Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2014 Aug 26;6(8):855-60.
doi: 10.4330/wjc.v6.i8.855.

Management of renal artery stenosis: What does the experimental evidence tell us?

Affiliations
Review

Management of renal artery stenosis: What does the experimental evidence tell us?

Mohammed Al-Suraih et al. World J Cardiol. .

Abstract

Optimal management of patients with renal artery stenosis (RAS) is a subject of considerable controversy. There is incontrovertible evidence that renal artery stenosis has profound effects on the heart and cardiovascular system in addition to the kidney. Recent evidence indicates that restoration of blood flow alone does not improve renal or cardiovascular outcomes in patients with renal artery stenosis. A number of human and experimental studies have documented the clinical, hemodynamic, and histopathologic features in renal artery stenosis. New approaches to the treatment of renovascular hypertension due to RAS depend on better understanding of basic mechanisms underlying the development of chronic renal disease in these patients. Several groups have employed the two kidney one clip model of renovascular hypertension to define basic signaling mechanisms responsible for the development of chronic renal disease. Recent studies have underscored the importance of inflammation in the development and progression of renal damage in renal artery stenosis. In particular, interactions between the renin-angiotensin system, oxidative stress, and inflammation appear to play a critical role in this process. In this overview, results of recent studies to define basic pathways responsible for renal disease progression will be highlighted. These studies may provide the rationale for novel therapeutic approaches to treat patients with renovascular hypertension.

Keywords: Atrophy; CCL2; CCR2; Inflammation; Kidney; Renovascular hypertension.

PubMed Disclaimer

Figures

Figure 1
Figure 1
Summary of hemodynamic and non-hemodynamic pathways responsible for development of chronic renal damage in renal artery stenosis.
Figure 2
Figure 2
Mediators persistently induced in the stenotic kidney and transiently induced in the contralateral kidney in murine renal artery stenosis.

References

    1. Ostchega Y, Yoon SS, Hughes J, Louis T. Hypertension awareness, treatment, and control--continued disparities in adults: United States, 2005-2006. NCHS Data Brief. 2008;(3):1–8. - PubMed
    1. Hansen KJ, Edwards MS, Craven TE, Cherr GS, Jackson SA, Appel RG, Burke GL, Dean RH. Prevalence of renovascular disease in the elderly: a population-based study. J Vasc Surg. 2002;36:443–451. - PubMed
    1. Iglesias JI, Hamburger RJ, Feldman L, Kaufman JS. The natural history of incidental renal artery stenosis in patients with aortoiliac vascular disease. Am J Med. 2000;109:642–647. - PubMed
    1. Valabhji J, Robinson S, Poulter C, Robinson AC, Kong C, Henzen C, Gedroyc WM, Feher MD, Elkeles RS. Prevalence of renal artery stenosis in subjects with type 2 diabetes and coexistent hypertension. Diabetes Care. 2000;23:539–543. - PubMed
    1. Textor SC. Managing renal arterial disease and hypertension. Curr Opin Cardiol. 2003;18:260–267. - PubMed

LinkOut - more resources