| Literature DB >> 28931393 |
Kaori Matsumoto1, Kazuhiko Imakawa2, Chuyu Hayashi3.
Abstract
BACKGROUND: The increase in serum estradiol (E2) concentrations during the follicular phase becomes the index of oocyte maturation in vivo. When ovarian stimulation is performed to hypogonadotropic hypogonadism (HH) patients with only follicle stimulating hormone (FSH), proper increase in serum E2 concentrations is not observed. Even if oocytes are obtained, which usually have low fertilization rate. In this report, we would like to present an unique case, in which under low E2 concentrations and without luteinizing hormone (LH) administration, numerous mature oocytes could be obtained and a healthy baby delivered. CASEEntities:
Keywords: Assisted reproductive technology; Controlled ovarian stimulation; Follicular fluids; High progesterone; Hypogonadotropic hypogonadism; Hypothalamic amenorrhea; Low estradiol; Luteinizing hormone
Mesh:
Substances:
Year: 2017 PMID: 28931393 PMCID: PMC5607600 DOI: 10.1186/s12884-017-1510-6
Source DB: PubMed Journal: BMC Pregnancy Childbirth ISSN: 1471-2393 Impact factor: 3.007
Fig. 1Follicular development following controlled ovarian stimulation (COS). Ovarian response was monitored through the use of transvaginal ultrasonography during COS. During the first COS, measurable follicles were not observed in either ovary on day 3 of the menstrual cycle (MC). On the same day, COS was initiated with daily administration of 225 international unit (IU) recombinant follicle stimulating hormone (rFSH). Follicular development and increased progesterone (P4) concentrations were observed, but estradiol (E2) concentrations were low on day 11. Although the right (R) and left (L) ovaries had over 30 follicles of 15–19 mm on day 13, serum E2 concentrations were low at 484 pg/ml and P4 concentrations were high at 2.09 ng/ml. COS was canceled due to the hormone concentration which did not reflect those of numerous follicular developments. From the day when the first COS was canceled, the patient took 10 mg synthetic progesterone (SP) orally for the next 14 days. The patient experienced withdrawal bleeding, and several small follicles were observed in both ovaries on day 3. From the same day, the daily dosage of 175 IU rFSH was administered for the first 5 days, followed by 200 IU for the remaining treatment period. Similar to the response seen at the first COS, high serum P4 concentrations, 2.11 ng/ml, were observed; however, serum E2 concentrations, 701 pg/ml, did not reflect those of numerous follicular developments
Transition in serum steroid hormone concentrations and follicular development during controlled ovarian stimulation
| First COS | |||||
| MC day | MC Day 3 | MC Day 8 | MC Day 11 | MC Day 13 | |
| (rFSH administration) | (0 IU) | (1125 IU) | (1800 IU) | (2250 IU) | |
| E2 | 10a | – | 219 | 484 | |
| (pg/ml) | |||||
| LH | 0.1a | – | 0.1a | 0.1a | |
| (mIU/ml) | |||||
| FSH | 0.1 | – | – | – | |
| (mIU/ml) | |||||
| P4 | – | – | 1.05 | 2.09 | |
| (ng/ml) | |||||
| Follicular diameter (mm) | NM | 6–8 | 9–12 | 15–19 | |
| Second COS | |||||
| MC day | MC Day 3 | MC Day 8 | MC Day 10 | MC Day 12 | MC Day 15 |
| (rFSH administration) | (0 IU) | (875 IU) | (1225 IU) | (1625 IU) | (2225 IU) |
| E2 | 10a | – | 60 | 201 | 701 |
| (pg/ml) | |||||
| LH | 0.1a | – | 0.1a | 0.1a | 0.1a |
| (mIU/ml) | |||||
| FSH | 0.2 | – | – | – | – |
| (mIU/ml) | |||||
| P4 |
| – | 0.40 | 0.53 | 2.11 |
| (ng/ml) | |||||
| Follicular diameter (mm) | 6–8 | 6–8 | 10 | 13–15 | 14–22 |
Note: COS controlled ovarian stimulation, MC menstrual cycle, IU international units, NM not measurable, bar no data, E estradiol, LH luteinizing hormone, FSH follicle stimulating hormone, P progesterone
aunder detection limit
Hormone concentrations throughout her pregnancy period
| estradiol (pg/ml) | androstenedione (ng/ml) | testosterone (ng/ml) | DHEA-S (μg/dl) | |
|---|---|---|---|---|
| 15w2d | 8,410 | 7.2 | 0.95 | 111 |
| 19w6d | 14,500 | 8.5 | 1.09 | 114 |
| 30w2d | 37,300 | 12.0 | 1.26 | 105 |
Note: w week, d day, DHEA-S dehydroepiandrosterone sulfate
Fig. 2Comparison of steroid hormone concentrations of this patient to those of infertile patients (Inf-), Inf-A and Inf-B. On day 4 of the menstrual cycle, these infertile women received daily administration of 100 mg clomifene citrate (CC) for 5 days. Follicular diameters were 25.2 mm and 18.1 mm for Inf-A and 22.8 mm for Inf-B on the day of induced ovulation. From the same day, serum hormone concentrations for Inf-A and Inf-B were 692 pg/ml and 745 pg/ml E2, 10.5 mIU/ml and 8.0 mIU/ml LH, and 0.40 ng/ml and 0.29 ng/ml P4, respectively. Ovulation was induced with 600 μg gonadotropin releasing hormone (GnRH) agonist, followed by oocyte pick-up (OPU), in vitro fertilization (IVF) and follicular fluids (FFs) cryopreservation in the same manner. However, no oocyte was collected from Inf-A, while one oocyte was collected from Inf-B, but its development ceased after fertilization. Although progesterone (P4), dehydroepiandrosterone sulfate (DHEA-S) and androstenedione (A2) concentrations in FFs of this patient did not differ from those of Inf-A and Inf-B, estrone (E1), testosterone (T) and estradiol (E2) concentrations were lower than those of Inf-A and Inf-B
Hormonal Precursor/Hormone Ratios
| A2/E1 | T/E2 | A2/T | E1/E2 | |
|---|---|---|---|---|
| Enzyme involved | Aromatase | Aromatase | 17β-HSD | 17β-HSD |
| Patient |
| 76,875.0 |
|
|
| Inf-A | 920.7 | 54,285.7 | 0.368 | 21.7 |
| Inf-B | 521.1 | 76,346.2 | 0.132 | 19.3 |
Note: Under bar denotes significantly lower in ratio than that of Inf-A and Inf-B
E estrone, E estradiol, A androstenedione, T testosterone, 17β-HSD 17β-hydroxysteroid dehydrogenase