AntiagingAtlanta

 
Hormone Replacement Therapy
     
 

by Dr. Randy Smith of Antiaging Atlanta

Advantages of treating LOH with HCG rather than Testosterone Hormone Replacement Therapy

 
   
 2016;19(1):34-9. doi: 10.3109/13685538.2015.1092021. Epub 2015 Oct 21.

Late-onset hypogonadism: the advantages of treatment with human chorionic gonadotropin rather than testosterone.

Abstract

The traditional pharmacological treatment of patients with late onset hypogonadism (LOH) is represented by different formulations of testosterone (T) or alternatively by the extractive human chorionic gonadotropin (HCG). The hormone replacement treatment (HRT) is associated with the potential increase of hematocrit, serum concentrations of prostate-specific antigen (PSA) and prostate volume. Moreover, the gynecomastia represent a condition frequently associated with HRT. Recent evidences showed the role of leydig cells in the 25-hydroxylation of vitamin D and the elevated frequency of hypovitaminosis D among LOH patients. Finally, another important aspect of LOH is represented by the frequency of secondary infertility due to age or to traditional HRT. This study evaluated 40 LOH patients treated for 6 months with extractive HCG (n = 10 patients) and three different formulations of T: transdermal (n = 10 patients), undecaonate (n = 10 patients) and enantate (n = 10 patients). Hormonal, anthropometric, metabolic and sperm parameters were evaluated and compared. Moreover, the main safety parameters and the results of the main questionnaires were evaluated. After treatment, HCG group showed serum concentrations of 25-OH-vitamin D significantly higher (p < 0.05) and serum concentrations of oestrogens significantly lower (p < 0.05) compared with other groups. Moreover, they showed a mean value of hematocrit, PSA and prostate volume significantly lower (p < 0.05) compared with other groups. Finally, all the groups treated with T showed a significant reduction (p < 0.05) of sperm density and of percentage of spermatozoa with progressive motility compared with HCG group.

KEYWORDS:

Human chorionic gonadotropin; late onset hypogonadism; testosterone

PMID:
 
26488941
 
DOI:
 
10.3109/13685538.2015.1092021
 
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