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Multi-modality MRI Study on Differences in Conversion of aMCI Patients With APOEε4 to AD

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02225964
Enrollment
200
Registered
2014-08-26
Start date
2014-01-31
Completion date
2018-12-31
Last updated
2020-07-02

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

Conditions

Mild Cognitive Impairment

Keywords

APOEε4

Brief summary

This study is to find out the imaging marker and the changing laws of the marker during the course of the disease. The final purpose is to provide scientific evidence for new prevention, diagnosis and treatment of Alzheimer's disease.

Detailed description

It is an urgent problem in the field of cognitive neuroscience to tell the conversion progression of amnestic mild cognitive impairment(aMCI) patients with Apolipoproteinε4(APOEε4) to Alzheimer's Disease(AD). Based on our preliminary work, we will study the special group of aMCI patients with APOEε4 with multi-modality magnetic resonance imaging (resting-state functional MRI, structural MRI and diffusion tensor imaging) longitudinally. Besides, we will also detect the APOE genotype of each sample and enlarge the sample size. According to situation of the conversion or non-conversion and differences in the conversion progression, we will analyze the data between the inter-groups and intra-groups, compare the imaging data of baseline and follow-up, find the prediction imaging marker of AD and optimize the reliability and validity.

Interventions

None listed

Sponsors

Xuanwu Hospital, Beijing
CollaboratorOTHER
XuanwuH 2
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Complaint about memory loss and confirmed by an informant * Cognitive impairment in single or multiple domains, adjusted for age and education * Normal or near-normal performance on general cognitive function and no or minimum impairment of daily life activities * A Clinical Dementia Rating (CDR) score is 0.5 * Failure to meet the criteria for dementia * Carrying susceptible gene APOEε4 * Must be able to accept examination of MRI, sight and hearing allow to complete test

Exclusion criteria

* Other diseases that cause cognitive impairment,such as thyroid disease,stroke and so on * people who have severe visual and hearing impairment

Design outcomes

Primary

MeasureTime frameDescription
the conversion of aMCI patients with APOEε4 to ADone yearAccording to situation of the conversion or non-conversion and differences in the conversion progression, we will analyze the data between the inter-groups and intra-groups, compare the imaging data of baseline and follow-up, find the prediction imaging marker of AD and optimize the reliability and validity.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026