Central Sensitization in Familial Mediterranean Fever (FMF)

Sponsor
Marmara University (Other)
Overall Status
Recruiting
CT.gov ID
NCT05177120
Collaborator
(none)
80
1
9
8.9

Study Details

Study Description

Brief Summary

Familial Mediterranean Fever (FMF) is an autosomal recessive inherited disease with a course of autoinflammation, which is characterized by the episodes of fever and serositis. Central sensitization (CS) is defined as increased response to normal or sub-threshold stimuli of central nervous system and its close relationship with many rheumatological diseases has been demonstrated in several studies. However, there are no data on the frequency of CS in FMF patients.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Central Sensitization Inventory
  • Other: Short form-36
  • Other: Pittsburgh Sleep Quality Index
  • Other: Health assessment questionnaire
  • Other: Hospital anxiety and depression scale
  • Diagnostic Test: Fibromyalgia rapid screening tool
  • Other: Familial Mediterranean Fever Quality of life scale

Detailed Description

Familial Mediterranean fever (FMF) is a self-limiting autoinflammatory disease with well-defined genetic and clinical features. Recurrent episodes of fever and serositis accompanied by increased acute phase reactants and good response to colchicine are the core components of the disease. The frequency of this disease, which is common in Eastern Mediterranean countries, is variable according to regions, but it is reported as 1/1000. In the pathogenesis of the disease, the mutation of the MEFV (Mediterranean Fever) gene, which is located on the 16th chromosome and encodes the pyrin protein, is known as the basic mechanism.In rheumatic diseases, inflammatory mediators cause CS by first creating changes in the regulation of pain in peripheral neurons and then in spinal and supraspinal pathways. Stimulation of peripheral nerves by mediators released during inflammation results in neurogenic inflammation, which is among the peripheral sensitization (PS) mechanisms. PS is defined as the increased sensitivity of nociceptive neurons to normal or below-threshold stimuli and constitutes the first step in the development of CS.Similar to other autoimmune diseases, it is possible that the neuroinflammatory process triggers peripheral and central sensitization mechanisms in FMF patients and affects pain pathways.

Study Design

Study Type:
Observational
Anticipated Enrollment :
80 participants
Observational Model:
Case-Only
Time Perspective:
Cross-Sectional
Official Title:
Central Sensitization in Familial Mediterranean Fever: A Cross-Sectional Observational Study
Actual Study Start Date :
Jun 1, 2021
Anticipated Primary Completion Date :
Dec 31, 2021
Anticipated Study Completion Date :
Mar 3, 2022

Arms and Interventions

Arm Intervention/Treatment
FMF patients

Patients with diagnosed FMF

Diagnostic Test: Central Sensitization Inventory
Standardized questionnaire to determine the level of central sensitization
Other Names:
  • CSI
  • Other: Short form-36
    Standardized questionnaire to investigate the quality of life in patients
    Other Names:
  • SF-36
  • Other: Pittsburgh Sleep Quality Index
    Standardized questionnaire to investigate the sleep quality and disturbance
    Other Names:
  • PSQI
  • Other: Health assessment questionnaire
    Standardized questionnaire used to detect the presence of disability
    Other Names:
  • HAQ
  • Other: Hospital anxiety and depression scale
    Standardized questionnaire to investigate the depression and anxiety
    Other Names:
  • HADS
  • Diagnostic Test: Fibromyalgia rapid screening tool
    Standardized questionnaire to determine the presence of fibromyalgia
    Other Names:
  • FIRST
  • Other: Familial Mediterranean Fever Quality of life scale
    Standardized questionnaire to investigate the quality of life in Familial Mediterranean Fever patients
    Other Names:
  • FMFQoL
  • Outcome Measures

    Primary Outcome Measures

    1. Central Sensitization Inventory (CSI) [6 months]

      25 somatic and psychosocial symptoms, which are frequently found in patients with central sensitization in part A, are questioned. In part B, the presence of diseases whose relationship with central sensitization is well defined is questioned in the patient without participating in scoring. Central sensitization is assumed in patients who score 40 or more over 100 points.

    Secondary Outcome Measures

    1. Short form-36 (SF-36) [6 months]

      The 36-Item Short Form Survey (SF-36) is an oft-used, well-researched, self-reported measure of health.The scale consists of 36 questions questioning 8 sub-parameters regarding the health status of the person.These parameters are physical function, pain, limitation due to physical and emotional problems, emotional well-being, social function, fatigue and general health perception. High scores are associated with improved quality of life.

    2. Familial Mediterranean Fever Quality of Life Scale (FMF-QoL) [6 months]

      FMF-QoL was developed to evaluate the quality of life in FMF patients. This scale consists of 20 questions in the form of a Likert scale and the total scoring is between 0-80. High scores indicate a decrease in quality of life.

    3. Health Assessment Questionnaire (HAQ) [6 months]

      n the scale, difficulty in performing 20 specific tasks from 8 categories is questioned and the scoring is between 0-60. High scores are associated with increased disability.

    4. Hospital Anxiety and Depression Scale (HADS) [6 months]

      This scale consists of 14 questions in total, and anxiety symptoms are questioned in half of the questions and depression-related complaints in the other half. A subscore of 8 or higher for depression or anxiety is considered a clinical case.

    5. Pittsburgh Sleep Quality Index (PSQI) [6 months]

      The questionnaire includes 21 questions covering 7 components that investigate the symptoms of sleep disturbances. Scores range from 0 to 21 and a score of >5 is considered as a sleep disorder.

    6. Fibromyalgia Rapid Screening Tool (FIRST). [6 months]

      This scale consists of 6 questions investigating the most relevant clinical features of fibromyalgia. The questions are answered as yes/no and 5 or more out of 6 points in total are in favor of fibromyalgia.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Agree to participate in the study
    Exclusion Criteria:
    • Had another systemic inflammatory rheumatic diseases

    • Using centrally acting pain medications (e.g., pregabalin, duloxetine, opioids) or glucocorticoids (>10 mg prednisone or its equivalent)

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Feyza Nur Yücel Sinop Turkey 57200

    Sponsors and Collaborators

    • Marmara University

    Investigators

    • Study Chair: Canan Sanal- Toprak, Asst.Prof, Marmara University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Marmara University
    ClinicalTrials.gov Identifier:
    NCT05177120
    Other Study ID Numbers:
    • 06.12.2019.1053
    First Posted:
    Jan 4, 2022
    Last Update Posted:
    Jan 4, 2022
    Last Verified:
    Dec 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Marmara University
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Jan 4, 2022