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
Cited by
196 articles.
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