Menopause Clinical Trial
Official title:
Vaginal Cytokines in Postmenopausal Women With Symptoms of Vulvovaginal Irritation
Many postmenopausal women suffer from vaginal symptoms such as dryness, itching, and painful intercourse. The underlying pathology is unknown. Since symptoms are comparable to those found in infectious vaginitis during the reproductive life stage, the investigators hypothesize that the vaginal milieu in symptomatic postmenopausal women is comparable to inflammation in vaginitis. The investigators therefore study vaginal cytokines in symptomatic and asymptomatic postmenopausal women.
Background
Vulvovaginal irritation is a frequent complaint among postmenopausal women who are not on
hormone therapy. Common symptoms include pruritus. Patients describe the irritation to be
similar to that of vulvovaginal candidiasis during their reproductive years. Clinical
improvement is seen with estrogen therapy. Most clinicians attribute the symptoms to vaginal
dryness secondary to estrogen deficiency. However, the underlying pathophysiology of this
clinical entity is not well defined. Since cytokines have been shown to play a significant
role in the pathogenesis of infectious vaginitis, and there is evidence to suggest that
estrogen influences cytokine production, we postulate that estrogen deficiency causes a
disturbance in the vaginal cytokine environment similar to that of infectious
vulvovaginitis.
Studies that investigate the pathogenesis of bacterial vaginosis, vulvovaginal candidiasis,
and vestibulitis have identified changes in the level of antibodies and cytokines in the
vagina during these processes. Donders and co-workers performed a study looking at the
correlation between disturbance of the lactobacillary flora, vaginal pH, interleukin 1beta
(IL-1b), and interleukin 8 (IL-8). Menopausal women were excluded from this study. Vaginal
pH, IL-8, and IL-1β concentrations increased linearly with decreasing lactobacilli by 4 to
10 fold. IL-1β concentration was most closely related to decreasing lactobacilli, and IL-8
concentration was most closely related to positive culture results. Regúlez, Garcia
Fernández, and co-worker performed a study to correlate the symptoms of vulvovaginal
candidiasis with vaginal IgE levels. Patients who have clinically overt vulvovaginal
candidiasis with classical symptomatology regardless of whether yeast or mycelia is
identified in fresh smear or culture had higher IgE levels in their vagina than asymptomatic
carriers or uninfected controls. This variation of host response has been proposed as one of
the mechanism why only some women with vulvovaginal candidiasis experience symptoms. This
concept of an imbalance between TH1 to TH2 cell reactivity with preference to the latter was
further suggested by Puccetti, Romani and Bistoni. In contrary to the findings by Regúlez,
Garcia Fernández and co-workers, Fidel, Ginsburg, and co-workers studied the
vaginal-associated immunity in women with recurrent vulvovaginal candidiasis and found that
Th-1 type response is increased. This area is certainly controversial and requires further
investigations. Since IL-6 has been suggested as one of the cytokines involved in Th-2 or
immediate-type hypersensitivity response, it will be of interest to study whether its level
is increased for patients with symptomatology. Foster and Hasday compared the levels of
IL-1b, and tumor necrosis factor-alpha (TNF-a) in perineal biopsy between women with vulvar
vestibulitis and pain-free subjects, and found an increase in both cytokines in the former
cases.
Estrogen has been shown to influence cytokine activity in the reproductive tract.
García-Velasco and Arici published a review article on chemokines and human reproduction. In
the article, the clinical relevance of chemokines in normal human reproductive events such
as ovulation, menstruation, and implantation were summarized. There was however little
information on their relevance in vaginal physiology. This is consistent with the little
information on the topic of vaginal physiology in the literature. A study by Franklin, and
Kutteh on the variation of immunoglobulins, and cytokines in cervical mucus in twelve women
on oral contraceptives (OCs), and fifteen naturally cycling women showed a definite
influence of exogenous and endogenous hormones on their levels. Cervical IgA, and IL-1b
levels in women taking Ortho Novum 777® paralleled the increasing dosage of oral
norethindrone, and the levels decreased after discontinuation of the oral contraceptive.
Cervical IL-1b, and IL-10 both peaked just before ovulation in natural cycles. Cervical
mucus IL-1b levels were found to correlate directly to changes in estrogen level during a
natural cycle. Vaginal cytokine levels were not investigated in the study. Al-Harth, and
co-workers measured cervicovaginal IL-1b, IL-4, IL-6, IL-8, IL-10, interferon-gamma
(INF-gamma), transforming growth factor-beta (TGF-b), tumor necrosis factor-alpha (TNF-a),
macrophage inflammatory protein-1alpha (MIP-1a) and TNG receptor II (TNFR II) during the
follicular, and luteal phases of ovulatory cycle of six premenopausal women. Cervicovaginal
IL-1b, and IL-6 were found to vary in level throughout the ovulatory cycle. Both IL-1b, and
IL-6 were 5-fold higher in the follicular phase than in the luteal phase. Other
cervicovaginal cytokines levels were not altered between the two phases. Plasma IL-8 level
was higher in the follicular than luteal phase. The investigators' hypothesis is that
postmenopausal estrogen deficiency causes changes in cytokine levels in the vagina similar
to that found with vaginal candidiasis and bacterial vaginosis. A common cytokine etiology
will account for the similarity of the symptomatology of infectious vaginitis and
postmenopausal vaginal irritation.
Unpublished preliminary data from a study done on premenopausal women by Ballagh in the
co-operating Howard and Georgeanna Jones Institute for Reproductive Medicine, Department of
Obstetrics and Gynecology, Eastern Virginia Medical School, Norfolk, Virginia, USA, has
shown that the mean levels of vaginal IL-1b and IL-8, as measured by ELISA, are higher in
the luteal phase than the follicular phase in naturally cycling women. The median level of
IL-1b is higher in the luteal phase than follicular phase but that of IL-8 is higher in the
follicular phase than luteal phase. These results show that vaginal interleukin environment
varies throughout the menstrual cycle to another. Women on oral contraceptive pills have
increased mean levels of both vaginal IL-1b, and IL-8 compared to naturally cycling women.
These data, though preliminary, support the theory that steroid hormone may play a role in
the regulation of vaginal cytokine levels.
Objective
The principal goal of this pilot study is to determine the correlation between
postmenopausal vulvovaginal irritative symptoms with vaginal interleukin levels. Cytokines
to be evaluated in vaginal lavage will include IL-1β, IL-6, IL-8 and TNF-α. Plasma
interleukin levels will be assessed concurrently, and compared to the vaginal levels to
ensure that the vaginal levels obtained are not a result of contamination by plasma
transudate. This study is thought to be the basis for a future randomised controlled trial
involving the treatment of symptomatic menopausal women for investigation whether the
resolution of the symptoms with e.g. estrogen and DHEA therapy is associated with a decrease
in the interleukin levels.
Methods
Screening Investigations (visit 1):
History and physical examination Vaginal pH, KOH prep, whiff test, and wet prep for
Trichomonas vaginalis Cervical sample for Neisseria gonorrhea & Chlamydia trachomatis assay
Enrollment Investigations (visit 2):
1. Vaginal pH
2. Vaginal smear for Nugent score and maturation index
3. Vaginal wet prep for Trichomonas vaginalis
4. Vaginal KOH prep and whiff test
5. Speculum examination and vaginal lavage
6. Leukocyte counts in vaginal samples
7. ELISA for serum IL-1b, IL-6, IL-8, TNF-a, IgE and estradiol
8. ELISA for IL-1b, IL-6, IL-8 TNF-a and IgE in vaginal lavage samples
;
Observational Model: Case Control, Time Perspective: Cross-Sectional
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