Testosterone replacement therapy in male hypogonadism is not associated with increase of endothelin-1 levels

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Abstract

Differences in endothelin-1 (ET-1) blood plasma levels were established between healthy men and women. Little is known about vascular effects of testosterone and the interactions between sex hormones and endothelin. In order to study the relationship between ET-1 and testosterone in more detail, we have investigated 33 male patients with various forms of hypogonadism (13 with hypergonadotropic hypogonadism and 20 with hypogonadotropic hypogonadism). Fourteen age-matched healthy males served as controls. The basal ET-1 levels in patients with hypogonadism (0.96 ± 0.12 fmol/mL) (mean ± SEM) were significantly higher in comparison with the controls (0.44 ± 0.04 fmol/mL), p < 0.01. Fifteen individuals of these patients were studied during the therapy with testosterone depot 250 mg i.m. The ET-1 levels decreased in this group from 0.99 ± 0.22 to 0.78 ± 0.14 fmol/mL at the third and to 0.76 ± 0.25 fmol/mL at the sixth month of the medication, respectively. The differences were not significant compared with the initial levels, but the concentrations at the sixth month of the treatment were not statistically different in comparison with the ET-1 levels of the controls. There was no significant difference in lipid data between patients before and during testosterone medication, except for the high-density lipoprotein cholesterol, which decreased at the third month of the treatment. Our results show that plasma ET-1 levels in males with hypogonadism are elevated with a tendency to decrease after testosterone administration. The optimum testosterone is not associated with enhanced cardiovascular risk as far as ET-1 plasma levels and lipids are concerned. © 2007 The Authors.

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Kumanov, P., Tomova, A., & Kirilov, G. (2007). Testosterone replacement therapy in male hypogonadism is not associated with increase of endothelin-1 levels. International Journal of Andrology, 30(1), 41–47. https://doi.org/10.1111/j.1365-2605.2006.00706.x

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