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P-value comparing
Clinical Ovulation Clinical Clinical Pregnancies
Age Natural Pregnancy NC Pregnancy Induction Pregnancy OI Pregnancy from NC vs.
(years) Cycles from NC per Cycle Cycles from OI per Cycle OI IUI (chi square)
O-44 Monday, October 8, 2018 11:00 AM A. David,b E. E. Marsh,a V. Padmanabhan,c A. Shikanov.b aObstetrics &
Gynecology, University of Michigan, Ann Arbor, MI; bBiomedical Engineer-
THE EFFICACY OF TESTOSTERONE OR ESTRADIOL ing, University of Michigan, Ann Arbor, MI; cPediatrics, University of Mich-
THERAPY WITHOUT A GNRH AGONIST OR PROGES- igan, Ann Arbor, MI.
TIN TO SUPPRESS ENDOGENOUS GONADAL ACTIV-
ITY IN TRANSGENDER PATIENTS. I. I. Stewart,a OBJECTIVE: Multiple national and international medical organizations,
L. V. Spratt,a W. Craig,b J. S. Olshan,c D. I. Spratt.a aThe Department of including ASRM, recommend fertility preservation counseling prior to start-
Obstetrics and Gynecology, Division of Reproductive Endocrinology and ing gender-affirming hormone therapy in transgender patients; however,
Infertility, Maine Medical Center, Portland, ME; bMaine Medical Center there is a paucity of data on the reproductive effects of long-term hormone
Research Institute, Scarborough, ME; cThe Department of Pediatrics, Divi- therapy, particularly in transgender men. The objective of this study was to
sion of Pediatric Endocrinology, Maine Medical Center, Portland, ME. develop a mouse model to investigate reproductive effects of T administra-
tion for female-to-male (FTM) gender transition.
OBJECTIVE: To determine the efficacy of testosterone (T) or estradiol DESIGN: Translational animal study.
(E2) therapy alone, without a GnRH agonist or progestin, to suppress endog- MATERIALS AND METHODS: Fifteen 8-9 week old adult female
enous gonadal activity in female-to-male (FTM) or male-to-female (MTF) C57BL/6J mice were injected with 0.9 mg, 0.45mg, or 0.225mg of T enan-
transgender patients. thate in sesame oil twice weekly; 10 controls were injected with vehicle.
DESIGN: A retrospective cohort study of transgender patients undergoing Daily vaginal cytology and weekly serum hormone analysis were performed.
routine therapy in the Reproductive Endocrinology Clinic at Maine Medical Mice were sacrificed after 6 weeks of injections, serum collected, and organs
Center. harvested. Data were analyzed with t-tests, Mann-Whitney, ANOVA, or
MATERIALS AND METHODS: Data were collected from all transgender Kruskal-Wallis with post-hoc tests, as appropriate, and nQuery Advisor
patients seen in the outpatient clinic between 03/2013 and 01/2018 who met used to calculate sample size with 85% power.
inclusion criteria: 1) age 18-40 years for FTM and 18-50 years for MTF; 2) RESULTS: Estrous cycles ceased in all T-treated mice within 1 week of
normal reproductive function prior to therapy; 3) total T within the normal initiating injections, while controls continued cycling normally. Mean termi-
adult male range (348-1197 ng/dL) in FTM patients while on T therapy; 4) nal T level (ng/mL) was increased in all T-treated mice (5.3, 5.7, and 7.7 for
serum E2 greater than 100 pg/mL in MTF patients while on E2 therapy unless 0.225mg, 0.45mg, 0.9mg T groups, respectively) compared to controls (0.05,
T was adequately suppressed at lower serum E2 concentrations; 5) no concur- p<0.05), and LH (ng/mL) was suppressed (0.04, 0.04, and 0.05 for 0.225mg,
rent therapy with a progestin or GnRH agonist; and 6) no history of oopho- 0.45mg, 0.9mg T groups, respectively) compared to controls (0.27, p<0.05).
