Exploring the Predicting Biomarkers From Mild Cognitive Impairment to Dementia (EBMID)

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age50-85
SponsorCuibai Wei,Clinical Professor

About this trial

Mild cognitive impairment (MCI) represents a transitional stage between healthy aging and dementia, and affects more than 15% of the population over the age of 60 in China. About 15% patients with MCI could progress into dementia after two years and about one-third develop into dementia within five years, which will lead to suffering, as well as staggering economic and care burden. So, exploring the predicting biomarkers from MCI to dementia to identify and delay progression to dementia at an early stage is of great social and clinical significance. Some reports based on a single neural biomarker suggest that risk models can predict the conversion of MCI to dementia, but no widely recognized prediction models basing on multiple complex markers have been used in clinical practice. The objectives of this study are to outline the spectrum of MCI transforming into dementia through a 5-year prospective longitudinal cohort study; Secondly, screening biomarkers for MCI transmit to dementia are based on clinical symptoms, neuropsychology, neuroimaging, neuroelectrophysiology, and humoral markers tests data.

Eligibility criteria

Qualifiers

Male or female patients aged ≥50 and ≤85 years;

Meet the diagnostic criteria for dementia or MCI; ③ Neuropsychological score: MMSE 15-28 points, CDR≤1 point; ④ The patients and their families were informed and signed the informed consent.

Disqualifiers

There are other neurological diseases that can cause brain dysfunction (such as depression, brain tumors, Parkinson's disease disease, metabolic encephalopathy, encephalitis, multiple sclerosis, epilepsy, traumatic brain injury, normal intracranial pressure hydrocephalus, etc.);

There are other systemic diseases that can cause cognitive impairment (such as hepatic insufficiency, renal insufficiency, Thyroid dysfunction, severe anemia, folic acid or vitamin B12 deficiency, syphilis, HIV infection, alcohol and drug abuse, etc.);

Suffering from a disease that cannot cooperate with the completion of cognitive examination; ④ There are contraindications to nuclear magnetic resonance;

There is mental and neurodevelopmental delay; ⑥ refuse to draw blood; ⑦ Refuse to sign the informed consent.

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

900 Participants
are grouped into 2 trial groups

Sponsors and collaborators

Cuibai Wei,Clinical Professor

Lead sponsor

Xuanwu Hospital, Beijing

Sponsor institution

Beihang University

Collaborator

Chinese PLA General Hospital

Collaborator

Chongqing Medical University

Collaborator

Tianjin Huanhu Hospital

Collaborator

Affiliated Zhongshan Hospital of Dalian University

Collaborator

First Hospital of Shijiazhuang City

Collaborator

Jilin University

Collaborator