Gout, inflammation, and metabolic health in French Polynesia
Official title: FENUA-METABOGOUT : Genetic Landscape of Gout, Inflammation and Metabolic Diseases in French Polynesia.
Run by Lille Catholic University · NCT07343336 · Data updated 2026-11-12
This project will collect blood, urine, and genetic information to see if specific genes and molecular markers explain gout, inflammation, and metabolic problems in adults with Polynesian ancestry in French Polynesia.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 75 Years |
| Sex | All |
| Enrollment | 2750 (estimated) |
| Sponsor | Lille Catholic University Academic / other |
| Locations | 6 sites (Faa'a and 5 other locations) |
| Status | Recruiting |
| Started | September 2, 2025 |
| Main results expected | September 2027 |
| Study ends | September 2027 |
| Registry record updated | January 15, 2026 |
| Trial ID | NCT07343336 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18 to 75 with self-declared Polynesian ancestry who can fast for sample collection and are affiliated to a social security scheme—including general practice visitors, patients followed at the Taaone rheumatology clinic, people with tophaceous gout, those within 48 hours of a gout attack, and prior TOPATA participants—are the intended participants.
✕Probably not a fit
People outside the 18–75 age range, those without Polynesian ancestry, those unwilling or unable to fast or provide biological samples, or those not affiliated with a social security scheme are not eligible and unlikely to benefit from participation.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is an observational, population-based effort to map the genetic and molecular landscape of hyperuricaemia, gout, and related metabolic and inflammatory traits in French Polynesia. Investigators will enroll adults of Polynesian ancestry from general practice visits, a rheumatology clinic cohort, people with tophaceous gout, recent gout attacks, and a 2021 TOPATA follow-up group, collecting blood and urine samples and clinical/anthropometric data. Laboratory analyses will include serum urate measurements, molecular assays and genetic analyses to look for variants and biomarkers linked to MSU crystal deposition and inflammatory response. The project aims to relate molecular and genetic findings to clinical patterns and cardiometabolic comorbidities in a population with very high hyperuricaemia prevalence.
Why it matters
Potential benefit: If successful, this work could reveal genetic or molecular markers that help predict who is at highest risk for gout or guide more targeted prevention and management for Polynesian patients.
How similar studies have gone: Prior work in French Polynesia (the 2021 TOPATA cohort) and international gout genetics studies have linked hyperuricaemia to cardiometabolic traits and identified some risk loci, but the genetic drivers of MSU deposition and variable inflammatory responses remain incompletely characterized, so this project builds on existing evidence while addressing unresolved questions.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: All participants: * Age between 18 and 75 years old inclusive * Signature of informed consent * Fasting for the collection of biological samples * Declared Polynesian ancestry * Affiliated to a social security scheme General population group : * Not having participated to the 2021 TOPATA study * Visiting a general practitioner (for whatever reason) Gout Group : * Managed at the rheumatology clinic of the Taaone Hospital Centre (CHT) in Papeete by Dr Baptiste Gérard. Tophaceous gout sub-group: * Present with tophaceous gout. Gout crisis subgroup: * Be within 48 hours of the onset of a gout attack * Agree to return 1 week after inclusion for the second blood and urine sample. 2021 follow-up group: * To have been included in the TOPATA study in 2021 * Have taken the genetic and biological samples that generated the genetic and serum urate data for the 2021 study * Have hyperuricaemia without signs of gout OR without hyperuricaemia or gout at the time of inclusion in TOPATA Exclusion Criteria: All participants : * Refusal or inability to understand or give consent * Physical inability to follow and respect the protocol * 1st degree relative\*, * Person under guardianship or trusteeship * Pregnant or breast-feeding woman \* If several relatives from the same household are eligible to participate, only one person may be included in the study. The choice is left to the discretion of the investigator or the first person met. However, both members of a couple (e.g. husband and wife) may participate. * General population group : * Unable to return for sampling if required. * Gout group : * Person wearing a knee prosthesis * People suffering from other inflammatory rheumatic diseases
Where it's running
-
Medical Office Dr Antoine Scuiller
Faa'a, French Polynesia Recruiting -
Medical Office Dr Cedric Gueguen
Papeete, French Polynesia Recruiting -
Medical Office Dr Voradeth Nouanesengsy
Papeete, French Polynesia Recruiting -
Medical Office Dr Nanethida Nouanesengsy
Pirae, French Polynesia Recruiting -
Medical Office Dr Raphael Habib
Pirae, French Polynesia Recruiting -
CH de Polynesie Française Papeete
Pirae, French Polynesia Not yet recruiting
Study contacts
- Principal investigator: Tristan Pascart, Professor — Ghicl
- Study coordinator: Marie De Solere
- Email: desolere.marie@ghicl.net
- Phone: +33 3 20 22 59 31
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
-
Registering medical data and care outcomes for ALS, SMA, and other motor disorders
This registry slowly collects routine-care information from adults with ALS, SMA, or other motor disorders to see how they’re treated and how care affects outcomes.
-
Myokines in metabolic and endocrine diseases linked to sarcopenia
This study tests whether myokines can serve as biomarkers or drivers of sarcopenia and sarcopenic obesity in people with metabolic or endocrine diseases.
-
AMX0035 in adults with Type 1 Diabetes
This study tests whether 24 weeks of the oral medication AMX0035 help improves metabolic health in adults with Type 1 Diabetes compared with a placebo.
-
A lifetime registry and imaging database for people with heart, kidney, and metabolic conditions
This project will see if creating a long-term clinical and imaging database for adults with heart, kidney, or metabolic conditions can improve prediction of outcomes and guide care.
-
Early pregnancy lifestyle patterns and glucose changes in a TOFFFY sub-study
This study tests whether daily patterns like sleep, activity, and meal timing in early pregnancy affect glucose levels and the risk of gestational diabetes, using CGM and wearable data in pregnant women in Singapore.
-
Measuring how well patients follow daily oral medicines in Necker’s inherited metabolic diseases department
This project will measure how well children, adolescents, and young adults with inherited metabolic diseases at Necker follow their daily oral medicines to see if a medication-education workshop is needed.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.