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Review

Hormone Replacement Therapy: Would it be Possible to Replicate a Functional Ovary?

by
Swati Agarwal
1,2,*,
Faisal A Alzahrani
3,4 and
Asif Ahmed
1,4
1
Aston Medical Research Institute, Aston Medical School, Aston University, Birmingham B4 7ET, UK
2
Department of Obstetrics and Gynecology, University of Toronto, Toronto, ON M5S 3H7, Canada
3
Department of Biochemistry, Faculty of Science, King Abdulaziz University, Jeddah 21589, Saudi Arabia, [email protected]
4
Embryonic Stem Cell Unit, King Fahad Center for Medical Research, King Abdulaziz University, Jeddah 21589, Saudi Arabia
*
Author to whom correspondence should be addressed.
Int. J. Mol. Sci. 2018, 19(10), 3160; https://doi.org/10.3390/ijms19103160
Submission received: 7 August 2018 / Revised: 2 October 2018 / Accepted: 3 October 2018 / Published: 14 October 2018
(This article belongs to the Section Molecular Pathology, Diagnostics, and Therapeutics)
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Versions Notes

Abstract

:
Background: Throughout history, menopause has been regarded as a transition in a woman’s life. With the increase in life expectancy, women now spend more than a third of their lives in menopause. During these years, women may experience intolerable symptoms both physically and mentally, leading them to seek clinical advice. It is imperative for healthcare providers to improve the quality of life by reducing bothersome menopausal symptoms and preventing disorders such as osteoporosis and atherosclerosis. The current treatment in the form of hormone replacement therapy (HRT) is sometimes inadequate with several limitations and adverse effects. Objective and rationale: The current review aims to discuss the need, efficacy, and limitations of current HRT; the role of other ovarian hormones, and where we stand in comparison with ovary-in situ; and finally, explore towards the preparation of an HRT model by regeneration of ovaries tissues through stem cells which can replicate a functional ovary. Search methods: Four electronic databases (MEDLINE, Embase, Web of Science and CINAHL) were searched from database inception until 26 April 2018, using a combination of relevant controlled vocabulary terms and free-text terms related to ‘menopause’, ‘hormone replacement therapy’, ‘ovary regeneration’, ‘stem cells’ and ‘ovarian transplantation’. Outcomes: We present a synthesis of the existing data on the efficacy and limitations of HRT. HRT is far from adequate in postmenopausal women with symptoms of hormone deprivation as it fails to deliver all hormones secreted by naïve ovarian tissue. Moreover, the pharmacokinetics of synthetic hormones makes them substantially different from natural ones. Not only does the number and type of hormones given in HRT matter, but the route of delivering and their release in circulation are also imperative. The hormones are delivered either orally or topically in a non-physiological uniform manner, which brings along with it several side effects. These identify the need for a hormone delivery system which replicates, integrates and reacts as per the requirement of the female body. Wider implications: The review outlines the strengths and weaknesses of HRT and highlights the potential areas for future research. There is a tremendous potential for research in this field to understand the collective roles of the various ovarian hormones and to devise an auto-regulated hormone delivery system which replicates the normal physiology. Its clinical applications can prove to be transformative for postmenopausal women helping them to lead a healthy and productive life.

