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Probiotics in Dementia (PIDE)

Primary Purpose

Dementia; Alzheimer, Mixed Type (Etiology)

Status
Recruiting
Phase
Not Applicable
Locations
Austria
Study Type
Interventional
Intervention
Omni-Biotic Stress Repair
placebo
Sponsored by
Medical University of Graz
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Dementia; Alzheimer, Mixed Type (Etiology)

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age >18 years
  • Dementia of Alzheimer type and mixed type (diagnosis by a board-certified neurologist/psychiatrist and according to ICD10)
  • Mini Mental State Examination 21-26
  • Stable treatment with anti-dementia drugs including phytotherapeutics (>3 months) or no intention to start anti-dementia drugs
  • Informed consent

Exclusion Criteria:

  • Other forms of dementia
  • Inflammatory bowel diseases
  • Liver cirrhosis
  • Antibiotic treatment within the last 4 weeks
  • Febrile illness within the last 4 weeks
  • Acute hospital admission for dementia-unrelated reasons within the last 4 weeks
  • Dysphagia
  • Any other condition or circumstance, which, in the opinion of the investigator, would affect the patient's ability to participate in the protocol

Sites / Locations

  • Medical University GrazRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Placebo Comparator

Arm Label

Probiotic

Placebo

Arm Description

Bifidobacterium bifidum W23, B. lactis W51, B. lactis W52, Lactobacillus acidophilus W22, L. casei W56, L. paracasei W20, L. plantarum W62, L. salivarius W24, Lactococcus lactis W19, 7.5 × 109 Colony Forming Units/g twice daily dissolved in water

3g of a similar looking and tasting powder, twice daily

Outcomes

Primary Outcome Measures

Butyrate producing bacteria
abundance of butyrate producing bacteria

Secondary Outcome Measures

Butyrate producing bacteria
abundance of butyrate producing bacteria
diaminooxidase concentration in serum
marker of intestinal permeability
diaminooxidase concentration in serum
marker of intestinal permeability
zonulin concentration in stool
marker of intestinal permeability
zonulin concentration in stool
marker of intestinal permeability
calprotectin concentration in stool
marker of intestinal inflammation
calprotectin concentration in stool
marker of intestinal inflammation
soluble CD 14 concentration in serum
marker of systemic inflammation
soluble CD 14 concentration in serum
marker of systemic inflammation
lipopolysaccharide binding protein concentration in serum
marker of systemic inflammation
lipopolysaccharide binding protein concentration in serum
marker of systemic inflammation
lipopolysaccharide concentration in serum
marker of bacterial translocation
lipopolysaccharide concentration in serum
marker of bacterial translocation
peptidoglycan concentration in serum
marker of bacterial translocation
peptidoglycan concentration in serum
marker of bacterial translocation
bacterial DNA concentration in serum
marker of bacterial translocation
bacterial DNA concentration in serum
marker of bacterial translocation
Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)
Questionnaire to assess cognitive function, 0-70 points
Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)
Questionnaire to assess cognitive function, 0-70 points
Mini mental state examination
Questionnaire to assess cognitive function, 0-30 points
Mini mental state examination
Questionnaire to assess cognitive function, 0-30 points
clinician's interview-based impression of change with caregiver input (CIBIC+)
Questionnaire to assess overall change during the study, 1-7 points
clinician's interview-based impression of change with caregiver input (CIBIC+)
Questionnaire to assess overall change during the study, 1-7 points
Barthel index
Assessment of activities of daily living, 0-100 points
Barthel index
Assessment of activities of daily living, 0-100 points

Full Information

First Posted
February 11, 2019
Last Updated
January 11, 2023
Sponsor
Medical University of Graz
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1. Study Identification

Unique Protocol Identification Number
NCT03847714
Brief Title
Probiotics in Dementia
Acronym
PIDE
Official Title
Probiotics in Dementia
Study Type
Interventional

2. Study Status

Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
June 15, 2019 (Actual)
Primary Completion Date
December 2023 (Anticipated)
Study Completion Date
December 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Medical University of Graz

