The goal of this observational study is to learn about neuroimage and biomarkers in the cerebral small vessel disease. The main questions it aims to answer are:
* How does neurovascular coupling change during the progression of CSVD?
* How is the pattern/mapping of alterations in CSVD biomarkers? Participants will be observed and visit the research center annually to perform multi-modal MRI, PET, neuropsychological tests, and blood tests.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
1. Age ≥18 years.
2. Evidence of cerebral small vessel disease (CSVD) on brain MRI, meeting at least one of the following imaging criteria:
* White matter hyperintensities (WMH) with a total Fazekas score ≥2;
* Fazekas score =1 with at least two vascular risk factors (hypertension, hyperlipidemia, diabetes mellitus, obesity, current smoking, or a history of vascular events other than stroke);
* Fazekas score =1 accompanied by the presence of lacunes;
* Imaging evidence of a recent subcortical lacunar infarction.
3. Independent in activities of daily living (modified Rankin Scale \[mRS\] ≤2).
4. Able and willing to provide written informed consent.
Exclusion Criteria:
1. Acute ischemic stroke with a diffusion-weighted imaging (DWI) lesion \>20 mm in diameter.
2. Acute intracerebral hemorrhage.
3. Acute subarachnoid hemorrhage, a history of aneurysmal subarachnoid hemorrhage or cerebrovascular malformation, or the presence of an untreated intracranial aneurysm \>3 mm in diameter.
4. Previously diagnosed neurodegenerative disorders, such as Alzheimer's disease (AD) or Parkinson's disease (PD).
5. Definite non-vascular white matter diseases, including multiple sclerosis, adult-onset leukodystrophy, metabolic encephalopathy, or other non-vascular white matter disorders.
6. Major psychiatric disorders diagnosed according to the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-5).
7. Contraindications to MRI (e.g., severe claustrophobia or MRI-incompatible implants).
8. Severe systemic diseases (e.g., active malignancy) with an expected life expectancy of less than 5 years.
9. Inability to complete scheduled follow-up because of geographic, logistical, or other reasons.
10. Concurrent participation in another interventional clinical trial.
Primary outcome measure(s)
Global cognitive ability — baseline, 1 year, 2-year, 3-year, 5-year,10-year Mini-mental state examination
Executive function — baseline, 1 year, 2-year, 3-year, 5-year,10-year Clock drawing test
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.
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