Cohort Follow-up of Patients With Renal or Craniocervical Fibromuscular Dysplasia (PROFILE)

Assistance Publique - Hôpitaux de Paris

Status

Completed

Conditions

Fibromuscular Dysplasia

Treatments

Other: Abdominal and supra-aortic trunks vascular imaging

Other: Urine sampling

Other: Blood sampling (biomarkers)

Genetic: Blood sampling (genetic)

Study type

Interventional

Funder types

Other

Identifiers

NCT02961868

PHRC-08-192 (Other Grant/Funding Number)

P071241 (Other Identifier)

2009-A00288-49 (Registry Identifier)

Details and patient eligibility

About

PROFILE is a cohort study evaluating the progression of fibromuscular dysplasia lesions. This study is the prospective dimension of ARCADIA registry (ClinicalTrials.gov Identifier: NCT02884141), which aims to document phenotypic and genetic traits in patients with renal and/or cervical artery fibromuscular dysplasia.

Full description

Background

Fibromuscular dysplasia (FMD) is a group of nonatherosclerotic, noninflammatory arterial diseases that usually involve renal and carotid arteries. Patients with FMD may present with renovascular hypertension and/or with cerebrovascular symptoms. The prevalence of FMD in hypertensive patients is estimated at 4/1000. Angiographic classification includes the multifocal type, with multiple stenoses and the 'string-of-beads' appearance that is related to medial FMD, and tubular and focal types which are not clearly related to specific histological lesions. FMD may affect one or more vascular beds and progress to more severe stenosis and to renal or cerebrovascular complications. FMD appears to be familial in 10% of cases (OMIM #135580).

Renal artery FMD may progress to more severe stenosis and to renal atrophy, and/or to stenoses affecting more arteries within or outside the renal vasculature. The risk of progression as assessed from available studies was probably overestimated because documentation of progression was obtained from angiography, a procedure which is not routinely undertaken in patients with favourable clinical and biological outcomes. The disease is progressive, however, and literature stated that patients with FMD should undergo yearly duplex ultrasonography to detect progression of disease, restenosis, or loss of kidney volume.

There are very few data on prognosis of patients with symptomatic carotid or vertebral artery FMD. The risk of arterial disease progression over time is unknown. The risk of ischemic stroke ranged from 0 to about 3% per year in the few studies which assessed that issue.

Objectives

The primary objective is to estimate the incidence and risk factors for progression of FMD lesions. This will be assessed by comparison between initial and 3 years abdominal and supra-aortic trunks vascular imaging (angiography, CT-angiography or Magnetic Resonance (MR) angiography), monitoring of downstream consequences development of lesions progression and clinical events.

The secondary objectives are:

to estimate rate of genetic polymorphism that may influence disease progression or be associated with complications
to assess the frequency of multi-site FMD (common objective with the ARCADIA study)
to collect standardized clinical, radiological, and biological data in patients with FMD through a national registry (common objective with the ARCADIA study)
to organize a clinical, radiological and biological database and a biobank that will constitute a unique resource to initiate further clinical research (common objective with the ARCADIA study).

Enrollment

340 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Patient with renal or craniocervical fibromuscular dysplasia diagnosed during the 2 years before inclusion
The fibromuscular dysplasia is documented by imaging (angiography, CT-angiography, MR-angiography) of less than 2 years and validated by a radiologist investigator
Patient who understood and signed inform consent form
Affiliated to the French health insurance system
Available for a 3 years follow-up

Exclusion criteria

Patient with renal or craniocervical atherosclerosis, or inflammatory vascular disease as dominant pathological features
Patient with renal or craniocervical arteries dissection or aneurysm without any other evidence of fibromuscular dysplasia
Patient under 18 or under tutorship
Known pregnancy