pSS: Immune Profile of Saliva and Serum of Patients With Primary Sjögren´s Syndrome

Sponsor
University of Sao Paulo General Hospital (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT03711214
Collaborator
(none)
80
3
2
49
26.7
0.5

Study Details

Study Description

Brief Summary

Primary Sjögren's syndrome (pSS) is a chronic systemic inflammatory disease, which mainly affects the lacrimal and salivary glands, leading to sicca syndrome. pSS has a probable autoimmune etiology, with the production of several autoantibodies such as antinuclear antibodies (ANA), anti-Ro/SS-A, anti-La/SS-B, rheumatoid factor (RF) and cryoglobulins. Recently, our group described a high frequency of antibodies directed to DNase I in the serum of pSS patients and these antibodies were associated with the presence of the anti-Epstein-Barr (EBV) early antigen diffuse (anti-EA-D). This finding becomes interesting considering the recent description of reduction of DNase I activity in the tear of patients with xerophthalmia of different causes, which would result in an accumulation of extracellular DNA and neutrophilic inflammatory infiltrate on the ocular surface. This hypothesis is reinforced by the observation that treatment with DNase I as eye drops results in clinical improvement of dry eye. In addition, it has been shown that periodontal disease is an aggravating factor of xerostomia in pSS, as it leads to a chronic inflammatory process and, consequently, to the destruction of minor salivary glands. Therefore, the objective of the present study will be to evaluate the presence of antibodies directed to DNase I in the saliva and serum of pSS patients and its possible capacity of inhibition of the enzyme before and after treatment of periodontal disease. Such findings will be correlated with the presence of periodontal disease, with the glandular and extraglandular manifestations of SSp and also with the presence of EBV DNA in the serum and oral lavage of these patients.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Periodontal scaling
N/A

Study Design

Study Type:
Interventional
Anticipated Enrollment :
80 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Intervention Model Description:
Clinical treatment of periodontal disease in pSS patients and healthy individualsClinical treatment of periodontal disease in pSS patients and healthy individuals
Masking:
None (Open Label)
Masking Description:
Open Label
Primary Purpose:
Treatment
Official Title:
Analysis of the Immune Profile of Saliva and Serum of Patients With Primary Sjögren´s Syndrome
Actual Study Start Date :
Dec 1, 2018
Actual Primary Completion Date :
Oct 13, 2021
Anticipated Study Completion Date :
Dec 31, 2022

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: pSS patients

We will evaluate 40 patients with pSS (EULAR/ACR Classification Criteria, 2016) of both sexes before and after periodontal disease treatment.

Procedure: Periodontal scaling
Periodontal scaling and root planing
Other Names:
  • Clinical periodontal disease treatment
  • Active Comparator: Healthy individuals

    We will evaluate 40 healthy controls before and after periodontal disease treatment.

    Procedure: Periodontal scaling
    Periodontal scaling and root planing
    Other Names:
  • Clinical periodontal disease treatment
  • Outcome Measures

    Primary Outcome Measures

    1. Change from baseline Xerostomia Inventory Score at 3 months [Change from baseline Xerostomia Inventory Score at 3 months]

      Change from baseline Xerostomia Inventory Score at 3 months. An international validated questionnaire of dry mouth symptoms ranging from 11 to 55 points.

    2. Change from baseline activity of DNAse I enzyme in saliva at 3 months [Change from baseline activity of DNAse I enzyme in saliva at 3 months]

      Change from baseline activity of DNAse I enzyme in saliva at 3 months measured by Enzyme-Linked Immunosorbent Assay (ELISA).

    Secondary Outcome Measures

    1. Change from baseline interleukin-1b (IL-1b) concentration in saliva at 3 months [Change from baseline interleukin-1b (IL-1b) concentration in saliva at 3 months]

      Change from baseline interleukin-1b (IL-1b) concentration in saliva at 3 months measured by Luminex Assay.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Patients with primary Sjögren's syndrome according to 2016 EULAR/ACR Classification Criteria, and healthy people without any rheumatic disease/symptoms of sicca syndrome

    • Patients regularly followed at the Sjögren's Syndrome outpatient clinic of Rheumatology Division

    Exclusion Criteria:
    • Use of drugs that cause oral dryness (mainly antidepressants and antihistamines).

    • Patients with history of head and neck radiation therapy.

    • Current smoking.

    • Pregnancy and/or lactation.

    • History of periodontal treatment for at least 6 months prior to enrollment.

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Rheumatology Division of Hospital das Clínicas da Faculdade de Medicina da Universidade de Sao Paulo São Paulo Sao Paulo Brazil 05403-000
    2 Hospital das Clínicas da Faculdade de Medicina da USP São Paulo Brazil 05403-000
    3 Hospital das Clínicas da Faculdade de Medicina da USP São Paulo Brazil

    Sponsors and Collaborators

    • University of Sao Paulo General Hospital

    Investigators

    None specified.

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    University of Sao Paulo General Hospital
    ClinicalTrials.gov Identifier:
    NCT03711214
    Other Study ID Numbers:
    • IPS - pSS
    • 2015/03756-4
    • 2018/09937-9
    First Posted:
    Oct 18, 2018
    Last Update Posted:
    Oct 15, 2021
    Last Verified:
    Apr 1, 2021
    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 Oct 15, 2021