Changes of androgens levels in menopausal women

Abstract

Androgens play an important role in women’s health. They are responsible for the sexual well-being and for maintaining proper structure and function of genitourinary woman’s tract. In menopausal period a relative increase in androgens level is observed as a result of dramatic demise of estrogens and increase of sex hormone-binding globulin (SHBG). However, the response of target tissue depends on its ability to control androgens availability. In menopausal women the symptoms of both hyperandrogenemia and of androgens deficiency may be observed. Hyperandrogenemia may result in discrete symptoms, such as slight terminal facial hair grow, or worsening of scalp hair loss. Those symptoms should not be belittled in any of the cases, especially when their severity increases one should seek possible causes of postmenopausal hyperandrogenemia.

Ovarian and adrenal aging, leading to a progressive decline in androgen levels, may exert detrimental effects on the quality of life. During menopause, changes in activation of particular brain spheres are connected with low sex hormone concentration and correlate with loss of sexual arousability. Hypoactive sexual desire dysfunction (HSDD) may be the direct result of androgens deficiency in menopausal women. It is the only evidence-based indication for the use of testosterone in women. However, before treatment, other diseases must be excluded that might alternatively be the cause of HSDD.

Introduction

Androgens play an important role in many aspects of women’s health and their well-being [1]. Luteinizing hormone (LH) stimulation has an impact on androgen secretion in pre- and post-menopausal women. After menopause, increased gonadotropin levels maintain ovarian androgen secretion besides the substantial estrogen demise [2, 3]. This imbalance between estrogens and androgens after menopause is strengthen by the evolving decrease in sex hormone-binding globulin (SHBG) concentrations and the subsequent increase in free androgen index (FAI) [4]. Ovarian and adrenal aging, leading to a progressive decline in androgen levels, may exert detrimental effects on the quality of life. Sexual function worsens with advancing menopause level. Declining levels of sex steroids play a major role in deterioration of sexual response [5]. What should be taken into consideration are psychological changes dependent on aging and an increase in metabolic and cardiovascular comorbidities in elderly. Furthermore, it should be recalled that human-specific and highly sophisticated mechanisms of intracrinology permit each cell to control androgen availability according to its own needs, independently from the remaining of the body, that may cause variable response to declining levels of androgens in women after menopause [6].

This review article is up to depict the physiological changes in androgens secretion and their impact on postmenopausal women.

Androgens in physiology of women

It is stated that the source of androgens in women – testosterone (T), dehydroepiandrosterone (DHEA), dehydroepiandrosterone sulphate (DHEAS), androstenedione (A4) and dihydrotestosterone (DHT) – are ovaries, adrenals and peripheral tissues (the skin). ACTH is in control of adrenal synthesis; though negative feedback regulation of ACTH secretion by androgens is not observed. Androgen secretion from ovaries is dependent on theca cells stimulation governed by LH. On the contrary to women, male androgens do not hamper LH secretion from the pituitary gland [1]. Androgens transported in blood occur mostly bound with SHBG or albumins, and as a result, those androgens do not show biological activity. Only DHEA and DHEAS exhibit little or no binding [7]. Approximately 0.5-7.5% of them arise in the free form (unbound), enabling their activity in target tissues [8]. Enzymes present in peripheral tissues have the ability to transform DHEAS into DHEA, next – into A4 and T, and further - T into the most active androgen - DHT (5-reductase is present in the skin). Other tissues and organs, like the liver, muscles, fat tissue, skin, kidneys or bones, retain enzymatic activity 17-hydroxysteroid dehydrogenase, allowing T conversion to estrone (E1), the latter exhibiting para- and interactive effects in tissues [9]. The skin is an important site for peripheral conversion of androgens; at least 50% of a woman’s androgen production occurs here, as DHEAS is converted to DHEA, the latter hormone to A4, A4 into T, and finally T to DHT [1].

