GADD34-LES: Prognosis Assessment of the Increase of GADD34 Gene Expression for Patient Suffering From Systemic Lupus Erythematosus

Sponsor
University Hospital, Grenoble (Other)
Overall Status
Completed
CT.gov ID
NCT02455089
Collaborator
(none)
143
7
1
44.1
20.4
0.5

Study Details

Study Description

Brief Summary

Given that GADD34 has been described as a potential key regulator of pro-inflammatory cytokine production in human and elevated blood marker in SLE patients, this study aim to prove that the GADD34 RNA level in mononuclear blood cells can be used as a prognostic marker to assess the risk of SLE flare.

Condition or Disease Intervention/Treatment Phase
  • Other: GADD34 RNA level measurement.
N/A

Detailed Description

Systemic lupus erythematosus (SLE) has a prevalence estimated between 1 and 6 per 10000 individuals and concerns over 30 000 patients in France for example. As of today, there isn't any reliable specific blood analysis that can be used to assess the prognosis of SLE, that means predict a SLE flare. The discovery of such a blood test could allow a better patients' monitoring in order to help doctors to better adapt treatments (lowering background treatments when they are not needed and increase them ahead of a potential flare when the risk assessment raises).

In SLE patients, a recent study shows elevated levels of GADD34 RNA in mononuclear blood cells : higher than twice the control levels for 36 of the 60 SLE patients and ten times higher than the control levels for 13 of the 60 SLE patients.

Given that GADD34 has been described as a potential key regulator of pro-inflammatory cytokine production in human and elevated blood marker in SLE patients, this study aim to prove that the GADD34 RNA level in mononuclear blood cells can be used as a prognostic marker to assess the risk of SLE flare.

Study Design

Study Type:
Interventional
Actual Enrollment :
143 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Prognosis Assessment of the Increase of GADD34 Gene Expression for Patient Suffering From Systemic Lupus Erythematosus
Actual Study Start Date :
Jun 1, 2015
Actual Primary Completion Date :
Feb 1, 2018
Actual Study Completion Date :
Feb 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Test group

250 SLE patients : All SLE patients included in the study. Intervention : Blood analysis including GADD34 RNA level measurement every 3 months up to 1 year. They will provided a blood sample every 3 months during a year. The result of GADD34 RNA level in mononuclear blood cells will be correlated to the clinical assessment of a SLE flare during the next 3 months. A flare occurence will the group

Other: GADD34 RNA level measurement.
Blood analysis including GADD34 RNA level measurement is performed every 3 months up to 1 year for SLE patients. A modal including physical exam, standard biological results and GADD34 RNA level is correlated to a SLE flare occurence in the next 3 months.
Other Names:
  • Experimental: Test group
  • Outcome Measures

    Primary Outcome Measures

    1. GADD34 RNA level [Measured every 3 months, up to 1 year (5 blood samples).The Last result before a SLE flare occurence will be used.]

      GADD34 RNA level in mononuclear blood cells in the last 3 months before a SLE flare occurence. RNA levels have no unit,they are rates compared with a housekeeping gene RNA level as unit. To avoid any bias in primary outcome, SLE Flare occurence is assessed with both patient and investigator blinded from Gadd34 RNA level.

    Secondary Outcome Measures

    1. Prognosis score of SLE flare occurence [Measured every 3 months, up to 1 year (5 blood samples).The Last result before a SLE flare occurence will be used.]

      Prognosis score of SLE flare occurence using a modal including GADD34 RNA increase, SLEDAI score and Physician Global Assessment (PGA). This modal is compared to the gold standard modal which use only PGA and SLEDAI Score in term of sensibility and specificity.

    2. Pro-inflammatory cytokine blood level. [Measured every 3 months, up to 1 year (5 blood samples).]

      Correlation between GADD34 RNA increase or decrease and interferon-alpha, interferon-beta, interleukin-6 and interleukine-17 levels.

    Other Outcome Measures

    1. GADD34 RNA level in each mononuclear blood cells (B cells, T cells and monocytes). [Measured once at the 2nd visit (3 months after the inclusion).]

      GADD34 RNA level is measured respectively in B cells, T cells and monocytes and is compared with each other. RNA levels have no unit,they are rates compared with a housekeeping gene RNA level as unit. This outcome is measured only for 30 patients.

    2. GADD34 RNA level in non-mononuclear blood cells [Measured once at the 2nd visit (3 months after the inclusion).]

      GADD34 RNA level is measured respectively in non-mononuclear blood cells and is compared with GADD34 RNA level in mononuclear blood cells. RNA levels have no unit,they are rates compared with a housekeeping gene RNA level as unit. This outcome is measured only for 30 patients.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    • Inclusion Criteria:

    • man and women over 18 Years old.

    • suffering from SLE (American College of Rheumatology criteria).

    • without SLE flare for 3 months.

    • with a signed consent and social security affiliation (required in France).

    • Exclusion Criteria:

    • Viral infection within 15 days.

    • Other chronic inflammatory disease.

    • People with special protection (defined in articles : L1121- §5-8 et articles L3212-§1-3 of French health care law).

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 CHU Grenoble Grenoble France 38000
    2 groupement hospitalier mutualiste de Grenoble Grenoble France 38000
    3 Hopital européen de Marseille Marseille France 13003
    4 CHU Marseille Marseille France 13005
    5 CHR Annecy Genevois Metz-Tessy France 74370
    6 CHU Lyon sud Pierre-Bénite France 69310
    7 CHU Saint Etienne Saint Etienne France 42000

    Sponsors and Collaborators

    • University Hospital, Grenoble

    Investigators

    • Principal Investigator: Jean-Yves Cesbron, MD, University Hospital of Grenoble, France.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University Hospital, Grenoble
    ClinicalTrials.gov Identifier:
    NCT02455089
    Other Study ID Numbers:
    • 38RC15.010
    • 2015-A00493-46
    First Posted:
    May 27, 2015
    Last Update Posted:
    Feb 21, 2019
    Last Verified:
    Feb 1, 2019
    Individual Participant Data (IPD) Sharing Statement:
    Yes
    Plan to Share IPD:
    Yes
    Keywords provided by University Hospital, Grenoble
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 21, 2019