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Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: For probands: 1. Aged 40-75 years; 2. Diagnosis of acute cerebral infarction; 3. Confirmed intracranial artery stenosis of more than 50 percent by CTA, MRA TOF or DSA ; 4. Should be recruited at least 90 days after stroke onset ; 5. Willingness of At least one sibling to participate in this study; 6. Willingness of the participant and all his/her guradians to provide written informed consent. For siblings: 1. 18 years of age or older; 2. At least one sibling diagnosed with cerebral infarction.
Exclusion criteria
Exclusion criteria: For probands: 1. Concurrent life-threatening disease including heart failure, respiratory failure, acute or chronic hepatic dysfunction, acute or chronic renal function, tumors and hematological disease; 2. History of psychiatric disorders; 3. Pregnancy; 4. Participating in other clinical studies concurrently. For siblings: 1. Concurrent life-threatening disease including heart failure, respiratory failure, acute or chronic hepatic dysfunction, acute or chronic renal function, tumors and hematological disease; 2. Allergy to contrast agent or inability to tolerant with head CTA ; 3. History of psychiatric disorders; 4. Pregnancy; 5. Participating in other clinical studies concurrently; 6. Inabililty to contact; 7. Unwillingness to provide written informed consent.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| frequency distribution of PDE4D genotypes and alleles;frequency distribution of ALOX5AP genotypes and alleles; | — |
Secondary
| Measure | Time frame |
|---|---|
| degree of intracranial arterial stenosis;location of intracranial arterial stenosis; | — |
Countries
China
Contacts
Huashan Hospital, Fudan University