To describe the clinical characteristics, management and pregnancy outcome of women with prepregnancy hypopituitarism (HYPO) that received care at our center.
Retrospective study describing 12 pregnancies in women with prepregnancy HYPO (two or more pituitary hormonal deficiencies under replacement treatment) that received care during pregnancy at Hospital Santa Creu i Sant Pau. Clinical characteristics, management and pregnancy outcome were systematically collected.
Average patients’ age was 35 years and HYPO duration at the beginning of pregnancy was 19 years. The most frequent cause of HYPO was surgical treatment of a sellar mass (8 pregnancies). Eight pregnancies were in primigravid women and 10 required assisted reproductive techniques. The hormonal deficits before pregnancy were as follows: GH in 12 women, TSH in 10, gonadotropin in 9, ACTH in 5 and ADH in 2. All deficits were under hormonal substitution except for GH deficit in 4 pregnancies. During pregnancy, 4 new deficits were diagnosed. The dosage of replacement treatment for TSH, ACTH and ADH deficits was increased and GH was stopped. Average gestational age at birth was 40 weeks, gestational weight gain was excessive in 9 women, 8 patients required induction/elective delivery and cesarean section was performed in 6. Average birthweight was 3227 g. No major complications were observed. Five women were breastfeeding at discharge.
In this group of women with long-standing HYPO, with careful clinical management (including treatment of new-onset hormonal deficits) pregnancy outcome was satisfactory but with a high rate of excessive gestational weight gain and cesarean section.
Hypopituitarism (HYPO) defined as the loss of function of one or more pituitary hormones, is a rare condition, with a reported prevalence between 300 and 355 per million inhabitants [1, 2]. The etiology is widely diverse, of which pituitary adenoma and its treatment-derived complications are the main causes followed by trauma, vascular injury, hypophysitis and infiltrative processes, among others . Clinical manifestations and decision to initiate hormonal replacement will depend on diverse factors such as sex, age, severity of damage, time of onset and the hormonal axes affected. Of note, a careful monitoring of the hormonal replacement is mandatory, since hormonal replacement interactions might occur, especially when several hormonal deficiencies exist . Globally, patients with HYPO have been shown to have reduced quality of life  along with higher rates of infertility  and mortality .
It is well known that not only the integrity of the pulsatile secretion of gonadotropin-releasing hormone and consequently of follicle-stimulating hormone and luteinizing hormone axis is needed to achieve pregnancy, but also the interaction of all pituitary hormones [6, 8, 9]. In this context, previous studies have reported that HYPO is often associated with lower pregnancy and live birth rates compared to women with either no hormonal deficits or with isolated hypogonadotropic hypogonadism .
During the last decades, the remarkable advance in assisted reproductive techniques (ART) has made it possible to significantly improve the fertility rate in patients with hypopituitarism. Despite the fact that the available data on this condition is scarce, a recent review based on retrospective studies  reported fertility rates of 81% in women with isolated hypogonadotropic hypogonadism and between 47 and 76% in women with HYPO.
Along with the development of ART, treatment with growth hormone (GH) may have concurred to the significant improvement of fertility and pregnancy outcomes during the last years . A large body of evidence supports that GH plays a fundamental role in the reproductive system [10, 12, 13]. However, the continuation of GH therapy during pregnancy remains a matter of discussion, and its use during pregnancy is not approved [11, 14]. It is well established that GH is secreted from placenta whose levels increase throughout pregnancy and progressively replace pituitary GH in the stimulation of insulin-like growth factor 1 (IGF1) . Of note, placental GH levels are similar in pregnant women with GH deficiency than in those without .
Pregnancy in hypopituitary women has classically been considered a high-risk condition based on the association with obstetrical complications such as higher rates of miscarriage, fetal growth restriction, cesarean section and post-partum hemorrhage [17, 18]. By contrast, recent studies have shown better results; such as those reported by Correa et al. , who described a 100% successful pregnancy rate in a case series of five women with childhood onset hypopituitarism after an optimized hormonal replacement, with no severe obstetrical complications.
Once pregnancy is achieved, a strict follow-up is needed for dosage replacement adjustment and early diagnosis of eventual new onset hormonal deficits. However, due to the lack of data based on randomized clinical trials, the actual clinical practice recommendations  are based on expert opinions and on the knowledge of hormonal physiology during pregnancy.
