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Unclassified GENotypes of Autoinflammatory Diseases and AA Amyloidosis

Physiopathological Investigation of Unclassified GENotypes of Autoinflammatory Diseases and AA Amyloidosis

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06354322
Acronym
IPHYGENI MAI
Enrollment
200
Registered
2024-04-09
Start date
2025-02-26
Completion date
2039-02-28
Last updated
2025-09-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

AA Amyloidosis, Autoinflammatory Disease

Keywords

Autoinflammatory disease, AA amylosis, Functional explorations, Unclassified genotypes

Brief summary

Patients with autoinflammatory diseases (AID) have recurrent episodes of systemic inflammation accompanied by nonspecific elevation of blood inflammation markers typically absent between attacks. A complication of autoinflammatory diseases is AA amyloidosis, which can lead to renal failure and dialysis. Advances in genetic analysis have led to the identification of new autoinflammatory diseases and thus new pathophysiological pathways. However, genetic analyses are sometimes confronted with results that are difficult to interpret. These are the Variants of Unknown Significance, for which genetic analysis alone does not allow to determine if the genetic mutation is responsible for the symptoms. genetic analysis sometimes has limitations in the diagnosis of AID which can only be overcome by pathophysiological studies of the variants found.

Detailed description

The study aim to explore variants of undetermined significance in major and minor patients with unclassified autoinflammatory disease or AA amyloidosis of undetermined etiology by studying their pathogenicity. National multicenter research: internal medicine department of Tenon Hospital, pediatric department of Versailles Hospital and pediatric dermatology department of Necker Enfants Malades Hospital in Paris Samples will be collected at the inclusion visit or at subsequent visits of the patient to the department during a blood draw performed as part of routine care by a registered nurse. The total volume of the sample will be 24 mL per 6 month period maximum, and will not exceed In case of skin involvement of the auto-inflammatory disease, a skin biopsy may be performed as part of the patient's follow-up care.

Interventions

None listed

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
3 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

Inclusion criteria for patients to be studied: * Patients over 18 years of age with the capacity to give express free and informed consent and; * Minor patients under 18 years of age with both parents or legal guardians giving consent; * Patients with unclassified IAD or AA amyloidosis of undetermined etiology; * Patients followed in one of the study departments; * Patients weighing more than 15 kg. Inclusion criteria for control patients: * Patients over 18 years of age with the capacity to give free and informed express consent; * Patients with IAD classified with well-defined international criteria or ; * Patients who have undergone cosmetic surgery or blood donors).

Exclusion criteria

* Patients unable to give express free and informed consent; * Subjects under guardianship, curatorship or safeguard of justice; * Subjects who do not speak French; * Subjects unable to answer questions or express themselves; * Patients weighing less than 15 kg; * Patients without social security coverage

Design outcomes

Primary

MeasureTime frameDescription
Exploration of VUS in AutoInflammatory DiseasesUp to 4 yearsTo explore variants of undetermined significance (VUS)in patients with unclassified autoinflammatory disease or AA amyloidosis of undetermined etiology by studying their pathogenicity.

Secondary

MeasureTime frameDescription
Pathophysiology of Autoinflammatory DiseasesUp to 4 yearsTo improve the knowledge on the pathophysiology of Autoinflammatory Diseases: to determine the role of new inflammation pathways in AutoInflammatory Diseases
Role of other innate immune cells in AutoInflammatory DiseasesUp to 4 yearsEvaluate the role of other innate immune cells (neutrophils, mast cells...) and their mediators
Improve knowledge of AA amyloidosisUp to 4 yearsImprove knowledge of AA amyloidosis, a complication of autoinflammatory diseases

Countries

France

Contacts

Primary ContactSophie GEORGIN-LAVIALLE, Professor
sophie.georgin-lavialle@aphp.fr00 33 1 56 01 72 04

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026