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Dementia is associated with changes in gut microbiome composition, gut barrier dysfunction, intestinal inflammation and systemic inflammation. Probiotics are a possibility to modulate the gut-brain axis. In this study the effect of probiotics on the gut microbiome and, gut barrier function, inflammation and cognitive dysfunction will be studied.
Detailed Description
Dementia is a disease that presents with deterioration in memory, thinking, behaviour and the ability to perform everyday activities. Worldwide 47.5 million people are affected and incidence of dementia is increasing. Dementia leads to disability and dependency among older people worldwide and thereby has a huge physical, psychological, social and economic impact on caregivers, families and society. Alzheimer's disease (AD) is the most common form of dementia accounting for 60-70% of the cases; other forms include Lewy body dementia, frontotemporal dementia, vascular dementia and Parkinson's disease with dementia. In AD, pathologic protein aggregates of amyloid beta and hyperphosphorylated tangles of tau-protein which deposit as neurofibrillary tangles are typical features. This leads to neuroinflammation, mainly mediated by the innate immune system. The most important cells in this process are microglia cells, which represent the resident macrophages of the brain. Although microglia is able to remove extracellular amyloid beta, in later stages of the disease cells remain in a dystrophic state and cannot exert their beneficial functions. Microglia maturation and function is critically dependent on short-chain fatty acids produced by the gut microbiome and therefore highlights the microbiome as a potential diagnostic and therapeutic target in dementia. The role of the commensal microbial population of the human body - especially the intestinal microbiome - in various diseases is emerging due to the development of advanced analysis techniques. Recently the concept of the gut brain-axis has been established. Several pathways including the autonomic nervous system, the enteric nervous system, the neuroendocrine system and the immune system allow a communication between gut and brain but may also be involved in disease development. During ageing, the gut microbiome composition undergoes changes. A decrease in diversity, a loss of beneficial taxa and an increase of facultative pathogens has been described. Diet and the place of residence play an important role in the shaping of the microbiome. Aging is also associated with inflammation - often termed as "inflammaging" associated with an increase in gut permeability, mucosal inflammation and bacterial translocation. Since the main risk factor for developing dementia, especially AD, is aging, it is very likely that the gut-brain axis is critically involved in dementia development. Animal studies so far suggest that AD is associated with changes in the gut microbiome composition with a decrease in beneficial, anti-inflammatory genera. Furthermore, genetic alterations in amyloid genes can influence microbiome composition in mice, pointing towards a vicious cycle in AD development. In humans, so far only limited evidence on the microbiome composition in patients with dementia is available. There is evidence that the composition of the microbiome in subgingival plaques is altered in dementia and associated with cognitive function. Recently the first human study identified phylum- through genus-wide differences in bacterial abundance including decreased Firmicutes, increased Bacteroidetes, and decreased Bifidobacterium in the stool of AD patients.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Dementia; Alzheimer, Mixed Type (Etiology)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
similar looking and tasting placebo
Allocation
Randomized
Enrollment
58 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Probiotic
Arm Type
Active Comparator
Arm Description
Bifidobacterium bifidum W23, B. lactis W51, B. lactis W52, Lactobacillus acidophilus W22, L. casei W56, L. paracasei W20, L. plantarum W62, L. salivarius W24, Lactococcus lactis W19, 7.5 × 109 Colony Forming Units/g twice daily dissolved in water
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
3g of a similar looking and tasting powder, twice daily
Intervention Type
Dietary Supplement
Intervention Name(s)
Omni-Biotic Stress Repair
Other Intervention Name(s)
Omni-Biotic SR-9, Winclove 825
Intervention Description
The probiotic supplement is a commercially available food for special medical purposes and includes 9 bacterial strains with at least 7.5 billion organisms (7.5 × 109 Colony Forming Units/g) per 1 portion (= 3 g).
