Advances in the treatment of functional male hypogonadism

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ABSTRACT

Introduction


Functional hypogonadism is frequently found in obese men, particularly those with metabolic complications. Several possible therapeutic approaches could be considered.


Areas covered

An extensive search on Medline, Embase, and Cochrane databases was performed to retrieve the available studies assessing the change of testosterone (T) and sexual function upon dieting or physical activity programs, as well as glucagon-like peptide 1 analogues. The role of lifestyle interventions associated with T replacement therapy (TRT) was also evaluated. The expert opinion provided here has been corroborated by meta-analyzing the results of the retrieved studies.


Expert opinion

Current evidence supports the beneficial role of lifestyle modifications in increasing T and improving sexual function as a function of weight loss. While dieting programs are associated with greater effects in younger populations, physical exercise has major effects in older ones. Among the dieting programs, a very low-calorie ketogenic diet shows the best results; aerobic or endurance physical exercise perform similarly. The advantages of functional hypogonadism in lifestyle modifications are empowered by the association with TRT. Therefore, TRT may be a valuable complementary strategy to increase muscle mass and facilitate physical exercise while improving sexual symptoms, thus favoring the motivation and compliance for lifestyle interventions.




4. Clinical data

4.1. Effect of lifestyle and pharmacologically induced weight loss on functional hypogonadism

4.1.1. Effect of diet
4.1.2. Effect of physical exercise
4.1.3. Effect of GLP-1 analogues
4.1.4. Weight loss and sexual function



4.2. Combined TRT and lifestyle




5. Conclusions


The present data indicate that lifestyle modifications are able to reverse overweight- and obesity-related functional hypogonadism in both preclinical and clinical studies. In clinical studies, the improvement in total T is tightly related to the entity of weight loss obtained over the lifestyle intervention period with comparable effects of a low-calorie diet and physical exercise. Conversely, no effect on LH levels was observed, at least when a low-calorie diet was considered. The increase in total and free T levels was more evident when a pharmacological approach with the use of GLP-1 analogues, was analyzed. However, even with the latter approach no significant modifications in LH levels at follow-up were observed, although there was a clear trend. It is important to note that LH is secreted in a pulsatile manner and, therefore, a single measurement (as often performed in the aforementioned studies) can be misleading. Interestingly, VLCKD resulted in better T improvement when compared to other dieting approaches. The latter observation was confirmed even after the adjustment for confounders, including the extent of weight loss. Similarly, to what was observed for the modification in the hormonal parameters, weight loss, whatever was obtained, was associated with an overall improvement in erectile function, as assessed by IIEF. The latter finding was more evident inpatients with lower baseline T levels, at least when a low calorie diet was considered. Unfortunately, no sufficient data to investigate the effect of weight loss on other sexual function domains, when IIEF was considered, were available. However, it should be recognized that weight loss has been shown to improve several aspects of male sexual function including libido and urinary symptoms [48,99,100]. When the combination of lifestyle interventions and TRT was compared to lifestyle alone, the former resulted in a larger improvement in body composition (including a greater reduction of fat mass and waist circumference and an increase of lean mass) as well as an overall improvement of insulin resistance as derived by surrogate markers (including the HOMA index and triglyceride levels). Finally, the use of TRT along with lifestyle showed a better IIEF score at the end of the trial when compared to that obtained with lifestyle modifications alone.




6. Expert opinion

In conclusion, the key message arising from the present paper is that lifestyle modifications and weight loss should be considered and strongly recommended for all subjects with functional hypogonadism. In symptomatic and uncomplicated patients with overweight or obesity, the combination of TRT and lifestyle can result in better outcomes. Accordingly, available guidelines recommend starting TRT in all symptomatic hypogonadal men, after contraindications are excluded, in whom a reversal of the condition cannot be expected in a reasonable timeframe [8]. It can be speculated that the observed improvement in fat mass after TRT can allow one to perform physical activity, eventually resulting in further weight loss and metabolic profile improvement.
 

