Phosphate and FGF23 in the renoprotective benefit of RAAS inhibition

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• 作者：Sophie de Seigneux^a ; ^b ; ^{Sophie.deseigneux@hcuge.ch" class="auth_mail" title="E-mail the corresponding author} ; Pierre-Yves Martin^a ; ^b
• 关键词：Ace inhibitors ; RAA system ; FGF23 ; Klotho ; Phosphate ; Chronic kidney disease
• 刊名：Pharmacological Research
• 出版年：2016
• 出版时间：April 2016
• 年：2016
• 卷：106
• 期：Complete
• 页码：87-91
• 全文大小：903 K

文摘

Renin angiotensin-aldosterone system (RAAS) blockade is a mainstay of chronic kidney disease (CKD) treatment given its beneficial effects on proteinuria, nephroprotection, heart disease and global mortality.

The FGF23/Klotho/phosphate axis is crucial for phosphate excretion. During CKD, loss of Klotho, decreased phosphate excretion and FGF23 elevation are early events contributing both to renal disease progression and to cardiovascular complications. Experimental evidence suggests that Klotho replacement may improve renal and cardiovascular disease during CKD.

Recent evidence suggests that both RAAS activation and proteinuria decrease Klotho expression and lead to phosphate retention and FGF23 elevation. In opposition RAAS blockade may reverse Klotho loss during CKD in both experimental and human studies, with direct and indirect expected beneficial effects on the kidney and cardiovascular system. This effect of RAAS blockade on the FGF23/Klotho/phosphate axis may participate in explaining some of the beneficial effects of these drugs during CKD.

In this article we review the evidence linking RAAS blockade to modulation of the FGF23/Klotho/phosphate axis and the beneficial effects of these regulations.