Hmong Microbiome ANd Gout, Obesity, Vitamin C (HMANGO-C)

Sponsor
University of Minnesota (Other)
Overall Status
Recruiting
CT.gov ID
NCT04938024
Collaborator
(none)
180
1
3
28.1
6.4

Study Details

Study Description

Brief Summary

Investigators seek to quantify the impact of vitamin C on patient outcomes, including serum urate level, gout-related symptoms, and obesity (measured by BMI) in both healthy Hmong adults and in Hmong patients with hyperuricemia (HU) and/or gout; identify associations between individuals' taxonomic and functional patterns of gut microbiota and its impact on the serum urate-lowering effect of vitamin C; compare taxonomic and functional patterns of gut microbiota between people with HU and/or gout and people without HU and gout; and identify associations between individuals' taxonomic and functional patterns of gut microbiota and self-reported acute gout trigger foods.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Vitamin C
N/A

Detailed Description

Gout, caused by chronic elevation of serum urate (SU), is the most common form of inflammatory arthritis worldwide. About 3.9% of adults in the U.S. suffer from gout and prevalence is even higher in certain ethnicities. Factors that may influence SU include patients' characteristics (gender, weight, renal function, etc.), genetics, and diet. Foods and beverages that have shown positive association with HU and gout are alcohol (particularly beer), purine-rich foods, red meat, seafood, and sugar-sweetened drinks, while inverse association has been found with dairy intake such as skimmed milk and low-calorie yoghurt, coffee and vitamin C. The gut microbiota composition and function have been linked to common chronic human disorders, such as obesity, diabetes, non-alcoholic fatty liver disease, and rheumatoid arthritis. Intestinal microbiota of gout patients were also found highly distinct from healthy individuals in both organismal and functional structures from a small study conducted in China. Strategies to use personal microbiome features to predict glucose response to specific food have been proposed. However, little is known about the impact of microbiota on food and urate-lowering therapy (ULT). The translational significance of a microbiota-guided approach to select appropriate foods and medications that could prevent the elevation of SU for individuals with gout or at high risk for gout is significant. The Hmong are a unique Asian sub-population. Hmong men exhibit a 2-fold higher prevalence of gout, manifesting it earlier in life and experiencing up to 5-fold increased risk of gout-associated complications, compared to non-Hmong in the US. This could lead to higher rates of cardiometabolic diseases (e.g. hypertension, renal disease, type 2 diabetes [T2DM]), which significantly impact morbidity, mortality and healthcare costs. Accordingly, the investigators seek to quantify the impact of vitamin C on patient outcomes, including serum urate level, gout-related symptoms, and obesity (measured by BMI) in both healthy Hmong adults and in Hmong patients with hyperuricemia (HU) and/or gout; identify associations between individuals' taxonomic and functional patterns of gut microbiota and its impact on the serum urate-lowering effect of vitamin C; compare taxonomic and functional patterns of gut microbiota between people with HU and/or gout and people without HU and gout; and identify associations between individuals' taxonomic and functional patterns of gut microbiota and self-reported acute gout trigger foods.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
180 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Hmong Microbiome ANd Gout, Obesity, Vitamin C (HMANGO-C)
Actual Study Start Date :
Mar 28, 2021
Anticipated Primary Completion Date :
Aug 1, 2023
Anticipated Study Completion Date :
Aug 1, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: People with hyperuricemia (HU) or gout without urate-lowering therapy (ULT)

Participants with HU or gout who are not treated with ULT will take 500 mg of vitamin C twice daily for 8 weeks.

Dietary Supplement: Vitamin C
Vitamin C is a commercially available over-the-counter food supplement.
Other Names:
  • L-ascorbic acid
  • Experimental: People with hyperuricemia (HU) or gout with urate-lowering therapy (ULT)

    Participants with HU or gout who are treated with ULT will take 500 mg of vitamin C twice daily for 8 weeks.

    Dietary Supplement: Vitamin C
    Vitamin C is a commercially available over-the-counter food supplement.
    Other Names:
  • L-ascorbic acid
  • Active Comparator: People without hyperuricemia (HU) or gout without urate-lowering therapy (ULT)

    Participants without HU or gout who are not treated with ULT will take 500 mg of vitamin C twice daily for 8 weeks.

    Dietary Supplement: Vitamin C
    Vitamin C is a commercially available over-the-counter food supplement.
    Other Names:
  • L-ascorbic acid
  • Outcome Measures

    Primary Outcome Measures

    1. Change in serum urate [8 weeks]

      Serum urate levels (mg/dL) will be measured from baseline to end, and the absolute difference will be reported.

    Secondary Outcome Measures

    1. Change in Gout Assessment Questionnaire 2.0 score [8 weeks]

      The Gout Assessment Questionnaire 2.0 (GAQ2.0) contains 25 items covering the following domains: gout overall concern, medication side effects, perception of unmet needs, wellbeing during acute gout attack, and concerns during gout attack. Items are rated on a 5-point likert scale. Total scores range from 25 to 125 with higher scores indicating more gout symptoms.

    2. Change in body mass index (BMI) [8 weeks]

      Change in body mass index (BMI) from baseline to end. BMI is calculated as body weight (in kg) divided by height (in cm) squared. BMI is reported in kg/m^2, and the change will be reported as an absolute value.

    3. Change in Swollen Joint Count (44 Joints) [8 weeks]

      Change in gout-related symptoms will be measured from baseline to end using the Swollen Joint Count (44 Joints) post-administration of vitamin C. Scores range from 0-44 with higher scores indicating more swollen joints.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Self-identified Hmong persons whose both parents are Hmong, with and without hyperuricemia (serum urate (UA) ≥ 6.8 mg/dL ) and/or gout (defined by 2020 American College of Rheumatology Guideline for the Management of Gout) are eligible for the study.

    • For those with gout, participants qualify if they have serum UA ≥ 6.8 mg/dL based on the baseline measurement or serum UA < 6.8 mg/dL based on the baseline measurement with at least 1 episode of peripheral joint or bursal swelling, pain, or tenderness (acute gout flare) in their lifetime, (with or without urate-lowering therapy)

    Exclusion Criteria:
    • Allergy or sensitivity to vitamin C

    • Diagnosis/history of:

    • Gastrointestinal surgery including colectomy, ileectomy, and gastrectomy

    • Inflammatory bowel disease

    • Auto-immune disease

    • Type I diabetes mellitus

    • Severe kidney disease (i.e., on dialysis)

    • End-stage liver disease (i.e. cirrhosis)

    • Glucose-6-phosphate dehydrogenase deficiency, (due to increased bleeding risk in those with G6PD deficiency when receiving vitamin C)

    • Pregnant or breastfeeding persons

    • Current use of:

    • Antibiotics

    • Probiotics supplement

    • Ketogenic diet

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 University of Minnesota Minneapolis Minnesota United States 55455

    Sponsors and Collaborators

    • University of Minnesota

    Investigators

    • Principal Investigator: Robert J Straka, PharmD, FCCP, Univeristy of Minnesota Department of Experimental and Clinical Pharmacology

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Minnesota
    ClinicalTrials.gov Identifier:
    NCT04938024
    Other Study ID Numbers:
    • PHARM-2020-29354
    First Posted:
    Jun 24, 2021
    Last Update Posted:
    Jan 6, 2022
    Last Verified:
    Jan 1, 2022
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 6, 2022