Intervention Type
Dietary Supplement
Intervention Name(s)
placebo
Intervention Description
similar looking and tasting powder
Primary Outcome Measure Information:
Title
Butyrate producing bacteria
Description
abundance of butyrate producing bacteria
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Butyrate producing bacteria
Description
abundance of butyrate producing bacteria
Time Frame
12 months
Title
diaminooxidase concentration in serum
Description
marker of intestinal permeability
Time Frame
6 months
Title
diaminooxidase concentration in serum
Description
marker of intestinal permeability
Time Frame
12 months
Title
zonulin concentration in stool
Description
marker of intestinal permeability
Time Frame
6 months
Title
zonulin concentration in stool
Description
marker of intestinal permeability
Time Frame
12 months
Title
calprotectin concentration in stool
Description
marker of intestinal inflammation
Time Frame
6 months
Title
calprotectin concentration in stool
Description
marker of intestinal inflammation
Time Frame
12 months
Title
soluble CD 14 concentration in serum
Description
marker of systemic inflammation
Time Frame
6 months
Title
soluble CD 14 concentration in serum
Description
marker of systemic inflammation
Time Frame
12 months
Title
lipopolysaccharide binding protein concentration in serum
Description
marker of systemic inflammation
Time Frame
6 months
Title
lipopolysaccharide binding protein concentration in serum
Description
marker of systemic inflammation
Time Frame
12 months
Title
lipopolysaccharide concentration in serum
Description
marker of bacterial translocation
Time Frame
6 months
Title
lipopolysaccharide concentration in serum
Description
marker of bacterial translocation
Time Frame
12 months
Title
peptidoglycan concentration in serum
Description
marker of bacterial translocation
Time Frame
6 months
Title
peptidoglycan concentration in serum
Description
marker of bacterial translocation
Time Frame
12 months
Title
bacterial DNA concentration in serum
Description
marker of bacterial translocation
Time Frame
6 months
Title
bacterial DNA concentration in serum
Description
marker of bacterial translocation
Time Frame
12 months
Title
Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)
Description
Questionnaire to assess cognitive function, 0-70 points
Time Frame
6 months
Title
Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)
Description
Questionnaire to assess cognitive function, 0-70 points
Time Frame
12 months
Title
Mini mental state examination
Description
Questionnaire to assess cognitive function, 0-30 points
Time Frame
6 months
Title
Mini mental state examination
Description
Questionnaire to assess cognitive function, 0-30 points
Time Frame
12 months
Title
clinician's interview-based impression of change with caregiver input (CIBIC+)
Description
Questionnaire to assess overall change during the study, 1-7 points
Time Frame
6 months
Title
clinician's interview-based impression of change with caregiver input (CIBIC+)
Description
Questionnaire to assess overall change during the study, 1-7 points
Time Frame
12 months
Title
Barthel index
Description
Assessment of activities of daily living, 0-100 points
Time Frame
6 months
Title
Barthel index
Description
Assessment of activities of daily living, 0-100 points
Time Frame
12 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age >18 years Dementia of Alzheimer type and mixed type (diagnosis by a board-certified neurologist/psychiatrist and according to ICD10) Mini Mental State Examination 21-26 Stable treatment with anti-dementia drugs including phytotherapeutics (>3 months) or no intention to start anti-dementia drugs Informed consent Exclusion Criteria: Other forms of dementia Inflammatory bowel diseases Liver cirrhosis Antibiotic treatment within the last 4 weeks Febrile illness within the last 4 weeks Acute hospital admission for dementia-unrelated reasons within the last 4 weeks Dysphagia Any other condition or circumstance, which, in the opinion of the investigator, would affect the patient's ability to participate in the protocol
Facility Information:
Facility Name
Medical University Graz
City
Graz
Country
Austria
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Vanessa Stadlbauer-Köllner, MD
Phone
0043 316 385
Ext
82282
Email
vanessa.stadlbauer@medunigraz.at

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Plan Description
microbiome sequencing data will be published at nucleotide archive
IPD Sharing Time Frame
at time of publication; no limit
IPD Sharing Access Criteria
open

Learn more about this trial

Probiotics in Dementia

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