1. Background

Throughout history, menopause has been regarded as a major transition in a woman’s life. With the increase in life expectancy, women now spend more than a third of their life in menopause. During these years, women experience intolerable symptoms and seek clinical advice. It is imperative for healthcare providers to improve the quality of lives by reducing bothersome menopausal symptoms and preventing disorders such as osteoporosis, atherosclerosis and coronary heart disease, dyslipidemia, and so on. However, a question that is yet to be determined is: “Is the age of natural menopause a marker of health and aging?” The onset of menopause has been considered as an ideal time to introduce preventative strategies to improve the longevity and quality of postmenopausal women’s lives. The current hormone replacement therapy (HRT), which is primarily based on estrogen and progesterone, has been prescribed over decades for the treatment of postmenopausal symptoms, and has been questioned time and again owing to its side effects and efficacy in substituting for a functional ovary. Recent developments in estrogen and progesterone-based drugs and mode of deliveries have extended the benefits of HRT; however, it is yet to be equivalent to functional ovaries of premenopausal women. Along with releasing eggs, ovaries secrete several hormones, including oestrogen, progesterone, testosterone, activin, inhibin, anti-Müllerian hormone (AMH) and insulin-like growth factor 1 (IGF-1), which have an immense significance on a woman’s physiology [1]. The secretion and functioning of these hormones are complexly integrated and intricately regulated by many positive and negative feedback loops (Figure 1). Hence, the ovary must not be regarded as a static endocrine organ, which expands at puberty and contracts with menopause, rather, it is a dynamic organ whose periodicity is measured in weeks. It has immensely beneficial effects on women’s health and is considered to be the prime attribute for lower morbidity and mortality, as evidenced in premenopausal women compared to men of the same age group. Later age at natural menopause has been found to be associated with plenty of benefits, including longevity and reduced all-cause mortality [2,3,4]. There is a decreased prevalence of atherosclerosis and cardiovascular events in women with late age at natural menopause [5,6,7,8,9]. Moreover, there are some additional benefits, such as a substantial increase in the bone density and consequently a reduction in the incidence of osteoporosis and fractures [10,11]. Nevertheless, it comes at a cost of increased risk of breast [12], ovarian [3,13] and endometrial [14] cancers. However, unlike a functional ovary, the exogenous hormones, oestrogen and progesterone, prescribed during the postmenopausal period in a stereotyped manner to replete the functioning of in situ ovary bring along several side effects.
The present review intends to discuss the need, efficacy, and limitations of current oestrogen- and progesterone-based HRT; where we stand in comparison with a functioning ovary in situ; and finally, to explore towards the preparation of an ideal HRT model which can truly replicate a functional ovary. We have evaluated the published literature on the benefits and risks associated with HRT, and the importance of other hormones secreted by the functioning premenopausal ovary which are not currently included in the HRT. We have further explored the emerging opportunities for the development of a flawless HRT model, which could help post-menopausal women to battle through this period, and which could be achieved by understanding the role, mode and regulation of all hormones secreted by functioning ovaries, improving the present oestrogen- and progesterone-based drugs and their delivery system.

2. Health Concerns with Menopause/Need for HRT

The health problems of women undergoing menopause are varied, ranging from mild mood issues to severe problems such as myocardial infarction, and are amenable to treatment to varying degrees by HRT. They are discussed in detail in the following paragraphs (Figure 2).

2.1. Coronary Artery Disease

Heart disease is the leading cause of death for women in the developed world [15]. Before the age of 40 years, women have a lower incidence of coronary heart disease (CHD) and myocardial infarction than men (WHO 2009). The lower incidence in premenopausal women is attributed to the favourable effect of oestrogen on the lining of the blood vessels, the endothelium [16,17]. However, following menopause, the benefit slowly fades, and women are at a similar risk of dying from cardiovascular diseases as men. Similarly, women with premature ovarian failure are at an increased risk of CHD [18]. The increased risk with HRT was unveiled by Women’s Health Initiative (WHI) and the Heart and Estrogen-progestin Replacement Study (HERS) I and HERS II studies [19,20,21]. In 2013, WHI investigators reported age as a major attribute in the benefit-risk balance following hormone use [22]. Presently, many observational studies suggest that if HRT is started immediately following menopause, it has more beneficial effects on the cardiovascular health and leads to decreased mortality. In contrast, the mortality due to heart diseases is increased if HRT is started more than 10 years after menopause or after the age of 60 years [23,24,25]. Thus, this ‘therapeutic window’ for starting HRT gives a limitation to the use of HRT in the prevention of cardiac disease [26]. The prothrombotic effects of oestrogen include a decrease in the levels of serum fibrinogen, factor VII, and antithrombin III. These effects are less pronounced in case of transdermal oestrogen but the evidence that transdermal oestrogen is safer for secondary prevention of CHD is lacking [27,28]. In addition, the choice and regimen of progesterone is important as there is some evidence that some progesterone like medroxy progesterone acetate (MPA) (used in WHI and HERS) might attenuate the cardiac benefit caused by oestrogen while norethindrone acetate or natural progesterone are not found to lessen the benefit of oestrogen. Studies have shown that combined oestrogen-progesterone therapy does not affect the incidence of peripheral arterial events [29].