In order to contribute to the extension of the available data, we describe the clinical aspects as well as management and pregnancy outcomes of a case series of women with HYPO followed at our center.
This is a retrospective descriptive study of patients with HYPO that were attended at the outpatient clinic for Endocrine Disorders and Pregnancy at the Endocrinology Department in Hospital Santa Creu i Sant Pau, between October 2001 and November 2019. The study was approved by the Hospital Ethics Committee that waived the requirement of an informed consent.
(1) Prepregnacy HYPO defined as the deficit of at least two pituitary hormones requiring substitutive treatment and (2) confirmed pregnancy.
Clinical data were obtained from electronic medical records including visits at primary care and endocrinology and obstetrics departments. Information on the following variables was collected:
*Pituitary disease and treatment: primary diagnosis and date, treatment received. *Hormonal status before pregnancy: type and number of hormonal deficits, need of replacement therapy and dosage, plasmatic and/or urine hormone levels. *Fertility: treatment used to achieve pregnancy, if needed. *Clinical assessment during pregnancy: anthropometrics, periodic hormonal status evaluation, substitutive treatment and dosage and presence of any complication. *Delivery: gestational age, induction, oxytocin use, type of delivery, pregnancy-induced hypertension, perinatal complications. *Postpartum: complications. *Neonatal: sex, birth weight, Apgar score at 5 and 10 min, arterial and venous pH, presence of any type of breastfeeding  at discharge and neonatal complications.
Customized birthweight centiles were calculated using gestational related optimal weight (GROW) software .
Data are expressed as median (percentile 25–75) using the SPSS version 20 statistical package.
Here we present the data of 12 pregnancies in 10 women with HYPO. The characteristics of each patient are summarized in Table 1. The most frequent cause of HYPO was a sellar mass that had undergone surgical treatment.
From the women with GH deficiency, 66.6% were under GH substitution therapy, with a median daily dosage of 0.51 mg (0.40–0.60). All women stopped GH treatment after pregnancy confirmation. All the other TSH, ACTH and ADH deficiencies were under substitution therapy with levothyroxine, hydrocortisone and desmopressin, respectively. No patients had concomitant hormonal hypersecretion.
Women were primigravida in 8 of the 12 pregnancies and patients with prior pregnancies had had 3 abortions and 2 live children. In order to achieve pregnancy, only 2 women did not require ART. Patient #3 was diagnosed of craniopharyngioma at 15 at another center and had postoperative deficiency of GH, TSH and gonadotropins. She received treatment with levothyroxine, had puberty induction at 17 and used long-term replacement therapy with oral estrogens and gestagens. She got spontaneously pregnant when she dropped replacement therapy for 2 months. Sixteen months after delivery and 2 months after stopping partial breastfeeding she initiated transdermal hormone therapy due to hypogonadotropic hypogonadism (estradiol 0.13 nmol/l, LH 7.9 IU/L, FSH 6.6 IU/L) with normal prolactin and severe vasomotor symptoms. Transdermal treatment was stopped 10 years after delivery, and she had regular menses for 3 years. Thus, even when this is an unusual clinical course, we consider that this patient had (intermittent) hypogonadotropic hypogonadism and had spontaneous pregnancy favored by stopping combination therapy. The situation would be parallel to that in subjects with idiopathic hypogonadotropic hypogonadism where reversal and relapse has been described, even in subjects with severe phenotype . In their article, Sidhoum et al. reported that up to 22% of subjects experienced reversal during their lifetime and one of the conclusions was to emphasize the need that these patients take contraceptive precautions despite apparent infertility. Patient #6 and #7 required ART due to PCOS.
All but 2 patients were under follow-up at the Endocrinology Department before conception. The dosage of hormonal substitution of each hormonal axis during pregnancy is represented in Fig. 1. During pregnancy follow-up, 4 patients had to initiate treatment for a de novo deficit: one for thyroid deficit (T4 7.5 pmol/L; reference range 9–19 pmol/L) at 32 weeks, one for ACTH at 24 weeks (sinusitis in a patient with prepregnancy partial deficit) and 2 patients for ADH deficit at 18 and 21weeks (diuresis 2860 mL/24 h and 5200 mL/24 h) respectively. In those patients on levothyroxine before pregnancy, the dose during pregnancy was increased by 71.7%. Weight increase during pregnancy was excessive in 9 women according to the Institute of Medicine guidelines . No patient developed apoplexy, visual impairment or any other acute complication in relation with the pituitary disease.
