NEUTROSAS2: Evaluation of Circulating Neutrophils in Antisynthetase Syndrome

Sponsor
Central Hospital, Nancy, France (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT05989399
Collaborator
(none)
150
22

Study Details

Study Description

Brief Summary

Antisynthetase syndrome (ASyS) is a rare and heteregeneous overlapping connective tissue disease, characterized by myositis, interstitial lung disease (ILD), joint involvement, Raynaud's phenomenon and cutaneous manifestations ("mechanic's hands"). Over 50% of patients develop ILD, which is the leading cause of death.

The role of neutrophils - innate immune cells involved in inflammatory processes and induced in particular by cytokines of the Th17 pathway - during AS is unknown. Direct pathogenic role of neutrophils has been described during idiopathic inflammatory myopathies, with an increase of netosis correlated with disease activity and muscle damage. During ASyS, a higher number of alveolar neutrophils has been observed in patients with rapidly progressive ILD.

There are few data on the specific evaluation of circulating neutrophils in ASyS. Investigators suppose that circulating neutrophils level could represent a simple and accessible severity biomarker in patients with ASyS.

The main objective is to evaluate the diagnostic performance of the circulating neutrophils level (> 7000/mm3) at diagnosis on ASyS severity.

The secondary objectives are:
  • to define a threshold for circulating neutrophils levels at diagnosis allowing to predict ASyS severity and to assess the diagnostic performance of this threshold.

  • to study the correlation between the level of circulating neutrophils and ASyS severity at diagnosis of the disease.

  • to compare the circulating neutrophils level at ASyS diagnosis and after 1 year of treatment.

  • to compare patients characteristics according to ASyS severity at diagnosis.

  • to compare BAL fluid neutrophils level according to ILD severity at ASyS diagnosis in patients with ILD.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: circulating neutrophils

Study Design

Study Type:
Observational
Anticipated Enrollment :
150 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Evaluation of Circulating Neutrophils in Antisynthetase Syndrome: a Multicenter Retrospective Study
Anticipated Study Start Date :
Jan 1, 2024
Anticipated Primary Completion Date :
Oct 31, 2025
Anticipated Study Completion Date :
Oct 31, 2025

Arms and Interventions

Arm Intervention/Treatment
ASyS patients

Patients with antisynthetase syndrome

Diagnostic Test: circulating neutrophils
evaluation of circulating neutrophils level

Outcome Measures

Primary Outcome Measures

  1. circulating neutrophils level > 7000/mm3 [baseline (J0)]

  2. global severity [baseline (J0)]

    global severity defined as presence of severe ILD (PaO2 < 600 mmHg or rapidly progressive ILD), and/or presence of severe myositis (bedrest, or MMT8 score < 30, or MRC muscle testing < 3/5, or swallowing disorers, or dysphagia) and/or presence of myocarditis on cardiac MRI

Secondary Outcome Measures

  1. circulating neutrophils level [baseline (J0)]

  2. FVC [baseline (J0)]

    FVC percentage

  3. DLCO [baseline (J0)]

    DLCO percentage

  4. MRC muscle testing [baseline (J0)]

  5. CK level [baseline (J0)]

  6. circulating neutrophils level [12 months]

  7. BAL fluid neutrophils level [baseline (J0)]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Patients with ASyS diagnosis according to Connors criteria
Exclusion Criteria:
  • Active infection at ASyS diagnosis

  • Evolutive cancer at ASyS diagnosis

  • Corticosteroid therapy initiation before circulating neutrophils evaluation

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Central Hospital, Nancy, France

Investigators

  • Principal Investigator: Paul Decker, MD, CHU Nancy

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Paul DECKER, MD, Principal Investigator, Central Hospital, Nancy, France
ClinicalTrials.gov Identifier:
NCT05989399
Other Study ID Numbers:
  • 2023PI083
First Posted:
Aug 14, 2023
Last Update Posted:
Aug 14, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of Aug 14, 2023