2.2. Metabolic Effects

The remarkable effects of oestrogen on women’s metabolism, and its elusive physiological shield against metabolic syndrome in women of reproductive age making oestrogen the most likely candidate for the HRT. The deficiency of oestrogen postmenopausally causes the development of metabolic syndrome (41.5%) and hypertriglyceridemia (56.9%) in almost half of menopausal women [30,31,32]. Women with metabolic syndrome have six times increased risk of developing CHD and the underlying pathophysiology could be related to insulin resistance or central obesity [33]. HRT, instead of restoring the imbalance, further worsens some of the metabolic effects like hypertriglyceridemia, while decreasing low-density lipoprotein and increasing high-density lipoprotein levels [34]. It is notable that HRT appears to decrease the risk of diabetes mellitus type 2; however, the impact is insufficient for HRT to be recommended for its prevention [35,36].

2.3. Osteoporosis

Osteoporosis is widely recognised as one of the most common bone problems in elderly females. It is a generalised skeletal disorder ascribed to decreased bone mass with increased susceptibility to fractures. Seventy-five percent or more of bone mass loss has been attributed to the declining oestrogen levels during the postmenopausal period, rather than aging [37]. Oestrogen exerts a constant suppressive action on the remodelling of bone and with reduced oestrogen levels in menopause. The bone resorption is enhanced by oestrogen. The risk of sustaining a fracture in a postmenopausal woman is almost twice the lifetime probability of developing breast cancer for a woman [38,39,40].
Although HRT is not the first line treatment in postmenopausal women for the prevention or treatment of osteoporosis, WHI study revealed a significant reduction in fractures in women on HRT compared to women on placebo [41]. While, HRT is effective in osteoporosis, it is not uniformly recommended by all the major societies for its prevention [42,43,44,45].

2.4. Vasomotor Symptoms (VMS)

Commonly known as hot flushes or night sweats (VMS) are experienced by about 60–80% of postmenopausal women during the perimenopausal phase [46,47,48]. Most importantly, VMS severely affect women’s sense of wellbeing and quality of life [49,50]. According to a Cochrane review, there was a significant reduction in the frequency and severity of hot flushes with HRT as compared to placebo [51,52]. HRT is recommended for women with moderate to severe symptoms and no contraindications for short-term symptom relief. It can be speculated that the other ovarian hormones also play a potential role in triggering these symptoms.

2.5. Vulvovaginal Atrophy (VVA)

Oestrogen deficiency results in atrophy of the vaginal mucosa, causing vaginal dryness, dyspareunia (painful intercourse), itching, vaginal stenosis and urinary incontinence. Similar to VMS, VVA is highly prevalent among postmenopausal women, with prevalence ranging from 4% in early menopause to 47% by three years after the last menses [53]. Low-dose vaginal oestrogen preparations are shown to be highly efficacious in treating VMS [54]. The American College of Obstetricians and Gynaecologists and North American Menopause Society recommend the indefinite use of low-dose vaginal therapy for as long as needed; however, there is limited evidence regarding the safety of vaginal preparations beyond one year of use [55,56]. Similarly, another study was recently published reassuring the long-term safety of vaginal oestrogen [57].
The incidence of urinary tract infections and the symptoms of overactive bladder are found to decrease with topical oestrogen therapy [54,58]. Urinary incontinence affects 26–40% of women beyond the age of 55 years [59]. It is hypothesised that oestrogen plays a vital role in the continence mechanism; however, randomised control trials (RCTs) have failed to demonstrate improvement in urinary incontinence in post-menopausal females following treatment with oestrogen [60,61,62]. In contrast, HERS reported an increase in incontinence with HRT [63]. The worsening of symptoms with exogenous administration of oestrogen is an enigma as biological oestrogen secreted by the ovary is protective, as evidenced by a lower incidence in younger women [59].

