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dc.contributor.authorMay, S
dc.contributor.authorAbbott, TEF
dc.contributor.authorGutierrez Del Arroyo, A
dc.contributor.authorReyes, A
dc.contributor.authorMartir, G
dc.contributor.authorStephens, RCM
dc.contributor.authorBrealey, D
dc.contributor.authorCuthbertson, B
dc.contributor.authorWijeysundera, D
dc.contributor.authorPearse, R
dc.contributor.authorAckland, G
dc.date.accessioned2020-11-18T11:44:56Z
dc.date.available2020-02-27
dc.date.available2020-11-18T11:44:56Z
dc.date.issued2020-07-25
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/68429
dc.description.abstractBackground: Elevated plasma/serum troponin, indicating perioperative myocardial injury (PMI), is common after non-cardiac surgery. However, underlying mechanisms remain unclear. Acute coronary syndrome (ACS) is associated with the early appearance of circulating microRNAs, which regulate post-translational gene expression. We hypothesised that if PMI and ACS share pathophysiological mechanisms, common microRNA signatures should be evident. Methods: Nested case-control study of samples obtained before and after non-cardiac surgery from patients enrolled in two prospective observational studies of PMI (postoperative troponin I/T>99th centile). In cohort one, serum microRNAs were compared between patients with/without PMI, matched for age, gender and comorbidity. Real-time polymerase chain reaction quantified relative microRNA expression (cycle quantification threshold <37) before and after surgery for microRNA signatures associated with ACS, blinded to PMI. In cohort two, we analysed (EdgeR) microRNA from plasma extracellular vesicles using next-generation sequencing (Illumina HiSeq500). microRNA-messenger RNA-function pathway analysis was performed (DIANA miRPath v3.0/TopGO). Results: MicroRNA were detectable in all 59 patients (median age:67yrs (61-75); 42% male), who had similar clinical characteristics independent of developing PMI. In cohort one, PMI was not associated with increased serum microRNA expression levels after surgery (hsa-miR-1-3p mean fold-change (FC): 3.99 (95%CI:1.95-8.19); hsa-miR-133-3p FC:5.67(95%CI:2.94-10.91); p<0.001). hsa-miR-208b-3p was more commonly detected after PMI (odd ratio (OR):10.0 (95%CI:1.9-52.6); p<0.01). Bioinformatic analysis of differentially expressed microRNAs from cohorts one and two identified pathways associated with adrenergic stress involving calcium dysregulation, rather than ischaemia. Conclusions: Circulating microRNAs synonymous with cardiac ischaemia were universally elevated in patients after surgery, independent of developing myocardial injury.en_US
dc.publisherElsevieren_US
dc.relation.ispartofBritish Journal of Anaesthesia
dc.titleMicroRNA signatures of perioperative myocardial injury after elective noncardiac surgery: a prospective observational mechanistic cohort studyen_US
dc.typeArticleen_US
dc.rights.holder(c) 2020
dc.identifier.doihttps://doi.org/10.1016/j.bja.2020.05.066
pubs.notesNot knownen_US
pubs.publication-statusAccepteden_US
dcterms.dateAccepted2020-02-27
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
qmul.funderParasympathetic modulation of perioperative myocardial injury.::Royal College Of Anaesthetists/ British Journal of Anaesthesiaen_US


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