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OpenTrials
Completed

NCT Number: NCT03847714

Probiotics in Dementia

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Medical University Graz

Graz, Austria

About this study

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.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Omni-Biotic Stress Repair

Dietary Supplement

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).

Other names: Omni-Biotic SR-9, Winclove 825

Placebo

Dietary Supplement

similar looking and tasting powder

Primary outcomes

  1. Butyrate producing bacteria

    Time frame: 6 months

    abundance of butyrate producing bacteria

Secondary outcomes

  1. Butyrate producing bacteria

    Time frame: 12 months

    abundance of butyrate producing bacteria

  2. diaminooxidase concentration in serum

    Time frame: 6 months

    marker of intestinal permeability

  3. diaminooxidase concentration in serum

    Time frame: 12 months

    marker of intestinal permeability

  4. zonulin concentration in stool

    Time frame: 6 months

    marker of intestinal permeability

  5. zonulin concentration in stool

    Time frame: 12 months

    marker of intestinal permeability

  6. calprotectin concentration in stool

    Time frame: 6 months

    marker of intestinal inflammation

  7. calprotectin concentration in stool

    Time frame: 12 months

    marker of intestinal inflammation

  8. soluble CD 14 concentration in serum

    Time frame: 6 months

    marker of systemic inflammation

  9. soluble CD 14 concentration in serum

    Time frame: 12 months

    marker of systemic inflammation

  10. lipopolysaccharide binding protein concentration in serum

    Time frame: 6 months

    marker of systemic inflammation

  11. lipopolysaccharide binding protein concentration in serum

    Time frame: 12 months

    marker of systemic inflammation

  12. lipopolysaccharide concentration in serum

    Time frame: 6 months

    marker of bacterial translocation

  13. lipopolysaccharide concentration in serum

    Time frame: 12 months

    marker of bacterial translocation

  14. peptidoglycan concentration in serum

    Time frame: 6 months

    marker of bacterial translocation

  15. peptidoglycan concentration in serum

    Time frame: 12 months

    marker of bacterial translocation

  16. bacterial DNA concentration in serum

    Time frame: 6 months

    marker of bacterial translocation

  17. bacterial DNA concentration in serum

    Time frame: 12 months

    marker of bacterial translocation

  18. Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)

    Time frame: 6 months

    Questionnaire to assess cognitive function, 0-70 points

  19. Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS cog)

    Time frame: 12 months

    Questionnaire to assess cognitive function, 0-70 points

  20. Mini mental state examination

    Time frame: 6 months

    Questionnaire to assess cognitive function, 0-30 points

  21. Mini mental state examination

    Time frame: 12 months

    Questionnaire to assess cognitive function, 0-30 points

  22. clinician's interview-based impression of change with caregiver input (CIBIC+)

    Time frame: 6 months

    Questionnaire to assess overall change during the study, 1-7 points

  23. clinician's interview-based impression of change with caregiver input (CIBIC+)

    Time frame: 12 months

    Questionnaire to assess overall change during the study, 1-7 points

  24. Barthel index

    Time frame: 6 months

    Assessment of activities of daily living, 0-100 points

  25. Barthel index

    Time frame: 12 months

    Assessment of activities of daily living, 0-100 points

Sponsors and collaborators

Lead sponsor

Medical University of Graz

Other

Registry information

Acronym: PIDE

Important dates

Study start
2019
Primary completion
2024
Study completion
2024
First posted
Feb 20, 2019
Registry last updated
Feb 12, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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