Impact of Diet on the Gut-Muscle Axis in Older Adults

Sponsor
Tufts University (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05549622
Collaborator
(none)
24
2
31

Study Details

Study Description

Brief Summary

Muscle health declines during aging. One factor that may impact muscle health is the community of bacteria that live in our intestines, but studies aimed at improving muscle health by targeting the gut in older adults are sparse. The primary goal of this study is to use a diet that is enriched in soluble fiber, which is exclusively utilized by gut bacteria to make substances that can impact muscle health, to improve muscle-related measures in older adults.

Condition or Disease Intervention/Treatment Phase
  • Other: Low-soluble fiber diet
  • Other: High-soluble fiber diet
N/A

Detailed Description

During aging, skeletal muscle mass and physical function decrease, whereas levels of lipids and adipocytes increase within and between muscle cells, thereby worsening muscle composition. As a result of these age-related changes, older adults are at a higher risk for frailty, falls and fracture, disability and hospitalization, and all-cause mortality. Accordingly, elucidation of mechanisms that underlie muscle mass, muscle composition, and physical function, and interventions that positively affect these variables will be important for addressing the public health priority of an improved quality of life and healthy aging in older adults.

The gut microbiome and its metabolic products are involved in mechanisms that impact skeletal muscle mass, muscle composition, and physical function, which has been defined as the gut-muscle axis. For example, muscle mass and physical function are reduced in animals that do not have a microbiome (germ-free mice), and in antibiotic-treated mice, an intervention that reduces gut bacterial content. Investigating further, gut bacteria-derived metabolites affect muscle mass, muscle composition, and physical function in young and aged animals, including positive effects for the short-chain fatty acids (SCFAs) acetate, propionate, and butyrate, and negative effects for indoxyl sulfate (IS) and para-cresol sulfate (PCS). Similarly, phenol sulfate (PS) and phenylacetylglutamine (PAG) are gut microbiome-derived metabolites that were associated with poor muscle composition and worse physical function in studies of older adult humans that were published by our group. Interestingly, higher colonic levels of SCFAs are associated with a lower pH, an important finding because growth of Enterobacteriaceae, a bacterial family that contains genes involved in the production of IS, PCS, PS, and PAG, is limited in an acidic environment and following exposure to physiological levels of SCFAs. Taken together, these data suggest that interventions aimed at increasing bacterial SCFA production may be an important approach for improving muscle-related measures in older adults.

Soluble fiber fermentation by gut bacteria results in the formation of acetate, propionate, and butyrate, and fecal SCFAs proportionally increase, whereas circulating levels of IS and PCS are reduced in response to high-soluble fiber diets. As a proof of concept, fecal and circulating levels of SCFAs, muscle mass, and aerobic exercise capacity were increased in young mice that were fed a relatively higher soluble fiber diet, but few studies have attempted this approach in older adult humans. When considering that fecal levels of SCFAs decrease during aging, whereas plasma levels of IS, PCS, PS, and PAG increase, these data collectively suggest that a high-soluble fiber diet may be an important approach for improving muscle-related measures in older adults humans. To test this hypothesis, older adults will be randomized to consume a high- or low-soluble fiber diet for 12-weeks.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
24 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
24 older adults (> 65y) will be randomized to consume a high- or low-soluble fiber diet24 older adults (> 65y) will be randomized to consume a high- or low-soluble fiber diet
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Impact of a High-Soluble Fiber Diet on the Gut-Muscle Axis in Older Adults
Anticipated Study Start Date :
Sep 15, 2022
Anticipated Primary Completion Date :
Apr 15, 2025
Anticipated Study Completion Date :
Apr 15, 2025

Arms and Interventions

Arm Intervention/Treatment
Other: Low-soluble fiber diet

Other: Low-soluble fiber diet
12 older adults (>65y) will be randomized to consume the USDA Guidelines for fiber intake (10g of total fiber/1000 calories), as the low-soluble fiber diet

Active Comparator: High-soluble fiber diet

Other: High-soluble fiber diet
12 older adults (>65y) will be randomized to consume 34-35g of total fiber/1000 calories, as the high-soluble fiber diet

Outcome Measures

Primary Outcome Measures

  1. Quantification of SCFAs in fecal samples [Change from baseline when compared with the Week-13 visit]

    Fecal levels of bacterial metabolites, including acetate, propionate, and butyrate will be determined at the baseline and week-13 study visits

  2. Quantification of whole-body lean mass with DXA [Change from baseline when compared with the Week-13 visit]

    Measurement of whole-body lean mass will be determined at the baseline and week-13 study visits

