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08.07.2020 | Review | Ausgabe 12/2020 Open Access

Osteoporosis International 12/2020

Is there a role for menopausal hormone therapy in the management of postmenopausal osteoporosis?

Zeitschrift:
Osteoporosis International > Ausgabe 12/2020
Autoren:
S. Rozenberg, N. Al-Daghri, M. Aubertin-Leheudre, M.-L. Brandi, A. Cano, P. Collins, C. Cooper, A. R. Genazzani, T. Hillard, J.A. Kanis, J.-M. Kaufman, I. Lambrinoudaki, A. Laslop, E. McCloskey, S. Palacios, D. Prieto-Alhambra, J.-Y. Reginster, R. Rizzoli, G. Rosano, F. Trémollieres, N.C. Harvey
Wichtige Hinweise

Key messages

• Overall the benefit-risk balance for MHT use is more favourable at the age of menopause or in the years thereafter, for example before the age of 60 years and/or within 10 years after menopause, and for unopposed oestrogen (used in hysterectomized women) compared with combined oestrogen plus progestogen in women with an intact uterus.
• There is some evidence that the risk of cardiovascular outcomes depends upon age/time from menopause, such that, particularly for oestrogen only therapy, the risk of such outcomes may be lower when hormone therapy is commenced early postmenopause compared with in older age. This temporal relationship is less well-defined for combined oestrogen-progestogen therapy.
• Transdermal preparations are associated with lower risk of thromboembolic outcomes and are as effective as oral preparations for maintenance of BMD, but their effect on fracture risk reduction is unproven.
• Overall, MHT may be considered as an option for the maintenance of bone health in menopausal women, as an additional benefit in the context of treatment of menopausal symptoms, amongst women who are at low risk of breast cancer and of cardiovascular, cerebrovascular and venous thromboembolic events and who do not warrant a specific skeletal therapy such as a bisphosphonate.

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Introduction

Over the last three decades, osteoporosis has progressed from being viewed as an inevitable consequence of ageing to being understood as a major non-communicable chronic disease, with an associated diagnostic definition and effective methods of detection, risk stratification and treatment [ 1, 2]. We are fortunate now to have a wide range of therapeutic strategies for managing osteoporosis, targeted at improving or maintaining bone mineral density [ 3, 4]. Across the various pharmaceutical interventions available, it is possible to view particular therapies as most appropriately targeted to particular stages of the risk spectrum. For example, oral bisphosphonate therapy may be appropriate where there is established osteoporosis and high risk of fracture [ 3]. In a recent position paper from the European Society for the Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO) and the International Osteoporosis Foundation (IOF), we described how this appreciation of stratification according to efficacy, costs and side effects, in relation to low, high and very high fracture risk, might be implemented in clinical practice [ 5]. A key consideration in this work was the approach to women who were currently at low risk but who might well become at high risk in older age and whether interventions based on the high lifetime risk of fracture, rather than the immediate low risk of fracture, might be advised. One class of medication that is highly relevant here is menopausal hormone therapy (MHT), given the clear evidence for its anti-fracture efficacy, regardless of baseline bone mineral density, and also for the relevant ameliorative effects on menopausal symptoms [ 6].
MHT was widely used in the 1980s and 1990s for the prevention of symptoms associated with the menopause, such as hot flushes, night sweats and sleep disturbance, with the widely prevailing view that prevention of cardiovascular disease and osteoporosis were additional benefits [ 7, 8]. The rationale for such an approach was an evidence-base consisting principally of observational studies, in which the use of hormone replacement therapy (as it was known at that time) was associated with generally improved health outcomes, particularly in relation to cardiovascular disease. This whole thesis was challenged by results from the large US Women’s Health Initiative (WHI) Hormone Therapy trials, the first of which compared a fixed composition of conjugated equine oestrogens (CEE) and medroxyprogesterone acetate (MPA) to placebo and was published in 2002 [ 7, 9]. This trial reported that, whilst this hormone therapy regimen did indeed lead to a decreased risk of fractures, it was associated with increased risks of cardiovascular and cerebrovascular events, as well as with increased risks of breast cancer and other adverse health outcomes [ 10]. Subsequently, the limitations of inadequately analysed, confounded observational studies and the potential for converse findings from well conducted randomized controlled trials have found a key exemplum in the MHT story [ 11]. Interestingly, when the original observational studies were re-analysed using state-of-the-art pharmacoepidemiology techniques, which much more effectively control problems such as confounding by indication, then findings more in line with the results from randomized trials were observed [ 11]. However, these remain analyses of observational studies and therefore should be viewed as less robust evidence than those derived from randomized trials. Subsequent re-analyses of the WHI trials, together with evidence from other trials, have suggested that the benefit-risk profiles of MHT differ according to the timing of use in relation to the menopause and chronological age and by MHT regimen (addition or not of progestogen, type of oestrogen and progestogen, dose of oestrogen and route of administration) [ 79].
There is clearly a complex evidential landscape in which to assess the role of MHT in the prevention/treatment of osteoporosis. In this position paper, based on a narrative literature review, we will use randomized controlled trial evidence and meta-analyses thereof, in order to use the best quality data. Additionally, we focus on the scenario of normal menopause, rather than premature ovarian insufficiency, for which MHT, to replace the hormone deficit, is generally appropriate [ 12]. We firstly describe the natural history of the menopause in terms of hormonal changes and consequent health outcomes; subsequently, we set out the evidence that MHT is effective in reducing the risk of incident fracture, the independence of this effect from baseline BMD and age. Thereafter, we aim to examine the overall benefit-risk profile of MHT, particularly with regard to cardiovascular outcomes, and to investigate the potential effects of timing in relation to menopausal transition, dose and route of administration as approaches to mitigate adverse effects. We conclude by assessing the potential health economic aspects of the use of MHT for fracture prevention and outline a potential clinical approach.

Natural history of hormonal changes at the menopause and associated health outcomes

Menopausal physiology

The menopause is defined as the permanent cessation of menstruation that results from loss of ovarian follicular activity. Clinically, in women in their 40s or 50s, it is recognized to have occurred after twelve consecutive months of amenorrhoea for which no other obvious pathological or physiological cause can be found. In most women, the menopause is preceded by a phase of about 4 years during which the endocrine, biological and clinical features of changing ovarian function occur [ 13, 14]. In a normal menstrual cycle, the ovaries produce oestrogens (i.e. oestradiol), androgens (i.e. testosterone) and progesterone in a cyclical pattern under the control of follicle stimulating hormone (FSH) and luteinizing hormone (LH), which are secreted by the pituitary gland. In the early menopausal phase (perimenopause), oestradiol levels may remain relatively similar to those in young women (or may even be higher), but cycles frequently become shorter or irregular. The depletion of the ovarian reserve with age, a consequence of the finite number of oocytes and the consequent reduced levels of oestrogen, leads to an increase in circulating follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels. In contrast to the relatively rapid decline in oestradiol during menopause, concentrations of total and free testosterone, as well as of dehydroepiandrosterone sulphate (DHEAS) and androstenedione, appear to fall rather more steadily with advancing age. Concentrations of progesterone are low postmenopause, and whilst circulating levels of oestrogen are markedly lower post- than premenopause, there may still be some oestrogenic activity at the intracellular level as a result of local aromatization of androgen precursors [ 15]. These hormonal changes lead to the wide range of symptoms associated with the menopause, such as hot flushes, sleep disturbance, mood changes and urogenital changes, which are described in detail elsewhere [ 16].

