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Journal of Clinical Endocrinology & Metabolism, doi:10.1210/jc.2007-1809
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The Journal of Clinical Endocrinology & Metabolism Vol. 93, No. 1 19-25
Copyright © 2008 by The Endocrine Society


EXTENSIVE CLINICAL EXPERIENCE

Long-Term Treatment of Transsexuals with Cross-Sex Hormones: Extensive Personal Experience

Louis J. Gooren, Erik J. Giltay and Mathijs C. Bunck

Department of Endocrinology (L.J.G., M.C.B.), Vrije Universiteit University Medical Center, 1081 HV Amsterdam, The Netherlands; and Leiden University Medical Center (E.J.G.), Department of Psychiatry, 2333 ZA Leiden, The Netherlands

Address all correspondence and requests for reprints to: Dr. L. J. Gooren, Department of Endocrinology, VU University Medical Center, De Boelelaan 1118, 1081 HV Amsterdam, The Netherlands. E-mail: ljgooren{at}truemail.co.th.

Context: Transsexuals receive cross-sex hormone treatment. Its short-term use appears reasonably safe. Little is known about its long-term use. This report offers some perspectives.

Setting: The setting was a university hospital serving as the national referral center for The Netherlands (16 million people).

Patients: From the start of the gender clinic in 1975 up to 2006, 2236 male-to-female and 876 female-to-male transsexuals have received cross-sex hormone treatment. In principle, subjects are followed up lifelong.

Interventions: Male-to-female transsexuals receive treatment with the antiandrogen cyproterone acetate 100 mg/d plus estrogens (previously 100 µg ethinyl estradiol, now 2–4 mg oral estradiol valerate/d or 100 µg transdermal estradiol/d). Female-to-male transsexuals receive parenteral testosterone esters 250 mg/2 wk. After 18–36 months, surgical sex reassignment including gonadectomy follows, inducing a profound hypogonadal state.

Main Outcome Measures: Outcome measures included morbidity and mortality data and data assessing risks of osteoporosis and cardiovascular disease.

Results: Mortality was not higher than in a comparison group. Regarding morbidity, with ethinyl estradiol, there was a 6–8% incidence of venous thrombosis, which is no longer the case with use of other types of estrogens. Continuous use of cross-sex hormones is required to prevent osteoporosis. Androgen deprivation plus an estrogen milieu in male-to-female transsexuals has a larger deleterious effect on cardiovascular risk factors than inducing an androgenic milieu in female-to-male transsexuals, but there is so far no elevated cardiovascular morbidity/mortality. Low numbers of endocrine-related cancers have been observed in male-to-female transsexuals.

Conclusions: Cross-sex hormone treatment of transsexuals seems acceptably safe over the short and medium term, but solid clinical data are lacking.




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Copyright © 2008 by The Endocrine Society