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Tahiti-families: Polynesian Families of Gout Patients

L

Lille Catholic University

Status

Completed

Conditions

Gout

Treatments

Other: Epidemiological study

Study type

Interventional

Funder types

Other

Identifiers

NCT04900090
RC-P00106

Details and patient eligibility

About

Gout is a chronic disease caused by the deposit of monosodium urate (MSU) crystals in body tissues secondary to hyperuricemia. Patients with gout suffer severe attacks of acute joint pain. As the disease progresses, the joint pain becomes chronic and associated with disabling and deformative manifestations called tophus. This disease is strongly associated with several comorbidities such as cardiovascular disease and chronic kidney failure. Gout is a very common disease, which is affecting 0.9% of the adult population in France and nearly 4% of the North-American population. Data from New Zealand show a particularly high prevalence of gout among Polynesians (minority populations in New Zealand and other islands of the South Pacific) that would be explained by genetic susceptibility and frequently interrelated metabolic diseases. Data on the Polynesian population in New Caledonia suggest prevalence figures close to 7% and prevalence in French Polynesia is assumed to be higher. International genomic studies of gout and hyperuricaemia have identified alleles associated with the occurrence of gout.

The aim is to focus on families with several gouty members (numerous in French Polynesia, and geographically clustered) in order to enable the study of individuals with monogenic gout or with a low number of variants (= cases) determining in the occurrence of gout, as well as a non-gouty family member (= controls).

Dual-energy CT scan (DECT) allows identification and quantification of UMS crystal deposits in the tissue. The volume of crystals correlates not only with the inflammatory activity of the disease but also with the comorbidities that complicate it. Dual-energy scanning has shown the presence of UMS crystals in some hyperuricemic individuals, which could help to identify those individuals most at risk of developing the disease as they already have the stigma of sub-clinical inflammatory activity.

Enrollment

33 patients

Sex

All

Ages

18 to 80 years old

Volunteers

Accepts Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria :

Case group :

  • Gout patients
  • Polynesian origin
  • Aged 18 to 80 years
  • Agreeing to participate in the study
  • Having a 1st or 2nd degree relative who is also gouty and a 1st degree relative of the same generation and sex who is not gouty

Control group :

  • Non-gouty individuals who are 1st degree relatives of a gouty patient of the same generation and sex
  • Aged 18 to 80 years
  • Agreeing to participate in the study

Exclusion Criteria :

  • Pregnant women
  • Persons under guardianship, curatorship or other legal incapacity
  • Persons with a contraindication to Magnetic resonance imaging (MRI) examination
  • For non-gouty controls : current hyperuricemic treatment (Allopurinol, Febuxostat, Probenecid or Benzbromarone)
  • For gouty case : not participating in the TOPATA study (NCT04812886)

Trial design

Primary purpose

Other

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

33 participants in 2 patient groups

Case group : gout patients
Experimental group
Description:
Epidemiological study
Treatment:
Other: Epidemiological study
Control group
Experimental group
Description:
Epidemiological study
Treatment:
Other: Epidemiological study

Trial contacts and locations

1

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Central trial contact

Amélie LANSIAUX, MD PhD; Jean-Jacques VITAGLIANO, PhD

Data sourced from clinicaltrials.gov

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