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Fiber and Calcium Absorption in Older Men

Modulation of the Gut Microbiome by Dietary Fiber to Improve Calcium Absorption and Bone Health in Older Men

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06519877
Enrollment
30
Registered
2024-07-25
Start date
2025-01-01
Completion date
2029-01-01
Last updated
2026-02-17

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

Conditions

Aging

Brief summary

Osteoporotic fractures are a major but underrecognized problem in men. There is growing evidence that low dietary fiber intake is a modifiable risk factor for age-related bone loss in men. Preclinical and human studies in adolescents and postmenopausal women suggest that dietary fiber intake influences bone metabolism by modulating the gut microbiome to augment intestinal calcium absorption, but it is unclear through what molecular mechanism and whether dietary fiber has the same effects in older men. In this crossover intervention study, the investigators will enroll and follow 30 older male Veterans to evaluate the effects of soluble corn fiber on intestinal calcium absorption and explore the contribution of the gut microbiome.

Detailed description

Osteoporosis and associated fractures are a major problem in older men. One in four men over the age of 60 will sustain an osteoporotic fracture during his lifetime. Moreover, the mortality rate in men after fractures is nearly twice that in women. Despite the burden of fractures, little is understood about the pathogenesis of progressive bone loss in men. Studies point to dietary fiber as a potentially important mitigator of decline in bone mass, likely through increased intestinal calcium absorption and retention, as studied in adolescents, young men, and postmenopausal women. However, the effects of dietary fiber in older men have not been tested and the mechanism by which dietary fiber influences calcium absorption is unclear. The gut microbiome, which is crucial for host nutrient metabolism and hormone modulation, is a likely but underexplored mechanism. The overall objective is to examine the effects of soluble corn fiber on intestinal calcium absorption with modulation of the gut microbiome in older men. The central hypothesis is that soluble corn fiber augments production of short-chain fatty acids by the gut microbiome, which modulates the production of systemic insulin-like growth factor 1 to increase calcium absorption and bone mass. This study is a crossover intervention study on the effects of soluble corn fiber vs. placebo on intestinal calcium absorption and gut microbiome composition and function in 30 older male Veterans 60 years of age. Participants will be randomized 1:1 to sequential soluble corn fiber 20g/day vs. placebo for4 weeks each with a 4-week washout period. Individualized doses of calcium and vitamin D supplementation will also be provided through out the study period. Study measurements at the end of each intervention include intestinal calcium absorption via a dual stable isotope method, detailed gut microbiome characterization with metagenomics and metabolomics, dietary assessment, calciotropic hormones, and bone turnover marker levels. Baseline bone density and microstructure will also be obtained.

Interventions

DIETARY_SUPPLEMENTSoluble corn fiber

Soluble corn fiber, also referred to resistant maltodextrin, is a type of dietary fiber made from corn starch. Soluble corn fiber is typically used to thicken processed foods and has been marketed as a prebiotic to improve digestive health.

Sponsors

VA Office of Research and Development
Lead SponsorFED
San Francisco VA Health Care System
CollaboratorFED

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
OTHER
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

Sachets of soluble corn fiber and placebo will be prepared and assigned randomization numbers by the investigational pharmacist at the San Francisco VA Health Care System. Participants, study staff, and those involved in outcome assessment will be blinded to the group assignment throughout the study.

Intervention model description

Participants will be randomized into one of two groups at a 1:1 ratio in random permutated blocks of size 6. Each group will undergo 2 phases of intervention with soluble corn fiber 20g/day for 4 weeks and placebo (maltodextrin) for 4 weeks, with 4-weeks of washout in between. Group 1 will receive soluble corn fiber first followed by placebo, whereas group 2 will receive placebo first followed by soluble corn fiber. Outcomes will be assessed at the end of each intervention phase.

Eligibility

Sex/Gender
MALE
Age
60 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Male Veterans 60 years of age

Exclusion criteria

* History of malabsorption * Hypercalcemia (corrected Ca \> 10.2 mg/dL) * Vitamin D insufficiency (25OHD \< 30 ng/mL) * Chronic kidney disease stage 3B or worse (CrCl \< 45 mL/min) * Severe hypogonadism (AM fasting serum total testosterone \< 150 ng/dL) * Daily use of proton pump inhibitor * Use of medication(s) known to affect calcium metabolism * Use of medications or supplements that could impact gut microbiota in the previous 3 months (antibiotics or commercially available probiotics or prebiotics. * Presence of a condition or abnormality that in the opinion of the Investigator that would compromise the safety of the patient or the quality of the data.

Design outcomes

Primary

MeasureTime frameDescription
Intestinal fractional calcium absorptionAt week 4 and week 12 of study participation (at the end of each treatment phase x2)Dual stable calcium isotopic tracer method

Secondary

MeasureTime frameDescription
Biochemical markers of bone turnoverAt week 4 and week 12 of study participation (at the end of each treatment phase x2)Blood draw
Calciotropic hormonesAt week 4 and week 12 of study participation (at the end of each treatment phase x2)Blood draw
Gut microbial profilingAt week 4 and week 12 of study participation (at the end of each treatment phase x2)Stool collection
Adherence, tolerability, and acceptabilityThroughout study period, an average of 12 weeksQuestionnaire

Countries

United States

Contacts

CONTACTKarin C Wu, MD
karin.Wu@va.gov(415) 221-4810
PRINCIPAL_INVESTIGATORKarin C Wu, MD

San Francisco VA Medical Center, San Francisco, CA

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026