Menopause and the skeleton

In 1947, Fuller Albright published his observations on the causal relationship between oestrogen deficiency following the menopause and impaired bone health [ 17]. His work established the principles that treatment with exogenous oestrogen can help to maintain bone mass and thus to reduce fracture risk. Oestrogen appears to have direct activity on osteoclasts, osteoblasts and osteocytes, with the principal effects as an antiresorptive agent through reduction of osteoclast numbers and function, mediated through various pathways including the receptor activator of nuclear factor kappa B ligand (RANKL) system [ 18]. Impaired osteoblast activity in oestrogen deficiency is reflected in reduced matrix production as measured by mean wall thickness on bone histology, an effect that is reversed by oestrogen replacement [ 19]. The increase in fracture risk associated with the menopausal transition is well established, together with a period of accelerated bone loss, particularly trabecular (with a loss of bone structure, for example increased trabecular perforations, as well as loss of bone mass [ 20]), which then settles to a more long-term age-related decline. Interestingly, the presence of menopausal symptoms has been shown to be associated with spinal osteoporosis, supporting a dual benefit of MHT on both outcomes [ 21]. The incidence of fracture varies by age and site, such that wrist fractures become notable around the age of menopause and in the years soon after, whereas the incidences of vertebral and then hip fractures rise sharply at older ages [ 22, 23]. A wrist fracture may well be the warning sign for impaired bone health in the recently menopausal woman, and thus indicate the urgent necessity for risk assessment and preventive action to prevent further fracture events [ 22].

Types of MHT (oestrogens, progestogens, dose, route of administration)

MHT in its simplest form consists of an oestrogen, given either alone (where a woman has undergone hysterectomy) or together with a progestogen to reduce the risk of endometrial cancer where the uterus is still present. For example, the combination used in the WHI was oral conjugated equine oestrogen (CEE) 0.625 mg/day and medroxyprogesterone acetate (MPA) 2.5 mg/day. However, there is now a wide range of options, including other more physiological oestrogen compounds, such as oral micronized 17β-oestradiol (typically at a dose of 1–2 mg/day), and other progestogens, such as norethisterone acetate, micronized progesterone or dydrogesterone. Additionally, there are preparations that can be administered via the transdermal or percutaneous route (for example transdermal 17β-oestradiol typically at 25–50 μg/day), and across routes of administration, various doses are now available [ 24]. Transdermal absorption of oestrogen bypasses first pass metabolism in the liver and appears not to alter the risk of venous thromboembolic disease and stroke, certainly much less than do oral oestrogens [ 25, 26]. Whilst the progestogen component of MHT is given to reduce the risk of endometrial cancer, it should be noted that the benefit-risk profile of unopposed and opposed oestrogen MHT is rather different [ 8]. Finally, for completeness, tibolone (a synthetic steroid with mixed oestrogenic, progestogenic and androgenic activity) [ 27] and TSEC (Tissue Selective Oestrogen complex containing CEE and bazedoxifene) are also available for menopause treatment, although, as with other medications, their use and availability vary from country to country [ 24]. Given these complexities, it is critical to take a particular MHT preparation on its own merits and individualize treatment as far as the evidence will permit. For more specific information regarding doses and preparations, the reader is directed elsewhere [ 16].

Efficacy of MHT for fracture prevention

The initial seminal intervention studies, undertaken by Christiansen and colleagues in relatively small numbers of women, demonstrated protective effects of oestrogen with or without progestogen on bone mass, assessed using single or dual photon absorptiometry [ 2830]. A US trial additionally demonstrated effects on bone histomorphometric parameters [ 31]. The first randomized trial evidence using dual-energy X-ray absorptiometry (DXA) to show that MHT maintains bone mineral density (BMD) after the menopause came from the Postmenopausal Oestrogen/Progestin Intervention (PEPI) trial, published in 1996 [ 32]. It was the results of the WHI that demonstrated the anti-fracture efficacy of MHT, a finding that applied to all osteoporosis-related fractures, including those at the hip, and importantly in a population that was unselected for low BMD. Thus, amongst the 16,608 women aged 50–79 years with an intact uterus at baseline who were randomized to either CEE+MPA or matching placebo, over a mean of 5.2 years follow-up, there was a 34% reduction in the incidence of hip fracture [Hazard Ratio (HR): 0.66; 95% CI: 0.45 to 0.98]. A very similar effect was observed on the incidence of clinical vertebral fractures and a reduction in other osteoporotic fractures was documented (HR: 0.77; 95% CI: 0.69 to 0.86) [ 10]. A second analysis with 5.6 years of follow-up on active treatment again demonstrated a statistically significant reduction in fracture risk for the CEE+MPA group compared with placebo (HR: 0.76; 95% CI: 0.69 to 0.83). This effect was not modified by a range of factors such as age, body mass index, smoking status, prior falls, personal/family history of fracture, total calcium intake, past use of hormone therapy and importantly was independent of baseline BMD. A 3.7% increase in total hip BMD was noted at 3 years of treatment compared with a 0.14% increase in the placebo group [ 33].
The persistence, or otherwise, of a bone protective effect of MHT is an important consideration for its place in osteoporosis management. In a small early study, women ( n = 347) who had previously been enrolled in one of four placebo-controlled MHT trials were re-examined at 5, 11 or 15 years after stopping MHT [ 34]. Here, although rates of bone loss after stopping MHT returned to normal postmenopausal values, the BMD of previously MHT-treated women continued, for many years after cessation of treatment, to be higher than that of women who had received placebo. Furthermore, the risk of all osteoporotic fractures was lower in the previously MHT-treated than previously placebo-treated group [ 34]. However, several other studies both at the mechanistic [ 35] and population level have suggested that protective skeletal effects of MHT do not convincingly persist after cessation of therapy. Thus, amongst 140,584 postmenopausal women who participated in the US National Osteoporosis Risk Assessment study, those women who had discontinued MHT in the past 5 years had a 1-year hip fracture risk similar to women who had never used MHT [ 36]. Similar findings came from a study using the US Southern California Kaiser Permanente health management organization database. A total of 80,955 postmenopausal women using MHT were followed for around 6.5 years [ 37]. Women who discontinued MHT were at 55% greater risk of hip fracture compared with those who continued, with the risk increasing as early as 2 years after cessation of MHT. Clearly, these observational studies may be more prone to bias and confounding than randomized trials. However, in the WHI, 3 years after cessation of the MHT intervention [ 38], in further analyses at a median follow-up of 4.8 years postintervention [ 39] and then in extended follow-up (8.2 years CEE+MPA and 6.6 years CEE only) postintervention, there was no evidence of any residual benefit from prior MHT for hip fractures, although rates were lower in the intervention than placebo group across the combined intervention and post-intervention follow-up [ 39, 40]. A further fracture-focused WHI analysis, examining women during 5 years of postintervention follow-up, who had been previously randomized to MHT or placebo again found that there was no evidence of either transiently or persistently decreased fracture risk amongst former MHT users compared with former placebo users. However, there was some evidence of a persisting benefit on total fractures amongst former MHT users who had taken part in the CEE-alone trial (who had undergone hysterectomy prior to baseline) but not in the CEE+MPA trial [ 41].
The WHI programme, with its several trials randomizing women to MHT versus placebo and calcium+vitamin D supplementation versus placebo, yielded a total of 16,089 women in whom an interaction between MHT and calcium+vitamin D supplementation on fracture risk reduction could be investigated. Indeed, there was evidence of an interaction between hormone therapy and calcium+vitamin D supplementation on hip fracture ( p-interaction = 0.01). The effect of calcium+vitamin D supplementation was greater amongst women assigned to MHT (HR: 0.59; 95%CI: 0.38 to 0.93) than placebo (HR: 1.20; 95%CI: 0.85 to 1.69). Furthermore, the effect of hormone therapy (vs hormone therapy placebo) on hip fracture was greater amongst women assigned to calcium+vitamin D supplementation (HR: 0.43; 95%CI: 0.28 to 0.66) than those women assigned to the placebo of the calcium+vitamin D randomization (HR: 0.87; 95%CI: 0.60 to 1.26). Interestingly, there was no apparent interaction of MHT with calcium+vitamin D supplementation on hip or spine BMD changes, leading to questions regarding the underlying mechanism. However, the findings do suggest a synergistic benefit between these two interventions on fracture reduction [ 42]. Finally, in a meta-analysis of 28 studies including 33,426 participants and 2516 fracture cases, bone protective effects were consistent with those observed in WHI, with the HR for all fractures (MHT vs placebo) 0.74; 95%CI: 0.69 to 0.80. Effect sizes were similar for hip (HR: 0.72; 95% CI: 0.53 to 0.98) and vertebral (HR: 0.63; 95% CI: 0.44 to 0.91) fractures [ 43]. Studies examining lower doses and transdermal applications (for example doses of 0.3 mg/day oral conjugated oestrogens, 0.25 mg/day oral micronized 17β-oestradiol or 14 μg/day transdermal oestradiol) have suggested positive effects on bone mineral density, but definitive fracture outcome data are scarce [ 24, 44].

