Alzheimers disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.Individuals presenting with subjective complaints of cognitive impairment and memory decline. 2.Patients with clinical features suggestive of Alzheimer’s disease or mild cognitive impairment (MCI). 3.High-risk individuals with a family history of Alzheimer’s disease. 4.Individuals who voluntarily agree to undergo blood testing and provide written informed consent.
Exclusion criteria
Exclusion criteria: 1.Patients with severe coagulation disorders. 2.Patients with major systemic diseases that may affect blood-based biomarkers (e.g., severe hepatic or renal insufficiency). 3.Patients who are unable to comply with sample collection procedures or who refuse testing. 4.Individuals who refuse to provide written informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Blood-based AD biomarkers (Aß1–42, Aß1–40, Aß42/40 ratio, p-tau181, and p-tau217);Diagnostic performance of blood-based AD biomarker testing (area under the curve, AUC).; | — |
Secondary
| Measure | Time frame |
|---|---|
| Correlation between blood-based AD biomarkers and Aß-PET or cerebrospinal fluid (CSF) findings.; | — |
Countries
China
Contacts
Zhejiang Provincial People's Hospital