Thethi Tina K, Bajwa Muhammad A, Ghanim Husam, Jo Chanhee, Weir Monica, Goldfine Allison B, Umpierrez Guillermo, Desouza Cyrus, Dandona Paresh, Fang-Hollingsworth Ying, Raghavan Vasudevan, Fonseca Vivian A
Tulane University Health Sciences Center, New Orleans, LA; Southeast Louisiana Veterans Health Care Systems, New Orleans, LA.
Joslin Diabetes Center, Boston, MA.
J Diabetes Complications. 2015 Apr;29(3):433-7. doi: 10.1016/j.jdiacomp.2015.01.004. Epub 2015 Jan 13.
Patients with type 2 diabetes (T2DM) and chronic kidney disease (CKD) have impaired endothelial function. Vitamin D and its analogs may play a role in regulation of endothelial function and inflammation. We studied effects of paricalcitol compared to placebo on endothelial function and markers of inflammation and oxidative stress in patients with T2DM and CKD.
A double blind, randomized, placebo-controlled trial was conducted in 60 patients with T2DM and stage 3 or 4 CKD. Paricalcitol 1 mcg or placebo was administered orally once daily for three months. Brachial artery flow mediated dilatation (FMD), nitroglycerine mediated dilation (NMD), and plasma concentrations of inflammatory cytokines, tumor necrosis factor -α and interleukin-6, highly-sensitive C-reactive protein; endothelial surface proteins, intercellular adhesion molecule -1 and monocyte chemo attractant protein-1, and plasma glucose, insulin, free fatty acids, and urinary isoprostane were measured at baseline and end of three months.
27 patients in the paricalcitol group and 28 patients in the control group completed the study, though analysis of FMD at both time points was possible in 23 patients in each group. There was no significant difference in the change in FMD, NMD or the biomarkers examined after paricalcitol or placebo treatment.
Treatment with paricalcitol at this dose and duration did not affect brachial artery FMD or biomarkers of inflammation and oxidative stress. The lack of significance may be due to the fact that the study patients had advanced CKD and that effects of paricalcitol are not additive to the effects of glycemic, lipid and anti-hypertensive therapies.
2型糖尿病(T2DM)合并慢性肾脏病(CKD)患者存在内皮功能受损。维生素D及其类似物可能在内皮功能调节和炎症反应中发挥作用。我们研究了与安慰剂相比,帕立骨化醇对T2DM合并CKD患者内皮功能以及炎症和氧化应激标志物的影响。
对60例T2DM合并3期或4期CKD患者进行了一项双盲、随机、安慰剂对照试验。帕立骨化醇1微克或安慰剂每日口服一次,持续三个月。在基线和三个月结束时测量肱动脉血流介导的血管舒张(FMD)、硝酸甘油介导的血管舒张(NMD)以及炎症细胞因子、肿瘤坏死因子-α和白细胞介素-6、高敏C反应蛋白的血浆浓度;内皮表面蛋白、细胞间黏附分子-1和单核细胞趋化蛋白-1,以及血浆葡萄糖、胰岛素、游离脂肪酸和尿异前列腺素。
帕立骨化醇组27例患者和对照组28例患者完成了研究,尽管每组23例患者在两个时间点均可进行FMD分析。帕立骨化醇或安慰剂治疗后,FMD、NMD或所检测的生物标志物的变化无显著差异。
在此剂量和疗程下,帕立骨化醇治疗并未影响肱动脉FMD或炎症和氧化应激生物标志物。缺乏显著性可能是由于研究患者患有晚期CKD,且帕立骨化醇的作用并非叠加于血糖、血脂和抗高血压治疗的作用之上。