scholarly journals Testosterone vs. aromatase inhibitor in older men with low testosterone: effects on cardiometabolic parameters

Andrology ◽  
2016 ◽  
Vol 5 (1) ◽  
pp. 31-40 ◽  
Author(s):  
J.P. Dias ◽  
M. D. Shardell ◽  
O. D. Carlson ◽  
D. Melvin ◽  
G. Caturegli ◽  
...  
Metabolism ◽  
2017 ◽  
Vol 69 ◽  
pp. 143-147 ◽  
Author(s):  
Jenny Pena Dias ◽  
Johannes D. Veldhuis ◽  
Olga Carlson ◽  
Michelle Shardell ◽  
Chee W. Chia ◽  
...  

JAMA ◽  
2017 ◽  
Vol 317 (7) ◽  
pp. 717 ◽  
Author(s):  
Susan M. Resnick ◽  
Alvin M. Matsumoto ◽  
Alisa J. Stephens-Shields ◽  
Susan S. Ellenberg ◽  
Thomas M. Gill ◽  
...  

2017 ◽  
Vol 103 (2) ◽  
pp. 681-688 ◽  
Author(s):  
Emile R Mohler ◽  
Susan S Ellenberg ◽  
Cora E Lewis ◽  
Nanette K Wenger ◽  
Matthew J Budoff ◽  
...  

Abstract Context Studies of the possible cardiovascular risk of testosterone treatment are inconclusive. Objective To determine the effect of testosterone treatment on cardiovascular biomarkers in older men with low testosterone. Design Double-blind, placebo-controlled trial. Setting Twelve academic medical centers in the United States. Participants In all, 788 men ≥65 years old with an average of two serum testosterone levels <275 ng/dL who were enrolled in The Testosterone Trials. Intervention Testosterone gel, the dose adjusted to maintain the testosterone level in the normal range for young men, or placebo gel for 12 months. Main Outcome Measures Serum markers of cardiovascular risk, including lipids and markers of glucose metabolism, fibrinolysis, inflammation, and myocardial damage. Results Compared with placebo, testosterone treatment significantly decreased total cholesterol (adjusted mean difference, −6.1 mg/dL; P < 0.001), high-density lipoprotein cholesterol (adjusted mean difference, −2.0 mg/dL; P < 0.001), and low-density lipoprotein cholesterol (adjusted mean difference, −2.3 mg/dL; P = 0.051) from baseline to month 12. Testosterone also slightly but significantly decreased fasting insulin (adjusted mean difference, −1.7 µIU/mL; P = 0.02) and homeostatic model assessment‒insulin resistance (adjusted mean difference, −0.6; P = 0.03). Testosterone did not change triglycerides, d-dimer, C-reactive protein, interleukin 6, troponin, glucose, or hemoglobin A1c levels more than placebo. Conclusions and Relevance Testosterone treatment of 1 year in older men with low testosterone was associated with small reductions in cholesterol and insulin but not with other glucose markers, markers of inflammation or fibrinolysis, or troponin. The clinical importance of these findings is unclear and requires a larger trial of clinical outcomes.


2008 ◽  
Vol 68 (1) ◽  
pp. 42-50 ◽  
Author(s):  
Laura A. Schaap ◽  
Saskia M. F. Pluijm ◽  
Dorly J. H. Deeg ◽  
Brenda W. Penninx ◽  
Barbara J. Nicklas ◽  
...  

2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. 471-471
Author(s):  
Shehzad Basaria

Abstract Serum testosterone concentrations decrease in men with age, but benefits and risks of raising testosterone levels in older men remain controversial. In the T-Trials, a total of 790 men, age 65 and older, with a serum testosterone concentration of < 275 ng/dL and symptoms of sexual dysfunction, fatigue or physical dysfunction were randomized to either testosterone gel or placebo gel for 1 year. Treatment in the testosterone arm increased serum testosterone levels to the mid-normal range for young men. Testosterone replacement was associated with a significant increase in sexual activity (p<0.001), libido and erectile function. In contrast, there was no improvement in vitality or physical function. Adverse findings included increases in non-calcified plaque formation and a higher rate of prostate events. In sum, testosterone treatment in older men was associated with modest benefits, while the risk on prostate and cardiovascular health remain unclear.


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