Steroid hormones are important for maintaining proper structure and function of genitourinary woman’s tract [10-14]. In healthy young women the vagina has a stratified squamous epithelium composed of 3 cell layers consisting of superficial and intermediate cells with few parabasal cells. Normal proliferation of the epithelium leads to the formation of moist and thick rugae on the mucosal surface of the vagina and glycogen released by exfoliated epithelial cells is hydrolyzed into glucose. Then, glucose is metabolized mainly by lactobacilli into lactic acid, creating an acidic environment that discourages the growth of pathogenic bacteria and fungi [13, 15]. In postmenopausal women, T and estrogens are synthesized locally in extragonadal tissues with circulating precursor androgens (DHEA and A4) [16, 17]. They manage cells proliferation and maintain vaginal epithelium condition [18]. The highest secretion of androgens and their precursors is observed in women who are in age between 20 and 30 years; later, their concentration gradually decreases by 50%, up to 40 years in T, DHEA and DHEAS spectrum [19, 20]. In the next years of life, androgens secretion is diminished by 25% (up to 50 years) and the process continues after 60 years, though is less intense comparing to the age of 50 [21].

Androgens in menopause

It is said that in post-menopausal women ovaries remain hormonally active, producing androgens even up to 10 years after menstruation end [22, 23]. Estrogen concentration decreases in an abrupt and drastic way within postmenopausal period, whereas androgen concentration gradually decreases over the years. Ovary androgens secretion, before menopause and directly after it, is dependent on ovaries stimulation, which is governed by LH, i.e. gonadotropin, the concentration of which at this period increases [23]. Additionally, decrease in concentration of SHBG in menopausal period is a consequence of the rapid slump in estrogen secretion and boosts the pool of available T, which is marked as FAI [22, 23]. Additionally, in women before and after menopause, especially those obese ones, androgen secretion can intensify conditions like insulin resistance and excessive insulin production which stimulates the ovaries to produce androgen [24].

What can be understood is that sudden estradiol (E2) concentration decrease, with resistant quantities of T and low SHBG concentration in post-menopausal women, in a natural manner directs the hormonal balance to hyperandrogenemia. It may result in discrete hyperandrogenemia symptoms, such as slight terminal facial hair grow, or worsening of scalp hair loss [25]. Those symptoms should not be belittled in any of the cases, especially when their severity increases one should seek possible causes of postmenopausal hyperandrogenemia [25, 26].

However, what is observed, is that androgen concentration in postmenopausal women may be significantly lower in comparison to women in their 20s/30s [10]. After menopause, structural and functional changes in genitourinary tract occur under the influence of decreased sex hormone production and lead to the situation that may be compared to pre-puberty period. Anatomic alterations in vulvar, clitoral, vestibular, urethral, vaginal, anterior vaginal wall, periurethral, and bladder tissues may be observed [10]. Vulvar tissue can appear diminished, obliterated, or even fused, and irritation or erythema can be evident [27]. The introitus becomes narrow with a loss of hymenal remnants, the cervix can become flush with the vaginal vault, and pelvic organ prolapse is not uncommon [27]. The vagina can become shortened and narrowed; its surface can appear thinner, less elastic, and smoother (fewer rugae) with visible petechiae from intradermal or submucosal bleeding or inflammation. Urethral changes can include development of a urethral caruncle with urethral prolapse when the mucosa is circumferentially everted at the meatus. The loss of acidity in the vagina is associated with decreased resistance to non-native bacterial or fungal infection and there could be subsequent development of ascending bladder infections, overactive bladder, or recurrent urinary tract infections [28].

Initial observations that vaginal atrophy was less prevalent in postmenopausal women with higher levels of A4 and T [29] left open the possibility that T could be converted to E2 by aromatase. However, in a study involving a small number of women with breast cancer undergoing aromatase inhibitor therapy, intravaginal (vaginal mucosa) application of T for 4 weeks was shown to ameliorate the signs and symptoms of vaginal atrophy (dyspareunia, vaginal dryness, vaginal pH, and epithelial maturation) [30], suggesting that androgens could have an independent effect on epithelial growth.

It is claimed that sexual behavior, mood and emotional condition and cognition abilities are modulated by sex hormones throughout woman’s life. During perimenopausal period, and especially after menopause, recession in sex hormone concentration may impact on woman’s well being. During menopause, changes in activation of particular brain spheres are connected with low sex hormone concentration and correlate with loss of sexual arousability [5]. It is believed that independently of age, once menopause progresses the sexual functions deteriorate. The most common symptoms are low libido (40-50%), vaginal dryness (25-30%)s, and pain experienced while sexual intercourse (12-45%), one of the complications of genitourinary syndrome of menopause (GSM) [31].