2.6. Cognition and Dementia

Studies have reported that dementia occurs less frequently in oestrogen users and the preventive effect is greater with increasing dose and duration of use [64,65,66]. Oestradiol replacement in rats found that it increases the activity of choline acetyltransferase in various parts of the brain related to memory and cognition [67]. Others have advocated a critical window period for starting HRT [68,69,70] for dementia. No such difference was found in studies where HRT was given to older postmenopausal females (>65 years) [71,72]. On the other hand, an increased risk of dementia was found when oestrogen was given in combination with progesterone (HRT) [73]. A Cochrane review in 2008 has refuted any benefits of HRT on cognition [74]. Another review reflected both possible beneficial and detrimental impact of oestrogen on memory in the aging brain [75]. There appears to be no conclusive study to give a definitive answer to this critical concern.

2.7. Sleep Disturbances

The quality of sleep deteriorates with aging [76], and menopause further contributes to it [77,78]. The Study of Women’s Health Across the Nation (SWAN) in the United States of America reported sleep disturbances in 36.6% of late perimenopausal or postmenopausal women [79]. The role of HRT is quite limited in treating sleep disorders associated with menopause.

2.8. Overall Effects of HRT

The ovary has an immense benefit for women’s health and is the primary organ responsible for lowering morbidity and mortality in premenopausal women compared to men of the same age group. However, the advantages gained through functioning ovaries, decline with menopause and HRT does not appear to reap the expected benefits. Moreover, HRT, when prescribed for a long duration, is associated with many side effects, some being life-threatening. Therefore, the benefits must be weighed against the risks before prescribing HRT. Though it should be noted that long-term exposure to endogenous hormones is also associated with increased risks. Further research is required not only to validate these findings but also develop a novel hormone replacement model which can replicate the natural functioning of ovary without causing the adverse effects.

3. Current Preparations of HRT in Clinical Practice

Current HRT mainly consists of oestrogen and progesterone in various preparations differing in their dosages and routes of administration, each having its benefits and risks (Table 1). However, with HRT, the menopausal symptoms can only be partially relieved, as present therapy fails to replicate the natural functioning of an ovary. The relative alleviation of menopausal symptoms is primarily due to oestrogen. The oestrogen only therapy is prescribed for a hysterectomised woman, but in a woman with an intact uterus, progestin is added to combat the increased risk of endometrial hyperplasia and even carcinoma.
Natural oestrogens are available in various plant sources like soy, but their efficacy is unclear. The modified oestrogens are called semisynthetic and include conjugated oestrogens (conjugated equine oestrogen, oestradiol valerate and oestrone sulphate) and micronized oestradiol. Conjugated equine oestrogen is prepared from the urine of pregnant mares and is composed of 50–60% oestrone sulphate along with other equine oestrogens like equilin and 17-dihydroequilin. Micronisation of oestradiol results in higher blood levels of oestrogen, but it is rapidly metabolised to less active forms like oestrone. Synthetic oestrogens such as ethinyl oestradiol have better potency and extended half-life.
Based on present evidence, physicians have unsuccessfully tried to tailor the HRT prescription as per the symptoms of menopausal women. Women are informed that their prescription for HRT has been individualised with the type and dosage of preparation being determined according to their specific requirements. However, in reality, there are no means of establishing the amount of hormones needed by a woman’s body to combat her postmenopausal symptoms. This is because the ovarian physiology is dynamic and the blood levels of hormones could be misleading since every woman develops symptoms at different hormone levels with varying severity.

