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Moyamoya Disease Biomarkers in Patients With Intracranial Atherosclerotic Stroke

Moyamoya Disease Biomarkers in Patients With Intracranial Atherosclerotic Stroke

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02074111
Enrollment
400
Registered
2014-02-28
Start date
2014-01-31
Completion date
2019-12-31
Last updated
2017-04-26

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

Conditions

Intracranial Atherosclerotic Stroke, Intracranial Steno-occlusive Disease, Moyamoya Disease

Keywords

Moyamoya disease, Intracranial atherosclerotic stroke, Intracranial steno-occlusive disease, ring finger 213 (RNF213) gene mutation, high-resolution MRI

Brief summary

The aim of this study is to investigate the proportion of patients with moyamoya disease among the patients who were diagnosed as having intracranial atherosclerotic stroke. To do this, biomarkers (gene and imaging) for moyamoya disease are tested and follow up angiography are performed during follow up (in selected patients).

Detailed description

1. Purpose Both moyamoya disease (MMD) and intracranial atherosclerotic stenosis (ICAS) are more prevalent in Asians than in Westerners, although the reason for the race-ethnic differences is unsettled. It is possible that patients with adult-onset MMD were misclassified as having ICAS, which may in part explain the high prevalence of intracranial atherosclerosis in Asians. It is important to differentiation between these two diseases because MMD and ICAS have differential therapeutic strategies (surgical revascularization in MMD vs. the use of antithrombotics/statins and stenting in ICAS). The ring finger 213 (RNF213) was recently identified as a susceptibility gene for MMD in East Asians. Characteristic high-resolution (HR) MRI findings of MMD and ICAS have recently been reported. The aim of this study is to investigate the proportion of patients with moyamoya disease among the patients who were diagnosed as having intracranial atherosclerotic stroke. To do this, biomarkers (gene and imaging) for moyamoya disease are tested and follow up angiography are performed during follow up (in selected patients). 2. Conditions: Stroke, intracranial occlusive lesion 3. Intervention: None 4. Study period: Jan 22, 2014 \ Dec 31, 2016 5. Study design: Observational model Time perspective: Retrospective-Prospective

Interventions

None listed

Sponsors

Samsung Medical Center
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
20 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

1. Intracranial atherosclerotic stroke * Patients with age over 20 years * Patients with focal neurological deficits presented within 7 days of symptom onset * Patients with acute ischemic lesions on diffusion-weighted image (DWI) * Patients with stenosis on the relevant intracranial vessels (distal ICA and/ or M1) 2. Moyamoya disease * Patients with age over 20 years * Patients who performed conventional angiography * Patients who are diagnosed as having either definite or probable Moyamoya disease 3. Healthy subjects * Subjects with age over 20 years * Subjects with no history of cerebrovascular disease

Exclusion criteria

* Patients with extracranial stenosis more than 50% * Patients with potential sources of cardio-aortic embolism * Patients with moderate to severe renal disease * Pregnancy or lactation * Patients with short life expectancy

Design outcomes

Primary

MeasureTime frame
Frequency of RNF213 gene variants and HR-MRI findings in patients with intracranial atherosclerosisAnytime during study period (in intracranial atherosclerosis, HR-MRI findings within 2 weeks)

Secondary

MeasureTime frame
Frequency of typical angiographic findings of moyamoya disease at follow up conventional angiography in patients with intracranial atherosclerosis who showed typical gene and imaging biomarkers of moyamoya diseaseWithin 2 years

Countries

South Korea

Contacts

Primary ContactOh Young Bang, MD PhD
nmboy@unitel.co.kr82-2-3410-3599

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026