The effects of vitamin D repletion on endothelial function and inflammation in patients with coronary artery disease

被引:69
|
作者
Sokol, Seth I. [1 ,2 ,3 ]
Srinivas, Vankeepuram [1 ,2 ]
Crandall, Jill P. [4 ]
Kim, Mimi [5 ]
Tellides, George [6 ]
Lebastchi, Amir [6 ]
Yu, Yiting [5 ]
Gupta, Alok K. [7 ]
Alderman, Michael H. [2 ,5 ]
机构
[1] Jacobi Med Ctr, Dept Med, Div Cardiol, Bronx, NY 10461 USA
[2] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
[3] Montefiore Med Ctr, Dept Med, Div Cardiol, Bronx, NY 10467 USA
[4] Albert Einstein Coll Med, Dept Med, Div Endocrinol, Bronx, NY 10467 USA
[5] Albert Einstein Coll Med, Dept Epidemiol & Populat Hlth, Bronx, NY 10467 USA
[6] Yale Univ, Sch Med, Dept Surg, New Haven, CT 06510 USA
[7] Louisiana State Univ Syst, Dept Clin Res, Pennington Biomed Res Ctr, Baton Rouge, LA USA
关键词
coronary disease; endothelium; inflammation; prospective studies; randomized controlled trials; vascular; vitamin D; SPONTANEOUSLY HYPERTENSIVE-RAT; RANDOMIZED CONTROLLED-TRIAL; SERUM; 25-HYDROXYVITAMIN-D; CARDIOVASCULAR-DISEASE; OLDER-ADULTS; D DEFICIENCY; 1,25-DIHYDROXYVITAMIN D-3; DEPENDENT CONTRACTIONS; VASCULAR HEALTH; D INSUFFICIENCY;
D O I
10.1177/1358863X12466709
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Adequate vitamin D levels may promote cardiovascular health by improving endothelial function and down-regulating inflammation. The objective of this pilot trial was to investigate the effects of vitamin D repletion on endothelial function and inflammation in patients with coronary artery disease (CAD). Using a double-blind placebo wait-list control design, 90 subjects with CAD and vitamin D deficiency (< 20 ng/ml) were randomized 1:1 to 50,000 IU of oral ergocalciferol or placebo weekly for 12 weeks. Endothelial function (reactive hyperemia peripheral arterial tonometry, RH-PAT), circulating adhesion molecules, and pro-inflammatory cytokines were measured at baseline and 12 weeks. The median increase in serum 25-vitamin D from baseline was 26 +/- 17 ng/ml in the active group and 4 +/- 8 ng/ml in the placebo group (between-group difference = 22 ng/ml, p < 0.001). The median within-subject change in RH-PAT score was 0.13 +/- 0.73 with active treatment and -0.04 +/- 0.63 with placebo (between-group difference = 0.17, p = 0.44). Within-group and between-group differences in intercellular adhesion molecule levels were greater with placebo (between-group difference = 6 ng/ml, p = 0.048). Vascular cell adhesion molecule levels decreased in both groups by a similar magnitude (median difference between groups = 8.5 ng/ml, p = 0.79). There was no difference between groups in magnitude of reduction in interleukin (IL)-12 (-8.6 ng/ml, p = 0.72) and interferon-gamma (0.52 ng/ml, p = 0.88). No significant differences in blood pressure, e-selectin, high-sensitivity c-reactive protein, IL-6 or the chemokine CXCL-10 were found with treatment. In conclusion, repleting vitamin D levels in subjects with CAD failed to demonstrate any benefits on surrogate markers of cardiovascular health. These results question the role of vitamin D supplementation in modifying cardiovascular disease. ClinicalTrials.gov Identifier: NCT01570309.
引用
收藏
页码:394 / 404
页数:11
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