Safety profile of MHT

Women’s Health Initiative: overview and key findings

The Women’s Health Initiative (WHI) hormone studies comprised two MHT randomized controlled trials, including 27,347 postmenopausal women age 50–79 years [ 7, 8]. Although these women were a generally healthy population, it should be noted that 35% had treated hypertension, 50% were past/current smokers and 34% had a body mass index greater than 30 kg/m 2 [ 10]. In order to accommodate the established risk of unopposed oestrogen for endometrial cancer, women with an intact uterus ( n = 16,608) were randomized to conjugated equine oestrogens (CEE) 0.625 mg/day, together with an oral progestin [medroxyprogesterone acetate (MPA) 2.5 mg/day) or placebo. Those women who had had a hysterectomy ( n = 10,739) were included in the oestrogen alone trial, with randomization to CEE 0.625 mg/day versus matched placebo. The aim of these trials was to assess the impact of MHT on chronic non-communicable diseases of ageing such as cardiovascular outcomes, and therefore the sample sizes were chosen to have sufficient power to detect an effect on a composite outcome of coronary heart disease [non-fatal myocardial infarction (MI) or coronary death] and to assess the balance of benefits and risks over an 8.5 year treatment period. In fact, the two trials were stopped earlier than planned with the oestrogen-progestin trial halted after a median of 5.6 years of treatment (as a result of an observed increase in risk of breast cancer); the oestrogen alone trial was stopped after median of 7.2 years because of an increased risk of stroke in the CEE arm. The investigators continued to follow the participants for several years after cessation of the intervention and thus in the combined trial, median follow-up post intervention was 8.2 years; in the CEE alone trial, median post-intervention follow-up was 6.6 years. The findings from WHI completely altered the clinical approach to MHT, with the prevalence of hormone therapy use in the US and Europe, declining sharply after publication of the first results in 2002. Data from the US National Health and Nutrition Examination Survey demonstrated a 22.4% prevalence of MHT use 1999 to 2000, declining to 11.9% in 2003–2004 with a more gradual further decline to 4.7% in 2009–2010 [ 45].
Thus, whilst the observational studies that preceded WHI had suggested a protective effect of MHT for cardiovascular outcomes; in the WHI trials, there was a modest increase in all cardiovascular events in women treated with hormone therapy. This was observed both with CEE+MPA (Hazard Ratio (HR): 1.13; 95%CI: 1.02 to 1.25) and with CEE alone (HR: 1.11; 95%CI: 1.01 to 1.22) during the intervention phases of the trials. The signal was also observed in the extended follow-up covering 13 years, with the HR (CEE+MPA): 1.08; 95% CI: 1.00 to 1.15 and HR (CEE alone): 1.06; 95%CI 0.98 to 1.15 [ 40]. Interestingly, during the first year of follow-up, there was an 80% increased risk of coronary heart disease events (non-fatal myocardial infarction or coronary death) with CEE+MPA compared with placebo, but which tapered off with time on treatment, a secular effect that was statistically significant ( p = 0.03) [ 8]. It should be noted that the original analyses also included adjusted 95% CI to account for the repeated assessments of coronary heart disease (and breast cancer) outcomes and that these confidence intervals generally spanned unity. However, the investigators emphasized the unadjusted confidence intervals as the primary outcomes, which appears appropriate given the potential evidence for adverse effects [ 10]. A similar pattern of findings was observed in the final analysis of cardiovascular outcomes in the CEE+MPA trial, published a year later, with the absolute event rates for coronary heart disease events demonstrating the small excess in terms of absolute risk with 39 cases per 10,000 person-years in the hormone therapy and 33 per 10,000 person-years in the placebo group [ 46]. Venous thromboembolism was increased with both types of MHT, although more so with CEE+MPA. Thus, the HR for pulmonary embolism in the CEE+MPA trial was 1.98; 95%CI: 1.36 to 2.87, and in the same trial, the HR for deep vein thrombosis was 1.87; 95%CI: 1.37 to 2.54. The corresponding HRs in the CEE alone trial were 1.35; 95%CI: 0.89 to 2.05 and 1.48; 95%CI: 1.06 to 2.07 for pulmonary embolism and deep-vein thrombosis, respectively [ 40]. The HR for stroke with CEE+MPA vs placebo was 1.37; 95%CI: 1.07 to 1.76 and with CEE alone vs placebo, 1.35; 95%CI: 1.07 to 1.70. The other major concern arising from WHI was the increased risk of breast cancer for women randomized to CEE+MPA compared with placebo (HR: 1.24; 95%CI: 1.01 to 1.53), which remained elevated during cumulative follow-up (HR: 1.28; 95%CI: 1.11 to 1.48). Interestingly (and consistent with other data) [ 24], randomization to CEE alone was associated with a reduced risk (HR: 0.79: 95%CI: 0.61 to 1.02), which persisted with time. Over the entire follow-up (after a mean of 10.7 years), lower breast cancer incidence in the CEE group persisted and was 0.27% compared with 0.35% in the placebo group (HR, 0.77; 95%CI: 0.62 to 0.95) [ 39]. Conversely, CEE+MPA was associated with a reduction in colorectal cancer (HR: 0.62; 95%I: 0.43 to 0.89) and evidence of a more modest reduction in endometrial cancer (HR: 0.83; 95%CI: 0.49 to 1.40). With both MHT regimens, there were reductions in the risk of hip fracture, all fractures and type II diabetes, but an increase in gall bladder disease, urinary incontinence and the risk of dementia (only assessed in an older subset). In neither trial was the MHT intervention associated with mortality [ 40].
Finally, the pattern of cardiovascular events following discontinuation of MHT deserves consideration. Thus, amongst 332,202 Finnish women discontinuing MHT between 1994 and 2009, with data derived from national registries, previous MHT users had greater risk of cardiac (standardized mortality ratio (SMR), 95%CI: 1.26; 1.16 to 1.37) and stroke death (1.63; 1.47 to 1.79) than expected over the first year post MHT cessation, but a lower risk thereafter (SMR: 0.75; 95%CI: 0.72 to 0.78 and 0.89; 0.85 to 0.94 respectively). Interestingly, the first year excess mortality seemed greater for women who had been < 60 years old at MHT initiation or been users for < 5 years, supporting the notion of differences in cardiovascular effects of MHT by age. The risk of both outcomes was consistently greater in those women who stopped MHT compared with those continuing [ 47]. A further analysis from the same group using national Finnish registry data and excluding women who experienced a cardiac or cerebrovascular event within the year before treatment cessation demonstrated similar excess mortality in the first year after stopping MHT compared with an age-matched female background population [ 48]. Although these observational findings do not prove a causal relationship and indeed may be influenced by, for example, cardiovascular/cerebrovascular related reasons for stopping (although the authors attempted to control for this in the later paper), these results do further support the vascular relevance of MHT.

