AI Article Synopsis

  • There is a high rate of treatment failure with leflunomide (LEF) in rheumatoid arthritis (RA) patients, prompting this study to assess the effectiveness of teriflunomide levels (A77 1726) in predicting disease activity outcomes.
  • The study involved comparing RA patients with low disease activity (DAS28-ESR ≤ 3.2) against those with moderate/severe disease activity (DAS28-ESR > 3.2) after LEF treatment in a sample of 115 patients.
  • Results indicated that higher A77 1726 levels correlated negatively with disease activity, enabling high sensitivity and specificity in identifying patients who achieved better outcomes, thus showcasing its potential as a useful biomarker

Article Abstract

There is a significant rate of therapeutic failure in rheumatoid arthritis (RA) patients treated with leflunomide (LEF). This study investigates the utility values of teriflunomide levels (A77 1726) in identifying RA patients who remained with moderate or severe disease activity after the treatment with LEF. In this cross-sectional study, we compared: (a) RA patients who achieved a DAS28-ESR ≤ 3.2, and (b) RA patients who maintained a DAS28-ESR > 3.2 after treatment. ROC curves determined the cut-off of A77 1726 with the better performance to identify patients achieving a DAS28-ESR ≤ 3.2. Of the 115 patients treated with LEF, 69 (60%) remained with moderate/severe disease activity and 46 (40%) achieved low disease activity/remission. Higher A77 1726 levels showed a negative correlation with DAS28-ESR (r = - 0.42, p < 0.001) and other parameters of disease activity. We obtained the following utility values with the cut-off of A77 1726 > 10 µg/mL to identify RA patients who achieved a DAS28-ESR ≤ 3.2: sensitivity of 91.31%; specificity of 73.91%; positive predictive value of 70.00%; and negative predictive value of 92.73%. Serum A77 1726 discriminated between RA patients who remained with moderate/severe disease activity despite the treatment with LEF both as monotherapy and LEF as combo therapy.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8814146PMC
http://dx.doi.org/10.1038/s41598-022-05644-7DOI Listing

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