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

A Longitudinal Study to Explore the Impact of Gut Microbiome on Brain Health in Alzheimer's Disease: China Healthy Brain and Gut Microbiome Study (CHBGMS)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06837272
Enrollment
285
Registered
2025-02-20
Start date
2024-01-01
Completion date
2029-12-31
Last updated
2025-02-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer Disease, Gut Microbiota, Magnetic Resonance Imaging, Metabonomics

Keywords

Subjective cognitive decline, Multi-omics

Brief 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.

Interventions

DIAGNOSTIC_TESTMulti-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.

Sponsors

Xuanwu Hospital, Beijing
CollaboratorOTHER
Jining Medical University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
60 Years to 80 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frameDescription
The changes of gut microbiome in the spectrum of AD5 yearUsing the 16S rRNA Illumina Miseq sequencing technique, the diversity and compositions of gut microbiome will be compared in different stages of AD, including cognitively normal individuals, SCD, MCI and AD dementia.
The changes of SCFAs in the spectrum of AD5 yearUsing the high-throughput target metabolomics technique, SCFAs will be compared in different stages of AD, including cognitively normal individuals, SCD, MCI and AD dementia.
Multi-omics biomarkers associated with conversion to cognitive impairment for SCD subjects5 yearsSCD subjects will be followed for five years. The investigators aim to characterize those who convert to MCI or AD dementia during the follow-up, and further find the multi-omics features associated with the progression of AD. 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.

Secondary

MeasureTime frameDescription
The interaction mechanisms of gut microbiota-SCFAs-brain networks5 yearsThe gut microbiome, SCFAs and multi-modal MRI techniques will be combined to elucidate potential interaction mechanisms of gut microbiota-SCFAs-brain networks.

Countries

China

Contacts

Primary ContactCan Sheng, PhD
canyeweiwu2013@163.com86-18701257298
Backup ContactYun Guo, Master
yun125985@163.com86-18863030588

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026