MHT and cardiovascular outcomes: does timing make a difference?

A key consideration in the interpretation of the results of the WHI trial is that the average age of the participants was 63 years, which is markedly older than the average age of menopause in North America or Europe (51 years) [ 8]. Indeed, the majority of the WHI participants did not have symptoms of the menopausal transition [ 7]. This contrasts with the majority of the preceding observational studies, which generally enrolled younger women closer to the onset of menopause and usually with menopausal symptoms. The WHI investigators undertook analyses stratified by age, that is, effectively by years since menopause [ 8, 40]. The findings, of a more favourable benefit-risk profile for those within 10 years of the menopause, compared with those women more than 10 years after menopause, have led to the concept of the “timing hypothesis” in relation to cardiovascular outcomes [ 8]. In this context, cardiovascular refers to arterial disease rather than to venous thromboembolism. Thus, in the WHI, when stratified by age, there was actually a reduction in myocardial infarction [HR: 0.55; 95%CI: 0.31 to 1.00) and all-cause mortality (HR: 0.70; 95%CI: 0.46 to 1.09) in the 50–59 year age band for CEE alone compared with placebo. In contrast, those in the oldest age band (70–79 years) tended towards increased risks of these outcomes (HR: 1.24; 95%CI: 0.88 to 1.75 and HR: 1.21; 95%CI: 0.95 to 1.56 for myocardial infarction and total mortality respectively). Although there were differences by age band for the CEE+MPA trial, these were not so obviously linear, with the lowest hazard ratios usually in the 60–69 year age band compared with 50–59 years and 70–79 years. Interestingly, there appeared to be no effect by age band on relationships with stroke, breast cancer, fractures, diabetes or thromboembolic disease across either of the two hormone therapy regimens [ 40]. Indeed, breast cancer remains the other particularly concerning side effect of opposed MHT, and although beyond the scope of this review, the relevant evidence is discussed in detail elsewhere [ 16, 24]. Figure 1 summarizes the absolute differences per 5000 person-years (1000 persons treated over 5 years) in number of events in the WHI hormone trials for women aged 50–59 years at enrolment.

