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Clinical Trials in China / NCT06837272
Recruiting Observational

A Longitudinal Study to Explore the Impact of Gut Microbiome on Brain Health in Alzheimer's Disease

NCT06837272 · tracked via the Priya Life Science China tracker
Sponsor
Jining Medical University
Phase
Observational
Started
2024-01-01
Last updated
2025-02-20

Condition(s) studied

Alzheimer DiseaseGut MicrobiotaMetabonomicsMagnetic Resonance Imaging

Investigational drug(s) / intervention(s)

Multi-omics features extraction

Multi-omics features extraction: Based on multi-omics features extracted from clinical data, gut microbiome, metabolomics, and multi-modal MRI, the diagnostic model of SCD due to preclinical AD will be established.

Study summary

Gut microbiota dysfunction is associated with Alzheimer's disease (AD). However, the potential modulatory mechanism remains unclear. Previous studies have shown that gut-derived metabolites short-chain fatty acids (SCFAs) may be the key mediators between gut microbiota and brain, participating in the modulatory pathway "gut microbiota-SCFAs-brain networks". In this project, high-throughput targeted metabolomics technique will be used to explore the differences of SCFAs in the spectrum of AD, including cognitively normal individuals, subjective cognitive decline (SCD), mild cognitive impairment (MCI), and AD dementia. Then, the gut microbiome and multi-modal MRI techniques will be combined to elucidate potential interaction mechanisms of "gut microbiota-SCFAs-brain networks". Finally, based on multi-omics features extracted from gut microbiome, metabolomics, and neuroimaging after five years, the diagnostic model of SCD due to preclinical AD will be established using machine learning methods.

Eligibility

Sex
ALL
Min age
60 Years
Max age
80 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Cognitively normal group: 1. normal performance on standardized cognitive tests; 2. with no cognitive complaints or any concerns (worries). * SCD group: 1. self-experienced persistent decline in memory, rather than other domains of cognition; 2. normal performance on standardized cognitive tests; 3. failure to meet the criteria for MCI or dementia; 4. age at onset of SCD ≥ 60 years old; 5. onset of SCD within the last 5 years; 6. concerns (worries) associated with SCD; 7. feeling of worse performance than others of the same age group. * MCI group: 1. having impaired scores on both measures in at least one cognitive domain (memory, language, or speed/executive function); 2. having impaired scores in each of the three cognitive domains (memory, language, or speed/executive function); 3. the Functional Activities Questionnaire (FAQ)≥9. * AD dementia group: 1. meet the criteria for dementia and have impaired daily functional activities; 2. episodic memory deficit; 3) Clinical Dementia Rating (CDR) ≥ 1. Exclusion Criteria: * a history of stroke; * major depression and anxiety; * other central nervous system disorders that may cause cognitive impairment, such as Parkinson's disease, tumors, encephalitis, and epilepsy; * cognitive impairment caused by traumatic brain injury; * systemic diseases, such as thyroid dysfunction, syphilis and HIV; * psychosis or congenital mental developmental delay; * a history of using antibiotics, probiotics, prebiotics, or synbiotics within 3 months; * the use of corticosteroid, immune stimulating medications, and immunosuppressive agents; * major gastrointestinal tract surgery in past 5 years; * severe gastrointestinal diseases, such as irritable bowel syndrome, infammatory bowel disease, severe gastritis, other dysfunction in digestion and absorption, which has been reported to infuence gut microbiota

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Department of Neurolgy, the Affiliated Hospital of Jining Medical University Jining Shandong Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06837272 on ClinicalTrials.gov ↗ ← All trials in China