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Investigation of the Effect of the Female Urinary Microbiome on Incontinence

Investigation of the Effect of the Female Urinary Microbiome on Incontinence

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02835846
Acronym
FUM
Enrollment
35
Registered
2016-07-18
Start date
2016-09-30
Completion date
2018-05-31
Last updated
2021-09-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Incontinence, Nocturia, Overactive Bladder

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 Long-standing medical dogma has been replaced by clear evidence that a female urinary microbiome (FUM) exists.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

Kimberly-Clark Corporation
CollaboratorINDUSTRY
Loyola University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
No

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

MeasureTime frameDescription
Change in the Relative Abundance of Lactobacillus0, 12 weeksThe 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

MeasureTime frameDescription
Change in OAB Symptoms0, 12 weeksOAB 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 Lactobacillus0, 12 weeksThe 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) Levels0, 12 weeksThe 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 Levels0, 12 weeksThe 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

ArmCount
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
Total35

Baseline characteristics

CharacteristicEstrogen Arm
Age, Continuous69 years
Body mass index28.5 kg/m^2
Number of vaginal deliveries3 deliveries
Ovaries removed
Ovaries not removed
26 Participants
Ovaries removed
Ovaries removed
7 Participants
Ovaries removed
Unknown
2 Participants
Postvoid residual40 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 typeEG000
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

Primary

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

ArmMeasureValue (MEAN)Dispersion
Estrogen ArmChange in the Relative Abundance of Lactobacillus0.275 proportion of total microbesStandard Deviation 0.345
Secondary

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

ArmMeasureValue (MEDIAN)
Estrogen ArmChange in OAB Symptoms-21 units on a scale
Secondary

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.

ArmMeasureValue (NUMBER)
Estrogen ArmChange in OAB Symptoms Associated With Change in AMP Levels-1 Spearman's rho
Secondary

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.

ArmMeasureValue (MEDIAN)
Estrogen ArmChange in Urothelial Antimicrobial Peptide (AMP) Levels0.14 normalized bacterial growth inhibition
Secondary

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

ArmMeasureValue (NUMBER)
Estrogen ArmOAB Symptoms Associated With Relative Abundance of Lactobacillus-0.32 Spearman's rho

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026