The timing hypothesis in trials subsequent to WHI

Other intervention studies have investigated whether use of MHT early after the menopause might have protective effects on coronary artery disease, using measures of atherosclerosis such as carotid intima-media thickness and coronary artery calcification (summarized in Table 1). The majority of these were conducted post-WHI, but the Heart and Estrogen/progestin Replacement Study (HERS) Research Trial yielded earlier relevant insights, albeit in the context of secondary prevention. A total of 2763 women with established coronary heart disease, who were younger than 80 years old (mean age 66.7 years) and postmenopausal with an intact uterus, were recruited across outpatient and community settings in 20 US clinical centres [ 49]. Women were randomized to either 0.625 mg CEE plus 2.5 mg of MPA ( n = 1380) or matched placebo ( n = 1383). Overall, there were no significant differences between groups in the primary outcome of non-fatal myocardial infarction or coronary heart disease (CHD) death [Relative hazard (RH), 0.99; 95% CI: 0.80 to 1.22] or in any of the secondary cardiovascular outcomes. There was a net 11% lower low-density lipoprotein cholesterol level and 10% higher high-density lipoprotein cholesterol level in the hormone group compared with the placebo group. Within the overall null effect, there was a statistically significant time trend, with more CHD events in the hormone group than in the placebo group in year one and fewer in years four and five. More women in the hormone group than in the placebo group experienced venous thromboembolic events (34 vs 12; RH: 2.89; 95% CI: 1.50 to 5.58) and gallbladder disease (84 vs 62; RH: 1.38; 95% CI: 1.00 to 1.92). So here across the mean 4.1 years follow-up, there was a null effect on cardiovascular endpoints overall but with evidence of greater risk early during follow-up and reduced risk later, as well as an increased risk for venous thromboembolic events [ 49]. Given the potential for loss to follow-up and reduced adherence with time (for example those who experienced a myocardial infarction in year 1 may have left the trial subsequently), any inferences about longer term treatment with MHT should be made with caution. However, 82% of those assigned to hormone treatment were taking it at the end of 1 year and 75% at the end of 3 years, and in fact outcome data were available on 100% participants. A total of 2321 women (93% of those surviving) consented to further unblinded follow-up over 2.7 years. The overall RHs for non-fatal myocardial infarction and death due to coronary heart disease, after adjustment for potential confounders and differential use of statins between treatment groups (RH: 0.97; 95% CI: 0.82 to 1.14), and in analyses restricted to women who were adherent to randomized treatment assignment (RH: 0.96; 95% CI: 0.77 to 1.19) did not provide any evidence of altered CHD risk during the additional follow-up [ 50]. It is notable that the percent participants who were > 80% adherent to allocated MHT fell from 81% at year one to 45% in year six, and MHT use in the placebo group increased from 0 to 8% over the same time period, indicating reduced power to detect differences by original treatment allocation.
Table 1
Non-WHI key randomized controlled trials of MHT and main outcomes
Trial
N
Intervention
Outcomes
Effect
Kronos Early Oestrogen Prevention Study (KEEPS) [ 51, 52]
Healthy menopausal women, aged 40–58 years; 4 years; n = 727
Randomized to either oral CEE (0.45 mg/day), or transdermal 17β-oestradiol (t-E2), 50 mcg/d, each with 200 mg of oral progesterone for 12 days per month, or placebo for 48 months
Annual change in coronary artery intima media thickness (CIMT); coronary artery calcium score
No differences between groups
Early versus Late Postmenopausal Treatment with Estradiol randomised trial (ELITE) [ 53]
643 healthy postmenopausal women; median 5 years
Randomly assigned to receive either oral 17β-oestradiol (1 mg/day, plus progesterone (45 mg) vaginal gel administered sequentially (once daily for 10 days of each 30-day cycle, intact uterus) or placebo (plus sequential placebo vaginal gel for women without a uterus)
Primary outcome: Change in CIMT every six months. Coronary atherosclerosis (cardiac computed tomography)
Early postmenopausal women: CIMT increased by 0.0078 mm per year in the placebo group compared with 0.0044 mm per year in the 17β-oestradiol group ( p = 0.008)
Late postmenopausal women, CIMT no difference ( p = 0.29)
Cardiac CT measurements not different
Danish Osteoporosis Prevention Study (DOPS) [ 54]
1006 healthy recently postmenopausal women aged 45–58 years
Randomized to MHT or placebo. MHT: triphasic oestradiol and norethisterone acetate (intact uterus); 2 mg/day oestradiol (hysterectomized)
Primary endpoint: composite of death, admission to hospital for heart failure and myocardial infarction.
After 10 years of intervention, HR: 0.48; 95% CI: 0.26 to 0.87
Mortality: HR: 0.57; 95%CI: 0.30 to 1.08
Breast cancer: HR: 0.58; 95%CI: 0.27 to 1.27
DVT: 2.01; 95%CI: 0.18 to 22.16
Stroke: HR: 0.77; 95%CI: 0.35 to 1.70.
Heart and Estrogen/progestin Replacement Study (HERS) Research Trial [ 49]
2763 women with coronary disease, <80 years old (mean 66.7 years), postmenopausal with an intact uterus.
Randomized to either 0.625 mg CEE plus 2.5 mg of MPA or matched placebo
Primary outcome: non-fatal myocardial infarction or coronary heart disease (CHD) death
Relative hazard (RH), 0.99; 95% CI: 0.80 to 1.22
DVT: RH: 2.89; 95% CI: 1.50 to 5.58
Gallbladder disease: RH: 1.38; 95% CI: 1.00 to 1.92
Women’s International Study of long Duration Oestrogen after Menopause (WISDOM) [ 55]
6498 women, mean age 62.8 years
2196 women were randomized to either oestrogen only therapy (CEE 0.625 mg orally daily) or combined hormone therapy (CEE plus MPA 2.5/5.0 mg orally daily) and 2189 to matched placebo
Major cardiovascular events, venous thromboembolism, cancer
Major cardiovascular events (7 vs 0; p = 0.016)
Venous thromboembolism HR: 7.36; 95% CI: 2.20 to 24.60
Cancer: HR: 0.88; 95%CI: 0.49 to 1.56
Cerebrovascular events: HR: 0.73; 95%CI: 0.37 to 1.46
Fractures: HR: 0.69; 95%CI: 0.46 to 1.03
Mortality: HR: 1.60; 95%CI: 0.52 to 4.89
CEE conjugated equine oestrogen, MPA medroxyprogesterone acetate, CIMT carotid intima media thickness, HR hazard ratio, DVT deep vein thrombosis, RH relative hazard
In the Kronos Early Oestrogen Prevention Study ( KEEPS), healthy menopausal women aged 40–58 years who were between 6 and 36 months from the last period and without previous cardiovascular events, were randomized to either oral CEE (0.45 mg/day) or transdermal 17β-oestradiol (t-E2), 50 mcg/d, each with 200 mg of oral progesterone for 12 days per month or placebo for 48 months [ 51, 52]. Over the 4-year treatment, amongst 727 women randomized, there was no evidence that hormone therapy, of either type, led to increases in carotid intima media thickness (CIMT) or in coronary artery calcium score, but the trial was not powered to detect differences in clinical outcomes. In this study, neither MHT intervention was associated with alterations to blood pressure, in contrast to oral CEE in WHI, although randomization to t-E2 was associated with decreased insulin resistance. The oral CEE dose in KEEPS (which was lower than that in WHI) was associated with a favourable change in lipid profile in the sense that there was an increase in high-density lipoprotein and decrease in low-density lipoprotein cholesterol; however, there was an associated increase in triglycerides [ 51, 52].
In the Early versus Late Postmenopausal Treatment with Estradiol randomised trial (ELITE), a total of 643 healthy postmenopausal women were randomly assigned to receive either oral 17β-oestradiol (1 mg/day) plus progesterone (45 mg) vaginal gel administered sequentially (once daily for 10 days of each 30-day cycle) for women with a uterus or placebo (plus sequential placebo vaginal gel for women without a uterus) [ 53]. Randomization was stratified according to time since menopause (less than six years or ≥ 10 years). Over a median of 5 years, the effect of 17β-oestradiol with or without progesterone on CIMT progression was different according to commencement early or late after the menopause. The interaction was statistically significant ( p = 0.007). Thus, for those women in the early postmenopausal stratum, the mean CIMT increased by 0.0078 mm per year in the placebo group compared with 0.0044 mm per year in the 17β-oestradiol group ( p = 0.008). In the late postmenopausal stratum, the rates of CIMT progression were similar between placebo and intervention groups ( p = 0.29). Measures of coronary artery calcification, total stenosis and plaque from the computed tomography assessments did not differ according to randomization group [ 53].
The Danish Osteoporosis Prevention Study ( DOPS) specifically addressed the issue of treatment with MHT soon after the menopause [ 54]. In this open-label, randomized controlled trial, 1006 healthy women aged 45–58 years (mean 50 years) who were recently postmenopausal (mean 7 months) were randomized to receive menopausal hormone therapy ( n = 502) or no treatment ( n = 504). In the treatment group, women with an intact uterus were treated with triphasic oestradiol and norethisterone acetate; women who had undergone hysterectomy received 2 mg oestradiol per day. The trial was stopped after around 11 years as a result of the adverse event signals from the WHI, but the DOPS investigators continued to follow participants for death, cardiovascular and cancer outcomes for up to 16 years. After 10 years of intervention, 16 women in the treatment group experienced the primary composite endpoint (death, admission to hospital for heart failure or myocardial infarction) compared with 33 in the control group (HR: 0.48; 95% CI: 0.26 to 0.87) and 15 vs 26 died (HR: 0.57; 95%CI: 0.30 to 1.08), consistent with a protective effect of MHT. There was no evidence of an increase in any cancer (intervention vs control: 36 vs 39; HR: 0.92; 95%CI: 0.58 to 1.45) or in breast cancer (10 vs 17; HR: 0.58; 95%CI: 0.27 to 1.27). The HR for deep vein thrombosis (2 vs 1) was 2.01; 95%CI: 0.18 to 22.16 and for stroke (11 vs 14) was 0.77; 95%CI: 0.35 to 1.70. After 16 years, the reduction in the primary composite outcome was still present and not associated with an increase in any cancer [ 54]. However, despite the use of hard endpoints, the open-label nature of the trial design does not necessarily warrant the same level of confidence as would be associated with a truly double-blind structure.
The Women’s International Study of long Duration Oestrogen after Menopause (WISDOM) trial was stopped early after a median of 11.9 months recruitment as a result of the findings from the WHI [ 55]. A total of 6498 women had been enrolled, with a mean age similar to that of women in the WHI (62.8 years). A total of 2196 women were randomized to either oestrogen only therapy (CEE 0.625 mg orally daily) or combined hormone therapy (CEE plus MPA 2.5/5.0 mg orally daily) and 2189 to matched placebo. Consistent with findings from the WHI, there was a significant increase in the number of major cardiovascular events (7 vs 0; HR p = 0.016) and venous thromboembolism (22 vs 3; HR: 7.36; 95% CI: 2.20 to 24.60) in the combined HT group vs placebo. There were no statistically significant differences in numbers of breast or other cancers (22 vs 25; HR: 0.88; 95%CI: 0.49 to 1.56), cerebrovascular events (14 vs 19; HR: 0.73; 95%CI: 0.37 to 1.46), fractures (40 vs 58; HR: 0.69; 95%CI: 0.46 to 1.03) and overall deaths (8 v 5; HR: 1.60; 95%CI: 0.52 to 4.89). Comparison of combined hormone therapy ( n = 815) versus oestrogen therapy ( n = 826) outcomes revealed no significant differences; the numbers of events were relatively low compared with WHI.
Finally a meta-analysis of 23 MHT trials, including 39,049 participants followed for 191,340 patient-years, showed that hormone therapy appeared to significantly reduce CHD events in younger (mean time postmenopause < 10 years or age < 60 years) women [Odds ratio (OR): 0.68; 95%CI: 0.48 to 0.96], but not in older women (OR: 1.03; 95%CI: 0.91 to 1.16). In older women, hormone therapy increased CHD events in the first year (OR: 1.47; 95%CI: 1.12 to 1.92) then reduced events after 2 years (OR: 0.79; 0.67 to 0.93) [ 56].

