Literature DB >> 32394149

Angiotensin Receptor-Neprilysin Inhibitors and the Natriuretic Peptide Axis.

Nestor Vasquez1, Spencer Carter2, Justin L Grodin3.   

Abstract

PURPOSE OF THE REVIEW: The purpose of this review is to describe the effects of angiotensin receptor neprilysin inhibitor (ARNI) therapy on the natriuretic peptide axis (NPA), with a particular focus on B-type natriuretic peptide (BNP), atrial natriuretic peptide (ANP), and C-type natriuretic peptide (CNP) to better understand the biology behind the improved outcomes in patients with heart failure with reduced ejection fraction (HFrEF). RECENT
FINDINGS: BNP, ANP, and CNP are the three main natriuretic peptides (NP); they share a common structure and ultimately mediate their actions by activating cyclic guanosine monophosphate (cGMP). ARNI therapy results in a decrease of N-terminal pro-BNP (NT-proBNP) and increase of BNP levels respectively. It is been questioned whether these changes may result from unique laboratory assays characteristics rather than actual biological implications. It appears to be that the prognostic accuracy of BNP for cardiovascular outcomes remains independent and comparable to that of NT-proBNP while on ARNI therapy. ANP levels also increase with ARNI therapy, but no consistent change has been described for CNP levels. There is evidence that the changes in BNP and NT-proBNP correlate with improvement in echocardiographic parameters of volume and function. The dual effect of neprilysin inhibition and angiotensin receptor blockade has substantial implications on the natriuretic peptide axis (NPA). The changes seen in BNP and NT-proBNP specifically have shown to correlate with improvement in echocardiographic parameters. Further results exploring the biologic effects of ARNI therapy on other NPs are still pending and likely will provide further insights in the mechanisms behind the improvement in cardiac function and clinical outcomes.

Entities:  

Keywords:  ANP; ARNI; BNP; CNP; NT-proBNP; Natriuretic peptides; Sacubitril/valsartan

Mesh:

Substances:

Year:  2020        PMID: 32394149     DOI: 10.1007/s11897-020-00458-y

Source DB:  PubMed          Journal:  Curr Heart Fail Rep        ISSN: 1546-9530


  3 in total

Review 1.  Angiotensin receptor neprilysin inhibitor as a novel antihypertensive drug: Evidence from Asia and around the globe.

Authors:  Donna S-H Lin; Tzung-Dau Wang; Peera Buranakitjaroen; Chen-Huan Chen; Hao-Min Cheng; Yook Chin Chia; Apichard Sukonthasarn; Jam Chin Tay; Boon Wee Teo; Yuda Turana; Ji-Guang Wang; Kazuomi Kario
Journal:  J Clin Hypertens (Greenwich)       Date:  2020-12-11       Impact factor: 3.738

2.  The Effect of Sacubitril/Valsartan Treatment on Cardiac and Renal Functions of a Patient With Cardiorenal Syndrome Type 4 and Stage 5 CKD After More Than Three Years of Follow-Up.

Authors:  Shuiqin Cheng; Tingting Zhou; Le Yu; Yunmin Chen; Zhihong Zhang; Jinquan Wang; Yusheng Yu
Journal:  Front Med (Lausanne)       Date:  2022-03-11

3.  Flow reduction of a high-flow arteriovenous fistula in a hemodialysis patient reveals changes in natriuretic and renin-angiotensin system hormones of relevance for kidney function.

Authors:  Christine L Meyer-Olesen; Kristine Lindhard; Niklas R Jørgensen; Jens P Goetze; Tobias Bomholt; Boye L Jensen; Ditte Hansen
Journal:  Physiol Rep       Date:  2021-10
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.