Effect of Aspirin on Gut Microbiome
| Status: | Active, not recruiting |
|---|---|
| Conditions: | Healthy Studies |
| Therapuetic Areas: | Other |
| Healthy: | No |
| Age Range: | 50 - 75 |
| Updated: | 4/17/2018 |
| Start Date: | August 2016 |
| End Date: | August 2018 |
Pilot Trial to Examine the Effect of Aspirin on the Gut Microbiome
Regular use of aspirin may reduce the incidence of colorectal cancer (CRC). However, it is
unclear through which mechanism aspirin exerts its effect, in whom it decreases CRC risk and
in whom it causes side effects. Recently, the imbalanced gut microbiome was linked to
inflammation and CRC risk. The main hypothesis for this study is that aspirin may decrease
CRC risk via targeting the gut microbiome. The study will be a randomized placebo-controlled
double-blinded design, recruiting 50 healthy subjects, 50-75 years old, from the PRospective
Evaluation of SEPTin 9 (PRESEPT) cohort living in the greater Twin Cities area, who will
receive either aspirin or placebo for 6 weeks.
unclear through which mechanism aspirin exerts its effect, in whom it decreases CRC risk and
in whom it causes side effects. Recently, the imbalanced gut microbiome was linked to
inflammation and CRC risk. The main hypothesis for this study is that aspirin may decrease
CRC risk via targeting the gut microbiome. The study will be a randomized placebo-controlled
double-blinded design, recruiting 50 healthy subjects, 50-75 years old, from the PRospective
Evaluation of SEPTin 9 (PRESEPT) cohort living in the greater Twin Cities area, who will
receive either aspirin or placebo for 6 weeks.
The pilot study will evaluate the feasibility of conducting a large randomized trial and
estimate the effects of aspirin on the gut microbiome. The study will recruit 50 healthy
subjects, 50-75 years old, from the PRospective Evaluation of SEPTin 9 (PRESEPT) cohort
living in the greater Twin Cities area.
The Primary Aim is to estimate the impact of a 3- and 6-week intake of once daily 325 mg
aspirin on the composition of the gut microbiome using a randomized placebo-controlled
double-blinded design, i.e. examine the change of microbiome over time within and between the
subjects. The hypothesis for this aim is that in the aspirin arm versus the placebo arm, gut
microbiome composition will shift towards a lower proportion of pro-inflammatory,
CRC-predisposing bacteria (e.g. Fusobacteria) and higher proportion of anti-inflammatory,
CRC-protective bacteria (e.g. butyrate-producing bacteria).
The Secondary Aims are to examine the correlation between the aspirin-related changes in
microbiome profile with the levels of circulating inflammatory biomarkers in urine and
plasma. Within-individual and between-arm differences in microbiome composition will be
compared after 3 and 6 weeks of aspirin intake. Also, the microbiome composition will be
compared after 3-week and 6-week wash-out periods to test whether these periods are
sufficient to restore gut microbiome composition to a pre-treatment level. This study will
inform future crossover randomized studies focusing on CRC preventive interventions that will
enable clinicians to identify optimal candidates for aspirin therapy for the purposes of CRC
prevention using this accessible and cheap drug.
estimate the effects of aspirin on the gut microbiome. The study will recruit 50 healthy
subjects, 50-75 years old, from the PRospective Evaluation of SEPTin 9 (PRESEPT) cohort
living in the greater Twin Cities area.
The Primary Aim is to estimate the impact of a 3- and 6-week intake of once daily 325 mg
aspirin on the composition of the gut microbiome using a randomized placebo-controlled
double-blinded design, i.e. examine the change of microbiome over time within and between the
subjects. The hypothesis for this aim is that in the aspirin arm versus the placebo arm, gut
microbiome composition will shift towards a lower proportion of pro-inflammatory,
CRC-predisposing bacteria (e.g. Fusobacteria) and higher proportion of anti-inflammatory,
CRC-protective bacteria (e.g. butyrate-producing bacteria).
The Secondary Aims are to examine the correlation between the aspirin-related changes in
microbiome profile with the levels of circulating inflammatory biomarkers in urine and
plasma. Within-individual and between-arm differences in microbiome composition will be
compared after 3 and 6 weeks of aspirin intake. Also, the microbiome composition will be
compared after 3-week and 6-week wash-out periods to test whether these periods are
sufficient to restore gut microbiome composition to a pre-treatment level. This study will
inform future crossover randomized studies focusing on CRC preventive interventions that will
enable clinicians to identify optimal candidates for aspirin therapy for the purposes of CRC
prevention using this accessible and cheap drug.
Inclusion Criteria:
- Healthy adults aged 50-75 years who reside within the greater Twin Cities area
- Capable and willing to comply with the entire study protocol
- Able to give voluntary written informed consent.
Exclusion Criteria:
- Use of any aspirin-containing products or other non-steroidal anti-inflammatory drugs
(NSAIDs) (≥ 2 days per week on a regular basis)
- Known hypersensitivity to NSAIDs
- Any active cancer, history of gastrointestinal cancer, or chronic disease such as
peptic ulcer, irritable bowel syndrome, inflammatory bowel disease, intestinal
malabsorption syndrome or other gastrointestinal disorder
- History of any coagulation, bleeding, or blood disorders (e.g. Anemia)
- History of stroke/ Transient Ischemic Attack
- Acute heart disease or history of heart attack, atrial fibrillation, or angina
- Diagnosis of dementia
- Use of antibiotics, antiplatelets (e.g. clopidogrel), or anticoagulants (e.g.
warfarin) within the last 3 months. A complete list of contraindicated medications
will be provided (Appendix A)
- Regular use of laxatives (e.g. Ex-lax, Dulcolax, Miralax) that may affect the
microbiome ≥2 days a week (Appendix B)
- Body mass index (BMI) greater than or equal to 40 or less than or equal to 17 kg/m2 at
screening visit
- Unexplained change in weight (>4.5 kg) within the past 6 months
- Major changes in eating habits within the past 3 months
We found this trial at
1
site
1100 South Washington Avenue
Minneapolis, Minnesota 55415
Minneapolis, Minnesota 55415
Phone: 612-626-0250
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