Incontinence, Nocturia, Overactive Bladder
Conditions
Keywords
Overactive Bladder Syndrome, Female Urinary Microbiome, Urinary Urgency, Estrogen, Nocturia, Incontinence
Brief summary
This purpose of this study is to understand the types of bacteria that are in the bladder and vagina in patients with overactive bladder (OAB) symptoms and understand if the types of bacteria change when with the use of estrogen in the vagina. The investigators are also trying to understand how estrogen influences the body's ability to make substances called peptides that can kill bacteria.
Detailed description
Overactive bladder (OAB) syndrome is characterized by the symptom complex of urinary urgency, usually with associated frequency and nocturia, with or without urgency urinary incontinence in the absence of infection or other pathology. OAB affects approximately 31% of women over the age of 65. Vaginal estrogen, a well-documented treatment for OAB in hypoestrogenic women, has been shown to improve symptoms of frequency, urgency and urgency urinary incontinence (UUI). Several theories have been proposed to explain the mechanism underlying estrogen's effect on lower urinary tract symptoms (LUTS). The investigators propose that estrogen treatment influences bacterial communities (microbiomes) in the vagina and bladder and alters urothelial and vaginal (AMPs) thereby improving OAB symptoms in hypoestrogenic women. Long-standing medical dogma has been replaced by clear evidence that a female urinary microbiome (FUM) exists. The investigators recently reported that the FUM in women without OAB is less diverse than the FUM of women with OAB. The investigators soon will report that FUM status stratifies women with OAB into treatment response groups and women with less diverse FUMs are more likely to respond to anti-cholinergic OAB therapy (Thomas-White et al., in preparation). This suggests that the FUM is a factor in lower urinary tract symptoms (LUTS) and that FUM diversity contributes to LUTS and treatment response, like the vaginal microbiome and its contribution to vaginal symptoms. In hypoestrogenic women, the vaginal microbiome shifts from low diversity communities, commonly dominated by Lactobacillus, to more diverse communities dominated by anaerobes; this change can be reversed with estrogen treatment. Since the FUM of women with OAB includes bacteria similar to those of the vaginal microbiome (e.g. Lactobacillus, Gardnerella, and diverse anaerobes), the investigators reason the FUM would respond similarly to estrogen and become less diverse. Although transvaginal medications likely alter nearby bacterial niches (e.g. the bladder), no study has reported the urinary microbiomic response to vaginal estrogen. While almost nothing is known about urinary/vaginal microbiome interplay, even less is known about immune response modulation in the bladder and vagina. However, estrogen reduces the subsequent urinary tract infection (UTI) rate in hypoestrogenic women affected by recurrent UTI, and estrogen induces urothelial antimicrobial peptide (AMP) expression. Since AMPs exhibit microbicidal activity, stimulate inflammation, and facilitate epithelial barrier homeostasis, estrogen may work through AMPs as mediators to optimize microbial equilibrium. The investigators hypothesize that, following estrogen treatment of hypoestrogenic women with OAB, symptom improvement will be associated with 1) reduced FUM diversity, 2) alteration of other FUM characteristics and 3) increased AMP levels. The investigators propose two specific aims: Aim 1: To compare pelvic floor microbiome (PFM) diversity and AMP levels before and after estrogen treatment in hypoestrogenic women with OAB symptoms. Aim 2: Determine if FUM characteristics correlate with OAB symptoms.
Interventions
Participants are provided a vaginal estrogen cream (i.e., Premarin Cream® 0.625 mg conjugated estrogen/gram) and instructed to use 0.5 grams with an applicator twice weekly for 12 weeks.
