Healthy Young Adults, Healthy Elderly
Conditions
Brief summary
The population is aging worldwide, which requires more attention to health needs and leads to a dramatic increase in health care costs. Prevention or delay of onset of disorders associated with aging is needed. Dietary intake of pectin, a dietary fiber, may have beneficial effects on gut health parameters, i.e. intestinal barrier function, immune function and microbial composition. As intestinal barrier function may be compromised in the elderly we will investigate whether the effects of pectin on selected parameters of gut health differ between young vs. older individuals. The primary objective of this study is to investigate the effects of aging on pectin-induced changes in intestinal permeability. Furthermore, this study has seven secondary objectives. This study conforms to a randomized, double-blind and placebo-controlled design including two parallel arms.The study population consists of Healthy human volunteers (male and female), 18-40 and 65-75 years old, BMI 20-30 kg/m2. One group will receive 7.5 grams of pectin supplements twice daily for four weeks. A second group will receive 7.5 grams of placebo supplements twice daily for four weeks. Before and after the supplementation period, several measurements will take place. The main study parameter is the change in urinary sugar excretion ratio before and after the intervention period.
Interventions
DIETARY_SUPPLEMENTPectin
This group will receive 7.5 grams of pectin supplements twice daily for four weeks.
DIETARY_SUPPLEMENTMaltodextrin
This group will receive 7.5 grams of maltodextrin supplements twice daily for four weeks.
Sponsors
Maastricht University Medical Center
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes
Inclusion criteria
* Based on medical history and previous self-admitted examination, no gastrointestinal complaints can be defined. * Age between 18 - 40 years and 65 - 75 years. * Body Mass Index (BMI) between 20 and 30 kg/m2. Normal BMI has been chosen because obesity is associated with an altered microbial composition and increased intestinal permeability.
Exclusion criteria
* History of severe cardiovascular, respiratory, urogenital, gastrointestinal/ hepatic, hematological/immunologic, HEENT (head, ears, eyes, nose, throat), dermatological/connective tissue, musculoskeletal, metabolic/nutritional, endocrine, neurological diseases, allergy, major surgery and/or laboratory assessments which might limit participation in or completion of the study protocol. * Use of proton-pump inhibitors, nonsteroidal anti-inflammatory drugs and/or vitamin supplementation, within 14 days prior to testing. Use of other medication will be reviewed by a medical doctor, who will decide on in- or exclusion based on the drug(s) used. * Administration of probiotic or prebiotic supplements, investigational drugs or participation in any scientific intervention study which may interfere with this study (to be decided by the principle investigator), in the 90 days prior to the study * Use of antibiotics in the 90 days prior to the study. * Abdominal surgery interfering with gastrointestinal function, upon judgment of the principle investigator). * Pregnancy, lactation. * Excessive alcohol consumption (\>20 alcoholic consumptions per week). * Smoking. * Blood donation within 3 months before or after the study period. * Self-admitted human immunodeficiency virus-positive state. * History of side effects towards intake of prebiotic supplements.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Sugar recovery in urine, as indicator of intestinal permeability | Change from Baseline to after 4 weeks of intervention |
Secondary
| Measure | Time frame |
|---|---|
| Ussing chamber experiments in colonic biopsies, as indicator of intestinal barrier function | After 4 weeks of intervention |
| Histology in colonic biopsies, as indicator of intestinal barrier function | After 4 weeks of intervention |
| MiR-29a in colonic biopsies, as indicator of intestinal barrier function | After 4 weeks of intervention |
| Zonulin in blood plasma, as indicator of intestinal barrier function | Change from Baseline to after 4 weeks of intervention |
| Immune infiltration cells in colonic biopsies, as indicator of immune system performance | After 4 weeks of intervention |
| T-cells and Natural Killer cells in blood plasma, as indicator of immune system performance | Change from Baseline to after 4 weeks of intervention |
| Cytokines Interleukin-10 and Interleukin-12 in blood plasma, as indicator of immune system performance | Change from Baseline to after 4 weeks of intervention |
| Tight junction structure and proteins in colonic biopsies, as indicator of intestinal barrier function | After 4 weeks of intervention |
| Secretory Immunoglobulin A in blood serum, as indicator of immune system performance | Change from Baseline to after 4 weeks of intervention |
| Microbial composition in luminal content and feces | Change from Baseline to after 4 weeks of intervention |
| Short-chain fatty acids in luminal content and feces, as indicator of microbial function | Change from Baseline to after 4 weeks of intervention |
| Volatile organic compounds in exhaled air, as indicator for metabolite production | Change from Baseline to after 4 weeks of intervention |
| Symptom diary questionnaire, as indicator of digestive parameters | Change from three days prior to the supplementation period to three days during the last week of the supplementation period |
| Stool frequency and consistency questionnaire, as indicator of digestive parameters | Change from Baseline to after 4 weeks of intervention |
| Gastrointestinal Symptom Rating Scale questionnaire, as indicator of digestive parameters | Change from Baseline to after 4 weeks of intervention |
| C-reactive protein in blood serum, as indicator of immune system performance | Change from Baseline to after 4 weeks of intervention |
Countries
Netherlands
Outcome results
None listed