Fig. 15.1
Schematic of the innervation of the vulva. A: Anterior cutaneous branches of the iliohypogastric nerve; B: Anterior labial branches of the ilioinguinal nerve; C: Genitofemoral nerve (both the genital and femoral braches); D: Dorsal nerve of the clitoris (continuation of pudendal nerve shown as dashed lines deeper in the muscles of the urogenital diaphragm.) Note: the course of the specified nerves is delineated based on quantitative sensory testing and selective nerve block in this individual patient
15.3 Quantitative Sensory Testing
QST was traditionally used to quantify sensory function in healthy people and in patients at risk for neurological impairment [1]. It also serves as a tool to investigate factors that affect pain perception [2–4]. In QST, a measurable stimulus is applied to the skin and the subject or patient reports his or her perception of it. The method employs calibrated instruments to deliver known intensities of physical stimuli, for example, mild electric current (by means of surface electrodes), temperature (via electric thermodes with controlled surface temperatures), touch (using filaments whose bending force depends on diameter and length), pressure (exerted by spring-loaded devices), and vibration (using tuning forks or vibrators that deliver sinusoidal stimuli at a given frequency). Stimulus of a given intensity is applied, and the subject reports whether or not the stimulus is perceived (or, in pain studies, whether or not the stimulus elicits pain). The lowest intensity that is perceptible (or, if pertinent, painful) is the detection threshold.
Two general methods are employed to determine these thresholds: the method of limits and the method of levels. With the method of limits, the stimulus is progressively increased and the subject declares when it first becomes perceptible. With the method of levels, stimulus of a defined intensity is applied and then increased or decreased by specific increments depending on whether or not the subject perceives it (protocols may differ in terms of the number of consistent responses required to progress upward or downward in stimulus intensity).
With the method of limits, sensory information is processed neurologically at the same time as the stimulus intensity is being changed. The inherent response lag leads to a small error in threshold measurement; consequently, thresholds measured with the level of limits skew higher than those measured with the method of levels [5, 6]. Moreover, the rate of change of the stimulus affects thresholds obtained by the method of limits.
The method of levels is known as “forced-choice,” as the subject must declare or “choose” whether or not the stimulus is perceived. Because this method takes longer and is more repetitive, error can result if the subjects become fatigued or distracted as the test proceeds.
Experimental variables such as the application site, the surface area of contact, the frequency of the stimulus (in the case of vibration), and the rate of change of stimulus intensity will affect the absolute value of thresholds measured. Consequently, the absolute values measured are a function of the experimental conditions employed and the lack of standardization complicates comparisons between experiments. Although this chapter reviews a number of published studies, it focuses on the relative thresholds assessed within experiments to draw conclusions about variables that affect sensory perception.
15.4 Sensory Thresholds on Extragenital Sites
Research on extragenital sites provides some general perspective on sensory perception thresholds. One general finding is that sensitivity to touch, vibration, and thermal stimuli varies by anatomical site. For example, the hands appear to be more sensitive to touch, and especially to vibration, than the feet [1, 7].
Besides the anatomical location itself, advancing age appears a most significant effect on perception of mechanical stimuli. For example, the sensitivity of the hands and feet to touch, skin indentation, and vibration declines with age. This decline becomes apparent by the fifth decade, progresses exponentially after age 65 or 70 [8, 9], and is more severe for the lower than the upper extremities [9, 10, 5]; the latter may reflect the longer distance of the neural pathway that the sensory input must travel.
By contrast, evidence for an age-related decline in the perception of thermal stimuli is inconsistent [5, 7, 8, 11]; some studies found an age-related decline, but several show no change. The disparate results may relate to the experimental conditions employed in each study: thermal stimuli are perceived more easily when a larger skin surface area is stimulated [11].
Gender differences in sensory perception have been found inconsistently. With respect to mechanical stimuli, several studies found no gender differences in perception thresholds on either the forehead [1], the hand and forearm [11], or the foot [10], regardless of age. However, a US study of 350 people found that, specifically among those aged over 50, women were more sensitive to vibration on the dorsum of the hands and feet than men [9]. A Taiwanese study among 484 subjects found vibratory thresholds to be lower in women than in men on the dorsum of foot, with no difference on the thenar eminence of the hand [5].
