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Cited by 253

The DOI matches its Crossref record; 47 of the 47 references it cites were found in a registry or an index.

Renin inhibition with aliskiren: where are we now, and where are we going?

Azizi, Michel, Webb, Randy, Nussberger, Juerg, Hollenberg, Norman K·2006·Journal of Hypertension

Abstract

With the development of aliskiren, blockade of the renin-angiotensin-aldosterone system (RAAS) at the level of the interaction of renin with a substrate has become a clinical reality. This review covers the specific features of the first agent likely to achieve widespread clinical exposure, aliskiren. The potential of renin inhibition must be viewed in the context of the remarkable efficacy of both angiotensin-converting enzyme (ACE) inhibition and angiotensin receptor blockers (ARBs). The implications of blockade of the renin system at its rate-limiting step are reviewed, with the therapeutic implications for both the renin inhibitor employed alone or the renin inhibitor combined with an ACE inhibitor or ARB. The relevant and necessary studies are ongoing.

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Crossref · 10.1097/01.hjh.0000202812.72341.99

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Metadata

Authors
Azizi, M., Webb, R., Nussberger, J., & Hollenberg, N. K.
Venue
Journal of Hypertension
Published
2006-02
Volume
24
Issue
2
Pages
243-256
ISSN
0263-6352 (ISSN-L)
OpenAlex
W1974174019
Cited by
253
References
47
FWCI
26.68
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Renin inhibition with aliskiren: where are we now, and where are we going? https://app.cochat.ai/papers/10.1097/01.hjh.0000202812.72341.99
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Azizi, M., Webb, R., Nussberger, J., & Hollenberg, N. K. (2006). Renin inhibition with aliskiren: where are we now, and where are we going? Journal of Hypertension. https://doi.org/10.1097/01.hjh.0000202812.72341.99

Data sources

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.