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Assessment of Vascular Function in Patients With Chronic Kidney Disease
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在脏和心血管疾病的交叉点FGF23和klotho
Daniel Edmonston1,2, Alexander Grabner1, Myles Wolf3,4
1Division of Nephrology, Department of Medicine, Duke University School of Medicine, Durham, NC, USA.
Nature reviews. Cardiology
|July 14, 2023
概括
心血管疾病是慢性病 (CKD) 的主要风险之一. 在CKD中,纤维细胞生长因子23 (FGF23) 和低克洛托导致心脏问题,需要对矿物质失衡进行整体治疗.
科学领域:
- 腎臟病學 (nephrology) 是一種醫學.
- 心脏病学 心脏病学
- 内分泌学 在内分泌学.
背景情况:
- 心血管疾病 (CVD) 是慢性病 (CKD) 患者的主要死亡原因.
- 慢性瘤的进展会通过慢性瘤特异性因素 (如 mineral homeostasis 失调) 加剧心血管疾病的风险.
- 纤维细胞生长因子23 (FGF23) 和klotho是矿物平衡的关键调节者,影响心血管健康.
研究的目的:
- 探索FGF23和klotho在CKD心血管并发症中的作用.
- 调查FGF23过量和klotho缺乏促进心脏功能障碍的机制.
- 评估向矿物质平衡的潜力,以改善CKD中的心血管结果.
主要方法:
- 对CKD相关心血管疾病中FGF23和klotho的新兴数据的审查.
- 分析FGF23,klotho和矿物代谢之间的相互作用.
- 讨论对治疗慢性脏病中心血管风险的临床影响.
主要成果:
- 随着FGF23的上升和CKD中klotho的下降,导致了klotho独立的,有害的心脏影响,包括左心室缩和心力衰竭.
- 溶性克洛托可以通过各种机制提供保护性心血管益处.
- 由于FGF23和klotho之间存在复杂的反循环,因此很难将病理的主要驱动因素分离出来.
结论:
- 针对整体地针对 mineral homeostasis 的疾病,对于改善 CKD 患者的心血管结果至关重要.
- 随机试验应侧重于解决矿物质不平衡的实际干预措施.
- 需要进一步的研究,以充分阐明FGF23和klotho在CKD的不同心血管并发症中的特定作用.
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