Bio-Identical HRT (BHRT)

Over the last two decades, many people are attracted by the idea of bio-identical hormones (BHRT). Bio-identical hormones are derived from plant extracts and chemically modified in the laboratory so as to be identical in molecular structure to natural female hormones [80]. There have been attempts to promote BHRT stating that these hormones are natural and, therefore, superior to synthetic HRT. Nevertheless, studies have failed to prove BHRT to be superior to conventional HRT [81,82,83].

4. Adverse Effects of HRT

It has been established that HRT is far from adequate in treating women with menopausal symptoms [52,84,85,86]. Moreover, it is associated with many unwanted and serious adverse effects, which are discussed subsequently. It is, however, important to note that these risks are also associated with delayed menopause.

4.1. Venous Thromboembolism (VTE) and Stroke

Venous thromboembolism is characterised by the formation of thrombus in deep veins of legs, which can embolise to the pulmonary circulation and even cause death. HRT increases the risk of VTE by 2-fold, mostly in the first and second years of treatment [87]. Studies have shown that transdermal oestrogen is associated with a lower risk while progesterone only HRT is not associated with an increased risk of VTE [88,89]. There is a wealth of literature showing the increased incidence of stroke in women on either oestrogen only or oestrogen-progestin HRT [90,91,92]. The current users of transdermal or oral HRT have a higher risk of stroke than non-users [93]. Hence, caution must be exercised in prescribing HRT to women with risk factors for stroke or VTE. The contention remains: why does oestrogen in HRT increase the risk of VTE while the presence of a functioning ovary does not?

4.2. Gynaecological Cancers

There is an increased risk of breast cancer in users of present HRT [94]. Recent studies have reported a hazard ratio of 1.24 to 2.74 in current users after 2 to 5 years of HRT use, which increases further with increasing duration of use [95,96].
A woman’s risk of having ovarian cancer during her lifetime is 1–1.5% and dying from the same disease is almost 0.5% [97]. A recent meta-analysis has revealed a relative risk of 1.43 in hormone users compared to non-users [98]. They reported increased risk, even with a limited period of use (less than five years), and the risk, although it declines, persists even ten years after discontinuing HRT. Women on unopposed oestrogen only therapy have a non-significant decrease in the incidence of breast cancer with a definite increased risk of endometrial cancer [22].
Endometrial carcinoma is the most common malignancy of the female genital tract, with 2–3% of women developing the cancer in their lifetime [99]. The risk increases manifold by taking unopposed oestrogen therapy; however, the threat of the cancer is almost entirely eliminated by the addition of progestins in a continuous fashion [100,101,102].

5. Caveats with HRT

There are many relative contraindications to HRT, although no absolute contraindications exist [103]. On the contrary, the presence of a normal functioning ovary in a woman causes less harm (if any) while offering plenty of benefits. There are hardly any indications for removing it. The contraindications of HRT are outlined in Figure 3.

6. The Role of Other Hormones Secreted by the Ovary

A functional ovary secretes several hormones, which play an essential role in the maintenance of women’s health and well-being; however, they are not a part of the current HRT regimens. The advancements in science and technology have helped us in identifying and isolating many of them. The ovarian hormones can be divided into two broad categories on the basis of their chemical structure. The first group is formed by the steroid hormones, which include oestrogens, androgens and progestins. The next group is the peptide hormones, which includes AMH, inhibin, activin, follistatin, IGF, relaxin, transforming growth factor-β (TGF-β), fibroblast growth factor (FGF), epidermal growth factor (EGF) and the oocyte-derived proteins GDF-9 and BMP-15. The levels of activin increase after menopause, follistatin concentrations remains the same [104,105] and the levels of all other hormones decrease. Most of them are released into the circulation and can be detected systemically. Factors such as IGF, GDF-9 and BMP-15 are released locally and act to promote follicular growth [1].

