Treatment of testosterone-induced gynecomastia with the aromatase inhibitor, anastroz

  1. Treatment of testosterone-induced gynecomastia with the aromatase inhibitor, anastroz

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    January 2004, Volume 16, Number 1, Pages 95-97
    Table of contents Previous Article Next PDF

    Case Report
    Treatment of testosterone-induced gynecomastia with the aromatase inhibitor, anastrozole

    E L Rhoden1,2 and A Morgentaler1

    1Division of Urology, Beth Israel Deaconess Medical Center, Men's Health Boston, Harvard Medical School, Massachusetts, USA

    Correspondence to: EL Rhoden, Rua Jaragua 370/302, Bela Vista 90450-140, Porto Alegre, RS, Brazil. E-mail: [email protected] or A Morgentaler, One Brookline Place, 624, Brookline, MA 02445, USA. E-mail: [email protected]

    2Supported by CAPES-Brazil (Government Foundation for Development of Postgraduation courses in Brazil).


    Gynecomastia is an unusual side effect associated with testosterone replacement therapy (TRT) that has been traditionally treated with surgery, radiation, or discontinuation of testosterone supplementation. We report here our experience with two cases of gynecomastia in men undergoing TRT who were successfully treated with the aromatase inhibitor anastrozole.

    International Journal of Impotence Research (2004) 16, 95-97. doi:10.1038/sj.ijir.3901154


    anastrozole; hypogonadism; testosterone; risks; gynecomastia; aging male


    Testosterone replacement therapy (TRT) in hypogonadal men has become more common as health care providers have become increasingly aware of andropause and the benefits of treatment. However, administration of exogenous testosterone can be associated with side effects that include effects on the prostate, hematocrit, fertility and the development of gynecomastia. Gynecomastia is believed to arise from peripheral conversion of testosterone to estradiol via the enzyme aromatase. The condition is embarrassing to men, and may cause discontinuation of testosterone treatment that has otherwise been successful.1

    Classically, male gynecomastia has been treated with radiotherapy or surgical resection of the breast gland tissue.2 The introduction of a new generation of aromatase inhibitors has created an opportunity to treat testosterone-induced gynecomastia with oral medications alone.

    We report here our experience with the use of an aromatase inhibitor, anastrozole, in the treatment of gynecomastia in hypogonadal men receiving testosterone supplementation.

    Case reports

    Case 1

    A 61-y-old man presented with a history of erectile dysfunction and reduction in libido, and difficulty achieving orgasm. Past medical history was notable for left gynecomastia in adolescence, which was treated surgically without further recurrence. The current physical examination was unremarkable. Blood tests showed FT of 0.8 ng/dl, TT of 295 ng/dl, luteinizing hormone (LH) of 3.4 mUI/l (normal: 2-18 mUI/l), follicle-stimulating hormone (FSH) of 3.4 mUI/l (normal: 2-18 mUI/l) and PSA of 1.5 ng/l (normal: 0-4 ng/l). Reduced peak rigidity was observed by NPTR. Intramuscular injections of testosterone enanthate 400 mg/3 weeks were started. The nadir total testosterone level was 287 ng/dl. The patient experienced significant symptomatic improvement with testosterone supplementation.

    At 6 months after beginning treatment, the patient noted gynecomastia on the right side, which had not received earlier surgical treatment as an adolescent. TRT was discontinued and 1 month later the patient reported complete resolution of the gynecomastia. Testosterone supplementation was resumed at the same schedule as before, and anastrozole (Arimidex“, AstraZeneca, London, UK) 1 mg/day orally was started as well. After 3 y, the patient continues to have clinical benefits from TRT without recurrence of gynecomastia.

    Case 2

    A 30-y-old man presented with a history of erectile dysfunction, reduced libido and fatigue. Physical examination was normal except for moderate obesity and mild bilateral gynecomastia. Blood tests revealed TT of 220 ng/ml, FT 1.1 ng/ml, FSH 0.9 mUI/l, LH 3.7 mUI/l and prolactin (PRL) 8.2 ng/ml (2.1-17.7 ng/ml). Poor erections were noted on NPTR. Treatment with intramuscular injections of testosterone enanthate 200 mg/2 weeks was initiated. After 6 months, the patient reported worsening of his baseline bilateral breast enlargement and new nipple tenderness. Peak serum levels of FT were 4 ng/dl. Estradiol levels were elevated at 103 pg/ml (normal: 10-52 pg/ml). Testosterone replacement was discontinued and anastrozole (Arimidex“, AstraZeneca, London, UK) 1 mg/day was initiated. After 1 month, the patient reported decreased breast size and resolution of his nipple tenderness. TRT was then re-introduced. After 5 months, the patient reported significant improvement in his baseline symptoms without return of any breast changes.


    We report here our successful experience using medical therapy with the aromatase inhibitor anastrozole for the treatment of gynecomastia induced by TRT in hypogonadal men.

