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Calcium phosphate metabolism and cardiovascular disease in patients with chronic kidney disease.

机译:慢性肾脏病患者的磷酸钙代谢和心血管疾病。

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摘要

Traditional risk factors for atherosclerotic cardiovascular disease (CVD) do not adequately explain the considerable increase in cardiovascular mortality observed among patients with end-stage renal disease (ESRD): these patients experience mortality rates 10-100 times those without ESRD. Disorders of mineral metabolism, including abnormalities in calcium, phosphorus, parathyroid hormone, and vitamin D, represent cardiovascular risk factors unique to the ESRD population. These disturbances manifest clinically through the promotion of extraskeletal calcification and disorders of bone remodeling, two processes which appear to share a common pathogenesis. This article presents evidence describing the impact of calcification-induced arterial stiffness on cardiovascular outcomes of patients with ESRD, along with data relating altered mineral metabolism to all-cause and cardiovascular mortality. Specific management recommendations include 1) early intervention to prevent the development of overt secondary hyperparathyroidism, 2) a more judicious strategy for vitamin D therapy, and 3) a thoughtful approach to the use of calcium-containing phosphate binders, taking into account the underlying bone remodeling disorder and the presence or absence of extraskeletal calcium accumulation.
机译:传统的动脉粥样硬化性心血管疾病(CVD)危险因素不足以解释患有终末期肾病(ESRD)的患者中心血管疾病死亡率的显着增加:这些患者的死亡率是没有ESRD的患者的10-100倍。矿物质代谢紊乱,包括钙,磷,甲状旁腺激素和维生素D异常,是ESRD人群独有的心血管危险因素。这些紊乱在临床上通过促进骨骼外钙化和骨骼重塑失调而表现出来,这两个过程似乎具有共同的发病机理。本文提供的证据描述了钙化诱导的动脉僵硬对ESRD患者心血管结局的影响,以及有关矿物质代谢改变与全因和心血管疾病死亡率相关的数据。具体的管理建议包括:1)早期干预以防止明显的继发性甲状旁腺功能亢进症发展; 2)更加明智的维生素D治疗策略; 3)考虑到基础骨骼的使用含钙磷酸盐结合剂的周到方法重塑障碍和骨骼外钙蓄积的存在与否。

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