Atrial nitroso-redox balance and refractoriness following on-pump cardiac surgery: a randomized trial of atorvastatin

Author:

Jayaram Raja1ORCID,Jones Michael2,Reilly Svetlana1ORCID,Crabtree Mark J1ORCID,Pal Nikhil1,Goodfellow Nicola1,Nahar Keshav1,Simon Jillian1ORCID,Carnicer Ricardo1ORCID,DeSilva Ravi3ORCID,Ratnatunga Chandana3,Petrou Mario3,Sayeed Rana3,Roalfe Andrea4ORCID,Channon Keith M1,Bashir Yaver2,Betts Timothy2,Hill Michael5ORCID,Casadei Barbara1ORCID

Affiliation:

1. Division of Cardiovascular Medicine, Radcliffe Department of Medicine, University of Oxford, L6, West Wing, Oxford OX3 9DU, UK

2. Cardiology, Oxford Heart Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK

3. Cardiothoracic Surgery, Oxford Heart Centre, Oxford University Hospitals NHS Foundation Trust, Oxford, UK

4. Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK

5. Clinical Trial Service Unit, Nuffield Department of Population Health, University of Oxford, Oxford, UK

Abstract

Abstract Aims Systemic inflammation and increased activity of atrial NOX2-containing NADPH oxidases have been associated with the new onset of atrial fibrillation (AF) after cardiac surgery. In addition to lowering LDL-cholesterol, statins exert rapid anti-inflammatory and antioxidant effects, the clinical significance of which remains controversial. Methods and results We first assessed the impact of cardiac surgery and cardiopulmonary bypass (CPB) on atrial nitroso-redox balance by measuring NO synthase (NOS) and GTP cyclohydrolase-1 (GCH-1) activity, biopterin content, and superoxide production in paired samples of the right atrial appendage obtained before (PRE) and after CPB and reperfusion (POST) in 116 patients. The effect of perioperative treatment with atorvastatin (80 mg once daily) on these parameters, blood biomarkers, and the post-operative atrial effective refractory period (AERP) was then evaluated in a randomized, double-blind, placebo-controlled study in 80 patients undergoing cardiac surgery on CPB. CPB and reperfusion led to a significant increase in atrial superoxide production (74% CI 71–76%, n = 46 paired samples, P < 0.0001) and a reduction in atrial tetrahydrobiopterin (BH4) (34% CI 33–35%, n = 36 paired samples, P < 0.01), and in GCH-1 (56% CI 55–58%, n = 26 paired samples, P < 0.001) and NOS activity (58% CI 52–67%, n = 20 paired samples, P < 0.001). Perioperative atorvastatin treatment prevented the effect of CPB and reperfusion on all parameters but had no significant effect on the postoperative right AERP, troponin release, or NT-proBNP after cardiac surgery. Conclusion Perioperative statin therapy prevents post-reperfusion atrial nitroso-redox imbalance in patients undergoing on-pump cardiac surgery but has no significant impact on postoperative atrial refractoriness, perioperative myocardial injury, or markers of postoperative LV function. Clinical Trial Registration https://clinicaltrials.gov/ct2/show/NCT01780740

Funder

British Heart Foundation (BHF) Programme Grant

(NIHR) Oxford Biomedical Research Centre

Pfizer Pharmaceuticals

BHF Intermediate Fellowship

BHF Chairholders

NIHR Oxford Biomedical Research Centre

Oxford University Hospital NHS Foundation Trust

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

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