|
|
|
|
The Internet Journal of Gynecology and Obstetrics™ ISSN: 1528-8439| Home | Editors | Current Issue | Archives | Instructions for Authors | Disclaimer |A Therapeutic Scheme For Oligospermia Based On Serum Levels Of FSH And EstradiolRelated Articles
Purushottam Sah D.G.O.
Citation: P. Sah : A Therapeutic Scheme For Oligospermia Based On Serum Levels Of FSH And Estradiol . The Internet Journal of Gynecology and Obstetrics. 2007 Volume 8 Number 1 Keywords: estrogen | testosterone | infertility Table of ContentsAbstractOligospermia is a major cause of infertility in couples. It is usually managed by assisted reproductive techniques. In these techniques the female partners are treated, while the male partners having this medical problem are left untreated! Though several empirical therapies are available to treat oligospermia, it is difficult to identify a therapy that is most likely to benefit a man having oligospermia. This leads to trial of different therapies resulting in varied success rates. These empirical therapies put emphasis on the stimulatory role of testosterone in the process of spermatogenesis while estrogens are considered inhibitory in this respect. In the last decade, however, positive role of estrogens in male reproduction has been reported by some authors. In view of this evidence, a therapeutic scheme for oligospermia based on serum levels of FSH and estradiol, is presented. Its aim is to develop a system by which a clinician may possibly identify a suitable therapy before starting the treatment of an infertile man. Thus it may reduce unnecessary trial of treatments and save on costs and time, and it may save some women from being treated for a problem of male infertility. IntroductionOligospermia is a major cause of infertility in large number of couples. It is usually managed by assisted reproductive techniques. In these techniques the female partners are treated, while the male partners having this medical problem are left untreated! Though several empirical therapies are available to treat oligospermia, it is difficult to identify a therapy that is most likely to benefit a man having oligospermia. This leads to trial of different therapies resulting in varied success rates. The empirical therapies to treat oligospermia include gonadotropins, androgens and antiestrogens 1. Most of these therapies put emphasis on the stimulatory role of testosterone in the process of spermatogenesis while estrogens are considered inhibitory to this process. In the last few years, however, some reports including 2, 3 have mentioned the positive role of estrogens in male reproduction. The author of this article too has reported the beneficial effects of low dose estrogen and testosterone combination therapy (ETCT) on the sperm count in men having oligospermia 4, 5, 6. In this article a therapeutic scheme for oligospermia, based on serum levels of FSH and estradiol, is presented. Its aim is to develop a system by which a clinician may possibly identify a suitable therapy before starting the treatment of an oligospermic man. Usually serum levels of FSH, LH and testosterone are measured in men having oligospermia. However, it is extremely uncommon to find clinically significant abnormalities in LH and testosterone levels in the presence of normal FSH levels 1 and FSH is also the most suitable hormone for diagnostic classification of oligospermia 7. Hence, LH and testosterone are not included in the proposed scheme and only FSH and estradiol are included. DiscussionTheoretically the maximum number of possible combinations of FSH and estradiol, depending on whether their serum levels are normal, elevated or depressed, is nine. But in practice all the possible combinations may not exist, six groups are identified remaining combinations are clubbed with other groups. These groups are as follows:
Furthermore, in all these aromatase deficient men serum FSH levels were elevated and serum estradiol levels were undetectable, but serum levels of testosterone and LH were variable 10, 11, 12. These evidences further emphasize the appropriateness of FSH and estradiol measurement in making a diagnostic and therapeutic scheme for oligospermia. The proposed treatments for the different groups are as follows:
It is obvious from the above observations that men having depressed or normal serum levels of estradiol may be treated with ETCT. Those having elevated serum levels of estradiol together with normal or depressed serum level of FSH shall benefit by treatment with antiestrogens (Tamoxifen, Clomiphene), because antiestrogens are known to stimulate FSH secretion. Others having elevated serum levels of estradiol together with elevated serum levels of FSH shall benefit by treatment with aromatase inhibitors (Testolactone, Anastrozole ), because FSH causes aromatisation of testosterone to estrogen 9. Thus it may be inferred that ‘Men having oligospermia can be divided in two clinical groups based on their serum levels of estradiol. The first group having normal or depressed serum levels of estradiol may benefit with low-dose estrogen-testosterone combination therapy, the second group having elevated serum levels of estradiol may benefit by treatment with antiestrogens or aromatase inhibitors depending on whether their serum levels of FSH are normal/ depressed or are elevated respectively'. In the above scheme antiestrogens and/ or aromatase inhibitors may be substituted with a combination of antiestrogen and androgen. In a prospective, randomized, placebo-controlled trial of 212 men with idiopathic oligozoospermia with a combination of tamoxifen citrate and testosterone undecanoate, the authors reported significant increase in the sperm counts of men in the active treatment group, but not in the placebo group 13. The doses used were tamoxifen citrate, 20 mg/d, and testosterone undecanoate, 120 mg/d for 6 months. In the active treatment group total sperm count , median [25th, 75th percentile] 27.1 x 10(6) cells/mL [9.4, 54.0 x 10(6) cells/mL] at baseline and 61.5 x 10(6) cells/mL [28.2, 119.6 x 10(6) cells/mL] at 6 months, were noted. The two combination therapies for oligospermia, mentioned above, are opposite in nature one contains estrogen and the other contains antiestrogen, together with testosterone. This interesting paradoxical observation further emphasizes the importance of serum estradiol estimation in making a therapeutic scheme. In the search for Cochrane reviews of therapies for idiopathic male factor subfertility, the only available review was that regarding the use of gonadotrophins in this condition. Here the authors could not reach a final conclusion about the efficacy of this treatment because the number of trials and participants was insufficient 14. Therefore it implies that an effective empirical therapy of oligospermia is yet to be determined. Our proposed scheme hopes to do so. Large multicentre controlled studies will be required to decide the utility of this therapeutic scheme in the management of oligospermia. Hopefully, this approach can evolve to more effective management of men having oligospermia and reduce unnecessary trial of treatments and save on costs and time. In some infertile couples this approach can possibly convert the choice of treatment from IVF/ICSI to less costly IUI, after the sperm count is suitably increased with treatment. Also it may save some women from being treated for a problem of male infertility.