Labor, delivery and pregnancy outcome
Pregnancy outcome is described in Table 2. Eight patients had labor induction/elective delivery and oxytocin was administered in about half of the patients for labor induction/augmentation. In the five patients using replacement treatment with hydrocortisone, stress dose was administered at delivery (four intravenous and one oral route). No patient developed adrenal crisis or problematic hypotension.
Cesarean section was performed in half of the patients. Birthweight centiles of the newborns were <10 in 2 babies and >P90 also in 2 babies. No episodes of intrapartum fetal distress nor major perinatal complications were present. Five women were breastfeeding at discharge.
Pregnancy in women with HYPO is infrequent. It is associated with a higher risk of maternofetal complications that requires a strict follow-up by a multidisciplinary team. Due to the lack of data from randomized clinical trials, clinical guidelines  mainly rely on pregnancy physiology and expert recommendations. In this report, we aimed to contribute with clinical data and pregnancy outcomes in 12 pregnancies in hypopituitary women. Overall, pregnancy outcome was satisfactory, supporting the close monitoring approach prior to and during pregnancy by a specialized and multidisciplinary team.
As previously mentioned, despite the fact that new ART have notably improved fertility rates in these patients, it has been widely reported that HYPO implies a poorer pregnancy potential. In the current study, most hypopituitary women presented gonadotropin deficit and in 10 out of 12 pregnancies some type of fertility treatment was required in order to achieve conception. Unfortunately, we do not have information on non-pregnant women with HYPO, therefore we cannot provide data about the fertility rate.
GH substitution during pregnancy in women with HYPO is controversial. Some hormonal interactions may occur and close monitoring of free T4 and cortisol status is advised once GH replacement is started. GH reduces the 11β-hydroxysteroid dehydrogenase (11βHSD) type 1 activity and increases the deiodinase type 1 activity that can decrease cortisol and free T4 levels [23, 24], and upward dose adjustments of hydrocortisone and levothyroxine might be required. The contrary situation could take place during pregnancy when GH treatment is stopped. While it is known that adequate substitution prior to pregnancy is needed, because GH deficiency is related to subfertility, the current recommendation is to stop treatment once pregnancy is confirmed . This recommendation is based on the physiological secretion of placental growth hormone from the 5th week of gestation , added to sufficient evidence regarding safety of exogenous hormone during this period. In the current study, all patients stopped GH replacement when pregnancy was confirmed. Along with several other benefits, it is generally established that despite the insulin antagonist action of GH, replacement therapy in patients with GHD, reverts almost all the metabolic alterations associated with this entity  by reducing fat mass, especially central adiposity and increasing lean body mass . Therefore, the suspension of GH replacement at the beginning of pregnancy could have a role in the weight gain observed during follow up. It has been suggested to continue GH therapy in the first trimester and at half the dose in the second, stopping it in the last trimester when placental GH levels reach the peak . Unfortunately, evidence regarding this issue ensuing from randomized controlled trials is not available.
During pregnancy, a strict follow up is essential to assess and adjust the dosage of every hormonal replacement treatment. Clinical practice guidelines on HYPO management  recommend to assess free T4 levels every 4–6 weeks in order to adjust levothyroxine dosage to maintain free T4 within normal ranges. Levothyroxine requirements during pregnancy might differ depending on the cause of hypothyroidism. Due to the TSH effect of hCG by binding to the TSH receptor, patients with secondary hypothyroidism could require a lower dose increment compared to those with primary hypothyroidism. Alternatively, thyroid gland may not respond appropriately to hCG due to chronic lack of TSH stimulus. In this report, the observed average increase in levothyroxine dose during pregnancy in women receiving prepregnancy treatment (71.7%) is well above reported values [29, 30], classically described as 25–30% . The stop of GH treatment should have little impact considering the progressive appearance of placental GH, but if any, the effect should be in the direction of a lower increment . Overall, current results do not suggest that women with hypothyroidism due to panhypopituitarism have lower requirements of levothyroxine during pregnancy.
