Key result
Decreased pre-operative mitochondrial respiration is linked to POAF in metabolic syndrome patients undergoing CABG.
Why the study?
Underlying mechanisms of postoperative atrial fibrillation remain largely unknown, prompting investigation into whether a causal link exists between POAF onset and preoperative function of cardiac mitochondria.
Is pre-operative mitochondrial dysfunction associated with the development of post-operative atrial fibrillation in patients with metabolic syndrome undergoing CABG?
Cohort (n=104)
Is pre-operative mitochondrial dysfunction associated with the development of post-operative atrial fibrillation in patients with metabolic syndrome undergoing CABG?
Pre-operative mitochondrial dysfunction in the atrial myocardium is independently associated with the development of post-operative atrial fibrillation in patients with metabolic syndrome undergoing CABG.
May inform preoperative risk stratification in metabolic syndrome; leaves open whether targeting mitochondrial dysfunction prevents post-operative atrial fibrillation.
OBJECTIVES: This study sought to provide bedside evidence of the potential link between cardiac mitochondrial dysfunction and arrhythmia as reported in bench studies. BACKGROUND: Atrial fibrillation (AF) is a frequent complication of cardiac surgery. Underlying mechanisms of post-operative atrial fibrillation (POAF) remain largely unknown. Because cardiac mitochondrial dysfunction has been reported in clinical conditions with a high risk of POAF, we investigated whether a causal link exists between POAF onset and pre-operative function of cardiac mitochondria. METHODS: Pre-operative mitochondrial respiration and calcium retention capacity, respiratory complex activity, and myocardial oxidative stress were quantified in right atrial tissue from 104 consecutive patients with metabolic syndrome, in sinus rhythm, and undergoing coronary artery bypass graft surgery. RESULTS: In this high-risk population, POAF occurred in 44% of patients. Decreased pre-operative mitochondrial respiration and increased sensitivity to calcium-induced mitochondrial permeability transition pore opening were significantly associated with POAF. Adenosine diphosphate-stimulated mitochondrial respiration supported by palmitoyl-l-carnitine was significantly lower in POAF patients and remained independently associated with AF onset after adjustment for age, body mass index, heart rate, beta-blocker use, and statin medication (multivariate logistic regression coefficient per unit = -0.314 ± 0.144; p = 0.028). Gene expression profile analysis identified a general downregulation of the mitochondria/oxidative phosphorylation gene cluster in pre-operative atrial tissue of patients in whom AF developed. CONCLUSIONS: Our prospective study identifies an association between pre-operative mitochondrial dysfunction of the atrial myocardium and AF occurrence after cardiac surgery in patients with metabolic disease, providing novel insights into the link between mitochondria and arrhythmias in patients.
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Montaigne et al. (2013) conducted a cohort in Post-operative atrial fibrillation (n=104). Pre-operative mitochondrial dysfunction was evaluated on Post-operative atrial fibrillation (POAF) (coefficient -0.314, p=0.028). Decreased pre-operative mitochondrial respiration was independently associated with post-operative atrial fibrillation in patients with metabolic syndrome undergoing CABG (p=0.028).
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