Testosterone Therapy and Cardiovascular Risk

Mayo Clinic Proceedings

February 23, 2015

Mayo Clinic Proceedings


TAKE-HOME MESSAGE

  • The authors performed an extensive literature search to examine the association between testosterone therapy and cardiovascular risk. In many studies, normal testosterone levels correlated with a decrease in cardiovascular risk and mortality. Serum testosterone concentrations were inversely associated with incident coronary artery disease, severity of coronary artery disease, and mortality. Compared with placebo, testosterone therapy was shown to improve cardiac function and glycemic control and reduced waist circumference, obesity, and fat mass.
  • Based on the published data, testosterone therapy was not associated with greater cardiovascular risk. Conversely, the literature suggests that normal testosterone levels benefit cardiovascular health.

 

Abstract

Two recent studies raised new concerns regarding cardiovascular (CV) risks with testosterone (T) therapy. This article reviews those studies as well as the extensive literature on T and CV risks. A MEDLINE search was performed for the years 1940 to August 2014 using the following key words: testosterone, androgens, human, male, cardiovascular, stroke, cerebrovascular accident, myocardial infarction, heart attack, death, and mortality. The weight and direction of evidence was evaluated and level of evidence (LOE) assigned. Only 4 articles were identified that suggested increased CV risks with T prescriptions: 2 retrospective analyses with serious methodological limitations, 1 placebo-controlled trial with few major adverse cardiac events, and 1 meta-analysis that included questionable studies and events. In contrast, several dozen studies have reported a beneficial effect of normal T levels on CV risks and mortality. Mortality and incident coronary artery disease are inversely associated with serum T concentrations (LOE IIa), as is severity of coronary artery disease (LOE IIa). Testosterone therapy is associated with reduced obesity, fat mass, and waist circumference (LOE Ib) and also improves glycemic control (LOE IIa). Mortality was reduced with T therapy in 2 retrospective studies. Several RCTs in men with coronary artery disease or heart failure reported improved function in men who received T compared with placebo. The largest meta-analysis to date revealed no increase in CV risks in men who received T and reduced CV risk among those with metabolic disease. In summary, there is no convincing evidence of increased CV risks with T therapy. On the contrary, there appears to be a strong beneficial relationship between normal T and CV health that has not yet been widely appreciated.


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