  3. Quantification of hand grip strength [Change from baseline when compared with the Week-13 visit]

    Grip strength will be determined at the baseline and week-13 study visits

  4. Chair stand test [Change from baseline when compared with the Week-13 visit]

    The number of chair stands that can be performed in 30 seconds will be determined at the baseline and week-13 study visits

Secondary Outcome Measures

  1. Quantification of thigh muscle composition with computed tomography [Change from baseline when compared with the Week-13 visit]

    Determined at the baseline and week-13 study visits

  2. 6-minute walk test [Change from baseline when compared with the Week-13 visit]

    The distance walked in 6 minutes will be determined at the baseline and week-13 study visits

  3. Quantification of gut bacterial metabolites in plasma [Change from baseline when compared with the Week-13 visit]

    Bacterial metabolites, including SCFAs but also indoxyl sulfate, p-cresol sulfate, phenol sulfate, and phenylacetylglutamine will be determined at the baseline and week-13 study visits

  4. Quantification of gut bacterial composition in fecal samples [Change from baseline when compared with the Week-13 visit]

    Determined at the baseline and week-13 study visits

  5. Quantification of pH in fecal samples [Change from baseline when compared with the Week-13 visit]

    Determined at the baseline and week-13 study visits

Eligibility Criteria

Criteria

Ages Eligible for Study:
65 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  1. Independently living older adults (> 65y)

  2. Sedentary (Godin-Shepard Leisure Time Physical Activity Questionnaire score < 10)

  3. Non-smoking

  4. Not already consuming a high-fiber diet (> 22, 28 g/day for women, men)

  5. Free of gastrointestinal disease (gastrointestinal cancer, inflammatory bowel disease, bariatric surgery, irritable bowel syndrome)

  6. Fluent in English

  7. Willing to attend three study visits (enrollment, baseline, and week-13)

  8. Willing to consume an abundance of fruits, vegetables, nuts/seeds

  9. Willing to consume an abundance of soluble fiber-rich foods (broccoli, brussels sprouts, flaxseeds sweetened with dates, lima beans, butternut squash, carrots, collard greens)

  10. Willing to tolerate mild gastrointestinal discomfort (bloating, belly grumbling, flatulence). Note that all attempts will be made to replace foods that may trigger these issues.

  11. Willing to not consume antibiotics during the 13-week study

  12. Willing to not schedule a colonoscopy during the 13-week study

Exclusion Criteria:
  1. Unwilling to visit the Tufts Human Nutrition Research Center on Aging (HNRCA) 3x/week to pick up the pre-prepared study diet

  2. Unwilling to only consume the provided food (unsweetened tea and/or black coffee are allowed)

  3. Food allergies related to foods that are included in the study

  4. Chewing problems

  5. Unwilling to wear a daily step counter (pedometer)

  6. Unwilling to complete a daily questionnaire that will assess gastrointestinal comfort

  7. Malnutrition (BMI < 18.5 kg/m2)

  8. Use of supplemental probiotics or antibiotics, participation in an investigational drug evaluation, or a recent change in habitual medication use within the 1 month-period prior to the screening visit

  9. 5% weight loss or weight gain within the past 6-months

  10. A recent history of alcohol abuse (within the past 5 years)

  11. A history of any significant injury or surgery that currently affects physical functioning and ability to perform physical function testing

  12. Treatment with immunosuppressive drugs

  13. A prior diagnosis of organ failure (heart, liver, renal, respiratory)

  14. Diabetes mellitus (type 1, or type 2 with insulin therapy)

  15. Chronic kidney disease (eGFR ≤ 30 mL/min/1.73 m2)

  16. Overt disease (cancer, dementia, cardiovascular disease)

  17. Chronic use of anti-inflammatory medication (corticosteroids)

  18. Already enrolled in another research study

  19. Active infection, including Tuberculosis , HIV, malaria, hepatitis, shingles, Methicillin-Resistant Staphylococcus Aureus (MRSA), SARS-CoV-2

  20. Any major illness or condition that may interfere with study outcomes at the discretion of the study physician

  21. Won't remain in Boston for the 13-week study duration

  22. Unwilling to complete a daily checklist aimed at quantifying the amount of food eaten on the study diet

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Tufts University

Investigators

  • Study Director: Michael S Lustgarten, PhD, Scientist II, NEPS Laboratory

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Michael Lustgarten, PhD, Principal Investigator, Tufts University
ClinicalTrials.gov Identifier:
NCT05549622
Other Study ID Numbers:
  • GRANT13386865
First Posted:
Sep 22, 2022
Last Update Posted:
Sep 23, 2022
Last Verified:
Sep 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Michael Lustgarten, PhD, Principal Investigator, Tufts University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 23, 2022