Volume 122, Issue 1, Supplement , Pages S1-S2, January 2009
Introduction
Article Outline
Atherosclerosis is the major cause of death in industrialized countries and is becoming dominant in other countries as they assume similar adverse diets and health practices. The challenge to researchers and clinicians is to develop and clinically apply treatments, including lifestyle changes, to prevent both secondary events and primary events of atherosclerotic cardiovascular disease. The rationale for these treatments is to favorably change the size, cellular and chemical composition, and biological activity of atherosclerotic plaques, thus resulting in a more favorable clinical course.
Our knowledge and understanding of the pathology of atherosclerosis development have advanced significantly in 3 aspects over the past 5 years. In 2008, rational medical treatments, based largely on 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins) available to every practitioner, can induce the regression of advanced-stage plaques of atherosclerosis and, concurrently, can reduce the risks of clinical disease. The rationale for these treatments is ultimately based on their effects on plaques, as documented by studies of plaque histopathology and morphology based on clinical imaging and on the results of clinical outcome studies.
The following 3 developments have been crucial to our enhanced understanding of the disease:
The purpose of this supplement to The American Journal of Medicine is to review for the practitioner major recent findings that support treatments to control advanced plaques of atherosclerosis, concluding with a checklist of key elements in the clinical management of atherosclerosis in 2008.
In the first article, Dr. William Insull, Jr., summarizes the pathology of lesions of atherosclerosis as they develop from initial lesions during the early teenage years to terminal events in late adulthood. The second article, by Dr. Borja Ibañez and colleagues, describes the role of clinical imaging in the diagnosis and evaluation of the burden of atherosclerosis for the individual patient.
In the third article, Dr. Harold E. Bays summarizes the practitioner's challenge to integrate the management of adipose tissue, obesity, and the metabolic syndrome into the management of atherosclerosis. In the fourth article, Dr. Sandra J. Lewis describes the practitioner's challenge to routinely and uniformly apply treatment for control of atherosclerosis in the office, aiming for the ideal of patient adherence to lifestyle changes and medical therapy.
The fifth article, by Dr. Michael H. Davidson and colleagues, provides a snapshot of medical treatment patterns in current clinical practice for the management of atherosclerosis and emphasizes the need for greater use of currently available treatments.
The supplement concludes with an article in which Drs. Insull and Lewis present a short checklist to aid the busy clinician in organizing and implementing an effective course of atherosclerosis evaluation and treatment for each patient.
Each article includes the authors' selected “clinical pearls,” which emphasize pivotal practical aspects of their topic. Two general conclusions are warranted:
Author disclosures
The author of this article has disclosed the following industry relationships:
William Insull, Jr., MD, serves on the Speakers' Bureau for Abbott Laboratories, Merck & Co., Inc., and Schering-Plough Corporation and as a consultant/advisory board participant for Daiichi Sankyo, Inc., Merck & Co., Inc., and Merck/Schering-Plough, Inc. He is an investigator for Pfizer Inc and has received research support from AstraZeneca Pharmaceuticals LP, Kos Pharmaceuticals, Inc., Merck & Co., Inc., and Pfizer Inc. In addition, Dr. Insull has received honoraria from Merck & Co., Inc., and from Merck/Schering-Plough, Inc., and is an editor/writer for AstraZeneca Pharmaceuticals LP.
Supplementary data
Supplementary material cited in this article is available online.
Supplementary data
Statement of author disclosure: Please see the Author Disclosures section at the end of this article.
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PII: S0002-9343(08)01016-4
doi:10.1016/j.amjmed.2008.10.012
© 2009 Published by Elsevier Inc.
Volume 122, Issue 1, Supplement , Pages S1-S2, January 2009


