Meta-analysis: Vitamin D compounds in chronic kidney disease

被引:191
作者
Palmer, Suetonia C.
McGregor, David O.
Macaskill, Petra
Craig, Jonathan C.
Elder, Grahame J.
Strippoli, Giovanni F. M.
机构
[1] Christchurch Sch Med, Dept Med & Hlth Sci, Christchurch 8001, New Zealand
[2] Christchurch Sch Med & Hlth Sci, Christchurch, New Zealand
[3] Univ Sydney, Ctr Transplant & Renal Res, Sch Publ Hlth, Westmead Millenium Inst, Sydney, NSW, Australia
[4] Natl Hlth & Med Res Council, Ctr Clin Res Excellence Renal Med, Westmead, NSW, Australia
关键词
D O I
10.7326/0003-4819-147-12-200712180-00004
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Vitamin D compounds are widely used to prevent and treat secondary hyperparathyroidism. Purpose: To determine whether vitamin D therapy improves biochemical markers of mineral metabolism and cardiovascular and mortality outcomes in chronic kidney disease. Data Sources: MEDLINE (January 1966 to July 2007), EMBASE (January 1980 to July 2007), and Cochrane databases were searched without language restriction. Study Selection: Randomized, controlled trials of vitamin D compounds in chronic kidney disease were identified. Data Extraction: Two authors independently extracted data. Data Synthesis: Seventy-six trials were identified for inclusion; 3667 participants were enrolled. Vitamin D compounds did not reduce the risk for death, bone pain, vascular calcification, or parathyroidectomy. Compared with placebo, established vitamin D sterols were associated with an increased risk for hypercalcemia (relative risk, 2.37 [95% Cl, 1.16 to 4.85]) and hyperphosphatemia (relative risk, 1.77 [Cl, 1.15 to 2.74]) but did not show a consistent reduction in parathyroid hormone (PTH) levels. Compared with placebo, more recently developed vitamin D analogues were associated with hypercalcernia (relative risk, 5.15 [Cl, 1.06 to 24.97]) but not hyperphosphatemia, and levels of PTH were reduced (weighted mean difference, -10.77 pmol/L [Cl, -20.51 to -1.03 pmol/L]). For suppression of PTH, intravenous administration was superior to oral vitamin D, but higher intravenous doses were used. Limitations: Few studies reported patient-level outcomes, including mortality (8 of 76 trials), and only 5 trials directly compared the effects of treatment with newer vitamin D compounds versus established ones. Heterogeneity in some comparisons remained unexplained by metaregression analyses. Conclusion: Vitamin D compounds do not consistently reduce PTH levels, and beneficial effects on patient-level outcomes are unproven. The value of vitamin D treatment for people with chronic kidney disease remains uncertain.
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页码:840 / 853
页数:14
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