As people around the world are living longer, the number of individuals with dementia, particularly Alzheimer's disease (AD), is expected to triple by 2050. There's growing evidence suggesting that our gut health might play a role in the prevention of dementia. The connection between our gut and brain, known as the gut-brain axis, is becoming an important area of study. Research in animals has shown that different types of dietary fibre can improve gut health, brain function, mood, blood sugar level and the immune system and may even prevent certain harmful brain changes seen in Alzheimer's disease. Subjective Cognitive Decline (SCD) is a condition where individuals notice a decline in their mental abilities, and it can be an early sign of Alzheimer's disease. The goal of this clinical trial is to learn if dietary fibres can improve gut and brain health in older individuals, between the ages of 60 and 79 years, who notice problems in their mental abilities, and meet the criteria of SCD. Three different dietary fibres will be given, and researchers will compare three different fibres to a placebo product to see if there is a difference between the fibres and the placebo. The main questions it aims to answer are: 1. Does dietary fibre improve working memory? 2. Does dietary fibre improve other markers of brain function? 3. Does dietary fibre improve gut health? 4. Does dietary fibre improve the immune system and blood glucose levels? 5. Does dietary fibre improve mood? Participants will: * Consume dietary fibres twice a day, mixed in water, tea or coffee, for a period of 26 weeks * Have two functional MRI scans, and three additional study visits, where blood, urine and feces will be collected * Undergo a number of neuropsychological tests, aimed at evaluating brain function * Fill out questionnaires on their general health, mood, dietary habits, gut health * Wear smartwatches for one week, at the beginning and the end of the study
Rationale: Due to the greying of society, a triplication of the number of people with dementia worldwide, with Alzheimer's disease (AD) as the commonest form, is expected by 2050. Compelling evidence points towards a crucial role of intestinal health as one potential etiological modifier of dementia, with the (microbiota) gut-brain axis (MGBA) receiving increasing attention. A number of preclinical studies have demonstrated benefit of various sources of dietary fibre for their capacity to improve gut health, cognitive functioning, general mood, glycaemia, immunogenicity, and, to inhibit tau phosphorylation, the latter which is a hallmark in AD brain. Subjective cognitive decline (SCD) lies on the continuum of AD, and subjects with this condition are at increased risk of further conversion to mild cognitive impairment (MCI) or AD. Currently, no cure is available for AD. Various symptomatic and a few disease-modifying treatments are available, but these treatments only have very limited or mild clinical effects and are often accompanied by severe side effects. Clinical follow-up studies to evaluate the effect of dietary fibre in older adults with suspected cognitive decline are required, but are still lacking to date. Objective: The primary objective of this study is to investigate the effect of 26 weeks of supplementation with three different dietary fibres (chicory inulin, resistant dextrin, and seaweed polysaccharide) compared to a placebo (maltodextrin) on microbiota gut-brain health effects in older adults (aged 60-79) with Subjective Cognitive Decline Plus (SCD+) by assessing changes in brain function and working memory by blood oxygen level dependant (BOLD) signal activity and task accuracy during n-back task functional magnetic resonance imaging (fMRI) assessment. The secondary objectives are to investigate the effects of 26 weeks of supplementation with dietary fibre (chicory inulin, resistant dextrin, and, seaweed polysaccharide) compared to placebo (maltodextrin) in older adults on the following parameters related to potential gut-brain pathways: 1. neuropsychological test battery scoring, 2. other relevant brain health parameters, 3. relevant intestinal health parameters, and 4. immune and metabolic parameters. Study population: 164 older adults (60-79 years) with SCD+. Study design implementation: Participants will undergo assessments at baseline (T0), mid-study (T1/2, after 13 weeks) and at study end (T1, after 26 weeks. Each participant will have five study visits in total: two at T0, one at T1/2 and two at T1. At each of the timepoints the following will be collected/performed at WUR: Sample collection (blood, urine (omitted in week 13), faeces); general cognitive assessments (see NTB; Cognitive Failure Questionnaire (CFQ) (baseline and end only), GDS-15, GAD-7); general physiological measures (blood pressure, BMI, grip-strength); dietary assessment (MIND-adjusted Eetscore, FFQ). At ZGV working memory will be evaluated using BOLD fMRI signalling and task accuracy using an n-back task paradigm. Additionally, high-resolution T1- and T2-weighted anatomical images of main regions of interest (hippocampi, (pre)frontal-, and temporal cortices) will be acquired. For two periods of one week, corresponding with the baseline and week 26 visits, participants will wear smartwatches. These watches will be worn continuously and data will be gathered regarding cardiovascular functioning (heart rate), physical activity and mood (push messages).
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
TRIPLE
Enrollment
164
Chicory inulin (12g/day) divided over two dosages (6g per dose)
Resistant dextrin (14g/day) divided over two dosages (7g per dose)
Seaweed polysaccharide (1g/day) divided over two dosages (0.5g per dose). Additionally contains 7g/day of placebo as a volumetric and isocaloric filler.
