Testosterone Suppression With Injectable Estrogen Therapy Alone in Male to Female Transgender Patients

2021 ◽  
Vol 45 (7) ◽  
pp. S40
Author(s):  
Joanna Igo ◽  
Hasina Visram
2019 ◽  
Vol 26 (2) ◽  
pp. 265-266 ◽  
Author(s):  
Miglena K. Komforti ◽  
Susan Fineberg ◽  
Tova Koenigsberg ◽  
Bryan E. Harmon

2013 ◽  
Vol 7 (7-8) ◽  
pp. 544 ◽  
Author(s):  
Rafal Turo ◽  
Samer Jallad ◽  
William Richard Cross ◽  
Stephen Prescott

The incidence of prostate cancer in transsexual patients is very low with only few reported cases. Many years before presenting with prostate cancer, these patients receive hormone ablation as a part of their gender therapy. Their disease is already defined as castrate resistant, and the treatment and follow-up of such patients remains a challenge. We report a case of a male-to-female transgender woman who was diagnosed with metastatic prostate cancer, 31 years post-feminization.


2020 ◽  
Vol 4 (Supplement_1) ◽  
Author(s):  
Maria João Ferreira ◽  
José Luis Castedo ◽  
Jorge Pires Pedro ◽  
Cristina Daniela Salazar ◽  
Cláudia Fernandes Costa ◽  
...  

Abstract Introduction: Gender dysphoria (GD) is a disease in which the patient's gender identity does not correspond to their biological gender. Traditionally, sex is assigned accordingly to the sexual organs as male or female, however these patients do not identify with this classification. A biological male who identifies himself as a female is referred to as transgender female or male to female GD (MtF) and a biological female who identifies herself as a male is referred to as a transgender male or female to male GD (FtM). In our center there is a multidisciplinary consultation to approach and follow up patients with GD. Our work is an analysis of the patients who are currently attending this consultation. Methods: Retrospective study of patients attending the Sexual Medicine Group Consultation with diagnosis of GD. Results: 100 patients diagnosed with GD, of which 65% had GD FtM and 35% MtF. The median age is 25 years (± 9.5 years). Regarding the onset of symptoms, 76% of patients report that it occurred in childhood (before age 10); 20% from 10 to 18 years old and only 4% reported having occurred after 18 years. The median age for starting treatment is at 22 years (± 7.5 years). About 83% of the patients start therapy on medical advice, the remaining are self-medicated; 86% of FtM GD patients are currently on testosterone therapy; 85% of MtF GD patients are on estrogen therapy and 71% on anti-androgens. Concerning co-morbidities: 22% of patients have depression; 39% smoke; 6% are HIV-infected; 4% dyslipidemia and 2% hypertension. 47 (47%) patients underwent at least one surgical treatment; the average time to the first surgery was 2 years. Of the FtM GD patients, 23 (35%) patients underwent mastectomy, 10 (15%) hysterectomy and oophorectomy and 3 (5%) neophaloplasty; of the MtF GD patients 8 (23%) underwent augmentation mammoplasty; 7 (20%) neovaginoplasty. Two patients had a family history of GD. One case of Klinefelter’s syndrome and one case of congenital adrenal hyperplasia was diagnosed during the study prior to therapy initiation. Discussion: There was a higher prevalence of FtM compared to MtF, unlike most centers reporting a higher prevalence of MtF. Regarding the proportion of patients on medical therapy, the data are in line with data from other centers already published, as well as the fact that most patients in our study are young. Conclusion: The demand for medical help from GD patients is increasing. The evaluation of these patients by endocrinology before and throughout treatment is essential, not only for the evaluation of contraindications or side effects of therapy, but also for the identification of endocrinological diseases. This is the first work, to our knowledge, to portray the case series of a consultation center dedicated to the treatment of patients with GD in Portugal.


1999 ◽  
Vol 277 (6) ◽  
pp. H2341-H2347 ◽  
Author(s):  
Gishel New ◽  
Stephen J. Duffy ◽  
Richard W. Harper ◽  
Ian T. Meredith

We have previously shown that chronic estrogen therapy improves endothelium-dependent vasodilation in the resistance vessels of biological males. Whether this is nitric oxide (NO) mediated and whether estrogen improves metabolic vasodilation is unknown. Resting forearm blood flow (FBF), ACh-induced vasodilation, and functional hyperemic blood flow (exercise) were assessed before and after the inhibition of NO with N G-monomethyl-l-arginine (l-NMMA) in 15 male-to-female transsexuals prescribed estrogen and in 14 age-matched males. Resting FBF was similar in the two groups and was similarly ( P = 0.44) but significantly reduced by 48% after infusion ofl-NMMA ( P < 0.0001). The ACh dose-response relationship was shifted upward and to the left in the transsexual compared with the male group ( P < 0.01). After the inhibition of NO, however, the difference in the ACh dose-response curve between the two groups was abolished ( P= 0.15). Peak functional hyperemic blood flow was similar for the two groups ( P = 0.94).l-NMMA produced a significant ( P < 0.01) but similar ( P = 0.64) reduction in peak hyperemia in the two groups. The volume of blood repaid to the forearm 1 and 5 min after exercise was also reduced by l-NMMA ( P < 0.0001); however, there were no differences between the two groups. This suggests that ACh-mediated NO-dependent vasodilation may be more sensitive to the effects of chronic estrogen than exercise-induced vasodilation. Long-term estrogen does not appear to improve exercise-induced metabolic vasodilation in biological males, despite the fact that NO contributes to this process.


1997 ◽  
Vol 29 (7) ◽  
pp. 1437-1444 ◽  
Author(s):  
Gishel New ◽  
Katrina L Timmins ◽  
Stephen J Duffy ◽  
Binh T Tran ◽  
Richard C O’Brien ◽  
...  

2006 ◽  
Vol 52 (7) ◽  
pp. 1356-1365 ◽  
Author(s):  
Margrita H Slagter ◽  
Louis JG Gooren ◽  
Willem de Ronde ◽  
Antoninus Soosaipillai ◽  
Andreas Scorilas ◽  
...  

Abstract Background: The expression of human tissue kallikrein genes is regulated by steroid hormones, but most studies have been conducted with cancer cell lines. Our purpose was to examine serum and urinary tissue kallikrein concentration changes in male-to-female transsexuals before and after treatment with antiandrogens and estrogens. Methods: Thirty-five male-to-female transsexuals receiving cyproterone acetate and estrogens (orally or transdermally) were included in this study. Serum and urine samples were collected before initiation of therapy and 4 and 12 months post therapy. ELISAs were used to measure multiple kallikreins in serum and urine. Results: After antiandrogen and estrogen therapy, serum testosterone concentrations decreased dramatically, as did serum and urinary concentrations of human glandular kallikrein (hK2) and prostate-specific antigen (PSA; hK3). Statistically significant but relatively small changes in serum and urinary concentrations of many other kallikreins were also seen. Kallikreins in serum and urine were correlated before and after treatment. Conclusions: The concentrations of hK2 and hK3, but not of any other kallikreins, decrease dramatically after combined antiandrogen and estrogen treatment in male-to-female transsexuals. The smaller responses of the other kallikreins presumably reflect their expression in multiple tissues.


The Prostate ◽  
2017 ◽  
Vol 77 (8) ◽  
pp. 824-828 ◽  
Author(s):  
Asma Sharif ◽  
Neha R. Malhotra ◽  
Andres M. Acosta ◽  
Andre A. Kajdacsy-Balla ◽  
Maarten Bosland ◽  
...  

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