How might MHT differentially influence ischaemic cardiovascular outcomes by age?

The concept that oestrogen might differentially influence cardiovascular risk depending upon time since menopause, or chronological age, originated in animal studies of non-human primates. Thus, in cynomolgus monkeys, conjugated oestrogens with or without MPA were not associated with any changes in coronary artery plaques when the hormone therapy was commenced at 2 years (equivalent to around 6 human years) after oophorectomy and in the presence of established atherosclerosis. In contrast, this intervention reduced plaque size by 70% when initiated immediately following oophorectomy in the early stages of atherosclerosis [ 57]. These findings are consistent with the results of the KEEPS, ELITE and DOPS trials described above and of human imaging trials in participants with significant coronary lesions at baseline in which oestrogen appeared not to slow the rate of arterial narrowing [ 5861]. In contrast, a protective effect of oestrogen on coronary artery atherosclerosis was observed in a further imaging trial in which severe coronary artery lesions were not a criterion for enrolment [ 62]. These findings suggest that oestrogen might have differential effects on the progression of atherosclerotic disease and/or thrombotic events depending upon the degree of baseline atherosclerotic disease. There is evidence that oestrogen may increase nitric oxide synthesis and thus vasodilation and potentially decrease inflammatory cell adhesion and thus slow the progression of atherosclerotic plaques, in the setting of healthy arteries, which of course are more likely in younger patients closer to the menopause. In older women with substantial atherosclerotic plaque, oestrogen receptors may become less responsive and there is some evidence that oestrogen may adversely affect established atherosclerotic plaques, rendering them more susceptible to rupture and subsequent thrombotic occlusion of the blood vessel [ 63]. Findings from WHI in relation to lipid status are consistent with these hypotheses. Thus, CEE with or without MPA was associated with a 40% lower risk of incident coronary heart disease amongst women with a favourable LDL/HDL ratio, but risk of these outcomes was greater in women with an adverse LDL/HDL ratio at baseline [ 64]. Furthermore, the risk of coronary heart disease outcomes associated with hormone therapy was more than double in those with metabolic syndrome compared to those without [ 65]. Again, within the WHI, measurements of coronary artery calcium amongst women aged 50–59 years were lower amongst women assigned to oestrogen alone than amongst those assigned to placebo [ 66]. As with all analyses of subsets within the overall randomized trial population, such investigation should be interpreted with caution given their secondary nature and that randomization of covariates may not be preserved.