6.1. Androgens

In premenopausal women, levels of free testosterone are found to correlate directly with libido [106]. After menopause, though the androgen production continues, its levels are much lower than the women of the reproductive age group. Supplementation of androgen has been found to increase not only the sexual desire but also improve the psychological well-being [107,108]. Along with that, androgen boosts have helped postmenopausal females to increase bone density more than oestrogen alone. However, the benefits of adding androgens must be weighed against their undesirable effects like hirsutism and hypercholesterolemia [109,110].

6.2. Anti-Müllerian Hormone

Anti-Müllerian hormone (AMH also called Müllerian inhibiting substance (MIS)) is secreted in the ovary by the granulosa cells of preantral and small antral follicles [111]. It regulates the follicular development in an autocrine and paracrine manner. Several studies on AMH have found that it inhibits the proliferation of all gynaecological cancers expressing MIS receptor such as cervical, endometrial, ovarian and breast cancers [112,113,114,115]. MIS inhibits the cancer cells by interfering with cell cycle progression and inducing apoptosis in them. The lack of AMH after menopause could be one of the contributors to the increased incidence of gynaecological carcinomas postmenopausally and its supplementation could have a preventable role in their development. It could also be contemplated that AMH may play a possible role in treating gynaecological conditions like endometriosis and adenomyosis. Pepin et al., have recently used adeno-associated virus (AAV9) to deliver MIS in mice which significantly inhibited the growth of ovarian cancer cells [116]. Papakostas et al., developed a novel and efficient way of producing highly pure and biologically active internally labelled form of MIS [117]. This provides a ray of hope that incorporating AMH in HRT in the near future could make it better and closer to a functional ovary.

6.3. Inhibin

Inhibin is secreted by the granulosa cells of small antral follicles during the follicular phase and helps in folliculogenesis [111]. It has been found that inhibin knockout mice have a higher susceptibility to developing tumours of gonads and adrenals. This suggests a potential tumour suppressive effect of inhibin in the body [118,119]. Recombinant human inhibin has long been synthesised [120] and its addition to HRT may prove beneficial. There have been no studies done thus far; however, there is a potential for research on the topic.

6.4. Insulin-Like Growth Factor

IGFs are single-chain polypeptides, which resemble insulin in structure and function and are secreted by granulosa cells in response to follicular stimulating hormone (FSH). In humans, IGF-II is more active in the embryonic period while IGF-I postnatally [1]. The ovary produces high amounts of IGF-I, next only to the liver. IGF along with TGF-β is required for maintaining healthy bone mass. Recombinant human IGF-I has been synthesised in the laboratory, and there are promising studies regarding its use in cardiovascular diseases [121] and diabetes mellitus [122]. It would also be worthwhile conducting further studies to explore the potential effects of supplementing IGF in the postmenopausal state.

6.5. Relaxin

Relaxin is a pleiotropic hormone secreted by ovary with a role in a multitude of physiological processes besides reproduction and pregnancy. It has positive effects on almost every organ system of the body, including the brain, heart and kidney. It has a central vasopressor effect and anti-ischemic effect on brain and myocardium [123,124]. It has a relaxant effect on the vasculature mediated by nitric oxide secreted from the endothelial cells [125,126,127]. Moreover, it induces angiogenesis and inhibits the activation of inflammatory cells thus playing a key role in the prevention of CHD [128]. It is found to impede myocardial damage induced by ischaemia and reperfusion [129,130,131]. It inhibits platelet aggregation [132] and neutrophil activation [133,134]. The loss of protection against CHD in postmenopausal women is partly attributed to the loss of relaxin. Relaxin is anti-asthmatic [135,136] and promotes ciliary beating in the respiratory pathways [137]. Recombinant human relaxin (Serelaxin) has been successfully tried in patients with acute heart failure, and resulted in reduced mortality, symptom relief and improvement in clinical outcomes [138,139].

