Abstract
Anabolic steroids are synthetic derivatives of testosterone that were developed as adjunct therapy for a variety of medical conditions. Today they are most commonly used to enhance athletic performance and muscular development. Both illicit and medically indicated anabolic steroid use have been temporally associated with many subsequent defects within each of the body systems. Testosterone is the preferred ligand of the human androgen receptor in the myocardium and directly modulates transcription, translation, and enzyme function. Consequent alterations of cellular pathology and organ physiology are similar to those seen with heart failure and cardiomyopathy. Hypertension, ventricular remodeling, myocardial ischemia, and sudden cardiac death have each been temporally and causally associated with anabolic steroid use in humans. These effects persist long after use has been discontinued and have significant impact on subsequent morbidity and mortality. The mechanisms of cardiac disease as a result of anabolic steroid use are discussed in this review.
Original language | English (US) |
---|---|
Pages (from-to) | 1-15 |
Number of pages | 15 |
Journal | Progress in Cardiovascular Diseases |
Volume | 41 |
Issue number | 1 |
State | Published - 1998 |
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ASJC Scopus subject areas
- Cardiology and Cardiovascular Medicine
Cite this
The cardiac toxicity of anabolic steroids. / Sullivan, M. L.; Martinez, C. M.; Gennis, P.; Gallagher, E. John.
In: Progress in Cardiovascular Diseases, Vol. 41, No. 1, 1998, p. 1-15.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - The cardiac toxicity of anabolic steroids
AU - Sullivan, M. L.
AU - Martinez, C. M.
AU - Gennis, P.
AU - Gallagher, E. John
PY - 1998
Y1 - 1998
N2 - Anabolic steroids are synthetic derivatives of testosterone that were developed as adjunct therapy for a variety of medical conditions. Today they are most commonly used to enhance athletic performance and muscular development. Both illicit and medically indicated anabolic steroid use have been temporally associated with many subsequent defects within each of the body systems. Testosterone is the preferred ligand of the human androgen receptor in the myocardium and directly modulates transcription, translation, and enzyme function. Consequent alterations of cellular pathology and organ physiology are similar to those seen with heart failure and cardiomyopathy. Hypertension, ventricular remodeling, myocardial ischemia, and sudden cardiac death have each been temporally and causally associated with anabolic steroid use in humans. These effects persist long after use has been discontinued and have significant impact on subsequent morbidity and mortality. The mechanisms of cardiac disease as a result of anabolic steroid use are discussed in this review.
AB - Anabolic steroids are synthetic derivatives of testosterone that were developed as adjunct therapy for a variety of medical conditions. Today they are most commonly used to enhance athletic performance and muscular development. Both illicit and medically indicated anabolic steroid use have been temporally associated with many subsequent defects within each of the body systems. Testosterone is the preferred ligand of the human androgen receptor in the myocardium and directly modulates transcription, translation, and enzyme function. Consequent alterations of cellular pathology and organ physiology are similar to those seen with heart failure and cardiomyopathy. Hypertension, ventricular remodeling, myocardial ischemia, and sudden cardiac death have each been temporally and causally associated with anabolic steroid use in humans. These effects persist long after use has been discontinued and have significant impact on subsequent morbidity and mortality. The mechanisms of cardiac disease as a result of anabolic steroid use are discussed in this review.
UR - http://www.scopus.com/inward/record.url?scp=0031880293&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0031880293&partnerID=8YFLogxK
M3 - Article
C2 - 9717856
AN - SCOPUS:0031880293
VL - 41
SP - 1
EP - 15
JO - Progress in Cardiovascular Diseases
JF - Progress in Cardiovascular Diseases
SN - 0033-0620
IS - 1
ER -