Overview
The goal of this clinical trial is to test the effect of a supplement called MitoQ (mitoquinol mesylate) on bladder symptoms such as urgency and frequency in women aged 50-75 years old who have the metabolic syndrome. The main questions it aims to answer are:
- Is the study design feasible and acceptable to participants?
- Do participants taking the study drug get any improvement to their bladder symptoms compared to participants taking a placebo (a look-alike substance that contains no drug)?
Participants will take 2 capsules of the study drug every morning for 4 months, answer many questions about their health including questions about their bladder health, perform physical and cognitive testing, give blood and urine samples, collect urine over 24 hour periods 3 times over the 4 months of the study, complete 3 day bladder diaries about how much they drink and void, undergo electrocardiograms, have their vitals and measurements (weight, height, waist circumference) taken, participate in 4 visits to the clinical research area and participate in many phone calls of varying length. Researchers will compare participants who were taking capsules containing MitoQ and participants taking capsules not containing MitoQ to see if MitoQ improves their bladder symptoms (urgency, frequency, nocturia, incontinence, etc.)
Description
Both aging and the metabolic syndrome are risk factors for lower urinary tract symptoms (LUTS, including urgency, frequency, nocturia (nighttime urination), and incontinence). This study aims to test whether an oral supplement that targets biological aging pathways can improve lower urinary tract symptoms (LUTS) in women aged 50-75 with the metabolic syndrome (a cluster of conditions that occur together, increasing the risk of heart disease, stroke and type 2 diabetes). MitoQ, a strong mitochondrial-targeted antioxidant molecule, has been shown to target mitochondrial dysfunction, oxidative stress, inflammation, and endothelial dysfunction, all aging pathways that are also found to be dysregulated in conditions that cause LUTS such as the overactive bladder syndrome. Women aged 50-75 who have the metabolic syndrome per the new International Diabetes Federation (IDF) definition and have had urinary urgency for at least 3 months will be invited to participate in the study. They will be screened by phone for major study inclusion/exclusion criteria and then invited for an in-person screening visit where blood will be drawn and measurements taken to confirm eligibility. Once eligible, participants will be randomly assigned to MitoQ or placebo (2MitoQ:1placebo) and asked to take 2 capsules daily (40mg MitoQ total) 30 minutes before breakfast for 4 months. Participants will come back for study visits at 8 and 16 weeks, and will receive two study data collection phone calls at 4 and 12 weeks, where they will answer questions about their bladder. There will be many other shorter phone calls throughout the study to check for adherence and adverse events. In addition to questionnaires assessing bladder function, participants will undergo tests of frailty, physical function, cognitive function and asked many questions about their health and medication. We will also draw blood for safety assessment and to measure aging molecules in the blood at each visit and see whether they change with treatment. Urine will also be collected at each study visit and participants will be asked to collect urine at home (first morning and 24-hour urine) and bring it to each of their study visits, which will be used for measuring aging molecules and testing how they change with the study drug. Participants will also fill out three-day voiding diaries to provide information about their voiding and LUTS.
Eligibility
Inclusion Criteria:
- Having the metabolic syndrome per the new International Diabetes Federation's 2006 consensus worldwide definition for metabolic syndrome.
- Having urgency with or without other urinary symptoms for at least 3 months.
- Women 50-75 years with metabolic syndrome and LUTS as defined above.
- Speak, read and understand English
- Willingness to provide consent and participate in all aspects of the trial including randomization to the intervention group
Exclusion Criteria:
- Frailty, defined as meeting 3 of 5 frailty indicators of the Fried Frailty Phenotype
- History of severe renal impairment and/or estimated glomerular filtration rate, eGFR ≤ 70 mL/min/1.73m2
- Excessive alcohol use (more than 14 alcoholic drinks/week)
- Clinical/laboratory evidence of hepatic disease (via medical history and/or Aspartate aminotransferase (AST) and/or alanine aminotransferase (ALT) ≥ 3 times upper limit of normal at screening)
- Diabetes mellitus (glycated hemoglobin or hemoglobin A1c, HbA1c >6.5%)
- Unwilling or unable (due to significant cognitive impairment) to provide informed consent.
- Terminal illness with life expectancy less than 12 months
- Advanced neurological disorder (Alzheimer's, Parkinson's, Amyotrophic lateral sclerosis (ALS), multiple sclerosis (MS), dementia, seizures)
- A score of 30 or less on the modified Telephone Screening of Cognitive Status administered during the in-person screening visit.
- Cancer or history of cancer.
- A history of gastric ulcers.
- Abnormal findings on endoscopy.
- Recent (within the last 2 weeks) or current chronic use of NSAIDs or other drugs or agents with the potential for gastric mucosal toxicity (except for daily use of baby aspirin or famotidine for which participants will not be excluded). Sporadic use of non-steroidal anti-inflammatory drugs (NSAIDs) will not be an exclusion criterion.
- Significant co-morbid disease (severe chronic obstructive pulmonary disease, active rheumatologic diseases, chronic infection (human immunodeficiency virus (HIV), tuberculosis), severe congestive heart failure (NYHA class 4), myocarditis, etc)
- Myocardial infarction, stroke or hospitalization for heart failure in the last 12 months
- Corrected QT interval, QTc >460 ms (milliseconds) at screening on electrocardiogram (ECG)
- Prior diagnosis of ventricular arrhythmia (e.g., ventricular tachycardia, ventricular fibrillation, torsades de pointes)
- Severe active psychiatric disorder (e.g. bipolar, schizophrenia)
- Unable to complete physical performance testing due to medical conditions (at discretion of the PI)
- Unintentional weight loss >15 lbs in past 12 months
- Immunosuppressive disorders or taking immunosuppressive medications (including oral prednisone > 10mg/day)
- Sub-cerebellar lesions
- Subjects must not be on warfarin or other blood thinning medications or have a known bleeding disorder.
- Conditions that might interfere with clinical diagnosis (such as pelvic organ prolapse ≥ stage 2, pelvic radiotherapy, any concurrent condition that could cause incontinence, hematuria, vaginitis, neurogenic lower urinary tract dysfunction); chronic pelvic pain syndrome, interstitial cystitis/bladder pain syndrome, pelvic malignancy.
- Active urinary tract infection (UTI).
- Recent urologic procedure (<6 months).
- Clean intermittent catheterization or indwelling catheter
- Current participation in another interventional study
- Pregnancy and nursing
- Subjects must not have used antibiotics for at least 3 weeks prior to visit 1, received a vaccination in the 2 weeks prior to visit 1 or used medicine that alters the immune response (eg high dose corticosteroids) in the 6 months prior to visit 1.
- Subjects must not have had an acute infection in the 3 weeks prior to visit 1 or had a major severe illness or been hospitalized in the 3 months prior to visit 1.
- Subjects must not be on or have taken anti-muscarinics or β3- adrenoreceptor agonists for 3 weeks prior to visit 1.