蛋白尿和损伤的进展:主要的致病基因机制和药理学方法
Elisa Longhitano1, Vincenzo Calabrese1, Chiara Casuscelli1
1Unit of Nephrology and Dialysis, Department of Clinical and Experimental Medicine, A.O.U. "G.Martino", University of Messina, 98125 Messina, Italy.
蛋白尿症表明损伤并使其恶化. 新的保护疗法,包括ACE抑制剂,ARB,SGLT2抑制剂,Finerenone和双抑制剂,为缓解慢性病进展提供了希望.
科学领域:
- 腎臟病學 (nephrology) 是一種醫學專業.
- 药理学 药理学是指药理学的学科.
背景情况:
- 蛋白尿症意味着膜过屏障受损.
- 尿中蛋白质水平升高不仅表明损伤,还通过球和管间介质机制积极促进损伤的进展.
研究的目的:
- 审查蛋白尿症加剧损伤的机制.
- 总结当前和新兴的保护性治疗策略,以减少蛋白尿和减缓慢性病 (CKD) 的进展.
主要方法:
- 对针对蛋白尿的既定和新型药理学药物的文献综述.
- 讨论治疗机制,包括ACE抑制,ARB,SGLT2抑制,矿物质皮质体受体对抗和双受体抑制.
主要成果:
- ангиотензин转化酶抑制剂 (ACEI) 和 ангиотензин受体阻断剂 (ARB) 是标准的治疗方法.
- -葡萄糖共运输体2 (SGLT2) 抑制剂在糖尿病和非糖尿病患者中显示出保护作用.
- 费内伦具有抗炎和抗纤维的益处,并具有有利的副作用.
- 斯帕森坦在IgA脏病和焦点细分质硬化症 (FSGS) 中表现出显著的抗蛋白尿作用.
结论:
- 减少蛋白尿对于保护至关重要.
- 药理疗法,生活方式改变和潜在疾病管理的组合对于缓解CKD进展至关重要.
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