Use of MHT for maintenance of bone health

Health economics

The cost-effectiveness of MHT has been examined in relation to the treatment of menopausal symptoms and for fracture prevention in asymptomatic women but who are at high risk of a fragility fracture. Zethraeus et al. incorporated the emerging data on efficacy and side effects from WHI into an individual state transition model of 50- to 60-year-old women with menopausal symptoms using a societal perspective in Sweden [ 67]. The group undertook a similar analysis for a population based in the UK using a Markov cohort simulation model in women aged 50 years with clinical effectiveness and side effects informed by the WHI [ 68]. In both of these studies, together with an analysis based on the US population [ 69], there was evidence of cost-effectiveness. The severity of menopausal symptoms was the most and only one important determinant of cost-effectiveness, but MHT remained cost-effective even where symptoms were mild or the effects on symptom relief was small [ 68]. A further analysis focused on women at high risk of fracture, but no menopausal symptoms, in Sweden, the US and the UK, with the clinical effects again based on the findings from the WHI [ 70]. The state transition model had a lifetime horizon with disease states across fracture, cancer and cardiovascular outcomes. The results demonstrated that MHT was cost-effective compared with no treatment for the majority of subgroups of hysterectomized women. In contrast, for women with an intact uterus without a prior fracture, the evidence for cost-effectiveness was less clear. In this analysis, fracture risk was the single most important determinant of the cost-effectiveness findings [ 70]. Thus, when fracture risk was taken into account rather than menopausal symptoms, use of MHT was cost-effective in women who had had a hysterectomy irrespective of prior fracture status. In contrast, amongst women with an intact uterus, opposed MHT was cost-effective only in those with a prior vertebral fracture. Overall then, these data favour the use of MHT for prevention of menopausal symptoms but do not clearly support a specific role in fracture prevention, particularly in low fracture risk individuals. A further caveat is that the analyses do not account for time since menopause, which would be expected to improve cost-effectiveness, and it is clearly important not to automatically conflate cost-effectiveness with clinical appropriateness.

Existing guidelines

The notion that MHT might be an appropriate first line therapy for the maintenance of bone health in recently postmenopausal women is consistent with that proposed in several current guidelines internationally. Thus the European Menopause and Andropause Society (EMAS) states that “Administration of systemic MHT has a favourable risk–benefit profile for women under the age of 60 years or within 10 years after menopause for menopausal symptoms and osteoporosis” [ 71]. The North American Menopause Society (NAMS) acknowledges the effect of age post menopause on the risk-benefit landscape and explicitly cites skeletal health as a consideration: “For women aged younger than 60 years or who are within 10 years of menopause onset and have no contraindications, the benefit-risk ratio is most favourable for treatment of bothersome vasomotor symptoms and for those at elevated risk for bone loss or fracture.” [ 72] This approach is also incorporated into guidance from the International Menopause Society (IMS) [ 73]. The American Association of Clinical Endocrinologists recommend that “MHT should be used for the prevention and treatment of osteoporosis within the context of the overall benefit-versus-risk analysis of each patient” but also that “MHT should be used in the lowest dose and for the shortest period necessary to control menopausal symptoms” [ 74]. In contrast, the American College of Obstetricians and Gynaecologists focuses on menopausal symptoms [ 75], and lowest dose, shortest time paradigm (to adequately control menopausal symptoms), with the US Endocrine Society suggesting that there is no support for using MHT to prevent coronary heart disease, breast cancer or dementia, but with ambivalence towards fracture prevention [ 76]. A 2016 Global Consensus Statement, endorsed by IMS, NAMS, The Endocrine Society, EMAS, The Asia Pacific Menopause Federation, The International Osteoporosis Foundation and The Federation of Latin American Menopause Societies, explicitly proposed that “MHT…can be initiated in postmenopausal women at risk of fracture or osteoporosis before the age of 60 years or within 10 years after menopause” but that “Initiation of MHT after the age of 60 years for the indication of fracture prevention is considered second-line therapy and requires individually calculated benefit/risk, compared to other approved drugs. If MHT is elected, the lowest effective dose should be used.” [ 77] Finally clinical guidance from the UK National Institute for Health and Care Excellence (NICE) focuses on the use of MHT for postmenopausal symptoms and suggests that under the age of 60 years, the risks of cardiovascular disease are negligible for oestrogen only MHT and that there is little or no increased risk of coronary heart disease with combined MHT. Again, an individualized approach accommodating baseline cardiovascular risk is recommended, together with consideration of other factors such as history of breast cancer and thromboembolic disease [ 16].

Clinical approach

Osteoporosis is now a well-defined morbidity, with associated diagnostic criteria, methods of detection and, importantly, a range of effective treatment modalities [ 22]. Approaches to detection and assessment of individuals at low, high and very high risk of experiencing an osteoporotic fracture have been recently set out in detail by the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO) and the International Osteoporosis Foundation (IOF) [ 5], building on the 2019 European Guidance for Assessment and Treatment of Postmenopausal Osteoporosis from the same societies [ 4]. The stratification of management approach according to risk level accommodates the nuances of the range of medications currently available, encompassing interventions including calcium and vitamin D supplementation all the way through bisphosphonates up to anabolic therapies. Within this framework, MHT is considered as a potential preventative intervention as the initial part of a longer term management strategy for those postmenopausal women found to be at low risk of fragility fracture over the next 10 years, using the FRAX® algorithm, but who of course may have a much greater remaining lifetime risk (Fig.  2) [ 5]. In this setting, a specific bone therapy (for example a bisphosphonate) may not be appropriate, and the question is, on the one hand, whether the use of MHT should be specifically indicated for the maintenance of bone health and prevention of fractures or, on the other hand, whether fracture risk reduction should be viewed as an additional benefit from a medication used for treatment of menopausal symptoms. Ultimately, this depends on the individual balance of benefits versus risks: the current literature suggests robust anti-fracture efficacy of MHT in patients unselected for low BMD, regardless of concomitant use with progestogens, but with little evidence for persisting benefits following cessation of therapy. The risks appear to vary according to age/time of use, with potential cardiovascular benefits for unopposed oestrogen (in hysterectomized women) used within 10 years after the menopause in WHI, and null effects for opposed oestrogen in KEEPS, but potential cardiovascular benefits when initiated close to the menopause in the ELITE and DOPS Trials. Other side effects such as deep-vein thrombosis, stroke and gall bladder disease are raised to a greater or lesser extent according to use of opposed or unopposed oestrogen, dose and route of administration, and should all be considered. Breast cancer remains a key consideration with combined MHT [ 16, 24]. Although there is clearly concern with regard to side effects of MHT, these must be understood in the context, firstly, of the absolute risks of such events in the menopausal population, and secondly, of the benefit-risk balance for other medications used in osteoporosis treatment. For example, a UK 50-year-old woman with no cardiovascular risk factors has a 2% chance of experiencing a myocardial infarction or stroke over the next 10 years (QRISK: https://​qrisk.​org/​three/​). In this context, a 34% CHD uplift (as noted in WHI for a women with an intact uterus treated with combined MHT [ 8]) will not be particularly clinically significant (final absolute risk 2.68%). Whilst the lifetime impact of, for example, a 5-year course of MHT from the age of menopause is not known, when absolute risks are considered, the use of MHT in menopausal women at low baseline cardiovascular risk seems a reasonable option. In terms of other medications used for bone protection, raloxifene is also associated with an increased risk of thromboembolic disease, at the same order of magnitude; bisphosphonates and denosumab have been associated with rare but serious side effects such as osteonecrosis of the jaw and atypical femoral fractures; intravenous bisphosphonates and denosumab may lead to symptomatic hypocalcaemia; romosozumab was associated with increased risk of cardiovascular side effects in one of its key trials [ 3, 78]. Finally, strontium ranelate, for which the licence was restricted by the European Medicines Authority on the basis of a signal for increased risk of myocardial infarction and subsequently voluntarily withdrawn (although now back on the market as a generic preparation), is also associated with increased risk of deep vein thrombosis [ 79]. This wider context, taken with the logistic issues and risks of oesophageal ulceration associated with improper use of oral bisphosphonates, should lead to a more nuanced appraisal of the benefit-risk balance for MHT. Taking all the evidence together then, MHT is most strongly supported for the primary indication of prevention of menopausal symptoms. Clearly in this context, it may also be viewed as having the added benefit of preventing bone loss and reducing fracture risk. The benefit-risk balance for a primary indication of fracture prevention is less clearly defined, and we suggest that in recently postmenopausal women for whom maintenance of skeletal health is a clinical priority, whilst MHT might be considered in those at low risk of cardiovascular disease, thromboembolic disease and breast cancer as a first line therapy, ultimately further research of MHT in the context of a long term osteoporosis management strategy is required. The detailed exposition of the clinical assessment of menopausal symptoms and their specific treatment (with associated risks) is beyond the scope of this article, but is very comprehensively summarized in the various sets of guidance from international and national bodies described in the preceding section.

