- ICH GCP
- US Clinical Trials Registry
- Klinisk utprøving NCT02215343
Effect of Prebiotic and PUFA on the Gut Microbiota and Metabolic Risk Markers (MyNewGut)
Effect of Prebiotic Fibre and Polyunsaturated Fatty Acid (PUFA) on the Gut Microbiota and Metabolic Risk Markers in a Metabolically Challenged Population
The main objective of this study is to investigate in detail how a high-(prebiotic)fibre diet and a high-PUFA diet affect the gut microbiota composition in a metabolic challenged population, and if the diet-induced modulation of the gut microbiota mediates changes in metabolic risk markers.
Intake of both experimental diets over 4 weeks are expected to induce beneficial changes in the gut microbiota composition and to affect markers for insulin sensitivity, lipid metabolism and inflammation. The investigators hypothesize that the effect of both interventions on the metabolic risk markers will be partly mediated by the diet-induced changes in the gut microbiota composition.
Studieoversikt
Status
Forhold
Intervensjon / Behandling
Studietype
Registrering (Faktiske)
Fase
- Ikke aktuelt
Kontakter og plasseringer
Studiesteder
-
-
-
Frederiksberg, Danmark, 1958
- Department of Nutrition, Exercise and Sports, University of Copenhagen
-
-
Deltakelseskriterier
Kvalifikasjonskriterier
Alder som er kvalifisert for studier
Tar imot friske frivillige
Kjønn som er kvalifisert for studier
Beskrivelse
Inclusion Criteria:
- BMI: 25-40 kg/m2
- Non-smoking
- Indices of the Metabolic Syndrome defined by the International Diabetes Federation (IDF 2006):
Central obesity (waist circumference; men: ≥94 cm and women: ≥80 cm) + any one of the following; raised triglyceride level (≥1.7 mmol/L), reduced HDL cholesterol (men: <1.03 mmol/L, women: <1.29 mmol/L), raised BP (systolic ≥130 mm Hg or diastolic ≥85 mm Hg) or raised fasting plasma glucose (≥5.6 mmol/L).
Exclusion Criteria:
- Use of antibiotics
- Weight change >3 kg 2 months prior to study start
- Intensive physical training/ elite athlete
- Medication for dyslipidemia, type 2 diabetes or elevated blood pressure
- Dietary supplements with pro/prebiotics, dietary fibre or fish oil supplement
- Lactation, pregnancy or planning of pregnancy during the study
- Gastro intestinal and liver disorders
- Chronic inflammatory disorders
- Diagnosed psychiatric disorder including treatment required depression
- Surgical treatment of obesity and abdominal surgery
Studieplan
Hvordan er studiet utformet?
Designdetaljer
- Primært formål: Forebygging
- Tildeling: Randomisert
- Intervensjonsmodell: Crossover-oppdrag
- Masking: Ingen (Open Label)
Våpen og intervensjoner
Deltakergruppe / Arm |
Intervensjon / Behandling |
---|---|
Eksperimentell: High fibre diet (wheat bran extract)
|
Patients will be provided with 15g of wheat bran extract (WBE) (Cargill R&D Centre Europe).
|
Eksperimentell: High PUFA diet (fish oil supplement)
|
Patients will be provided with a fish oil supplement (capsules), containing 3-4g of N-3 fatty acids (Axellus A/S, Ishøj, Denmark).
|
Hva måler studien?
Primære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Change in gut microbiota composition
Tidsramme: Week 0, 4, 8, 12
|
Gut microbiota composition will be analyzed by use of fecal samples.
|
Week 0, 4, 8, 12
|
Sekundære resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Change in markers for insulin sensitivity
Tidsramme: Week 0, 4, 8, 12
|
Will be measured by use of fasting blood samples
|
Week 0, 4, 8, 12
|
Change in markers for lipid metabolism
Tidsramme: Week 0, 4, 8, 12
|
Will be measured by use of fasting blood samples
|
Week 0, 4, 8, 12
|
Change in markers for inflammation
Tidsramme: Week 0, 4, 8, 12
|
Will be measured by use of fasting blood samples
|
Week 0, 4, 8, 12
|
Faecal SCFA and bile acid composition
Tidsramme: Week 0, 4, 8, 12
|
Will be analyzed by use of fecal samples.