Sponsors
Study design
Eligibility
Inclusion criteria
* Women who present with symptoms of OAB, defined as a condition characterized by urgency, with or without urgency incontinence, usually with frequency and nocturia in the absence of obvious pathology or infection \[9\], with atrophic vaginitis. * Postmenopausal by history (i.e., defined as twelve months or greater since last menstrual period), surgical menopause with removal of bilateral ovaries, or age over 55 with a previous hysterectomy (without removal of bilateral ovaries). * English language skills sufficient to complete questionnaires * Clinical indication for vaginal estrogen use (i.e., hypoestrogenic findings on physical examination) * Patients not currently receiving vaginal estrogen therapy
Exclusion criteria
* Patients currently on systemic hormone replacement therapy (HRT) or who have been on HRT within the past three months * Patients with current diagnosis or history of estrogen dependent malignancies (e.g., breast or endometrial malignancies) * Contraindication or allergy to estrogen therapy * Insufficient English language skills to complete study questionnaires * Women with active, standard culture positive urinary tract infection at baseline assessment, or those with a urine dip positive for leukocytes and nitrates on straight catheterized sample. * Patients who have received antibiotics within the past two weeks * Patients with stage 3 or 4 pelvic organ prolapse based on the pelvic organ prolapse quantitation system (POP-q) * Patients unwilling to use vaginal estrogen preparation * Patients currently on anticholinergic medications or who have received anticholinergic medications within the past three months * Patients who have previously failed two medications for treatment of OAB or have previously received more advanced treatment for OAB including intra-vesicle botulinum toxin injections, posterior tibial nerve stimulation, or implantation of a sacral neuromodulator * Patients wishing to start anticholinergic medication at the initial encounter * Undiagnosed abnormal genital bleeding * Active deep vein thrombosis (DVT), pulmonary embolism (PE), or a history of these conditions * Active arterial thromboembolic disease (for example, stroke and MI), or a history of these conditions * Known liver dysfunction or disease * Known protein C, protein S, or antithrombin deficiency or other known thrombophilic disorders
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Change in the Relative Abundance of Lactobacillus | 0, 12 weeks | The relative abundance of Lactobacillus to total microbes per sample was measured before and after treatment. The within-participant change in relative abundance of Lactobacillus was calculated subtracting pre-treatment from post-treatment. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Change in OAB Symptoms | 0, 12 weeks | OAB symptoms are measured using the Overactive Bladder Questionnaire (OAB-q). The OAB-q symptom score ranges from 0-100 with higher scores indicating greater symptom severity. A change score is calculated as the post-treatment score minus the pre-treatment score. |
| OAB Symptoms Associated With Relative Abundance of Lactobacillus | 0, 12 weeks | The investigators will determine whether change in OAB symptoms using the OAB-q before and after treatment is associated with the change in participants' relative abundance of Lactobacillus before and after treatment. The OAB-q symptom score ranges from 0-100 with higher scores indicating greater symptom severity. |
| Change in Urothelial Antimicrobial Peptide (AMP) Levels | 0, 12 weeks | The investigators will compare participants' AMP activity levels before and after treatment. AMP activity level is measured as the diffusion of AMPs in bacterial agar from the center of the well to which the patient's purified biological sample is applied. The diffusion of AMPs in the agar results in the killing of bacteria and a clearing around the well. This clearing of bacterial growth is measured in square millimeters and then normalized to the total peptide concentration. Change is calculated as the post-treatment AMP activity level minus the pre-treatment AMP activity level. |
| Change in OAB Symptoms Associated With Change in AMP Levels | 0, 12 weeks | The investigators will determine whether any change in OAB symptoms using the OAB-q before and after treatment is associated with the change in participants' AMP levels before and after treatment. |
Countries
United States
Participant flow
Participants by arm
| Arm | Count |
|---|---|
| Estrogen Arm The intervention for this study is an estrogen cream (i.e., Premarin Cream®). Women in this study will receive this estrogen cream and apply it to their vagina twice weekly for 12 weeks
