Influence of a Delivery System on the Efficacy of a Probiotic Intervention

NCT ID: NCT01399996

Last Updated: 2023-08-21

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

PHASE1

Total Enrollment

36 participants

Study Classification

INTERVENTIONAL

Study Start Date

2012-04-30

Study Completion Date

2014-08-31

Brief Summary

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In the proposed work we will evaluate the efficacy of a probiotic bacterium (Bifidobacterium animalis subsp. lactis BB12) delivered in a yogurt smoothie (organism to be added before or after fermentation) or as a supplement (tablet) by assessing 1) bowel habits (transit time); 2) the ecology of the bacterial community in the GIT; and 3) immune status of healthy human volunteers. In addition to providing information about the relative efficacy of the delivery vehicles on probiotic function it will provide novel information about the influence of the yogurt smoothie alone (control) on all the parameters measured.

Detailed Description

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Probiotics (health-promoting bacteria) are often considered "functional ingredients" that act independently of the matrix used to deliver them to the human host. This thinking ignores the impact the delivery matrix (food or dietary supplement) may have on both the physiology of the probiotic organism and on the human host and is likely not true.

Historically the most common "probiotic foods" have been fermented dairy products, particularly yogurts. Since yogurts are commonly understood to contain live "good" bacteria they are well accepted by consumers. However, increasingly over the last decade, probiotics are being added to non-dairy-based foods (juice, chocolate, cookies, etc) or consumed as supplements (tablets/capsules). While this expands the options for people to obtain probiotic organism, it is not clear whether probiotics delivered in these products are as efficacious as when delivered in a dairy food. In fact, the buffering capacity and nutrient composition of milk products may directly influence efficacy of the probiotic by increasing survival during passage through the gastrointestinal tract (GIT) and by modifying the physiology of the probiotic organism. In addition, fermentation products produced by the probiotic during manufacture of yogurt may also have an influence on the efficacy of probiotic bacteria.

Our hypotheses are:

1. The vehicle used to deliver probiotic bacteria into the body influences the performance of the probiotic in vivo. Specifically, consumption of yogurt-based smoothie containing probiotic bacteria will result in greater decrease in fecal transit time, and have a greater effect on the composition of the fecal microbiota and on markers of immune status than the same probiotic bacteria delivered at the same level in the form of a dietary supplement (tablet).
2. Timing of the addition of probiotic organism to the yogurt smoothie (pre or post fermentation) will not change the efficacy of the probiotic with respect to the outcomes being assessed.

Conditions

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Delayed Transit Time Irregular Bowel Function

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

CROSSOVER

Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

TRIPLE

Participants Investigators Outcome Assessors

Study Groups

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Yogurt smoothie without probiotic.

Group Type PLACEBO_COMPARATOR

Yogurt smoothie without probiotic

Intervention Type DIETARY_SUPPLEMENT

A daily 8 oz (240 mg) serving will provide 10x\^y5 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

Probiotic added post fermentation.

Group Type EXPERIMENTAL

Yogurt smoothie with probiotic added post fermentation

Intervention Type DIETARY_SUPPLEMENT

A daily 8 oz (240 mg) serving will provide 10x\^y5 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

Probiotic added pre-fermentation.

Group Type EXPERIMENTAL

Yogurt smoothie with probiotic added pre-fermentation

Intervention Type DIETARY_SUPPLEMENT

A daily 8 oz (240 mg) serving will provide 10x\^y5 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

A capsule containing the probiotic.

Group Type EXPERIMENTAL

A capsule containing the probiotic

Intervention Type DIETARY_SUPPLEMENT

A capsule taken daily will provide between 10x\^y9 and 10x\^y10 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

Interventions

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Yogurt smoothie without probiotic

A daily 8 oz (240 mg) serving will provide 10x\^y5 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

Intervention Type DIETARY_SUPPLEMENT

Yogurt smoothie with probiotic added post fermentation

A daily 8 oz (240 mg) serving will provide 10x\^y5 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

Intervention Type DIETARY_SUPPLEMENT

Yogurt smoothie with probiotic added pre-fermentation

A daily 8 oz (240 mg) serving will provide 10x\^y5 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

Intervention Type DIETARY_SUPPLEMENT

A capsule containing the probiotic

A capsule taken daily will provide between 10x\^y9 and 10x\^y10 cfu/ml of the probiotic (Bifidobacterium animalis subsp. lactis BB12).

