Impact of Oral Probiotics on Oral Homeostasis

Sponsor
University of Copenhagen (Other)
Overall Status
Completed
CT.gov ID
NCT04071210
Collaborator
(none)
110
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2
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Study Details

Study Description

Brief Summary

Aim:

To evaluate the effect of three months use of tablets containing probiotics on the composition of the supragingival plaque microbiota and salivary levels of inflammation-related proteins in oral healthy individuals.

Hypothesis:

Three months use of tablets containing probiotics will induce quantifiable changes to the composition of the supragingival plaque microbiota and salivary levels of inflammation-related proteins in oral healthy individuals.

Perspectives:

Data from the present study will be able to reveal the impact of regular use of probiotics on oral homeostasis in oral healthy individuals. Specifically, simultaneous registration of clinical, microbial and inflammatory characteristics will provide comprehensive information on the potential beneficial effect of regular use of oral probiotics on maintenance of oral homeostasis. Thus, data from the present study will provide a scientific platform, which dentist and dental hygienist can utilize when deciding if oral healthy individuals may benefit from using oral probiotics as a supplement to regular oral hygiene.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Probiotic tablet
  • Dietary Supplement: Placebo tablet
N/A

Detailed Description

Oral health is built upon a symbiotic relationship between the resident oral microbiota and the immune system of the host. Therefore, structural or functional changes to either the microbiota or the immune system may result in dysbiosis, which in turn can lead to oral diseases such as gingivitis, periodontitis and dental caries.

The composition of the resident oral microbiota in oral health is shaped by ecological properties found at various sites of the oral cavity, which is why major site-specific variations are observed. Interestingly, the composition of the oral microbiota is individualized and relatively time stable as long as oral homeostasis is maintained. However, structure and function of the oral microbiota can be altered by internal and external perturbations. For example, it has previously demonstrated that oral hygiene discontinuation induces structural changes to the supragingival plaque microbiota, whereas non-surgical periodontal treatment has deep impact on the composition of the subgingival plaque microbiota. Interestingly, a recent study demonstrated that the composition of the resident oral microbiota may also be influenced by external perturbations. Specifically, daily use of ZendiumTM toothpaste for 12 weeks was reported to induce significant changes to the supragingival plaque microbiota in oral healthy individuals with an increase in health-associated bacterial species.

Probiotics is the term used when a harmless effector strain is implanted in the host's microbiota to maintain or restore a natural microbiome by interference and/or inhibition of other microorganisms, and especially pathogens. In a recent study, it was demonstrated an effect of using tablets containing a mix of Lactobacillus rhamnosus PB01, DSM 14869 and Lactobacillus curvatus EB10, DSM 32307 on gingival inflammation. Specifically, daily use of this probiotic candidate for four weeks resulted in significant reduction in clinical parameters such as bleeding on probing (BOP) and amount of gingival crevicular fluid (GCF).

However, at present it is not known if daily use of a probiotic tablet containing a mix of L. rhamnosus PB01, DSM 14869 and L. curvatus EB10, DSM 32307 is able to induce shifts to the composition of the oral microbiota, or cause a decrease in salivary levels of inflammation-related proteins such as neutrophil gelatinase-associated lipocalin (NGAL) and transferrin, which is the purpose of the present study.

Study Design

Study Type:
Interventional
Actual Enrollment :
110 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Randomized double blind clinical trialRandomized double blind clinical trial
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Masking Description:
PI are the only one aware of participant status.
Primary Purpose:
Prevention
Official Title:
Impact of Oral Probiotics on Oral Homeostasis - a Randomized Double Blind Study
Actual Study Start Date :
Oct 1, 2019
Actual Primary Completion Date :
Mar 10, 2020
Actual Study Completion Date :
Mar 10, 2020

Arms and Interventions

Arm Intervention/Treatment
Experimental: Experimental

Probiotic tablets (containing a mix of Lactobacillus rhamnosus PB01, DSM 14869 and Lactobacillus curvatus EB10, DSM 32307, 1*10(9) CFU) 2 times/day for 12 weeks

Dietary Supplement: Probiotic tablet
Probiotic tablet twice a day for 12 weeks

Placebo Comparator: Placebo Comparator

Placebo tablets 2 times/day for 12 weeks

Dietary Supplement: Placebo tablet
Placebo tablet twice a day for 12 weeks

Outcome Measures

Primary Outcome Measures

  1. Change in bacterial diversity of supragingival plaque microbiota from baseline to week 12 [Baseline alpha-diversity vs. alpha-diversity at week 12]

    Alpha-diversity measured by shannon index

Secondary Outcome Measures

  1. Change in salivary levels of neutrophil gelatinase-associated lipocalin (NGAL) from baseline to week 12 [Baseline levels vs. leves at week 12.]

    Mean levels of NGAL (mg/mL) measured by ELISA

  2. Change in Salivary levels of transferrin from baseline to week 12 [Baseline levels vs. leves at week 12.]

    Mean levels of transferrin (mg/mL) measured by ELISA

Other Outcome Measures

  1. Change in plaque index (PI) from baseline to week 12 [Baseline recordings vs. recordings at week 12.]

    Mean levels of PI (% of sites with positive recordings)

  2. Change in gingival inflammation index (GI) from baseline to week 12 [Baseline recordings vs. recordings at week 12.]

    Mean levels of GI (% of sites with positive recordings)

  3. Change in bleeding index (BI) from baseline to week 12 [Baseline recordings vs. recordings at week 12.]

    Mean levels of BI (% of sites with positive recordings)

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 40 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • age > 18 yrs.
Exclusion Criteria:
  • gingivitis

  • periodontitis

  • dental caries

  • systemic disease

  • current medication

  • antibiotic treatment within the latest 3 months.

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Copenhagen, Dept. of Odontology Copenhagen Denmark 2200

Sponsors and Collaborators

  • University of Copenhagen

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Daniel Belstrøm, DDS, PhD, Associate professor, Principal Investiator, dr. odont., PhD, DDS, University of Copenhagen
ClinicalTrials.gov Identifier:
NCT04071210
Other Study ID Numbers:
  • UCPH_OI_003
First Posted:
Aug 28, 2019
Last Update Posted:
Oct 11, 2021
Last Verified:
Oct 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Oct 11, 2021