Rethinking Low Sexual Desire in Women 2001
Rethinking Low Sexual Desire in Women 2001
REVIEW
these engorging structures is not appreciated as pleasurable Women with sudden complete loss of ovarian androgen
sexual arousal. The genital physiological response would
appear to be an involuntary reflex mediated by the (uncon- The woman with premature, surgical or medical meno-
scious) autonomic nervous system3 (note the occurrence of pause is more distressed by her inability to respond to
genital response in situations of genital assault and rape)3. formerly effective sexual stimuli than her lack of sponta-
Clearly, the subject of sexual arousal and any lack thereof neous sexual thoughts and fantasies. The androgen needed
is highly complex, with the result that the role of genital for processing the stimuli in generating subjective arousal
vasoactive medication in women complaining of arousal is insufficient. She may also suffer the consequences of
difficulties is far from clear20,22,23. To date, the only lack of peripheral testosterone action on the smooth muscle
large placebo controlled studies of sildenafil given to response involved in vulval and vaginal congestion. The
women have failed to show benefit over placebo23. Of couple’s emotional intimacy may suffer from both the lack
note, these studies (one on oestrogenised and one on non- of rewarding physical times together and the confusion and
oestrogenised women), included women with a broad misunderstanding as to its cause. The breaks in her cycle
range of sexual dysfunction which included lack of arousal. are shown in Fig. 6. In one study28 47 consecutive couples
The arousal disorder was not analysed in any way (e.g. to referred for female low sexual desire were assessed.
determine whether the women were complaining of lack of Although lack of testosterone was felt to be a factor in
subjective arousal or lack of both subjective and genital some 20%, many other breaks in the women’s (alternative)
arousal)22. Current research is attempting to focus on the cycles were also apparent. Of note, in a recent placebo-
use of vasoactive drugs in women with an acquired reduc- controlled study of transdermal testosterone replacement in
tion in genital response and a smaller placebo controlled
study showing benefit of sildenafil in premenopausal
women has been recently published24. The traditional view
that vaginal lubrication constitutes sexual arousal in
women is thus not only restrictive but misleading when
arousal disorder is under discussion. Women tend to focus
mostly on how mentally exciting they find the stimulus
when they rate their sexual arousal18. Future research may
profitably focus on those women who reliably respond
genitally throughout the experience of sexual stimulation
but have no subjective arousal. In other words, there is a
need to identify the mechanisms of the disconnection
between mind and genitalia.
These models of blended intimacy-based and ‘drive-
based’ sexual response cycles with ongoing modulation
from emotional, cognitive and physical feedback include
many concepts of previous authors3,6 – 8,25 – 27. However,
the traditional model familiar to gynaecologists still Fig. 6. The repercussions of sudden complete loss of ovarian androgen on
remains that of Kaplan, Masters and Johnson where con- the woman’s sex response cycle.
women whose surgical menopause was thought to be the associated with dyspareunia38. Tibolone’s androgenic
cause of acquired low sexual desire and response, benefit activity is thought to account for increased sexual desire
only was seen in the older women and only if they achieved and responsiveness in women receiving tibolone, compared
high normal (as opposed to mid-normal) premenopausal with those receiving either conjugated oestrogen plus
testosterone levels29. No therapy other than testosterone medroxyprogesterone acetate39, or oestradiol plus norethis-
replacement was given. terone40,41. Also, tibolone allowed comparable increases
Little detail is known about the exact role of testosterone in sexual responsiveness compared with oestradiol plus
in either innate sexual need or in the processing of sexual dihydro-androsterone, the latter causing untoward lipid
stimuli. Post mortem evidence of uptake of androgen (and effects42. Of note, these studies were of otherwise healthy
oestrogen) in various areas of the brain has shown highest postmenopausal women rather than women complaining of
levels in the medial preoptic area, medial and basal hypo- sexual dysfunction.
thalamus and the substantia nigra30. Whether testosterone Women of all ages are currently requesting (and in some
needs to be converted in brain cells to both dihydrotestos- centres being given)43,44 testosterone supplementation in
terone via 5a hydroxylase and aromatised to oestradiol to various forms, without safety and efficacy data, and with-
exert its action, as is necessary in rodents, is not clear. The out the documentation that sexual desire and responsive-
practice of giving women aromatase inhibitors after a ness correlate with testosterone (or any other androgen)
diagnosis of breast cancer, may clarify this question. levels, other than those in the supraphysiological range.
Adrenal androgen is nevertheless sufficient for many Additional basic requirements include a testosterone assay
women. Clearly, the sensitivity of androgen receptors sensitive and accurate in the female range. More data are
(currently not measurable in clinical practice) is likely as needed of androgen levels in women of different ages (and
important as blood levels. health status), who do not have sexual dysfunction. Scien-
tific studies of testosterone replacement in peri and na-
turally postmenopausal women are needed, including the
Women with gradual loss of testosterone use of local testosterone in restoring vulval congestion
without necessarily achieving high normal premenopausal
The usual slow decline in testosterone levels from the testosterone levels systemically. Replacing testosterone in a
early 40s onwards appears to be far less often associated pattern that varies through the four-week period to mimic a
with unresponsiveness to formerly effective stimuli31. younger premenopausal ovulating cycle would be a useful
Beginning in the early 40s, some but not all studies strategy to study.
indicate testosterone levels decline progressively but not Discussion of the alternative cycle is helpful in identify-
usually to undetectable levels32,33. Although this slow ing the subgroup of menopausal women who previously
decline appears often to be asymptomatic, certainly some experienced conscious intrinsic sexual desire, and were less
peri and naturally postmenopausal women do complain of aware of beginning a sexual experience from a state of
loss of genital response and mental response comparable sexual neutrality. This particular subgroup acknowledges
with the loss experienced by some women with surgical that their sexual response can still occur but they are
menopause. For both groups of women, loss of energy may dissatisfied; they mourn the loss of their former ‘hunger’,
also be linked to the androgen lack34. Unfortunately, that appeared to be spontaneous rather than triggered.
scientific study of androgen replacement therapy in women Fortunately, adaptation to the need for creating a sexual
is minimal35. We lack both efficacy and safety data. Prior
to the study by Shifren et al.29, there were minimal data on
physiological as opposed to pharmacological doses of
prescribed androgen. Sexual benefit was seen in the oes-
trogen versus oestrogen plus testosterone controlled study
by Davis et al.36 using testosterone implants designed to
give high normal premenopausal testosterone levels; but
interestingly, the women were recruited for bone density
reasons rather than sexual dysfunction. Non-physiological
androgen administration (i.e. methyl testosterone), acting
via the androgen receptor and via reduction of sex hormone
binding globulin (SHBG), has also been associated with
sexual benefit in postmenopausal women but the dose
needed (2.5mg) is associated with unwanted reduction of
high density lipoprotein cholesterol37. Tibolone has oes-
trogenic properties as well as some androgenic activity via
its D4 metabolites and its ability to reduce SHBG. It also
has been shown to improve the effects of lack of oestrogen Fig. 7. The repercussions of infertility on the woman’s sex response cycle.
context (and removing their often self-imposed label of A much-needed area of psychosexual research is the dis-
dysfunction) is possible. connection between subjective arousal and genital conges-
tive response.
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