rectomy or orchiectomy. Consistent with Endocrine Society guidelines, AMH levels were increased in the 0.225mg (1.6x) and 0.45mg (1.5x) T
effective suppression of ovarian function in FTM patients was assessed by groups, compared to controls (p<0.05). There were no differences in FSH,
cessation of menses and a serum E2 of (<50 pg/mL). In MTF patients, testic- estradiol, or progesterone levels. Clitoral area was significantly increased
ular suppression was assessed by total serum T concentrations below the up- in T-treated mice compared to controls (9.5 vs 5.2mm2, p<0.0001). Ovaries
per limit of the premenopausal adult female normal range (<55 ng/mL)1. of all T-treated mice had a multi-follicular appearance and complete absence
RESULTS: FTM patients (n¼50) were aged 26.25.9 years and received of corpora lutea. Liver weight was significantly increased in mice receiving
T through subcutaneous (SC, n¼58) or intramuscular (IM, n¼2) injections. T 0.45 or 0.9mg T (1.1 and 1.18g, respectively, vs 0.96g in controls, p<0.05).
doses ranged from 40-100 mg per week. All FTM patients were amenorrheic There were no significant differences between groups in body weight change,
on T therapy alone. The mean serum E2 concentration was 39.821.4 pg/ or uterine, ovarian or brain weights. Two mice in the 0.9mg T group had
mL. Among these 50 patients, 36 (72%) had serum E2 <50 pg/mL. The me- vaginal prolapse.
dian serum E2 value for the 14 patients with E2 R50 pg/mL was 55 pg/mL CONCLUSIONS: T treatment of adult female mice mimicking hormone
(range, 55-130). Thus, 36 out of 50 (72%) FTM patients had effective therapy in FTM patients resulted in reproductive as well as metabolic pertur-
biochemical suppression of ovarian function without a GnRH agonist or pro- bations, manifested at the level of the ovaries and liver. Due to vaginal pro-
gestin therapy and all FTM patients had clinical suppression of ovarian func- lapse in the 0.9mg T group, possibly due to higher serum T levels, 0.225mg or
tion (amenorrhea). MTF patients (n¼24) were aged 29.79.0 years and 0.45mg T are more suitable for a FTM mouse model, which can be used to
received oral (n¼25), SC (n¼1), or IM (n¼1) E2 as well as spironolactone. further elucidate the consequences of chronic T administration on fertility
Oral E2 doses ranged from 3-12 mg per day. Serum total T values for the 24 and metabolic health, for which there is currently only sparse data.
MTF patients were all within the target range (median 8.2, range 2.7-36 ng/
dL). Thus, all MTF patients had effective biochemical suppression of testic-
ular function without GnRH agonist or progestin therapy. O-46 Monday, October 8, 2018 11:30 AM
CONCLUSIONS: Our results indicate that most transgender patients do
not need GnRH agonist or progestin treatment in addition to T or E2 therapy FEMALE TO MALE TRANSGENDER PATIENTS HAVE
to suppress endogenous gonadal activity. Additional unnecessary endocrine GOOD EGG YIELDS WITH CONTROLLED OVARIAN
therapies to suppress ovarian or testicular function incur a significant expense HYPERSTIMULATION. A. Leung,a,b D. Sakkas,a
and potential adverse effects without providing a clear change in clinical S. Pang,a K. Thornton,a,c N. Resetkova.a,c aBoston IVF, Wal-
outcome. tham, MA; bOb/Gyn, Beth Israel Deaconess Medical Center, Boston, MA;
c
References: Ob/Gyn, Beth Israel Deaconess Medical Center, Boston, MA.
1. J Clin Endocrinol Meta (2017), 102:3869-3903.
OBJECTIVE: The transgender population is increasingly seeking access
to assisted reproductive technologies (ART). However, there are no studies
O-45 Monday, October 8, 2018 11:15 AM of substantial sample size that examines ovarian hyperstimulation outcomes
in this underserved patient population. Given the increasing demand for ART
DEVELOPMENT OF A MOUSE MODEL TO INVESTI- services by transgender patients and lack of information for providers treat-
GATE THE REPRODUCTIVE EFFECTS OF TESTOS- ing these patients, we seek to inform this area of medicine. This information
TERONE (T) ADMINISTRATION IN TRANSGENDER will serve to counsel transgender patients and their providers on ART out-
MEN. M. B. Moravek,a H. M. Kinnear,b E. S. Constance,a comes in this population.