTOR-23; RANDOMIZED CONTROLLED-TRIAL; GLOMERULAR-FILTRATION-RATE; FGF23; GENE-EXPRESSION; VITAMIN-D THERAPY; INSULIN-RESISTANCE; SECONDARY HYPERPARATHYROIDISM; HEMODIALYSIS-PATIENTS; 1,25-DIHYDROXYVITAMIN D-3; INTRAVENOUS CALCITRIOL;
D O I
10.1038/ki.2012.311
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
Patients with chronic kidney disease are often insulin resistant and glucose intolerant abnormalities that promote cardiovascular disease. Administration of 1,25-dihydroxyvitamin D (calcitriol) has improved glucose metabolism in patients with end-stage renal disease. We conducted a randomized, placebo-controlled clinical trial to test whether paricalcitol, a 1,25-dihydroxyvitamin D analog, changes glucose tolerance in earlier stages of chronic kidney disease. In a crossover design, 22 nondiabetic patients with estimated glomerular filtration rates of stage 3-4 chronic kidney disease and fasting plasma glucose of 100-125 mg/dl were given daily oral paricalcitol for 8 weeks and matching placebo for 8 weeks, separated by an 8-week washout period. The order of interventions was random and blinded to both participants and investigators. Paricalcitol significantly reduced serum concentrations of parathyroid hormone, 1,25-dihydroxyvitamin D, and 25-hydroxyvitamin D while significantly increasing serum concentrations of fibroblast growth factor-23 and 24,25-dihydroxyvitamin D. Paricalcitol, however, had no significant effect on glucose tolerance (the primary outcome measure), insulin sensitivity, beta-cell insulin response, plasma free fatty acid suppression, or urinary F2-isoprostane excretion. Thus, despite substantial effects on vitamin D metabolism, paricalcitol did not improve glucose metabolism in nondiabetic patients with stage 3-4 chronic kidney disease. Kidney International (2013) 83, 323-330; doi:10.1038/ki.2012.311; published online 22 August 2012
引用
收藏
页码:323 / 330
页数:8
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