Study on Susceptibility Genes and Pathogenic Mechanism of Non-syndromic Familial Aortic Dissection

NCT ID: NCT04439565

Last Updated: 2020-06-19

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2020-06-17

Study Completion Date

2023-07-17

Brief Summary

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Aortic dissection is dangerous and difficult to predict, so it is particularly important to carry out early prevention, diagnosis and rational treatment for high-risk groups. The related genes found in previous studies can not be detected in all patients with dissection; at present, the pathogenesis of non-syndromic aortic dissection is not clear, of which about 20% of patients have family aggregation and have the general representative characteristics of non-syndromic dissection. In this project, the peripheral blood samples of core family subjects were detected by sequencing technique. analyze disease-related susceptibility genes; 2 determine the effect of susceptibility genes on the incidence of dissection in mice through animal experiments; and 3 explore the effect of susceptibility genes on cell function at the cellular level.

Detailed Description

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Conditions

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Aortic Dissection Family Research Aortic Dissection, Familial, With or Without Aortic Aneurysm

Study Design

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Observational Model Type

FAMILY_BASED

Study Time Perspective

OTHER

Interventions

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movement

aortic dissection or aneurysm patients this is an observation cohort study about a Non-syndromic Familial Aortic Dissection without intervention.

Intervention Type GENETIC

Eligibility Criteria

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Inclusion Criteria

Inclusion Criteria:

* Family inclusion criteria: 1 at least one person in each generation of a family has aortic dissection, and at least two generations of members can be included;

Exclusion Criteria:

* Pedigree exclusion criteria: pedigree members have marfan syndrome, Loeys-Dietz syndrome, Ehler-Danlos syndrome, aneurysm-Osteoarthritis syndrome and other syndroms
Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Chinese Medical Association

NETWORK

Sponsor Role lead

Responsible Party

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Zaiping Jing

professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Locations

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Changhaihospital

Shanghai, Shanghai Municipality, China

Site Status RECRUITING

Countries

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China

Central Contacts

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Jing Zaiping, professor

Role: CONTACT

02131161670

Facility Contacts

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Jing Zaiping, MD

Role: primary

Other Identifiers

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https://orcid.org/0000-0002-05

Identifier Type: -

Identifier Source: org_study_id

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