Intervention Type DIETARY_SUPPLEMENT

Other Intervention Names

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Yogurt Yogurt with probiotic Yogurt with probiotic Probiotic capsule

Eligibility Criteria

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Inclusion Criteria

* Generally healthy
* Men and women
* 18-40 years of age
* Body mass index between 20 and 35 kg/m\^2
* Persons with irregular bowel function as determined using the Rome III criteria (1) which is used to classify functional gastrointestinal disorders.
* Increased gastrointestinal transit time \> 60 hours.

Exclusion Criteria

* Smoking and/or use of other tobacco products
* Blood pressure greater than 140/90 mm Hg
* A history of myocardial infarction, stroke, diabetes mellitus, liver disease, kidney disease and thyroid disease (unless controlled by medication and blood results within the previous 6 months are provided).
* Lactation, pregnancy or desire to become pregnant during the study
* Use of cholesterol-lowering medication
* Refusal to discontinue intake of putative cholesterol-lowering supplements (psyllium, fish oil capsules, soy lecithin, niacin, fiber, flax, phytoestrogens, stanol/sterol supplemented foods
* Refusal to discontinue probiotics,nutritional supplements, herbs or vitamins
* Vegetarianism/Veganism
* Lactose intolerance
* Clinical diagnosis of Inflammatory Bowel Disease (IBD), e.g. Crohn's Disease or ulcerative colitis
* Excessive alcohol consumption (\> 14 standard drinks per week)
* Chronic use of anti-inflammatory medications (unless able to discontinue)
* Individuals taking stool softeners or enemas on a regular basis.
* Allergy to polyvinyl chloride (PVC) or any other type of plastic
* Individuals with a bowel transit time of \< 60 hours at time of screening
* Individuals with swallowing disorders or dysphagia to food or pills
* Suspected strictures, fistulas, or physiological GI Obstruction
* GI surgery within the past three months
* Refusal to agree to give blood or plasma for the length of the study.

Note: If a participant experiences a delay in passing the capsule (beyond five days) they will be treated accordingly and excluded from future participation in the study.
Minimum Eligible Age

18 Years

Maximum Eligible Age

40 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Dairy Management Inc.

INDUSTRY

Sponsor Role collaborator

Penn State University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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Penny M Kris-Etherton, PhD

Role: PRINCIPAL_INVESTIGATOR

Penn State University

Locations

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Penn State University

University Park, Pennsylvania, United States

Site Status

Countries

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United States

References

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Drossman DA, Dumitrascu DL. Rome III: New standard for functional gastrointestinal disorders. J Gastrointestin Liver Dis. 2006 Sep;15(3):237-41.

Reference Type BACKGROUND
PMID: 17013448 (View on PubMed)

Ba Z, Lee Y, Meng H, Kris-Etherton PM, Rogers CJ, Lewis ZT, Mills DA, Furumoto EJ, Rolon ML, Fleming JA, Roberts RF. Matrix Effects on the Delivery Efficacy of Bifidobacterium animalis subsp. lactis BB-12 on Fecal Microbiota, Gut Transit Time, and Short-Chain Fatty Acids in Healthy Young Adults. mSphere. 2021 Aug 25;6(4):e0008421. doi: 10.1128/mSphere.00084-21. Epub 2021 Jul 7.

Reference Type DERIVED
PMID: 34232082 (View on PubMed)

Lee Y, Ba Z, Roberts RF, Rogers CJ, Fleming JA, Meng H, Furumoto EJ, Kris-Etherton PM. Effects of Bifidobacterium animalis subsp. lactis BB-12(R) on the lipid/lipoprotein profile and short chain fatty acids in healthy young adults: a randomized controlled trial. Nutr J. 2017 Jun 29;16(1):39. doi: 10.1186/s12937-017-0261-6.

Reference Type DERIVED
PMID: 28662676 (View on PubMed)

Meng H, Lee Y, Ba Z, Peng J, Lin J, Boyer AS, Fleming JA, Furumoto EJ, Roberts RF, Kris-Etherton PM, Rogers CJ. Consumption of Bifidobacterium animalis subsp. lactis BB-12 impacts upper respiratory tract infection and the function of NK and T cells in healthy adults. Mol Nutr Food Res. 2016 May;60(5):1161-71. doi: 10.1002/mnfr.201500665. Epub 2016 Mar 1.

Reference Type DERIVED
PMID: 26821116 (View on PubMed)

Other Identifiers

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PKE PROBIOTIC

Identifier Type: -

Identifier Source: org_study_id

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