Psoriasis, Synovitis
Conditions
Brief summary
In this cross-sectional study, it was planned to compare the frequency of subclinical synovitis in the distal interphalangeal joints of the hands in psoriasis patients. 28 patients followed up by the Dermatology Department with a diagnosis of psoriasis and referred to us and 28 healthy volunteers were included in the study. Participants' age, gender, body mass index (BMI), year of psoriasis diagnosis, treatments they received, and comorbid diseases were recorded as demographic information. Psoriasis Area and Severity Index (PASI) and Nail Psoriasis Severity Index (NAPSI) were calculated by a dermatologist. Tenderness in the distal interphalangeal joints of both hands was evaluated by palpation. Subsequently, the presence of ultrasonographic synovitis findings of the participants was examined by a physician who was experienced in musculoskeletal ultrasonography and was blind to clinical evaluations. Scoring was done with the EULAR GS / PD joint scoring system and EULAR-OMERACT composite scoring system. The scores of the most affected joint were used in statistical analysis. Comparisons were made between psoriasis and control groups in terms of scores. Relationships between variables in the psoriasis group were examined.
Interventions
DIAGNOSTIC_TESTmusculoskeletal ultrasonography
The presence of subclinic synovitis findings in the hand joints was evaluated with musculoskeletal ultrasonography.
Sponsors
Ufuk University
Study design
Observational model
OTHER
Time perspective
CROSS_SECTIONAL
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
For patient group 1. Being over the age of 18 2. Being followed up by the Dermatology Department with a diagnosis of psoriasis and receiving topical or systemic treatment for this 3. Absence of clinically detected signs of arthritis 4. Absence of serious trauma, surgical intervention or injection in the joint areas to be evaluated. 5. Absence of any known inflammatory rheumatic disease For control group 1.\> 18 years old 2. Absence of clinically detected signs of arthritis 3.Lack of clinical signs suggestive of psoriasis
Exclusion criteria
For patient group 1. To be \<18 years old 2. Clinically detected evidence of arthritis 3. History of serious trauma, surgical intervention or injection in the joint areas to be evaluated 4. Having a known inflammatory rheumatic disease For control group 1\. To be \<18 years old 2. Having clinical signs suggestive of psoriasis 3. Having clinically detectable signs of arthritis 4. History of known inflammatory disease, severe trauma in the joint areas to be evaluated, surgical intervention, injection \-
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| GS/PD score | 8 month | Intaarticular fluid (0 = absent, 1 = present), synovial hypertrophy (0 = absent, 1 = mild, 2 = moderate, 3 = severe), bone erosion (0 = absent, 1 = 2 erosion, 2 = More than 2 erosion), surrounding soft tissue swelling (0 = absent, 1 = mild, 2 = moderate) with gray scale; the presence of blood flow in the area with synovial proliferation with power Doppler (0 = no signal, 1 = less signal in one vessel, 2 = moderate signal at vascular intersections, 3 = intense signal on more than half of the joint surface) are evaluated and scored. GS and PD scores of the joint with the greatest involvement are used in statistical analysis. |
Countries
Turkey (Türkiye)
Outcome results
None listed