Regarding the glucocorticoid axis adjustment, the recommendation is that during pregnancy only hydrocortisone should be used , since it is akin to the natural hormone, it is deactivated by the enzyme 11βHSD type 2 and cannot cross the placenta into the fetal circulation, preventing any undesirable effects of fetal exposure to glucocorticoid excess , contrary to dexamethasone, which is not inactivated. However, the best regime recommendation on hydrocortisone dose adjustment is still lacking. Furthermore, some hormonal replacement interactions may reduce cortisol levels, such as an increase in renal 11βHSD type 2 activity or an increased cortisol clearance due to levothyroxine therapy , and the previously mentioned effects of GH substitution. The suggestion from the abovementioned guideline  is to adjust dose after clinical judgment or to increase the hydrocortisone 20-40% in the third trimester. In the pregnancies herein reported, we observed that 3 out of the 5 pregnant women under hydrocortisone treatment did not require a dose increase during pregnancy, and the other 2 required a small increase of only 16.0% (3.2 mg/day) during the third trimester. The graph depicting median hydrocortisone dose during pregnancy (Fig. 1) is remarkably flat. It is well known that pregnancy could be considered a “physiological” state of hypercortisolism, based on the higher levels of cortisol binding globulin enhanced by placental estrogen and placental corticotropin-releasing hormone that lead to an increase of free and total plasma cortisol levels . Our therapeutic decision was based on clinical judgment as the measurement of plasma cortisol levels during pregnancy is not performed as part of our regular clinical practice. Since the women’s clinical condition and pregnancy outcome were uneventful, this suggests either that before pregnancy their deficit was over-replaced to some extent or that the dose increment required for pregnancy is less than usually assumed and GH cessation could have contributed. Overall, it seems clear that in women requiring glucocorticoid replacement, a systematic dose increase during pregnancy is not needed. In this line, even when information of the glucocorticoid dose given during pregnancy is usually not reported in articles dealing with adrenal insufficiency during pregnancy , in a recent report of 128 pregnancies, glucocorticoid dose was decreased after initial increase in some women and was not modified during pregnancy in a sizeable subgroup of women. In this study only 25% of the participants had secondary insufficiency. The increase in hydrocortisone equivalent during pregnancy was similar in women with Addison’s disease and secondary adrenal insufficiency but this observation might not be fully applicable to our study (i.e. information on concomitant treatment with GH was lacking) .
During follow-up, we detected 4 new hormonal deficits that were not present at the beginning of pregnancy and 3 of them resolved after delivery: One patient-initiated treatment with hydrocortisone, one patient required thyroid substitution at week 32 as the free T4 levels were below the normal range, and 2 patients required vasopressin substitution as they developed diabetes insipidus (DI). The patient with a diuresis >5000 mL/24 h, continued requiring desmopressin treatment after delivery, suggesting that diabetes insipidus was already present before pregnancy. Regarding vasopressin substitution, all the patients with ADH deficit diagnosed before or during pregnancy, needed to increase the desmopressin dosage during follow up. In women already treated before pregnancy, the dose increment at the end of pregnancy was 40% (60 mcg). It is remarkable that one of the patients initiating treatment during pregnancy, required up to 360 mcg/day at the time of delivery. It is well-known that pregnancy may unmask a partial DI not clinically relevant before gestation. Several possibilities might explain why pregnancy itself may cause exacerbation of DI. On the one hand, the higher levels of progesterone and steroids antagonize ADH . On the other hand, placental vasopressinase leads to accelerated metabolism of endogenous ADH and vasopressin requirements increase . Additionally, compression of the posterior pituitary by the enlarged anterior pituitary has also been described, aggravating situations of partial DI .
