A Registry Study on Biomarkers of Takayasu's Arteritis (ARSBTA)

NCT03372980 | Recruiting

• 1 other identifier: ARSBTA
• Study Type: observational
• Target: 1,000
• Locations: 1 country
• Sites: 1

Brief Summary

Takayasu arteritis is a chronic vasculitis mainly involving the aorta and its main branches such as the brachiocephalic, carotid, subclavian, vertebral, and renal arteries, as well as the coronary and pulmonary arteries. Inflammation causes segments of the vessels to become narrowed, blocked, or even stretched, possibly resulting in aneurysms. The disease is very rare but most commonly occurs in young Asian women. However, there is a considerable lack of understanding of the disease mechanism of Takayasu arteritis. Initially, the disease remains clinically silent (or remains undetected) until the patients present with vascular occlusion. Additionally, many individuals with Takayasu arteritis, however, have no apparent symptoms despite disease activity. Therefore, biomarkers for diagnosis and monitor disease activity in individuals with Takayasu arteritis are needed. In this study, the investigators therefore to use different methods to identify new biomarkers for diagnosing or monitoring the disease activity in individuals with Takayasu arteritis. These biomarkers may provide valuable insights into the underlying biochemical processes and aid the understanding of the pathophysiology of this disease.

Conditions

Takayasu's Arteritis

Keywords

Biomarkers

Outcome Measures

Primary Outcomes (2)

• Diagnosis of each participant

  Participant with Takayasu arteritis had image information from vascular magnetic resonance angiography (MRA) or computed tomography angiography (CTA) to confirm the final diagnosis.

  These data is collected from the cases' medical record in an average of 3 month after the sample recruiting.

• Disease activity of each participant

  Criteria for Disease Activity：Criteria for active disease are detection of new vascular lesion or lesions in arteries on vascular Imaging in participants who had undergone magnetic resonance angiography (MRA) or computed tomography angiography (CTA) examination in the month before evaluation, or at least 2 of the following: 1) new onset of carotodynia or pain over large vessels, 2) transient ischemic episodes not attributable to other factors, 3) new bruit or new asymmetry in pulses or blood pressure determination, 4) ischemic symptoms (including new-onset claudication), and 5) fever in absence of infection. Criteria defined inactive disease: 1) absence of the features of active disease for at least the previous 3 months; 2) absence of new vascular lesions and stability or improvement of previous vascular lesion or lesions on an imaging study performed up to 1 month before evaluation.

  These data is collected from the cases' medical record or during follow-up visit in an average of 6 month after the sample recruiting.

Study Arms (2)

Case

Control

Eligibility Criteria

• Age: 18 Years - 70 Years
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

Case group consists of patients who was diagnosed as Takayasu's Arteritis; control group is general population without Takayasu's Arteritis.

You may qualify if:

• Subjects who met the American College of Rheumatology 1990 classification criteria for Takayasu arteritis:
• Age of onset ≤40 years,
• Claudication of upper or lower extremities,
• Decreased pulsation of 1 or both brachial arteries,
• Difference of ≥ 10 mmHg in systolic blood pressure between arms,
• Bruit over subclavian arteries or aorta,
• \*Arteriographic evidence showing a branch of the aorta stenosis or occlusion.
• Meeting more than 3 of 6 criteria suggests the diagnosis of Takayasu arteritis.
• \*Angiography in this study was replaced by vascular magnetic resonance angiography(MRA)or computed tomography angiography(CTA).

You may not qualify if:

• Arteriographic lesions that could be entirely due to atherosclerosis,
• Suffer from other autoimmune diseases (eg, ANCA-associated vasculitis, systemic lupus erythematosus, etc.) besides Takayasu arteritis,
• Cogan's syndrome,
• Behcet's disease,
• Subjects with any serious acute or chronic infection,
• Giant cell arteritis (large vessel vasculitis and at least 50 years old) or other infectious forms of large vessel vasculitis.
• Prospective
• Subjects with initial suspicion of having Takayasu arteritis or patients with Takayasu arteritis need assessment of disease activity were prospectively enrolled.
• Patients without image studies.
• Patients with confirmed other autoimmune diseases (eg, ANCA-associated vasculitis, systemic lupus erythematosus, etc.)

Sponsors & Collaborators

• Beijing Institute of Heart, Lung and Blood Vessel Diseases: lead
• Shanghai Zhongshan Hospital: collaborator
• Peking University People's Hospital: collaborator

Study Sites (1)

Beijing Anzhen Hospital

Beijing, Beijing Municipality, 100029, China

RECRUITING

Biospecimen

Retention: SAMPLES WITH DNA

Blood samples，Cells，Tissues

MeSH Terms

Conditions

Takayasu Arteritis

Condition Hierarchy (Ancestors)

Aortic Arch Syndromes; Aortic Diseases; Vascular Diseases; Cardiovascular Diseases; Arteritis; Vasculitis; Skin Diseases, Vascular; Skin Diseases; Skin and Connective Tissue Diseases

Central Study Contacts

Yuan WANG, PhD

CONTACT

86-010-64456169; wangyuan980510@163.com

Fengjuan LI, PhD

CONTACT

86-010-64456165; lifjgogo@163.com

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: OTHER
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: December 4, 2017
• First Posted: December 14, 2017
• Study Start: January 1, 2016
• Primary Completion (Estimated): December 1, 2026
• Study Completion (Estimated): December 1, 2026
• Last Updated: April 12, 2022

Record last verified: 2022-04

Locations

CN (1)