Conclusion

The evidence surrounding the use of MHT is complex and spans a wide range of often conflicting findings from observational studies and randomized trials. The field has been beset with highly publicized controversies, which have seen MHT use decline sharply following initial WHI results, with something of a move towards rehabilitation of this intervention through subsequent analyses. MHT has a clear role in the treatment of menopausal symptoms and for many menopausal women, use of MHT commenced at the time of, or shortly after, menopause, under the age of 60 years, may be considered as an option, in this context, to achieve the additional benefit of maintenance of bone health where specific bone active medications are not warranted. Risk assessment should be individualized, taking into account baseline risk of breast cancer, together with that of cardiovascular, cerebrovascular and thromboembolic events, in addition to fracture risk. Such assessment should be undertaken in the context of menopausal symptoms and detailed discussion with the patient to reach an optimal understanding of the benefit-risk balance. Nuances such as the distinction in associations with outcome according to whether oestrogen is opposed or unopposed, and thus the relevance of prior hysterectomy and the use of different oestrogens and progestogens, doses and routes of administration, are all important considerations. Clearly, it is important to use preparations that have documented anti-fracture efficacy if bone protection is desired, and the approach chosen should be tailored to the individual benefit-risk balance. Used in this way, we suggest that the evidence supports the consideration of MHT as a means of achieving bone protection and fracture prevention in the context of a primary indication for menopausal symptom treatment, in recently postmenopausal women at low baseline risk of cardiovascular disease, cerebrovascular disease, thromboembolic disease and breast cancer.

Compliance with ethical standards

Conflicts of interest

N. Al-Daghri has no disclosures. M. Aubertin-Leheudre has no disclosures. M-L. Brandi reports honoraria from Amgen, Bruno Farmaceutici, Calcilytix and Kyowa Kirin; academic grants and/or speaker fees from Abiogen, Alexion, Amgen, Bruno Farmaceutici, Eli Lilly, Kyowa Kirin, MSD, NPS, Servier, Shire and SPA; and consultancy fees from Alexion, Bruno Farmaceutici, Kyowa Kirin, Servier and Shire outside the scope of the submitted work. A. Cano reports consultancy, honoraria and lecture fees from Theramex and Italfarmaco outside the scope of the submitted work. P. Collins reports consultancy, lecture fees and honoraria from Eli Lilly, Abbott, Novo Nordisk and Bayer outside the scope of the submitted work. C. Cooper reports consultancy, lecture fees and honoraria from AMGEN, GSK, Alliance for Better Bone Health, MSD, Eli Lilly, Pfizer, Novartis, Servier, Medtronic and Roche outside the scope of the submitted work. A. Genazzani has no disclosures. N. Harvey reports consultancy, lecture fees and honoraria from Alliance for Better Bone Health, AMGEN, MSD, Eli Lilly, Servier, Shire, UCB, Kyowa Kirin, Consilient Healthcare, Radius Health and Internis Pharma outside the scope of the submitted work. T. Hillard reports lecture fees and honoraria from Shionogi, Novo Nordisk and Theramex outside the scope of the submitted work. J. Kanis reports grants from UCB, grants from Amgen and grants from Radius Health outside the submitted work, and Dr. Kanis is a member of the National Osteoporosis Guideline Group (NOGG) and the principal architect of FRAX but derives no financial benefit. J-M. Kaufman is board member (treasurer) of ESCEO. I. Lambrinoudaki has no disclosures. A. Laslop has no disclosures. E. McCloskey reports consultant/advisor/speaker fees or research funding from Agnovos, Amgen, AstraZeneca, Consilient Healthcare, Fresenius Kabi, GSK, Hologic, I3 Innovus, Internis, Lilly, Merck, MRC, Novartis, Pfizer, Roche, Sanofi-Aventis, Servier, Synexus, UCB, Unilever, Versus Arthritis and Warner Chilcott outside the scope of the submitted work. S. Palacios has received consultancy, lecture fees, honoraria and grants from Serelys, Pfizer, Amgen, Gedeon Ritcher, Exeltis, Bayer Schering, MSD, Procare Health, Mylan and Shionogi outside the scope of the submitted work. D. Prieto-Alhambra’s research group reports research grants from Amgen, Servier and UCB; speaker tuition fees and advisory or consultancy fees (all paid to his department) from Amgen and UCB outside the scope of the submitted work. J-Y. Reginster reports consulting fees or paid advisory boards from IBSA-Genevrier, Mylan, Radius Health and Pierre Fabre; lecture fees when speaking at the invitation of sponsor from IBSA-Genevrier, Mylan, CNIEL and Dairy Research Council (DRC); and grant support from Industry (All through Institution) from IBSA-Genevrier, Mylan, CNIEL and Radius Health outside the scope of the submitted work. R. Rizzoli reports fees for advisory board or lectures from Abiogen, Amgen, CNIEL, Danone, Echolight, Effryx, EMF, Mithra, Mylan, Nestlé, ObsEva, Radius Health, Rejuvenate, Sandoz and Theramex outside the scope of the submitted work. G. Rosano has no disclosures. S. Rozenberg reports consultancy, lecture fees, honoraria and grants from Mylan, Abbott, Gedeon-Richter, UCB and Amgen outside the scope of the submitted work. F. Trémollieres reports lecture and/or consultancy fees from Amgen, Arrow, Lilly France and Theramex and non-financial support for meeting from Besins Healthcare France outside the scope of the submitted work.

Consents and ethics approval

This review article reports previously published findings and does not include any new research.
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