Please note that participants who completed the EP and were taking CS at Baseline (all participants in the CSD-RP [n = 8], and 83.3% [n = 5/6] of participants in the A-RP) were able to taper and/or discontinue using CS by the end of the EP (i.e., the end of the study) without recurrence or pericarditis symptomatology (e.g., patient-reported pericardial pain) or inflammation (e.g., elevated CRP level). This evidence concerns the gene CRP and pericarditis.