Abstract

Anabolic-Androgenic Steroids (AAS) are a group of organic compounds that include testosterone, or related compounds that induce similar effects by serving as structural analogues. Because of their propensity to induce gene expression that promotes protein synthesis, increased lean body mass, and strength, they have found utility in medicine to aide patients with chronic wasting syndromes, deficiencies in growth stature, and trauma recovery (e.g., burns). Contemporary off-label use of these classes of agents are also being used in anti-aging capacities under clinical supervision, and those with cardiovascular deficits related to metabolic derangement. Nevertheless, as hormones, testosterone and its analogues have systemic effects and their glut can be deleterious to global organs, namely the heart. Chronic utilization of these agents can be seen in domains of competitive physical activities given their performance enhancing effects. Associated with this abuse in particular have been ubiquitous clinical accounts of Major Adverse Cardiovascular Events (MACE), chronic hypertension, dyslipidemia, and left ventricular remodeling given the pleiotropic effects of testosterone and its analogues. One agent in particular, oxandrolone, a synthetic AAS, has an interesting profile as it has a biological disposition to more anabolic and metabolic effects compared to other AAS, with less profuse androgenic properties. There has been evidence to show that even oxandrolone supplementation may show promise in improving peripheral homeostasis conducive to positive cardiovascular health, especially in obese patients with features of metabolic syndrome, a condition related to endocrinological dysfunction and aberrant adiposity. In this commentary we will review the effects of this AAS with a commentary on cardiovascular physiology constructed around translational biology and clinical data. Commentaries such as the latter are scant in the literature and offer perspectives crucial to understanding the intersections between habitus, physiologic status, and the heart. Overall, oxandrolone shows promise related to its pharmacology in patients with low muscle tone and significant adiposity, namely cardiometabolic profiles if administered with clinical prudence due to its novel structure, metabolism, and effects.

Highlights

  • Testosterone is a steroid derivative from cholesterol that serves multiple biological functions such as the induction of protein synthesis in myocytes, the mitigation of protein loss, promotion of bone density, and the development of secondary sexual characteristics in pubertal stages [1,2]

  • Evidence for this phenomenon can be appreciated by Srikanthan et al who showed that graded levels of increase skeletal muscle mass to total body weight was inversely proportional to homeostatic models of insulin resistance [32]

  • While estradiol has been shown to aide in myocardial ischemia, its role is more in ischemic-reperfusion applications and there has been some speculation that as an estrogen group, there is an increased increase of venous thromboembolism which may lead to Acute Coronary Syndrome (ACS) itself, another reason why to mitigate estradiol if possible alternatives impervious to aromatization exist [121,122]

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Summary

Review Article

Cardiovascular Health, Testosterone, and Oxandrolone: Leveraging the Myotrophic-Androgenic Ratio in Males with a Sarcopenic Obese Phenotype. Nashawi M1*, Ahmed MS1, Ahmad M2, Issa O2 and Abualfoul M3 1Department of Medicine-Cardiology, University of Texas Health Science Center San Antonio, Terxas 2Department of Biology, The University of Texas at Arlington, Texas 3Department of Internal Medicine, Methodist Dallas Medical Center, Texas

Introduction
Austin Publishing Group
The Sarcopenic Obesity Phenotype and Testosterone
Findings
Oxandrolone Side Effects and Looking Forward
Full Text
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