Author [Reference] |
Main Findings |
King et al. [7] |
This study demonstrated a positive correlation between the concentration of WBCs and ratio of anti-inflammatory IL-1RA to pro-inflammatory IL-1β in the APS formulation and the WOMAC pain score. Additionally, 85.7% of the subjects whose IL-1RA to IL-1β ratio was greater than 1,000 or a WBC count >30,000/µl were OMERACT-OARSI responders at six months' follow-up. |
Drumpt et al. [8] |
Administration of IA APS is safe and led to significant improvement in all WOMAC subscales and attainment of OMERACT-OARSI high pain responder status at 18 months ' follow-up. |
Kon et al. [9] |
Administration of IA APS is safe and led to significant improvement in WOMAC, SF-36 bodily pain subscale, SF-36 role emotional health subscale, and CGI-S/C scores compared to the saline group at 12 months' follow-up. |
Kon et al. [10] |
Administration of IA APS is safe and led to significant improvement in VAS, all KOOS and WOMAC subscales, and SF-36 physical component compared to the baseline at 36 months' follow-up. The number of responders also increased from seven at 12 months' follow-up to nine at 24 and 36 months' follow-up. |
Genechten et al. [11] |
Administration of IA APS led to significant improvement in NPRS, KOOS, and Kujala scores at 12 months' follow-up. Additionally, MRI analysis showed significant improvement in KOOS symptoms and ADL subscales, and Kujala score in patients with major synovitis compared to patients with non-synovitis at 12 months' follow-up. Additionally, an overall responder rate of 53.7% was observed. |
Kuwasawa et al. [12] |
Administration of IA APS is safe and led to significant improvement in KOOS subscales compared to the baseline at 12 months' follow-up. The subgroup analysis showed that improvement in severe grades, that is, grade IV (on KL grade), was inferior to mild-to-moderate grades (grade II or III). The improvement in KOOS for KL grade II was significantly higher than in KL grade IV at 12 months' follow-up. |