Oxytocin is a neuropeptide synthetized in the hypothalamus and released to the neurohypophysis, that stimulates uterine smooth muscle contraction during labor. In recent years several case series have reported spontaneous labor initiation in pregnant women with HYPO and ADH deficiency [40, 41], without requiring oxytocin administration for labor initiation or augmentation in some women, suggesting that endogenous pituitary oxytocin may not be mandatory for spontaneous labor initiation or that it was (partially) preserved. Our results differ from previously mentioned data. Four patients had spontaneous initiation of labor but none of them had ADH deficiency. In the 4 patients with ADH deficiency delivery took place either through elective cesarean section or through vaginal delivery that required labor induction as well as oxytocin administration for augmentation, pointing to a likely deficit of endogenous and necessary oxytocin. Overall, the rate of elective delivery was 67%, nearly double that reported for Spain for the period 20101–2018  but close to the 57% in the center for high-risk pregnancies. Reasons were varied but in one third of cases, it was prompted by the endocrinological condition of the mother.
There is a general consensus on the association of HYPO with maternal-fetal complications such as high rate of miscarriage, pregnancy-induced hypertension, placental abruption, premature birth, and postpartum hemorrhage . However, in this study we did not observe major obstetrical or fetal complications.
We observed no miscarriage in the study group. It is certainly possible that this occurred if some pregnancies went unnoticed to the woman or were not reported to the health care provider. But considering that most patients were under follow-up in the department since before pregnancy, we consider this was likely not a common situation.
Weight gain was excessive in 9 women and adequate in 3. In particular, the patient who gained the most weight (#7) during pregnancy (up to 27 kg), was not on hydrocortisone replacement since she did not have adrenal insufficiency. On the other hand, the second patient (#1) who gained more weight during pregnancy (19.3 kg) presented with panhypopituitarism and hydrocortisone doses remained unchanged throughout all pregnancy. Certainly, inadequate hormonal replacement therapy (cortisol, T4, GH) could potentially have an influence on excessive weight gain; however, in our series, hydrocortisone dose was not high and its increment during pregnancy was negligible, so it is unlikely to be related to excessive weight gain. Additionally, stopping GH therapy at pregnancy confirmation might have a role in weight gain as discussed above. To our knowledge, our study reports and evaluates maternal weight during pregnancy in women with HYPO according to Institute of Medicine guidelines for the first time. This data emphasizes the importance of close maternal weight monitoring during pregnancy, as well as more studies addressing this outcome and related variables such as hormone substitution.
Moreover, all but one delivery was at term and birth weight centiles displayed a normal distribution. Our observation is similar to other studies showing normal weight in the majority of the newborns [6, 12, 14] notwithstanding, other studies in hypopituitary women reported up to half of the newborns small for gestational age [17, 18]. In this regard, it is relevant that in their systematic review, Vila et al. mention that most reports did not provide details on birthweight and gestational age . At delivery, no intrapartum fetal distress was observed, and the median arterial/venous cord blood pH were within the normal range. Nearly half of the reported arterial cord pH values were lower than 7.20, which is clearly higher than the published rates  but none was below the 7.10 or 7.00 problematic cut-offs [44, 45]. Regarding hypertensive disorders of pregnancy, it was diagnosed in only two patients.
Our observations are comparable to those of Correa et al. , and Sowithayasul et al.  who both described a 60% rate of cesarean deliveries. Nevertheless, we consider that the rate of cesarean section in this series was high, considering that the rate in the background obstetric population in the corresponding period was 24.8%.
At the time of hospital discharge, half of the patients were breastfeeding. This figure compares with other reports in the literature [14, 46] and even when the rate is far from satisfactory and that we do not have data on breastfeeding at longer term, women can be reassured that breastfeeding can be possible. In fact, in the last years, women have actively asked this question during pregnancy follow-up. We do not have information about breastfeeding being exclusive, predominant or mixed. But even if rates of exclusive breastfeeding were low, benefits are probably present .
The present study has some limitations such as the limited sample size and the descriptive methodology. Further studies with a larger number of patients and whenever possible, randomized trials are needed in order to determine if the actual practical recommendations for pregnant women with HYPO should be modified.
In conclusion, in this case-series of 12 pregnancies of women with HYPO, no relevant maternal-fetal complications were observed apart from a high rate of excessive gestational weight gain and cesarean section. Hormonal dosage adjustment was performed mainly according to clinical judgment without hormonal measurement, except for the thyroid axis. Our findings reinforce the idea that a strict follow up is needed during pregnancy in hypopituitary women in order to diagnose early any eventual new onset hormonal deficit.
