4.8 Article

C-reactive protein elevation in patients with atrial arrhythmias - Inflammatory mechanisms and persistence of atrial fibrillation

Journal

CIRCULATION
Volume 104, Issue 24, Pages 2886-2891

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1161/hc4901.101760

Keywords

fibrillation; arrhythmia; inflammation; C-reactive protein

Funding

  1. NHLBI NIH HHS [R01 HL-65412] Funding Source: Medline

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Background-Atrial Fibrillation (AF) may persist due to structural changes in the atria that are promoted by inflammation. C-reactive protein (CRP), a marker of systemic inflammation, predicts cardiovascular events and stroke, a common sequela of AF. We hypothesized that CRP is elevated in patients, with atrial arrhythmias. Methods and Results-Using a case-control study design, CRP in 131 patients with atrial arrhythmias was compared with CRP in 71 control patients. Among arrhythmia patients, 6 had frequent atrial ectopy or tachycardia, 86 had paroxysmal AF, 39 had persistent AF lasting > 30 days, and 70 had lone arrhythmias. CRP was higher in arrhythmia than in control patients (median, 0.21 versus 0.096 mg/dL; P <0.001). Arrhythmia patient,, in AF within 24 hours before sampling had higher CRP than those in sinus rhythm (0.30 versus 0.15 mg/dL; P <0.001). CRP in controls was not different than in patient,, with atrial ectopy or tachycardia. Lone arrhythmia patients had a CRP of 0.21 mg/dL, which was not significantly lower than arrhythmia patients with structural heart disease (CRP, 0.23 mg/dL) but higher than controls (P=0.002). Persistent AF patients had a higher CRP (0.34 mg/dL) than paroxysmal AF patients (0. 18 mg/dL, P=0.008); both groups had higher CRP levels than controls (P less than or equal to0.005). Conclusions-CRP is elevated in AF patients. This study is the first to document elevated CRP in non-postoperative arrhythmia patients. These findings are reinforced by stepwise CRP elevation with higher AF burden. Although the cause of elevated CRP levels in AF patients remains unknown, elevated CRP may reflect Lin inflammatory state that promotes the persistence of AF.

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