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
. 2013 Dec;15(6):681-95.
doi: 10.1007/s11936-013-0268-z.

Inflammation and atherosclerosis: disease modulating therapies

Affiliations

Inflammation and atherosclerosis: disease modulating therapies

Mahesh J Patel et al. Curr Treat Options Cardiovasc Med. 2013 Dec.

Abstract

Advances in the mechanistic understanding of atheroma initiation, repair, progression, and rupture have solidified the pivotal role played by the immune system in the pathophysiology of atherosclerotic vascular disease. These mechanistic findings have been extended into humans, with a strong evidence basis for the independent association between elevated blood markers of inflammation and future cardiovascular (CV) events. Investigations with statins as well as more conventional anti-inflammatory medications provide indirect evidence to support the concept that modifying immune responses can improve CV outcomes; however, robust evidence to support the use of anti-inflammatory treatment strategies to manage atherosclerotic vascular disease is still lacking. Such evidence may emerge from a new wave of clinical trials directly exploring the effects of targeted immune modulation on CV risk. These trials will provide key additional insights into atherosclerosis and will help determine the fate of immune modulation as a new treatment strategy in atherosclerotic vascular disease.

PubMed Disclaimer

References

    1. Nature. 2010 Apr 29;464(7293):1357-61 - PubMed
    1. Nat Med. 2006 Sep;12(9):1075-80 - PubMed
    1. Circulation. 2008 May 20;117(20):2577-9 - PubMed
    1. Lancet. 1981 Mar 21;1(8221):653-7 - PubMed
    1. BMJ. 2011 Feb 15;342:d548 - PubMed

LinkOut - more resources