The datasets generated during and/or analyzed during the current study will be publicly available.
Regal M, Páramo C, Sierra JM, García-Mayor RV (2001) Prevalence and incidence of hypopituitarism in an adult Caucasian population in northwestern Spain. Clin Endocrinol (Oxf) 55:735–740. https://doi.org/10.1046/j.1365-2265.2001.01406.x
Ehrnborg C, Roijen LH-V, Jonsson B et al (2000) Cost of illness in adult patients with hypopituitarism. PharmacoEconomics 17:621–628. https://doi.org/10.2165/00019053-200017060-00008
Tanriverdi F, Dokmetas HS, Kebapcı N et al (2014) Etiology of hypopituitarism in tertiary care institutions in Turkish population: analysis of 773 patients from Pituitary Study Group database. Endocrine 47:198–205. https://doi.org/10.1007/s12020-013-0127-4
Fleseriu M, Hashim IA, Karavitaki N et al (2016) Hormonal replacement in hypopituitarism in adults: an endocrine society clinical practice guideline. J Clin Endocrinol Metab 101:3888–3921. https://doi.org/10.1210/jc.2016-2118
Ajmal A, McKean E, Sullivan S, Barkan A (2018) Decreased quality of life (QoL) in hypopituitary patients: involvement of glucocorticoid replacement and radiation therapy. Pituitary 21:624–630. https://doi.org/10.1007/s11102-018-0918-y
Vila G, Fleseriu M (2020) Fertility and pregnancy in women with hypopituitarism: a systematic literature review. J Clin Endocrinol Metab 105:e53–e65. https://doi.org/10.1210/clinem/dgz112
Tomlinson JW, Holden N, Hills RK et al (2001) Association between premature mortality and hypopituitarism. West Midlands Prospective Hypopituitary Study Group. Lancet Lond Engl 357:425–431. https://doi.org/10.1016/s0140-6736(00)04006-x
Krassas GE, Poppe K, Glinoer D (2010) Thyroid function and human reproductive health. Endocr Rev 31:702–755. https://doi.org/10.1210/er.2009-0041
Barreca A, Artini PG, Del Monte P et al (1993) In vivo and in vitro effect of growth hormone on estradiol secretion by human granulosa cells. J Clin Endocrinol Metab 77:61–67. https://doi.org/10.1210/jcem.77.1.8325961
Hall R, Manski-Nankervis J, Goni N et al (2006) Fertility outcomes in women with hypopituitarism. Clin Endocrinol (Oxf) 65:71–74. https://doi.org/10.1111/j.1365-2265.2006.02550.x
Vila G, Akerblad AC, Mattsson AF et al (2015) Pregnancy outcomes in women with growth hormone deficiency. Fertil Steril 104:1210. https://doi.org/10.1016/j.fertnstert.2015.07.1132. 1217.e1
Milardi D, Giampietro A, Baldelli R et al (2008) Fertility and hypopituitarism. J Endocrinol Invest 31:71–74
Park JK, Murphy AA, Bordeaux BL et al (2007) Ovulation induction in a poor responder with panhypopituitarism: a case report and review of the literature. Gynecol Endocrinol 23:82–86. https://doi.org/10.1080/09513590601137533
Correa FA, Bianchi PHM, Franca MM et al (2017) Successful pregnancies after adequate hormonal replacement in patients with combined pituitary hormone deficiencies. J Endocr Soc 1:1322–1330. https://doi.org/10.1210/js.2017-00005
Karaca Z, Tanriverdi F, Unluhizarci K, Kelestimur F (2010) Pregnancy and pituitary disorders. Eur J Endocrinol 162:453–475. https://doi.org/10.1530/EJE-09-0923
Lønberg U, Damm P, Andersson A-M et al (2003) Increase in maternal placental growth hormone during pregnancy and disappearance during parturition in normal and growth hormone-deficient pregnancies. Am J Obstet Gynecol 188:247–251. https://doi.org/10.1067/mob.2003.82
Overton CE, Davis CJ, West C et al (2002) High risk pregnancies in hypopituitary women. Hum Reprod 17:1464–1467. https://doi.org/10.1093/humrep/17.6.1464
Kübler K, Klingmüller D, Gembruch U, Merz WM (2009) High-risk pregnancy management in women with hypopituitarism. J Perinatol 29:89–95
