Calcium Pyrophosphate Deposition (CPPD) Disease (PYC-OMIC)

Lille Catholic University

Status: Not yet enrolling

Conditions: Calcium Pyrophosphate Deposition Disease; Rheumatic Diseases

Treatments: Genetic: transcriptomic and metabolomic analysis

Study type: Interventional

Funder types: Other

Identifiers

NCT07005804

RC-P00127

Details and patient eligibility

About

The goal of this clinical trial is to describe the transcriptomic and metabolomic profile of patients with chronic Calcium Pyrophosphate Deposition (CPPD) compared to those with acute CPPD.

The hypotheses are as follows :

• It is hypothesised that there is a transcriptomic and metabolomic signature of CPPD which explains why therapeutic responses to different anti-inflammatory treatments differ from one phenotype to another one
• It is hypothesised that the acute and chronic clinical phenotypes of CPPD have different clinical, biological and imaging characteristics, as well as a differing predisposition toward crystalline deposition and inflammatory pathway activation.

The management of participants with chronic forms of the disease included in this research was modelled on the usual recommended management, including a biological workup, joint puncture, ultrasound and radiographic workup. Double-energy CT scans and transcriptomic and metabolomic analyses on plasma are not routine tests.

Enrollment: 137 estimated patients

Sex: All

Ages: 65+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria - Acute forms of CPPD: retrospective part of the study

• Cases included in the COLCHICORT cohort (NCT03128905), for whom this was the first acute episode of CPPD

Inclusion Criteria - Chronical forms of CPPD : prospective part of the study

• Patients affiliated to the French social security system
• Age ≥ 65 years
• Diagnosis of chronic CPPD (recurrent acute or persistent arthritis), meeting ACR/EULAR 2023,11 classification criteria after evaluation by a rheumatologist in the rheumatology department
• Progression of CPPD rheumatism for at least 3 months and still active CPPD rheumatism, defined by a visual analogue scale (VAS) of disease activity ≥ 40 and/or presentation of at least 1 crisis over the last 3 months
• Glomerular Filtration Rate (GFR) in Chronic Kidney Disease Epidemiology (CKD EPI Collaboration) ≥ 30ml/min/1.73m2
• Minimum time between the last intake of a crisis treatment and inclusion in the study, depending on their half-life, in order to not interfere with the results of the omics analyses: 2 weeks (Nonsteroidal Anti-Inflammatory Drugs Per Os (PO) or Intramuscular (IM) or Intravenous (IV); corticosteroids PO or IV; colchicine PO; anakinra Subcutaneous (SC), 1 month (methotrexate PO, tocilizumab SC), 3 months (canakinumab SC, tocilizumab IV)
• Signed written consent for study participation

Exclusion Criteria - Acute forms of CPPD:

• Missing data concerning transcriptomic and metabolomic analyses.
• Opposition

Exclusion Criteria - For chronic forms of CPPD:

• History of gout or presence of monosodium urate (MSU) crystals on joint fluid,
• Cognitive decline (confusion and neurodegenerative diseases)
• Inability to provide informed consent and disease VAS
• Patient under guardianship or curatorship

Trial design

Primary purpose: Basic Science

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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137 participants in 1 patient group

Patients with a chronic CPPD

Experimental group

Description:

Patients with diagnosis of chronic calcium pyrophosphate crystal arthritis (either acute recurrent or persistent arthritis), meeting the 2023 American College of Rheumatology/European League Against Rheumatism (ACR/EULAR) classification criteria, after evaluation by a rheumatologist from the rheumatology department.

Treatment:

Genetic: transcriptomic and metabolomic analysis