Issue: December 2012
November 08, 2012
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Safety of testosterone questioned in veterans with diabetes, CAD

Issue: December 2012
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LOS ANGELES — The use of testosterone replacement therapy in veterans with CAD who underwent coronary angiography is associated with an increased risk for MI and death, when compared with no testosterone therapy use, according to data presented here.

Perspective from Robert W. Yeh, MD, MSc

However, this risk has only been associated with those who had obstructive CAD, not less-severe CAD.

Rebecca Vigen, MD, MPA, from the cardiology section of VA Eastern Colorado Health Care System in Denver, Colorado, and colleagues used the VA CART-CL registry to find veterans who underwent coronary angiography between 2005 and 2011 and had total testosterone levels ≤250 ng/dL following their procedure.

The researchers studied 3,375 veterans, 461 (12%) of whom were administered testosterone replacement therapy an average of 546 days following coronary angiography.

Vigen reported a significant correlation between testosterone and CAD strata (P=.04). In patients with no CAD or nonobstructive CAD, no link was found between testosterone and MI (P=.46) or death (P=.3). Additional data showed that patients with obstructive CAD treated with testosterone were at an increased risk for MI and death (HR=2.51; 95% CI, 1.6-3.94).

“A significant portion of men undergoing angiography, who had levels checked, had a total testosterone level of <300 mg/dL. Testosterone replacement therapy use was associated with all-cause mortality and acute MI in veterans. This relationship was stronger among patients with no CAD vs. those with CAD on angiography,” Vigen said.

Prescriptions for testosterone replacement therapy increased from about 700,000 in 2000 to more than 2.5 million in 2008, according to Vigen.

“These findings may have potential implications for targeting testosterone use among selected patient populations,” the researchers said. – by Samantha Costa

For more information:

Vigen R. Abstract #19261. Presented at: the American Heart Association Scientific Sessions; Nov. 3-7, 2012; Los Angeles.

Disclosure: Vigen reports no relevant financial disclosures.