Obesity Clinical Trial
Official title:
Testosterone Replacement in Metabolic Syndrome and Inflammation of Fat Tissue
Hypogonadism (HG) frequently complicates the Metabolic Syndrome (MetS), whether testosterone replacement (TRT) is beneficial has not been clearly ascertained. This study was designed to address the effects of TRT on insulin resistance, body composition and pro-inflammatory status in naïve patients with MetS and HG.
The features of Metabolic Syndrome (MetS) include abdominal obesity, atherogenic
dyslipidemia, raised blood pressure, insulin resistance or glucose intolerance. These
symptoms are also frequently found in hypogonadal men.
Adipose tissue and androgens in male obesity are reciprocally linked. Total and free
testosterone (T) are decreased in proportion to the degree of body fatness while T regulates
insulin sensitivity and body composition. As a consequence, hypoandrogenism carries an
additional independent risk for cardiovascular and metabolic disorders. Men with type 2
diabetes mellitus (T2D) exhibit lowered T levels that are inversely correlated to HbA1c. In
addition, abdominal adiposity causes an impairment of testicular steroidogenesis that is
directly linked to circulating adipokines; enhanced cytokine release from
macrophage-infiltrated adipose tissue is pivotal to the pathogenesis of insulin resistance
and atherosclerosis. Both MetS and T2D share with hypogonadism such a proinflammatory state.
For this reason we performed a randomized controlled trial on the effects of TRT on insulin
resistance and circulating inflammatory markers in a cohort of middle-aged men with mild
hypogonadism and MetS at first diagnosis, that were not taking medications known to
influence the investigated outcomes. We established strict criteria for enrollment and used
a physiological replacing therapy.
Given that testosterone replacement therapy (TRT) determines a reduction of body fat mass
paralleled by an increase in fat free mass (6), and that TRT exerts an anti-inflammatory
role inhibiting interleukins (IL), in particular the IL-6 gene (14), it remains to be
established whether these independent effects also reflect in an improvement in insulin
resistance.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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