Correspondence toPurushottam Sah References1. Sigman M and Howards SS (1992) Male infertility. In Walsh PC, Retik AB, Stamey TA, Vaughan Jr ED (eds) Campbell's Urology. W B Saunders' Co., Philadelphia, USA, pp. pp. 664,665,675,680,689. (s) 2. Rochira V, Balestrieri A, Madeo B, Baraldi E, Faustini-Fustini M, Granata A R M, Carani C (2001) Congenital estrogen deficiency: in search of the estrogen role in human male reproduction. Mol Cell Endocrinol 178,107-115. (s) 3. Pentikainen V, Erkkila K, Suomalainen L, Parvinen M, Dunkel L (2000) Estradiol Acts as a Germ Cell Survival Factor in the Human Testis in Vitro. J Clin Endocrinol Metab 85(5), 2057- 2067. (s) 4. Sah P (1998) Role of low-dose estrogen-testosterone combination therapy in men with oligospermia. Fertil Steril 70, 780-781. (s) 5. Sah P (2002) Oligospermia due to partial maturation arrest responds to low dose estrogen-testosterone combination therapy resulting in live-birth: a case report. Asian J Androl 4 (4), 307-308 (s) 6. Sah P (2005) Oligospermia in a man with small testes and elevated serum FSH responds to low dose estrogen-testosterone combination therapy, resulting in his wife's pregnancy and live birth. The Internet Journal of Endocrinology 2(1). (s) 7. Rowe PJ, Comhaire FH, Hargreave TB, Mahmoud AMA, editors (2000) Who Manual for the Standardized Investigation, Diagnosis and Management of the Infertile Male. Cambridge University Press, Cambridge p.28 (s) 8. Smith EP, Boyd J, Frank GR, Takahashi H, Cohen RM, Specker B, Williams TC, Lubahn DB, Korach KS (1994) Estrogen resistance caused by a mutation in the estrogen-receptor gene in a man. N Engl J Med 331,1056- 1061. (s) 9. Kula K and Chilarski A (1987) The GnRH test reveals changes in readiness of testosterone and estradiol secretion in boys with bilateral cryptorchism. Pediatr Pol 62(9), 623-627. (s) 10. Carani C, Qin K, Simoni M, Faustini-Fustini M, Serpente S, Boyd J, Korach KS, Simpson ER(1997) Effect of testosterone and estradiol in a man with aromatase deficiency. N Engl J Med 337, 91- 95. (s) 11. Herrman BL, Saller B, Janssen OE, Gocke P, Bockish A, Sperling H, Mann K, Broecker M (2002) Impact of estrogen replacement therapy in a male with congenital aromatase deficiency caused by a novel mutation in the CYP19 gene. J Clin Endocrinol Metab 87, 5476 -5484. (s) 12. Morishima A, Grumbach MM, Simpson ER, Fisher C, Qin K (1995) Aromatase deficiency in male and female sibling caused by a novel mutation and the physiological role of estrogens. J Clin Endocrinol Metab 80, 3689- 3699. (s) 13. Adamopoulos DA, Pappa A, Billa E, Nicopoulou S, Koukkou E, Michopoulos J (2003) Effectiveness of combined tamoxifen citrate and testosterone undecanoate treatment in men with idiopathic oligozoospermia. Fertil Steril 80(4), 914-920. (s) 14. Attia AM, Al-Inany HG, Proctor ML (2006) Gonadotrophins for idiopathic male factor subfertility. Cochrane Database of Systematic Reviews, Issue 1. Art. No.: CD005071. DOI:10.1002/14651858.CD005071.pub2 (s) This article was last modified on Fri, 13 Feb 09 13:32:51 -0600 This page was generated on Tue, 09 Feb 10 14:38:19 -0600, and may be cached. |
|
Home |
Journals |
Sponsors |
Books |
PubMed |
Editorial Help |
Privacy Policy |
Disclaimer |
Job Opportunities |
Contact
Copyright Internet Scientific Publications, LLC., 1996 to 2010. |
|