With respect to thermal stimuli, women exhibited higher sensitivity in a subset of studies. For example, a Dutch study found women to be more sensitive to thermal stimuli on the foot [7]; a Taiwanese study found women to be more sensitive to warm thresholds on both the hand and the dorsal surface of the foot [5]; and a British study found women to be more sensitive than men to heat and cold stimuli on the thenar eminence of the hand, the distal phalanx of the middle finger, and the dorsal surface of the forearm [11]. However, a North American study of 48 people found young men aged 19–31 to be more sensitive than women in the same age group to warm stimuli on the plantar surface of the feet, but found no difference on the thenar eminence of the hand [10]. The variability in results among different studies may relate to the range of the age groupings analyzed or to differences in the types of thermal probe employed.
In summary, anatomical sites vary in their sensitivity to sensory stimuli. Advancing age has been shown to reduce sensory perception of mechanical stimuli on extragenital sites, but limited evidence exists for age-related reductions in the perception of thermal stimuli. Some evidence exists that women are more sensitive than men to mechanical and thermal stimuli, but this may depend on the body site stimulated, the exposure conditions, and the age range of the subjects studied.
15.5 Sensory Perception on the Vulva
15.5.1 Quantitative Sensory Thresholds with Age and Menopausal Status
Published quantitative testing on vulvovaginal sensory thresholds is summarized in Table 15.1. Studies that compared vulvovaginal sensory perception to that of other anatomical sites suggest that the vulva and vagina are relatively less sensitive to sensory stimuli. For example, among 58 premenopausal women in the Netherlands, the labia majora, labia minora, and clitoris were less sensitive to mild electric current than the lower abdomen or the dorsum of the hand; the vaginal wall was the least sensitive site studied [12]. A Canadian study of 40 premenopausal women found the labium minus and the mucosa of the vulvar vestibule to be less sensitive than the forearm to filament touch and pressure, although the labium minus was more sensitive to pain than the forearm [13]. Similarly, a Canadian study of 13 premenopausal women found the vulvar vestibule to be less sensitive to filament touch and pressure than either the deltoid muscle, the forearm, or the thigh [14].
Table 15.1
Factors affecting vulvovaginal sensory thresholds
Population | N | Stimulus | Method | Anatomical location | Results | Comments | References |
---|---|---|---|---|---|---|---|
USA | |||||||
Healthy and neurologically impaired women | 38 | Pressure/touch | Pressure esthesiometer: Semmes-Weinstein monofilaments | Vulva/perineum | Significant loss of sensitivity to pressure/touch in postmenopausal women, hypoestrogenic women, women with vulvar atrophy, neurologically impaired women, and women with impaired sexual function | A clear effect of estrogen on vulvar sensitivity was demonstrated: menopause, nonuse of ERT, and vulvovaginal atrophy were associated with decreased sensitivity to pressure/touch | Doeland et al. [7] |
32 healthy | Method of limits: sequential application of pressure filaments to point of detection | Clitoral glans | Although the vulva has lower density of estrogen receptors than the vagina, effect of estrogen on touch sensitivity appears profound | ||||
5 impaired | Labium minus (right and left) | ||||||
Premenopausal (17) | Perineum (right and left) | ||||||
Postmenopausal (15) | Anal verge | ||||||
6 with ERT | Average vulvar score (all sites) | ||||||
9 without ERT | |||||||
Normoestrogenic (premenopausal and postmenopausal women on ERT) | |||||||
23 (Hypoestrogenic: (postmenopausal women not on ERT)) | |||||||
Impaired sexual function (by questionnaire) | |||||||
Postmenopausal hypoestrogenic women with lower genitourinary tract complaints (e.g., urinary incontinence, frequency, urgency, nocturia, vaginal atrophy) | 39 (30 completed study) | Pressure/touch | Protocol | Vulvar vestibule | Estradiol treatment significantly increased sensitivity of the vestibule to pressure/touch relative to placebo at 4 and 6 weeks | Mechanism of estrogen action on sensory function of the vestibule not known. Potential sensorineural targets may be C fibers or Merkel cells | Foster et al. [19] |