Estrogen Cream: Participants are provided a vaginal estrogen cream (i.e., Premarin Cream® 0.625 mg conjugated estrogen/gram) and instructed to use 0.5 grams with an applicator twice weekly for 12 weeks. | 35 |
| Total | 35 |
Baseline characteristics
| Characteristic | Estrogen Arm |
|---|---|
| Age, Continuous | 69 years |
| Body mass index | 28.5 kg/m^2 |
| Number of vaginal deliveries | 3 deliveries |
| Ovaries removed Ovaries not removed | 26 Participants |
| Ovaries removed Ovaries removed | 7 Participants |
| Ovaries removed Unknown | 2 Participants |
| Postvoid residual | 40 mL |
| Previous incontinence surgery No previous incontinence surgery | 33 Participants |
| Previous incontinence surgery Previous incontinence surgery | 2 Participants |
| Prior hysterectomy No prior hysterectomy | 19 Participants |
| Prior hysterectomy Prior hysterectomy | 16 Participants |
| Race/Ethnicity, Customized African American | 8 Participants |
| Race/Ethnicity, Customized Asian | 1 Participants |
| Race/Ethnicity, Customized Hispanic | 2 Participants |
| Race/Ethnicity, Customized Other | 1 Participants |
| Race/Ethnicity, Customized White | 23 Participants |
| Region of Enrollment United States | 35 participants |
| Sex: Female, Male Female | 35 Participants |
| Sex: Female, Male Male | 0 Participants |
| Stage of prolapse 0 | 9 Participants |
| Stage of prolapse 1 | 11 Participants |
| Stage of prolapse 2 | 15 Participants |
Adverse events
| Event type | EG000 affected / at risk |
|---|---|
| deaths Total, all-cause mortality | 0 / 35 |
| other Total, other adverse events | 0 / 35 |
| serious Total, serious adverse events | 0 / 35 |
Outcome results
Change in the Relative Abundance of Lactobacillus
The relative abundance of Lactobacillus to total microbes per sample was measured before and after treatment. The within-participant change in relative abundance of Lactobacillus was calculated subtracting pre-treatment from post-treatment.
Time frame: 0, 12 weeks
Population: Participants with catheterized urine samples taken pre-treatment and post-treatment
| Arm | Measure | Value (MEAN) | Dispersion |
|---|---|---|---|
| Estrogen Arm | Change in the Relative Abundance of Lactobacillus | 0.275 proportion of total microbes | Standard Deviation 0.345 |
Change in OAB Symptoms
OAB symptoms are measured using the Overactive Bladder Questionnaire (OAB-q). The OAB-q symptom score ranges from 0-100 with higher scores indicating greater symptom severity. A change score is calculated as the post-treatment score minus the pre-treatment score.
Time frame: 0, 12 weeks
Population: All participants who completed the OAB symptoms questionnaire at baseline and after treatment
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Estrogen Arm | Change in OAB Symptoms | -21 units on a scale |
Change in OAB Symptoms Associated With Change in AMP Levels
The investigators will determine whether any change in OAB symptoms using the OAB-q before and after treatment is associated with the change in participants' AMP levels before and after treatment.
Time frame: 0, 12 weeks
Population: Assays were performed on a subset of participants due to resource constraints.
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Estrogen Arm | Change in OAB Symptoms Associated With Change in AMP Levels | -1 Spearman's rho |
Change in Urothelial Antimicrobial Peptide (AMP) Levels
The investigators will compare participants' AMP activity levels before and after treatment. AMP activity level is measured as the diffusion of AMPs in bacterial agar from the center of the well to which the patient's purified biological sample is applied. The diffusion of AMPs in the agar results in the killing of bacteria and a clearing around the well. This clearing of bacterial growth is measured in square millimeters and then normalized to the total peptide concentration. Change is calculated as the post-treatment AMP activity level minus the pre-treatment AMP activity level.
Time frame: 0, 12 weeks
Population: Assays were performed on a subset of participants due to resource constraints.
| Arm | Measure | Value (MEDIAN) |
|---|---|---|
| Estrogen Arm | Change in Urothelial Antimicrobial Peptide (AMP) Levels | 0.14 normalized bacterial growth inhibition |
OAB Symptoms Associated With Relative Abundance of Lactobacillus
The investigators will determine whether change in OAB symptoms using the OAB-q before and after treatment is associated with the change in participants' relative abundance of Lactobacillus before and after treatment. The OAB-q symptom score ranges from 0-100 with higher scores indicating greater symptom severity.
Time frame: 0, 12 weeks
Population: All participants who completed the OAB symptoms questionnaire and have catheterized urine samples at baseline and after treatment
| Arm | Measure | Value (NUMBER) |
|---|---|---|
| Estrogen Arm | OAB Symptoms Associated With Relative Abundance of Lactobacillus | -0.32 Spearman's rho |