|
Week 0, 4, 8, 12
|
Lipidomics
Tidsramme: Week 0, 4, 8, 12
|
Will be analyzed by use of fasting blood samples and fecal samples.
|
Week 0, 4, 8, 12
|
Metabolomics
Tidsramme: Week 0, 4, 8, 12
|
Will be analyzed by use of fasting blood samples, urine and fecal samples.
|
Week 0, 4, 8, 12
|
Andre resultatmål
Resultatmål |
Tiltaksbeskrivelse |
Tidsramme |
---|---|---|
Change in energy expenditure
Tidsramme: Week 0, 4, 8, 12
|
Resting energy expenditure will be measured by indirect calorimetry in a ventilated hood system
|
Week 0, 4, 8, 12
|
Gene expression
Tidsramme: Week 0, 4, 8, 12
|
Adipose tissue biopsies will be used for epigenetic analyses, gene and protein expression (no whole genome or exome sequencing).
|
Week 0, 4, 8, 12
|
Compliances markers
Tidsramme: Week 0, 4, 8, 12
|
Compliance will be evaluated from 3-days diet registration and self-reported intake of dietary supplements, PUFA complance markes (fatty acid composition) and body composition
|
Week 0, 4, 8, 12
|
Samarbeidspartnere og etterforskere
Sponsor
Samarbeidspartnere
Etterforskere
- Hovedetterforsker: Lesli H Larsen, PhD, Department of Nutrition, Exercise and Sports, University of Copenhagen
Publikasjoner og nyttige lenker
Generelle publikasjoner
- Benitez-Paez A, Kjolbaek L, Gomez Del Pulgar EM, Brahe LK, Astrup A, Matysik S, Schott HF, Krautbauer S, Liebisch G, Boberska J, Claus S, Rampelli S, Brigidi P, Larsen LH, Sanz Y. A Multi-omics Approach to Unraveling the Microbiome-Mediated Effects of Arabinoxylan Oligosaccharides in Overweight Humans. mSystems. 2019 May 28;4(4):e00209-19. doi: 10.1128/mSystems.00209-19.
- Kjolbaek L, Benitez-Paez A, Gomez Del Pulgar EM, Brahe LK, Liebisch G, Matysik S, Rampelli S, Vermeiren J, Brigidi P, Larsen LH, Astrup A, Sanz Y. Arabinoxylan oligosaccharides and polyunsaturated fatty acid effects on gut microbiota and metabolic markers in overweight individuals with signs of metabolic syndrome: A randomized cross-over trial. Clin Nutr. 2020 Jan;39(1):67-79. doi: 10.1016/j.clnu.2019.01.012. Epub 2019 Feb 19.
Hjelpsomme linker
Studierekorddatoer
Studer hoveddatoer
Studiestart
Primær fullføring (Faktiske)
Studiet fullført (Faktiske)
Datoer for studieregistrering
Først innsendt
Først innsendt som oppfylte QC-kriteriene
Først lagt ut (Anslag)
Oppdateringer av studieposter
Sist oppdatering lagt ut (Faktiske)
Siste oppdatering sendt inn som oppfylte QC-kriteriene
Sist bekreftet
Mer informasjon
Begreper knyttet til denne studien
Ytterligere relevante MeSH-vilkår
Andre studie-ID-numre
- MyNewGut, Task 3.3
- Grant Agreement no: 613979 (Annet stipend/finansieringsnummer: EU 7th Framework Programme)
Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .
Kliniske studier på Wheat bran extract
-
University Hospitals Cleveland Medical CenterUkjentAstma | Allergisk rhinitt | Allergisk konjunktivittForente stater
-
University of GuelphFullført
-
SeppicFullført
-
Hugh A Sampson, MDFullført
-
Rabin Medical CenterRekruttering
-
Pusan National University Yangsan HospitalFullførtHudoverfølsomhetKorea, Republikken
-
TCI Co., Ltd.Fullført
-
Jeeyoun MoonHar ikke rekruttert ennåFasettleddsyndrom
-
SeppicFullført
-
SeppicFullførtFriske FrivilligeItalia