Unlocking RA Mysteries: Can Disease Activity Scores Predict Cartilage Damage?
"New research from Indonesia explores the link between DAS28 and COMP levels in rheumatoid arthritis patients, offering insights into monitoring and managing this chronic condition."
Rheumatoid arthritis (RA) is a persistent autoimmune condition marked by symmetrical erosive arthritis in the synovial joints. This leads to pain, joint damage, impaired function, reduced quality of life, and even physical deformities. RA affects between 0.5% and 1.0% of the general population, with rates between 0.1% and 0.3% reported in Indonesia. Early diagnosis and treatment are vital for preventing joint deterioration.
Cartilage oligomeric matrix protein (COMP) has emerged as a promising biomarker to support RA diagnosis. COMP plays a role in assembling collagen type II fibers in cartilage and interacts with other matrix proteins to stabilize the collagen network. Previous research has suggested a correlation between serum COMP levels and the Disease Activity Score (DAS) 28-erythrocyte sedimentation rate (ESR) in the early stages of RA.
The Disease Activity Score (DAS) is essential for assessing RA stability, guiding treatment decisions to alleviate inflammation, and preventing further joint damage, which reduces pain and disability. Given the limited existing research on the relationship between DAS 28 and serum COMP levels, a study was conducted to investigate their correlation in RA patients.
Decoding the DAS28 and COMP Connection: What the Study Reveals

A cross-sectional study was conducted with prospective data collection, involving patients from a rheumatology clinic at a government hospital in Bandung, Indonesia. Thirty RA patients and a control group were recruited through consecutive sampling after providing informed consent. The study was approved by the Health Research Ethics Committee of Dr. Hasan Sadikin Hospital, Indonesia.
- DAS28 Assessment: Disease Activity Score 28 (DAS28) was calculated using the QxMD Software, integrating joint condition data, ESR, and subjective patient assessments.
- Serum COMP Measurement: Blood samples were collected, and serum was separated and stored at -80°C. COMP levels were determined using the Human COMP/TSP5 enzyme-linked immunosorbent assay.
- Statistical Analysis: The correlation between DAS28 and serum COMP levels was analyzed using IBM SPSS Statistics 23.
The Implications: Why This Research Matters
This study found no direct correlation between DAS 28 scores and serum COMP levels in RA patients. This may be because DAS 28 calculations include ESR, which is not specific to RA inflammation and can be influenced by other inflammatory conditions. Further research is needed to identify more specific biomarkers for assessing disease activity and cartilage damage in RA, potentially improving treatment strategies and patient outcomes.