7. Limitations of Current HRT

Hormone replacement therapy is undoubtedly beneficial in postmenopausal women with symptoms of hormone deprivation, but it has its own limitations. Although the ovary secretes a multitude of hormones, only two of them, oestrogen and progesterone, are replaced by HRT. Also, the pharmacokinetics of the synthetic hormones makes them substantially different from the natural ones. Not only does the number and type of hormones given in HRT matter, but the route of delivering these hormones so as to resemble physiologically is also imperative. The oral preparations of oestrogen and progestin have a significant first-pass metabolism, which decreases the bioavailability of the hormones. Once oestrogen is metabolised in the liver, it gets converted to oestrone sulphate (a weak oestrogen), and subsequently, only 10% of it reaches the circulation [140]. Orally administered oestrogen also increases sex hormone binding globulin (SHBG) levels [141,142], which further reduces the bioavailability, not only of the exogenous hormone but also of the residual endogenous one. Although HRT could, to some extent, compensate for the loss of ovarian hormone production, the delivery of constant amount via pharmacological means leads to substantially higher concentrations of the hormones, causing various side effects. In the body, the levels of different hormones secreted by the ovary vary not only with the phase but also within each day of the menstrual cycle, regulated by various feedback mechanisms.

8. Emerging Opportunities

8.1. Cell-Based Hormone Delivery

An approach to providing all the ovarian hormones physiologically without causing any side effects would be cell-based hormone delivery. This concept of designing an artificial ovary involves dissecting all the cells in the ovary and subsequently amalgamating them. This would unveil the contribution of each component of the ovary and may prove clinically useful in devising an optimal HRT. Though several types of research have been undertaken, the complex, cyclical and dynamic functioning of the ovary makes the formation of an artificial ovary a tough task. In a study, theca and granulosa cells, after being isolated, were seeded into micro-moulded gels and self-assembled into complex 3D microtissue [143]. The oocytes thus created from this construct of artificial ovary were functional and could be used to replace the lost ovarian function in postmenopausal women, as they can secrete hormones in response to gonadotropins.
Sittadjody et al., devised an in vitro tissue-based technique of hormone delivery that used a functional construct manufactured utilising encapsulation technology [144]. They consolidated theca and granulosa cells isolated from rat ovaries to form the native follicular structure using multi-layered alginate microcapsules. The encapsulated cells were viable and secreted adequate levels of oestradiol, progesterone, activin and inhibin in response to FSH and luteinising hormone (LH). This suggested that the multilayer microcapsules could function as a potential tissue-engineered endocrine ovary by synchronizing with the innate hypothalamic-pituitary-ovarian (HPO) axis. The same authors also suggested that the addition of a layer of poly l-ornithine around the theca cells will protect the construct from the host immune system and enable its in vivo use as a graft in postmenopausal women. The cell encapsulation technique may prove to be efficient in delivering the cultured cells into the body. This opens a whole new platform for further research in administering HRT. A similar experiment done in ovariectomized mice using granulosa cells grown on microcarriers, enclosed with theca cells in alginate-chitosan-alginate microcapsules have shown normal levels of serum estradiol and progesterone [145]. Another group has successfully used allografted microencapsulated ovarian cells in vivo to prevent the risk of osteoporosis after ovariectomy in mice [146]. The tissue engineering approaches might prove promising to provide endogenous female hormones in symptomatic post-menopausal females.

8.2. Brain-Selective Oestrogen Therapy

Recently, Merchenthaler et al. discovered that oral administration of a human oestrogen precursor—10β,17β-dihydroxyestra-1,4-dien-3-one (DHED) alleviates hot flushes and restores the oestrogen deprivation-induced loss of diurnal rhythm in rat models of thermoregulatory dysfunction of the brain [147,148]. Oestrogen is selectively generated in the brain, independent of the route of administration, and thus avoids the detrimental effects of the hormone exposure in the rest of the body, including the uterus, and circumventing the need for progesterone supplementation. However, further studies are required in the field before it can be clinically applied.

