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Vitamin-K-Dependent Protection of the Renal Microvasculature: Histopathological Studies in Normal and Diseased Kidneys

机译:维生素K依赖的肾脏微脉管系统的保护:正常肾脏和患病肾脏的组织病理学研究

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摘要

Vitamin-K-dependent carboxylation of matrix Gla protein (MGP) protects the macrocirculation against calcification. We recently reported in a multiethnic population study that the estimated glomerular filtration rate, a microvascular trait, decreased and the risk of chronic kidney disease increased with higher circulating levels of inactive dephospho-uncarboxylated MGP, a marker of vitamin K deficiency. These findings highlighted the possibility that vitamin K might have a beneficial effect on the renal microcirculation. To substantiate these epidemiological findings, we undertook a pilot study, in which we stained renal tissue samples obtained by biopsy from 2 healthy kidney donors and 4 patients with nephropathy for carboxylated and uncarboxylated MGP and calcium deposits. Three patients had renal calcifications, which were consistently associated with carboxylated and uncarboxylated MGP. Normal renal tissue was devoid of microcalcifications and staining for carboxylated and uncarboxylated MGP. Pending confirmation in a larger study covering a wider range of renal pathologies, these histopathological findings suggest that MGP might inhibit calcification not only in large arteries, as was known before, but in renal tissue as well, thereby highlighting potentially new avenues for promoting renal health, for instance by vitamin K supplementation.
机译:基质Gla蛋白(MGP)的维生素K依赖性羧化作用可保护大循环免受钙化。我们最近在一项多族裔人群研究中报告说,随着循环中较高水平的无活性脱磷非羧化MGP(维生素K缺乏症的标志),估计的肾小球滤过率,微血管特征降低,慢性肾脏疾病的风险增加。这些发现凸显了维生素K可能对肾脏微循环产生有益作用的可能性。为了证实这些流行病学发现,我们进行了一项前期研究,在该研究中,我们对2位健康的肾脏供体和4位肾病患者的活检组织中的肾脏组织样本进行了染色,以分析其羧化和非羧化的MGP和钙沉积。三例患者出现肾钙化,与钙化和非羧化MGP持续相关。正常的肾组织没有微钙化和羧基化和未羧基化的MGP染色。这些尚待进一步研究证实,MGP可能不仅抑制大动脉的钙化,而且抑制了肾组织的钙化,从而突出了促进肾脏健康的新途径,例如补充维生素K。

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