Maltodextrin (7g/day) will be provided in two divided doses (3.5g per dose)
Wageningen University
Wageningen, Netherlands
Effect on working memory during n-back task fMRI
Effects on working memory will be assessed by blood-oxygen level dependant (BOLD) signal activity during 2-back task performed during fMRI scanning
Time frame: Measured at baseline and week 26
Effect on working memory performance during n-back task fMRI
Effects on working memory performance will be assessed by task accuracy during 2-back task performed during fMRI scanning
Time frame: Measured at baseline and week 26
Effect on cognitive functioning as measured by a neuropsychological test battery
Effect on z-scoring of cognitive domains- episodic memory, executive function and working memory as measured by Cognitive Function Composite test battery
Time frame: Measured at baseline, week 13 and week 26
Effect on ADAS-Cog Word Recall cognitive assessment (episodic memory)
Mean number of correct responses across three trials; Score 0 to 10. Higher score indicates better outcome.
Time frame: Measured at baseline, week 13 and week 26
Effect on ADAS-Cog Word Recognition cognitive assessment (episodic memory)
Mean number of correct responses across three trials. Score 0 to 12. Higher score indicates better outcome.
Time frame: Measured at baseline, week 13 and week 26
Effect on Digit Symbol Substitution Test cognitive assessment (executive function)
Amount of symbols correctly substituted. Score 0 - 90. Higher score indicates better outcome
Time frame: Measured at baseline, week 13 and week 26
Effect on Digit Span Backward Task cognitive assessment (working memory)
Longest span of digits correctly recalled. Score 2-8. Higher score indicates better outcome
Time frame: Measured at baseline, week 13 and week 26
Effect on Category Fluency Test cognitive assessment (executive function)
Number of uniquely named items from category within 60 seconds. Higher score indicates better outcome
Time frame: Measured at baseline, week 13 and week 26
Effect on ADAS-Cog Orientation cognitive assessment (episodic memory)
The number of correct responses on orientation. Score 0 to 8. Higher score indicates better outcome
Time frame: Measured at baseline, week 13 and week 26
Effect on tryptophan metabolites
Tryptophan related neurotransmitters and metabolites (plasma)
Time frame: Measured at baseline and week 26
Effect on amyloid-beta (Aβ) biomarker
Aβ1-42/Aβ1-40 ratio (plasma)
Time frame: Measured at baseline and week 26
Effect on neuroplasticity
Brain-derived neurotrophic factor (BDNF) levels (serum)
Time frame: Measured at baseline and week 26
Effect on brain regions of interest
Structural MRI with T1- and T2-weighted anatomical images of regions of interest (hippocampi, (pre)frontal-and temporal cortices)
Time frame: Measured at baseline and week 26
Effect on hypothalamic-pituitary adrenal axis
Cortisol levels (serum)
Time frame: Measured at baseline and week 26
Effect on intestinal barrier integrity
Assay-based panel of intestinal barrier integrity markers measured in blood
Time frame: Measured at baseline, week 13 and week 26
Effect on intestinal inflammation
Assay-based panel of intestinal inflammatory markers measured in faeces
Time frame: Measured at baseline, week 13 and week 26
Effect on gastrointestinal transit time
Gut transit time measured by blue muffin consumption and appearance of blue colour in faeces
Time frame: Measured at baseline, week 13 and week 26
Effect on gastrointestinal symptoms
Self-rated gastrointestinal symptoms as measured by the Gastrointestinal Symptom Rating Scale (GSRS) questionnaire
Time frame: Measured at baseline, week 13 and week 26
Effect on self-reported stool consistency
Effect on stool consistency as measured by Bristol Stool Scale (BSS)
Time frame: Measured at baseline, week 13 and week 26
Effect on stool consistency
Effect on stool consistency as measured by faecal water content
Time frame: Measured at baseline, week 13 and week 26
Effect on qualitative faecal microbiota composition
Qualitative faecal microbiota composition as measured by 16s rRNA sequencing
Time frame: Measured at baseline, week 13 and week 26
Effect on quantitative faecal microbiota composition
Quantitative faecal microbiota composition as measured by digital droplet PCR
Time frame: Measured at baseline, week 13 and week 26
Effect on faecal metabolites
Faecal short-chain fatty acids (acetic acid, propionic acid, butyric acid, valeric acid, hexanoic acid, heptanoic acid) and branched-chain fatty acids (isobutyric acid, isovaleric acid, 4-methyl valeric acid) as measured by gas chromatography-flame ionization detection (GC-FID)
Time frame: Measured at baseline, week 13 and week 26
Effect on faecal pH
Faecal pH measurement
Time frame: Measured at baseline, week 13 and week 26
Effect on immune parameters
Inflammatory cytokine panel measured in blood
Time frame: Measured at baseline, week 13 and week 26
Effect on glucose homeostasis
Assay-based panel of markers to evaluate glucose homestasis in blood
Time frame: Measured at baseline, week 13 and week 26
Effect on lipid profile
Assay-based panel of markers to analyse lipid profile in blood
Time frame: Measured at baseline, week 13 and week 26
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