    Aromatase is the enzyme responsible for converting androgens to estrogens, and is widely distributed in several tissues such as brain, liver and reproductive tissue.1 In men, estrogen production occurs mainly by extratesticular aromatization of androstenedione to estrone and of testosterone to estradiol.1

    Aromatase inhibitors have been used primarily in the adjuvant treatment of breast cancer by reducing estrogen levels and consequently causing reduced stimulation of estrogen receptors in this disease. Anastrozole is a fourth-generation nonsteroidal competitive aromatase inhibitor with potent suppression of serum estradiol levels. It was approved by the Food and Drug Administration in 1995 for the treatment of estrogen receptor-positive breast cancer in postmenopausal women in whom the disease has progressed despite tamoxifen treatment.3 Serum estradiol was reduced by up to 80% in patients with breast cancer treated with this drug.4 Other aromatase inhibitors, such as the first-generation aminoglutethimide, have limited use due to toxicity and lack of selectivity for the aromatase enzyme, necessitating concomitant corticosteroid supplementation in some cases.5

    In men, aromatase inhibitors have been used in the treatment of male infertility, in the hopes of achieving an improved testosterone-to-estradiol ratio. Raman and Schlegel3 noted significant improvement in sperm concentration, motility and morphology in a group of men treated with anastrozole. No benefit was noted in azoospermic individuals. Gillam et al6 recently reported a case of a giant prolactinoma treated with bromocriptine and cabergoline. The associated hypogonadism was successfully managed with TRT and anastrozole. Herzog et al7 reported beneficial effects on sexual function and control of seizures in men using the aromatase inhibitor testolactone with TRT.

    Theoretical adverse effects of aromatase inhibition in men include effects on body composition, carbohydrate/lipid metabolism, muscle strength, bone density and infertility.7,8 Estrogens have been shown to have important beneficial effects on bone density, even in males;8 however, the long-term effects on bone density in men receiving both testosterone supplementation and an anti-estrogen such as anastrozole are uncertain. However, no large-scale studies of anastrozole have been performed in men, and so there is limited information regarding its side effects in this population. In a series of infertile men treated with anastrozole, an asymptomatic increase in serum liver enzymes was observed in 7.4% cases, which returned to baseline levels after discontinuation of the medication.3

    The development of gynecomastia in hypogonadal men undergoing TRT can be very troubling to affected individuals, and may result in cessation of therapy. Since TRT is generally considered elective because it is administered for quality of life rather than for a life-threatening illness, both radiation therapy and surgical treatment are often regarded by patients and physicians alike as being too invasive a treatment for gynecomastia and, instead, testosterone treatment is often discontinued by patients if they are embarrassed by the breast enlargement. Successful treatment with an oral medication such as an aromatase inhibitor thus represents an attractive alternative therapy, and should be considered for symptomatic men.


    1 Taplin ME, Ho S-M. The endocrinology of prostate cancer. J Clin Endocrinol Metab 2001; 86: 3467-3477. PubMed

    2 Gruntmanis U, Braunstein GD. Treatment of gynecomastia. Curr Opin Invest Drugs 2001; 2: 643-649.

    3 Raman JD, Schlegel PN. Aromatase inhibitors for male infertility. J Urol 2002; 167: 624-629. Article PubMed

    4 Geisler J et al. Influence of anastrozole (Arimidex), a selective, non-steroidal aromatase inhibitor on in vivo aromatization and plasma estrogen levels in postmenopausal women with breast cancer. Br J Cancer 1996; 74: 1286. PubMed

    5 Buzdar AU, Riobertson JFR, Eliermann W, Nabholtz J-M. An overview of the pharmacology and pharmacokinetics of the newer generation aromatase inhibitors anastrozole, letrozole, and exemestane. Pharmacol Pharmacokinet 2002; 95: 2006-2016. Article

    6 Gillam MP, Middler S, Freed DJ, Molitch ME. The novel use of very high doses of cabergoline and combination of testosterone and an aromatase inhibitor in the treatment of a giant prolactinoma. J Clin Endocrinol Metab 2002; 87: 4447-4451. Article PubMed

    7 Herzog AG, Klein P, Jacobs AR. Testosterone and testolactone in treating reproductive and sexual dysfunction in men with epilepsy in men with epilepsy and hypogonadism. Neurology 1998; 50: 782-784. PubMed

    8 Taxel P et al. The effect of aromatase inhibition on sex steroids, gonadotropins, and markers of bone turnover in older men. J Clin Endocrinol Metab 2001; 86: 2869-2874. PubMed

    Received 20 August 2003; revised 2 October 2003; accepted 14 October 2003

    January 2004, Volume 16, Number 1, Pages 95-97

    Table of contents Previous Article Next PDF

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  5. Isn't gyno just a build up of calcium deposits under the nipple that causes it to get hard. If one coulld find the correct frequency of ultrasound in which calcium deposits break wouldn't that resolve the problem. kidney stones are broken up by ultra sound why couldn't the calcium deposits in the breast be broken down the same way and then reabsorbed back in the body for deposal. Just a thought. Since molecular everything vibrates at a certain frequecy finding the right pitch my be all that would needed to break them up.

    Phil the study really never indicated what there levels of estroge, free -t and testosterone was after the 5 months of therapy will armidex. Becurious to see the changes that occurred before reinstating the TRT



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