Interleukin‐1 Blockade Inhibits the Acute Inflammatory Response in Patients With ST‐Segment–Elevation Myocardial Infarction

Author:

Abbate Antonio12,Trankle Cory R.1,Buckley Leo F.3,Lipinski Michael J.4,Appleton Darryn5,Kadariya Dinesh1,Canada Justin M.1,Carbone Salvatore1,Roberts Charlotte S.1,Abouzaki Nayef1,Melchior Ryan15,Christopher Sanah1,Turlington Jeremy1,Mueller George15,Garnett James5,Thomas Christopher15,Markley Roshanak1,Wohlford George F.3,Puckett Laura15,Medina de Chazal Horacio1,Chiabrando Juan G.1,Bressi Edoardo1,Del Buono Marco Giuseppe1,Schatz Aaron1,Vo Chau1,Dixon Dave L.13,Biondi‐Zoccai Giuseppe G.67,Kontos Michael C.1,Van Tassell Benjamin W.13

Affiliation:

1. Virginia Commonwealth University Pauley Heart Center MedStar Washington Hospital Center Washington DC

2. “Kenneth and Dianne Wright” Center for Clinical and Translational Research MedStar Washington Hospital Center Washington DC

3. Department of Pharmacotherapy and Outcomes Science MedStar Washington Hospital Center Washington DC

4. Medstar Heart and Vascular Institute MedStar Washington Hospital Center Washington DC

5. Virginia Cardiovascular Specialists Richmond VA

6. Department of Medico‐Surgical Sciences and Biotechnologies Sapienza’ University of Rome Latina Italy

7. Mediterranea Cardiocentro Napoli Italy

Abstract

Background ST ‐segment–elevation myocardial infarction is associated with an intense acute inflammatory response and risk of heart failure. We tested whether interleukin‐1 blockade with anakinra significantly reduced the area under the curve for hsCRP (high sensitivity C‐reactive protein) levels during the first 14 days in patients with ST ‐segment–elevation myocardial infarction (VCUART3 [Virginia Commonwealth University Anakinra Remodeling Trial 3]). Methods and Results We conducted a randomized, placebo‐controlled, double‐blind, clinical trial in 99 patients with ST ‐segment–elevation myocardial infarction in which patients were assigned to 2 weeks treatment with anakinra once daily (N=33), anakinra twice daily (N=31), or placebo (N=35). hsCRP area under the curve was significantly lower in patients receiving anakinra versus placebo (median, 67 [interquartile range, 39–120] versus 214 [interquartile range, 131–394] mg·day/L; P <0.001), without significant differences between the anakinra arms. No significant differences were found between anakinra and placebo groups in the interval changes in left ventricular end‐systolic volume (median, 1.4 [interquartile range, −9.8 to 9.8] versus −3.9 [interquartile range, −15.4 to 1.4] mL; P =0.21) or left ventricular ejection fraction (median, 3.9% [interquartile range, −1.6% to 10.2%] versus 2.7% [interquartile range, −1.8% to 9.3%]; P =0.61) at 12 months. The incidence of death or new‐onset heart failure or of death and hospitalization for heart failure was significantly lower with anakinra versus placebo (9.4% versus 25.7% [ P =0.046] and 0% versus 11.4% [ P =0.011], respectively), without difference between the anakinra arms. The incidence of serious infection was not different between anakinra and placebo groups (14% versus 14%; P =0.98). Injection site reactions occurred more frequently in patients receiving anakinra (22%) versus placebo (3%; P =0.016). Conclusions In patients presenting with ST ‐segment–elevation myocardial infarction, interleukin‐1 blockade with anakinra significantly reduces the systemic inflammatory response compared with placebo. Clinical Trial Registration URL : https://www.clinicaltrials.gov/ . Unique identifier: NCT 01950299.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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