The Endocrine Society Guidelines [32] do not recommend the use of clinical diagnosis of “androgen deficiency syndrome” in healthy women, mainly because standardized and exact measuring methods checking T level in blood are not available. Moreover, the concentration of circulating androgens does not reflect final individual exposition and peripheral tissues sensitivity.

The hypoactive sexual desire dysfunction (HSDD) is defined as stagnation in sexual desire, which is not connected with other medical conditions, physiology or conditions resulting in taking medicaments. It is observed that in women who are between 20 and 70, HSDD occurred more often as a result of surgical menopause rather than of physiological menopause. It is suggested that predispositions or other physiological or socio-cultural factors may affect sexual dysfunctions during menopause [33, 34]. It is stated that other diseases may co-exist with menopause time such as hyperprolactinemia [35], hypopituitarism, adrenal insufficiency, and chemical ovarian suppression during which the concentration of androgens is lowered. Other conditions as overt [36-38] or subclinical [36, 39] hypothyroidism and hyperthyroidism have been associated with reduced sexual desire in themselves. Low androgens level may be directly connected with impaired synthesis of sex hormones, or indirectly with increase of SHBG as in hyperthyroid patients. In depressive states the growth of sexual disorders is noticed (50% to 70% increased risk of sexual dysfunction, and the occurrence of sexual dysfunction is associated with a 130% to 210% increased risk of depression [40, 41]; on the other hand, sexual disorders may intensify depressive states. Additionally, taking antidepressant medicaments may perturb sexual desire [42-45]. Other common pathology connected with menopause may be carbohydrate metabolism disorders in the state of pre-diabetes, insulin resistance or diabetes, which hamper sexual desire [46]. Reduced sexual desire and sexual satisfaction were strongly associated with insulin resistance and, therefore, susceptible to changes in insulin sensitivity [46]. Obesity and metabolic condition in that time may affect sexual dysfunctions. Data proved that the sexual desire is inversely associated with body mass index [47-49]. Both obesity and metabolic syndrome have been associated with increased baseline clitoral vascular resistance and impaired sexual arousal, suggesting that the negative impact of these metabolic phenotypes on sexual function is primarily at the genital level rather than a central effect [50]. What is stated is that co-existence of other diseases in menopausal women may strengthen the effects of low androgen concentration, or alternatively be the cause of HSDD in this population [51]. It is thought that HSDD, in accordance with the Endocrine Society recommendations 2019, is the only indication to use T in menopausal women. There is not sufficient data confirming the efficacy of such treatment for other indications. HSDD diagnosis must be deliberated, based on excluding other factors which may lead to sexual disorders in that women population [52].

Conclusions

After menopause, estrogens fall to undetectable levels. Consequently, the small amount of remaining T may predispose to androgenic symptoms, especially acne, increased facial hair growth and male pattern baldness [23]. Androgens contribute to libido, sexual arousal and orgasm by increasing dopamine levels in the central nervous system. Testosterone also maintains normal metabolic function, muscle and bone strength, genitourinary health, mood and cognitive functions [33].

Androgens deficiency can lead to a number of distressing sexual symptoms. An “androgen deficiency syndrome” with loss of libido and sense of well-being is well recognized but these symptoms have many other causes. The occurrence, diagnosis and significance of androgen deficiency in women both clinically and biochemically needs to be further clarified [51].

According to the recent consensus referring to testosterone therapy for women (2019) the only evidence-based indication for the use of testosterone in women is for the treatment of postmenopausal women who have been diagnosed as having HSDD after formal bio-psychosocial assessment [52]. Patients should be monitored for their clinical response to treatment and assessed for signs of androgen excess with a serum total T concentration every 6 months, to screen for overuse. If no benefit is experienced by this time, treatment should be ceased. Systemic DHEA is not associated with significant improvement in libido or sexual function in postmenopausal women with normal adrenal function and cannot be recommended for women with HSDD [52].

Disclosure

The authors report no conflict of interest.