[age - rage系统在CKD-MBD中的作用]

Hironobu Fujisawa, Yosuke Nakayama, Kaoru Ueda, Kei Fukami
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引用次数: 0

摘要

异常,如甲状旁腺功能亢进、血管钙化和骨质疏松症,是终末期肾病(ESRD)患者的毁灭性并发症。这些异常显著影响生活质量和预后。因此,控制慢性肾脏疾病的异常-矿物质和骨代谢在这些患者中起着重要的作用。通常认为钙磷代谢异常主要归因于血管钙化的发生,但即使钙磷水平得到控制,预防血管钙化仍然是一件困难的事情。此外,ESRD患者血管钙化的发生和进展机制尚不清楚。近年来,晚期糖基化终产物(AGEs)已被发现参与骨异常的发展和促进,如骨脆化和血管钙化。因此,阻断AGEs和AGE受体(RAGE)系统可能是一种新的治疗策略,通过抑制骨脆化和血管钙化来改善ESRD患者的预后。
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[Role of AGEs-RAGE system in CKD-MBD.]

Abnormalities, such as hyperparathyroidism, vascular calcification, and osteoporosis, are devastating complications in patients with end-stage renal disease(ESRD). These abnormalities significantly affect the quality of life and prognosis. Therefore, controlling the abnormalities of chronic kidney disease-mineral and bone metabolism play an important role in these patients. Conventionally, calcium and phosphorus metabolism abnormalities have been mainly attributed to the development of vascular calcification, but preventing vascular calcification is still difficult even if calcium and phosphorus levels are controlled. Additionally, the mechanisms of the development and progression of vascular calcification in patients with ESRD are still unknown. Recently, advanced glycation end products(AGEs)have been known to be involved in the development and promotion of bone abnormality, such as bone embrittlement and vascular calcification. Therefore, blockade of AGEs and the receptor for AGE(RAGE)system may be a novel therapeutic strategy to improve the prognosis of patients with ESRD by inhibiting bone embrittlement and vascular calcification.

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