Labbok MH, Starling A (2012) Definitions of breastfeeding: call for the development and use of consistent definitions in research and peer-reviewed literature. Breastfeed Med 7:397–402. https://doi.org/10.1089/bfm.2012.9975
Gardosi J, Clausson B, Francis A (2009) The value of customised centiles in assessing perinatal mortality risk associated with parity and maternal size. BJOG Int J Obstet Gynaecol 116:1356–1363. https://doi.org/10.1111/j.1471-0528.2009.02245.x
Sidhoum VF, Chan Y-M, Lippincott MF et al (2014) Reversal and relapse of hypogonadotropic hypogonadism: resilience and fragility of the reproductive neuroendocrine system. J Clin Endocrinol Metab 99:861–870. https://doi.org/10.1210/jc.2013-2809
Institute of Medicine (US) and National Research Council (US) Committee to Reexamine IOM Pregnancy Weight Guidelines (2009) Weight gain during pregnancy: reexamining the guidelines. National Academies Press (US), Washington (DC)
Jørgensen JO, Møller J, Laursen T et al (1994) Growth hormone administration stimulates energy expenditure and extrathyroidal conversion of thyroxine to triiodothyronine in a dose-dependent manner and suppresses circadian thyrotrophin levels: studies in GH-deficient adults. Clin Endocrinol (Oxf) 41:609–614. https://doi.org/10.1111/j.1365-2265.1994.tb01826.x
Gelding SV, Taylor NF, Wood PJ et al (1998) The effect of growth hormone replacement therapy on cortisol-cortisone interconversion in hypopituitary adults: evidence for growth hormone modulation of extrarenal 11 beta-hydroxysteroid dehydrogenase activity. Clin Endocrinol (Oxf) 48:153–162. https://doi.org/10.1046/j.1365-2265.1998.3641180.x
Chellakooty M, Skibsted L, Skouby SO et al (2002) Longitudinal study of serum placental GH in 455 normal pregnancies: correlation to gestational age, fetal gender, and weight. J Clin Endocrinol Metab 87:2734–2739. https://doi.org/10.1210/jcem.87.6.8544
Chein E, Vogt DG, Terry C (2011) Clinical experiences using a low-dose, high-frequency human growth hormone treatment regimen. https://www.semanticscholar.org/paper/Clinical-Experiences-Using-a-Low-Dose-%2 C-Human-Chein-Vogt/a0209f2b6166ad08ef4bd8ee6721433ae9c52c6e. Accessed 4 Nov 2021
Hoffman AR, Kuntze JE, Baptista J et al (2004) Growth hormone (GH) replacement therapy in adult-onset gh deficiency: effects on body composition in men and women in a double-blind, randomized, placebo-controlled trial. J Clin Endocrinol Metab 89:2048–2056. https://doi.org/10.1210/jc.2003-030346
de Zegher F, Vanderschueren-Lodeweyckx M, Spitz B et al (1990) Perinatal growth hormone (GH) physiology: effect of GH-releasing factor on maternal and fetal secretion of pituitary and placental GH. J Clin Endocrinol Metab 71:520–522. https://doi.org/10.1210/jcem-71-2-520
Alexander EK, Pearce EN, Brent GA et al (2017) 2017 guidelines of the American thyroid association for the diagnosis and management of thyroid disease during pregnancy and the postpartum. Thyroid 27:315–389. https://doi.org/10.1089/thy.2016.0457
Caixàs A, Albareda M, García-Patterson A et al (1999) Postpartum thyroiditis in women with hypothyroidism antedating pregnancy? J Clin Endocrinol Metab 84:4000–4005. https://doi.org/10.1210/jcem.84.11.6144
Behan LA, Monson JP, Agha A (2011) The interaction between growth hormone and the thyroid axis in hypopituitary patients. Clin Endocrinol (Oxf) 74:281–288. https://doi.org/10.1111/j.1365-2265.2010.03815.x
Langlois F, Lim DST, Fleseriu M (2017) Update on adrenal insufficiency: diagnosis and management in pregnancy. Curr Opin Endocrinol Diabetes Obes 24:184–192. https://doi.org/10.1097/MED.0000000000000331
