Mathew Suresh, Lund Richard J, Chaudhary Lala R, Geurs Theresa, Hruska Keith A
Department of Pediatrics, Washington University School of Medicine, St. Louis, Missouri 63110, USA.
J Am Soc Nephrol. 2008 Aug;19(8):1509-19. doi: 10.1681/ASN.2007080902. Epub 2008 Apr 30.
An apparent conflict exists between observational studies that suggest that vitamin D receptor (VDR) activators provide a survival advantage for patients with ESRD and other studies that suggest that they cause vascular calcification. In an effort to explain this discrepancy, we studied the effects of the VDR activators calcitriol and paricalcitol on aortic calcification in a mouse model of chronic kidney disease (CKD)-stimulated atherosclerotic cardiovascular mineralization. At dosages sufficient to correct secondary hyperparathyroidism, calcitriol and paricalcitol were protective against aortic calcification, but higher dosages stimulated aortic calcification. At protective dosages, the VDR activators reduced osteoblastic gene expression in the aorta, which is normally increased in CKD, perhaps explaining this inhibition of aortic calcification. Interpreting the results obtained using this model, however, is complicated by the adynamic bone disorder; both calcitriol and paricalcitol stimulated osteoblast surfaces and rates of bone formation. Therefore, the skeletal actions of the VDR activators may have contributed to their protection against aortic calcification. We conclude that low, clinically relevant dosages of calcitriol and paricalcitol may protect against CKD-stimulated vascular calcification.
观察性研究表明维生素D受体(VDR)激活剂能为终末期肾病(ESRD)患者带来生存优势,而其他研究则表明它们会导致血管钙化,这两者之间存在明显冲突。为了解释这种差异,我们在慢性肾脏病(CKD)引发动脉粥样硬化性心血管矿化的小鼠模型中,研究了VDR激活剂骨化三醇和帕立骨化醇对主动脉钙化的影响。在足以纠正继发性甲状旁腺功能亢进的剂量下,骨化三醇和帕立骨化醇对主动脉钙化具有保护作用,但更高剂量则会刺激主动脉钙化。在具有保护作用的剂量下,VDR激活剂可降低主动脉中通常在CKD时会增加的成骨细胞基因表达,这或许可以解释对主动脉钙化的这种抑制作用。然而,使用该模型获得的结果解读因动力缺失性骨病而变得复杂;骨化三醇和帕立骨化醇均刺激了成骨细胞表面和骨形成速率。因此,VDR激活剂的骨骼作用可能有助于其对主动脉钙化的保护。我们得出结论,临床相关的低剂量骨化三醇和帕立骨化醇可能预防CKD引发的血管钙化。