8.3. Ovarian Tissue Transplantation

Furthermore, studies conducted using mice models have shown that transplantation of young ovaries to old mice increases their lifespan [149,150]. The same authors also found that mice that had ceased cycling before ovarian transplantation showed an increase in lifespan compared with mice still cycling at transplantation. Shikanov et al., transplanted ovarian cortical tissue in mice. The cortical tissue was vitrified, thawed and then encapsulated in fibrin-alginate hydrogels. It was loaded with vascular endothelial growth factor (VEGF) and then placed the tissue in the bursal sac [151,152]. The biomaterial supported cell infiltration and thus promoted the integration of the graft with the host. VEGF enhanced angiogenesis with vessel growth primarily from the bursa and thus, they obtained a high degree of graft revascularisation. Few studies have also been conducted in humans, transplanting young healthy ovaries using cortical grafting technique from premenopausal monozygotic twins discordant for premature ovarian failure and successful fertility outcomes were reported [153]. There was a case reported in which a woman with Hodgkin’s lymphoma was auto-transplanted her own ovary heterotopically subcutaneously in the abdomen after receiving hematologic stem cell transplantation. She successfully regained her fertility and had three babies [154]. The technique can be used in a postmenopausal woman by removing and cryopreserving one of her ovaries after she completes the childbearing process and then auto-transplanting the ovarian tissue at menopause. It is too early to say whether the benefits of such techniques outweigh the risks. This area needs to be studied further and could prove to be a breakthrough in the treatment of postmenopausal women.

9. Conclusion

The review outlines the strengths and weaknesses of HRT and highlights the potential areas for future research. The inadequate symptom relief and side effects associated with current HRT continues to set new riddles and opens a whole era to explore options to reformulate the current HRT. An ideal HRT should supplement all the hormones secreted by a functional ovary in a physiological manner without any side effects. There is tremendous potential for research in this field to understand the collective roles of the various ovarian hormones and to devise an auto-regulated hormone delivery system which replicates the normal physiology. Its clinical applications can prove to be transformative for postmenopausal women helping them to lead a healthy and productive life.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Schematic representation of the level of various ovarian hormones in reproductive age, post-menopausal and in women on HRT.
Figure 1. Schematic representation of the level of various ovarian hormones in reproductive age, post-menopausal and in women on HRT.
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Figure 2. Schematic figure depicting various symptoms of menopause.
Figure 2. Schematic figure depicting various symptoms of menopause.
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Figure 3. Relative contraindications to HRT.
Figure 3. Relative contraindications to HRT.
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Table
Table 1. Different preparations of oestrogen and progesterone.
Table 1. Different preparations of oestrogen and progesterone.
HormonePreparation
Oral OestrogenConjugated oestrogen
Ethinyloestradiol
Esterified oestrogens
17β-oestradiol
Transdermal Oestrogen17β-oestradiol patch
17β-oestradiol gel
17β-oestradiol emulsion
17β-oestradiol spray
Vaginal Oestrogen17β-oestradiol cream
Conjugated oestrogen cream
17β-oestradiol ring
17β-oestradiol tablet
Oral ProgestogenMedroxyprogesterone acetate
Norethindrone acetate
Megestrol acetate
Drosperinone
Micronised progesterone
Transdermal ProgestogenNorethindrone acetate
Levonorgoestrel
Progestin: Intrauterine SystemLevonorgoestrel IUS

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Agarwal, S.; Alzahrani, F.A.; Ahmed, A. Hormone Replacement Therapy: Would it be Possible to Replicate a Functional Ovary? Int. J. Mol. Sci. 2018, 19, 3160. https://doi.org/10.3390/ijms19103160

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Agarwal S, Alzahrani FA, Ahmed A. Hormone Replacement Therapy: Would it be Possible to Replicate a Functional Ovary? International Journal of Molecular Sciences. 2018; 19(10):3160. https://doi.org/10.3390/ijms19103160

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Agarwal, Swati, Faisal A Alzahrani, and Asif Ahmed. 2018. "Hormone Replacement Therapy: Would it be Possible to Replicate a Functional Ovary?" International Journal of Molecular Sciences 19, no. 10: 3160. https://doi.org/10.3390/ijms19103160

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