Testosterone Therapy Decreased Adiponectin and Subcutaneous Fat in Aging Men

2011 ◽  
pp. P3-470-P3-470
Author(s):  
Louise Frederiksen ◽  
Kurt Hojlund ◽  
David M Hougaard ◽  
Thomas H Mosbech ◽  
Rasmus Larsen ◽  
...  
2012 ◽  
Vol 166 (3) ◽  
pp. 469-476 ◽  
Author(s):  
L Frederiksen ◽  
K Højlund ◽  
D M Hougaard ◽  
T H Mosbech ◽  
R Larsen ◽  
...  

ObjectiveTestosterone therapy increases lean body mass and decreases total fat mass in aging men with low normal testosterone levels. The major challenge is, however, to determine whether the metabolic consequences of testosterone therapy are overall positive. We have previously reported that 6-month testosterone therapy did not improve insulin sensitivity. We investigated the effect of testosterone therapy on regional body fat distribution and on the levels of the insulin-sensitizing adipokine, adiponectin, in aging men with low normal bioavailable testosterone levels.DesignA randomized, double-blinded, placebo-controlled study on 6-month testosterone treatment (gel) in 38 men, aged 60–78 years, with bioavailable testosterone <7.3 nmol/l, and a waist circumference >94 cm.MethodsCentral fat mass (CFM) and lower extremity fat mass (LEFM) were measured by dual X-ray absorptiometry. Subcutaneous abdominal adipose tissue (SAT), visceral adipose tissue (VAT), and thigh subcutaneous fat area (TFA) were measured by magnetic resonance imaging. Adiponectin levels were measured using an in-house immunofluorometric assay. Coefficients (b) represent the placebo-controlled mean effect of intervention.ResultsLEFM was decreased (b=−0.47 kg, P=0.07) while CFM did not change significantly (b=−0.66 kg, P=0.10) during testosterone therapy. SAT (b=−3.0%, P=0.018) and TFA (b=−3.0%, P<0.001) decreased, while VAT (b=1.0%, P=0.54) remained unchanged. Adiponectin levels decreased during testosterone therapy (b=−1.3 mg/l, P=0.001).ConclusionTestosterone therapy decreased subcutaneous fat on the abdomen and lower extremities, but visceral fat was unchanged. Moreover, adiponectin levels were significantly decreased during testosterone therapy.


2014 ◽  
Vol 171 (1) ◽  
pp. 77-88 ◽  
Author(s):  
Stine J Petersson ◽  
Louise L Christensen ◽  
Jonas M Kristensen ◽  
Rikke Kruse ◽  
Marianne Andersen ◽  
...  

ObjectiveRecent studies have indicated that serum testosterone in aging men is associated with insulin sensitivity and expression of genes involved in oxidative phosphorylation (OxPhos), and that testosterone treatment increases lipid oxidation. Herein, we investigated the effect of testosterone therapy on regulators of mitochondrial biogenesis and markers of OxPhos and lipid metabolism in the skeletal muscle of aging men with subnormal bioavailable testosterone levels.MethodsSkeletal muscle biopsies were obtained before and after treatment with either testosterone gel (n=12) or placebo (n=13) for 6 months. Insulin sensitivity and substrate oxidation were assessed by euglycemic–hyperinsulinemic clamp and indirect calorimetry. Muscle mRNA levels and protein abundance and phosphorylation of enzymes involved in mitochondrial biogenesis, OxPhos, and lipid metabolism were examined by quantitative real-time PCR and western blotting.ResultsDespite an increase in lipid oxidation (P<0.05), testosterone therapy had no effect on insulin sensitivity or mRNA levels of genes involved in mitochondrial biogenesis (PPARGC1A,PRKAA2, andPRKAG3), OxPhos (NDUFS1,ETFA,SDHA,UQCRC1, andCOX5B), or lipid metabolism (ACADVL,CD36,CPT1B,HADH, andPDK4). Consistently, protein abundance of OxPhos subunits encoded by both nuclear (SDHAandUQCRC1) and mitochondrial DNA (ND6) and protein abundance and phosphorylation of AMP-activated protein kinase and p38 MAPK were unaffected by testosterone therapy.ConclusionThe beneficial effect of testosterone treatment on lipid oxidation is not explained by increased abundance or phosphorylation-dependent activity of enzymes known to regulate mitochondrial biogenesis or markers of OxPhos and lipid metabolism in the skeletal muscle of aging men with subnormal bioavailable testosterone levels.


Andrology ◽  
2017 ◽  
Vol 5 (5) ◽  
pp. 946-953 ◽  
Author(s):  
L. V. Magnussen ◽  
L. G. Hvid ◽  
A. P. Hermann ◽  
D. M. Hougaard ◽  
B. Gram ◽  
...  

2008 ◽  
Vol 93 (1) ◽  
pp. 139-146 ◽  
Author(s):  
C. A. Allan ◽  
B. J. G. Strauss ◽  
H. G. Burger ◽  
E. A. Forbes ◽  
R. I. McLachlan

AGE ◽  
2011 ◽  
Vol 34 (1) ◽  
pp. 145-156 ◽  
Author(s):  
Louise Frederiksen ◽  
Kurt Højlund ◽  
David M. Hougaard ◽  
Kim Brixen ◽  
Marianne Andersen

2012 ◽  
Vol 2012 ◽  
pp. 1-20 ◽  
Author(s):  
Prasanth N. Surampudi ◽  
Christina Wang ◽  
Ronald Swerdloff

Hypogonadism in older men is a syndrome characterized by low serum testosterone levels and clinical symptoms often seen in hypogonadal men of younger age. These symptoms include decreased libido, erectile dysfunction, decreased vitality, decreased muscle mass, increased adiposity, depressed mood, osteopenia, and osteoporosis. Hypogonadism is a common disorder in aging men with a significant percentage of men over 60 years of age having serum testosterone levels below the lower limits of young male adults. There are a variety of testosterone formulations available for treatment of hypogonadism. Data from many small studies indicate that testosterone therapy offers several potential benefits to older hypogonadal men. A large multicenter NIH supported double blind, placebo controlled study is ongoing, and this study should greatly enhance the information available on efficacy and side effects of treatment. While safety data is available across many age groups, there are still unresolved concerns associated with testosterone therapy. We have reviewed the diagnostic methods as well as benefits and risks of testosterone replacement therapy for hypogonadism in aging men.


Metabolism ◽  
2020 ◽  
Vol 112 ◽  
pp. 154347
Author(s):  
Rikke Kruse ◽  
Stine J. Petersson ◽  
Louise L. Christensen ◽  
Jonas M. Kristensen ◽  
Rugivan Sabaratnam ◽  
...  

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