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Figure 1. Effect of feeding a regular diet (RD) or a high-fat diet (HFD) without or with performing physical exercise (HFD+phyex) on the hypothalamic mRNA expression of Kiss-1 (panel a) or gonadotropin releasing hormone (GnRH; Panel b). Panel c and d show in the same groups of rabbits the effect of the aforementioned treatments on circulating luteinizing hormone (LH; panel c) or testosterone (panel d). Number of rabbits analyzed are in brackets. Data were obtained from references #18–20.
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Figure 2. Effect of feeding a regular diet (RD) or a high-fat diet (HFD) on the responsiveness to increasing doses of Ach (area under the curve, Panel a) or of the phosphodiesterase type 5 (PDE5) inhibitor sildenafil (area under the curve, panel b) upon electrical field stimulation (EFS) of penile strips. Results obtained in HFD rabbits treated with testosterone (T; HFD+T) or performing physical exercise (Phy Ex; HFD+Phy Ex) are also showed in both panels. Number of rabbits analyzed are in brackets. Data were obtained from references #18–20.
1714945447169.png
 
Table 1. Moderators and outcome variables in individual studies included in the meta-analysis. All data are reported as mean ± standard deviation. FU= follow up (weeks); DM= diabetes mellitus; BMI= body mass index; TT= total testosterone; *low calorie diet only group; ** high volume intensity exercise ^ low energy diet group, ^^ obese group, ^^^ non ketogenic diet, *** ketogenic diet. BA= Controlled cohort before-and-after comparisons in the same group of patients; RCT= randomized controlled trials CBA= Controlled before-and-after study between two or more groups of participants receiving different interventions
1714945519370.png
 
Figure 3. Weighted standardized (stand) mean differences (with 95%CI) before and after weight loss intervention as derived from studies included in the analysis. UL= upper limit LL= lower limit
1714945600711.png
 
Figure 4. Impact of Д weight loss (a) diabetes mellitus (b) and trial duration (c) on total testosterone increased levels after low calorie diet.
Screenshot (35466).png

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Table 2. Moderators and outcome variables in individual studies included in the meta-analysis. All data are reported as mean. FU= follow up (weeks); BMI= body mass index; TT= total testosterone; FT= free testosterone; BA= Controlled cohort before-and-after comparisons in the same group of patients; RCT= randomized controlled trials CBA= Controlled before-and-after study between two or more groups of participants receiving different interventions. IIEF= international index of erectile function. EFD= erectile function domain, *Middle age subjects; ** elderly subjects, *** aerobic exercise only; ^exercise only group; ^^ placebo and exercise group, § moderate-intensity exercise of low volume (<150 minutes/week); §§ moderate-intensity exercise of high volume (200–300 minutes/week): ° SSC, exercise training using stretch-shortening cycle; °° exercise training using eccentric contractions.
Screenshot (35469).png

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Table 3. Moderators and outcome variables in individual studies included in the meta-analysis. All data are reported as mean ± standard deviation. FU= follow up(weeks); DM= diabetes mellitus; BMI= body mass index; TT= total testosterone; IIEF= international index of erectile function. BA= Controlled cohort before-and-after comparisons in the same group of patients; RCT= randomized controlled trials CBA= Controlled before-and-after study between two or more groups of participants receiving different interventions.
1714945935483.png
 
Table 4. Characteristics of the clinical studies included in the meta-analysis. BMI= body mass index; T= testosterone; TU= testosterone undecanoate; BMI= body mass index; NR= not reported. RCT= randomized controlled trial. ID/C: investigational Drug/Comparator. HG = hypogonadism.
1714946018687.png
 
Figure 5. Weighted standardized (stand) mean differences (with 95% CI) of combination testosterone replacement therapy and lifestyle versus lifestyle alone from studies included in the analysis. UL= upper limit LL= lower limit.
1714946082821.png
 
Article highlights


● The beneficial role of lifestyle modifications in increasing testosterone levels and improving sexual function is dependent upon weight loss obtained

● Dieting programs have greater effects on testosterone levels in younger populations

● Among different dieting protocols, very low-calorie ketogenic diet obtains the best results

● Physical exercise is more effective in increasing serum testosterone in older populations

● Aerobic or endurance physical exercise have similar performance in improving testosterone levels

● Testosterone replacement therapy empowers the results obtained by lifestyle interventions
 
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