RCT: topical application of estradiol cream to the vulvar vestibule and vagina, nightly for 2 weeks, 3× weekly for 2 weeks, and 2× weekly for 2 more weeks, with or without pelvic muscle biofeedback | Vaginal wall | The greatest improvements occurred in women aged 70–79 years | |||||
Intervention groups | |||||||
(1) Active cream with biofeedback, (2) active cream with sham biofeedback, (3) placebo cream with biofeedback, (4) placebo cream with sham biofeedback | |||||||
Outcome measure | |||||||
Method of limits | |||||||
(1) Von-Frey monofilament thresholds (mN) at the vulvar vestibule | |||||||
(2) Maximum intravaginal pressure | |||||||
Women aged 20–78 | 58 | Vibration | Method of limits | Vulva | Age | Age affected both genital and peripheral sensation | Connell et al. [16] |
Examined variables of age, menopause, prior vaginal delivery, and history of neurological disorder | 10 (aged 20–29) | Commercially available 120 Hz biothesiometer | Clitoris | Vibratory sensation thresholds progressively increased with age at the vulva, clitoris, external urethral meatus, and ankle | Menopause affected genital sensation only | ||
13 (aged 30–39) | External urethral meatus | Menopause | |||||
17 (aged 40–49) | Right and left perineum | Sensitivity to vibration decreased after on genital sites but not on the ankle | |||||
8 (aged 50–59) | Medial right ankle | ||||||
10 (aged 60–79) | |||||||
Israel | |||||||
Healthy women aged 18–78 | 89 | Thermal (warm, cold) | Method of limits | Clitoris | Thermal thresholds with age | A smaller age effect on vibratory threshold was seen on the clitoris compared to the vagina | Vardi et al. [18] |
Vibratory | Thermal | Vagina | Sensitivity to warmth decreased with age at the clitoris but was constant on the anterior vagina | ||||
Cylindrical clitoral thermal probe, 25 mm diameter, with contact element on end; vaginal thermal probe with thermal contact on outer cylindrical surface (28 mm diameter) | Sensitivity to cold decreased with age at the anterior vagina but remained constant on the clitoris | ||||||
Vibratory | Vibratory thresholds with age | ||||||
Vibrameter, 100 Hz, amplitude 0–130 μm | Sensitivity to ascending vibration decreased with age on both the vagina and clitoris | ||||||
Method of limits (linear change): 1 ºC/s for thermal, 1 μm/s for vibratory | |||||||
Sweden | |||||||
Healthy women aged 27–44 | Aged 35–45 | Vibration | Method of limits | Clitoris | Vibratory thresholds by site | No change in sensitivity with menstrual cycle | Helstrom and Lundberg [15] |
n = 95 (examined once) | Commercially available 100 Hz vibrameter | Hands (dorsum) | The clitoris less sensitive than the hands but more sensitive than the feet | ||||
Aged 27–44 | Feet (dorsum) | ||||||
n = 8 (examined over the menstrual cycle) | |||||||
Turkey | |||||||
Women with diabetes (aged 39–50) and without diabetes (aged 35–42) | 30 with diabetes | Vibration | Method of limits | 9 genital sites | Genital sites, the nipples and fingers did not differ in sensitivity; the ears and lips were least sensitive extragenital sites | Absolute threshold values are highly dependent on type of equipment used | Connell et al. [16] |
Sexual function (questionnaire) and genital and extragenital sensory function assessed | 20 without diabetes | Commercially available 120 Hz biothesiometer, 300 mm2 surface area | Right and left labia majora, right and left labia minora, left and right side of clitoris, glans clitoris, and superior and inferior vaginal introitus | Women with diabetes were less sensitive to vibration at all anatomical sites tested | |||
500 ms stimulus duration | 14 extragenital sites | In women with diabetes, genital sites with the greatest deficit in sensitivity to vibration were the vaginal introitus, followed by the labia minora and clitoris | |||||
Right and left nipple, upper and lower lip, right and left ear lobe, first and second fingers of right and left hand, first and second toes of right and left feet | |||||||
Netherlands | |||||||
Healthy women | 60 | Electric current | Method of limits | Genital sites
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