Benediktsson R, Calder AA, Edwards CR, Seckl JR (1997) Placental 11 beta-hydroxysteroid dehydrogenase: a key regulator of fetal glucocorticoid exposure. Clin Endocrinol (Oxf) 46:161–166. https://doi.org/10.1046/j.1365-2265.1997.1230939.x
Kamoun M, Mnif MF, Charfi N et al (2014) Adrenal diseases during pregnancy: pathophysiology, diagnosis and management strategies. Am J Med Sci 347:64–73. https://doi.org/10.1097/MAJ.0b013e31828aaeee
Björnsdottir S, Cnattingius S, Brandt L et al (2010) Addison’s disease in women is a risk factor for an adverse pregnancy outcome. J Clin Endocrinol Metab 95:5249–5257. https://doi.org/10.1210/jc.2010-0108
Bothou C, Anand G, Li D et al (2020) Current management and outcome of pregnancies in women with adrenal insufficiency: experience from a multicenter survey. J Clin Endocrinol Metab 105:e2853–e2863. https://doi.org/10.1210/clinem/dgaa266
Scheer RL, Raisz LG, Lloyd CW (1959) Changes in diabetes insipidus during pregnancy and lactation. J Clin Endocrinol Metab 19:805–811. https://doi.org/10.1210/jcem-19-7-805
Ananthakrishnan S (2016) Diabetes insipidus during pregnancy. Best Pract Res Clin Endocrinol Metab 30:305–315. https://doi.org/10.1016/j.beem.2016.02.005
Hime MC, Richardson JA (1978) Diabetes insipidus and pregnancy. Case report, incidence and review of literature. Obstet Gynecol Surv 33:375–379. https://doi.org/10.1097/00006254-197806000-00001
Shinar S, Many A, Maslovitz S (2016) Questioning the role of pituitary oxytocin in parturition: spontaneous onset of labor in women with panhypopituitarism—a case series. Eur J Obstet Gynecol Reprod Biol 197:83–85. https://doi.org/10.1016/j.ejogrb.2015.11.028
Volz J, Heinrich U, Volz-Köster S (2002) Conception and spontaneous delivery after total hypophysectomy. Fertil Steril 77:624–625. https://doi.org/10.1016/S0015-0282(01)03198-3
Ministerio de Sanidad (2021) Atención perinatal en España. Análisis de los recursos físicos, humanos, actividad y calidad de los servicios hospitalarios, 2010–2018. Available at: https://www.mscbs.gob.es/estadEstudios/estadisticas/docs/Informe_Atencion_Perinatal_2010-2018.pdf
Lee JH, Jung J, Park H et al (2020) Umbilical cord arterial blood gas analysis in term singleton pregnancies: a retrospective analysis over 11 years. Obstet Gynecol Sci 63:293–304. https://doi.org/10.5468/ogs.2020.63.3.293
Malin GL, Morris RK, Khan KS (2010) Strength of association between umbilical cord pH and perinatal and long term outcomes: systematic review and meta-analysis. BMJ 340:c1471. https://doi.org/10.1136/bmj.c1471
Yeh P, Emary K, Impey L (2012) The relationship between umbilical cord arterial pH and serious adverse neonatal outcome: analysis of 51519 consecutive validated samples. BJOG 119:824–831
Sowithayasakul P, Boekhoff S, Bison B, Müller HL (2021) Pregnancies after childhood craniopharyngioma: results of KRANIOPHARYNGEOM 2000/2007 and review of the literature. Neuroendocrinology 111:16–26. https://doi.org/10.1159/000506639
Victora CG, Bahl R, Barros AJD et al (2016) Breastfeeding in the 21st century: epidemiology, mechanisms, and lifelong effect. Lancet Lond Engl 387:475–490. https://doi.org/10.1016/S0140-6736(15)01024-7
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RC has received fees from Merck as a consultant and to write patient information. All the other authors have no conflicts of interest to declare that are relevant to the content of this article.
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Aulinas, A., Stantonyonge, N., García-Patterson, A. et al. Hypopituitarism and pregnancy: clinical characteristics, management and pregnancy outcome. Pituitary (2021). https://doi.org/10.1007/s11102-021-01196-7
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