Rheumatoid Arthritis (RA) and Osteoarthritis (OA)
Conditions
Brief summary
The total number of the included subjects was 120 in 3 equal groups (RA, OA and control). All subject was subjected to serum IL17 level measurement. MSK US (of both wrists, MCPs, PIPs and DIPs) was done to all patients in RA and OA groups. Disease activity was measured by disease activity score (DAS28) for RA patients. Visual analogue scale for pain (VAS) was obtained from patients in RA and OA groups. Functional assessment was done using health assessment questionnaire (HAQ) for RA patients and the Australian/Canadian (AUSCAN) Osteoarthritis Hand Index for OA patients
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
* A patient is considered having definite RA if he/she scores at least 6 points in the established classification system * A patient is considered having Hand OA if he /she Hand pain, aching, or stiffness plus 3 or 4 of hard tissue enlargement of 2 or more of 10 selected joints or hard tissue enlargement of 2 or more DIP joints or fewer than 3 swollen MCP joints, or deformity of at least 1 of 10 selected joints which are are the second and third distal interphalangeal (DIP), the second and third proximal interphalangeal, and the first carpometacarpal joints of both hands
Exclusion criteria
* Any subject with liver diseases, coronary artery diseases, kidney diseases or other inflammatory conditions was excluded from the study.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Clinical disease activity in Rheumatoid Arthritis (RA) and hand Osteoarthritis (OA) patients | 12 months | During the whole course of the study, disease activity of the patients was measured by disease activity score (DAS28) for RA patients. Visual analogue scale for pain (VAS) was obtained from patients in RA and OA groups. Functional assessment was done using health assessment questionnaire (HAQ) for RA patients and the Australian/Canadian (AUSCAN) Osteoarthritis Hand Index for OA patients. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| IL-17 serum levels in RA and OA patients | 2 weeks | IL-17 will be measured by enzyme linked immunosorbent assay from collected serum samples from the study participants |
Other
| Measure | Time frame | Description |
|---|---|---|
| Radiologic bony changes in RA and OA patients | 12 months | During the whole course of the study period, recruited participants undergone musculoskeletal (MSK) ultrasound to assess the bony changes. |
Countries
Egypt