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dc.contributor.authorChan, K
dc.contributor.authorWahome, E
dc.contributor.authorTsiachristas, A
dc.contributor.authorAntonopoulos, AS
dc.contributor.authorPatel, P
dc.contributor.authorLyasheva, M
dc.contributor.authorKingham, L
dc.contributor.authorWest, H
dc.contributor.authorOikonomou, EK
dc.contributor.authorVolpe, L
dc.contributor.authorMavrogiannis, MC
dc.contributor.authorNicol, E
dc.contributor.authorMittal, TK
dc.contributor.authorHalborg, T
dc.contributor.authorKotronias, RA
dc.contributor.authorAdlam, D
dc.contributor.authorModi, B
dc.contributor.authorRodrigues, J
dc.contributor.authorScreaton, N
dc.contributor.authorKardos, A
dc.contributor.authorGreenwood, JP
dc.contributor.authorSabharwal, N
dc.contributor.authorDe Maria, GL
dc.contributor.authorMunir, S
dc.contributor.authorMcAlindon, E
dc.contributor.authorSohan, Y
dc.contributor.authorTomlins, P
dc.contributor.authorSiddique, M
dc.contributor.authorKelion, A
dc.contributor.authorShirodaria, C
dc.contributor.authorPugliese, F
dc.contributor.authorPetersen, SE
dc.contributor.authorBlankstein, R
dc.contributor.authorDesai, M
dc.contributor.authorGersh, BJ
dc.contributor.authorAchenbach, S
dc.contributor.authorLibby, P
dc.contributor.authorNeubauer, S
dc.contributor.authorChannon, KM
dc.contributor.authorDeanfield, J
dc.contributor.authorAntoniades, C
dc.contributor.authorORFAN Consortium
dc.date.accessioned2024-06-04T13:42:31Z
dc.date.available2024-03-22
dc.date.available2024-06-04T13:42:31Z
dc.date.issued2024-05-29
dc.identifier.citationKenneth Chan, Elizabeth Wahome, Apostolos Tsiachristas, Alexios S Antonopoulos, Parijat Patel, Maria Lyasheva, Lucy Kingham, Henry West, Evangelos K Oikonomou, Lucrezia Volpe, Michail C Mavrogiannis, Edward Nicol, Tarun K Mittal, Thomas Halborg, Rafail A Kotronias, David Adlam, Bhavik Modi, Jonathan Rodrigues, Nicholas Screaton, Attila Kardos, John P Greenwood, Nikant Sabharwal, Giovanni Luigi De Maria, Shahzad Munir, Elisa McAlindon, Yogesh Sohan, Pete Tomlins, Muhammad Siddique, Andrew Kelion, Cheerag Shirodaria, Francesca Pugliese, Steffen E Petersen, Ron Blankstein, Milind Desai, Bernard J Gersh, Stephan Achenbach, Peter Libby, Stefan Neubauer, Keith M Channon, John Deanfield, Charalambos Antoniades, Sheena Thomas, Jon Denton, Robyn Farral, Carolyn Taylor, Wendy Qin, Mary Kasongo, Susan Anthony, Adrian Banning, Cheng Xie, Rajesh K Kharbanda, Amy Pritchard, Thomas Halborg, Nigar Syed, Sam Fry, Chris Mathers, Anne Rose, George Hudson, Amrita Bajaj, Intrajeet Das, Aparna Deshpande, Praveen Rao, Dan Lawday, Saeed Mirsadraee, Benjamin Hudson, Colin Berry, Mohamed Marwan, Pál Maurovich-Horvat, Guo-Wei He, Wen-Hua Lin, Li-Juan Fan, Naohiko Takahashi, Hidekazu Kondo, Neng Dai, Junbo Ge, Bon-Kwon Koo, Marco Guglielmo, Gianluca Pontone, Daniel Huck, Theodora Benedek, Ronak Rajani, Dijana Vilic, Haleema Aljazzaf, Mak S Mun, Giulia Benedetti, Rebecca L Preston, Zahra Raisi-Estabragh, Derek L Connolly, Vinoda Sharma, Rebecca Grenfell, William Bradlow, Matthias Schmitt, Fabiano Serfaty, Ilan Gottlieb, Mario FT Neves, David E Newby, Marc R Dweck, Stéphane Hatem, Alban Redheuil, Georgios Benetos, Meinrad Beer, Gastón AR Granillo, Joseph Selvanayagam, Francisco Lopez-Jimenez, Ruben De Bosscher, Alain Tavildari, Gemma Figtree, Ibrahim Danad, Ronney Shantouf, Bas Kietselaer, Dimitris Tousoulis, George Dangas, Nehal N Mehta, Christos Kontanidis, Vijay Kunadian, Timothy A Fairbairn, Inflammatory risk and cardiovascular events in patients without obstructive coronary artery disease: the ORFAN multicentre, longitudinal cohort study, The Lancet, 2024, , ISSN 0140-6736, https://doi.org/10.1016/S0140-6736(24)00596-8. (https://www.sciencedirect.com/science/article/pii/S0140673624005968) Abstract: Summary Background Coronary computed tomography angiography (CCTA) is the first line investigation for chest pain, and it is used to guide revascularisation. However, the widespread adoption of CCTA has revealed a large group of individuals without obstructive coronary artery disease (CAD), with unclear prognosis and management. Measurement of coronary inflammation from CCTA using the perivascular fat attenuation index (FAI) Score could enable cardiovascular risk prediction and guide the management of individuals without obstructive CAD. The Oxford Risk Factors And Non-invasive imaging (ORFAN) study aimed to evaluate the risk profile and event rates among patients undergoing CCTA as part of routine clinical care in the UK National Health Service (NHS); to test the hypothesis that coronary arterial inflammation drives cardiac mortality or major adverse cardiac events (MACE) in patients with or without CAD; and to externally validate the performance of the previously trained artificial intelligence (AI)-Risk prognostic algorithm and the related AI-Risk classification system in a UK population. Methods This multicentre, longitudinal cohort study included 40 091 consecutive patients undergoing clinically indicated CCTA in eight UK hospitals, who were followed up for MACE (ie, myocardial infarction, new onset heart failure, or cardiac death) for a median of 2·7 years (IQR 1·4–5·3). The prognostic value of FAI Score in the presence and absence of obstructive CAD was evaluated in 3393 consecutive patients from the two hospitals with the longest follow-up (7·7 years [6·4–9·1]). An AI-enhanced cardiac risk prediction algorithm, which integrates FAI Score, coronary plaque metrics, and clinical risk factors, was then evaluated in this population. Findings In the 2·7 year median follow-up period, patients without obstructive CAD (32 533 [81·1%] of 40 091) accounted for 2857 (66·3%) of the 4307 total MACE and 1118 (63·7%) of the 1754 total cardiac deaths in the whole of Cohort A. Increased FAI Score in all the three coronary arteries had an additive impact on the risk for cardiac mortality (hazard ratio [HR] 29·8 [95% CI 13·9–63·9], p<0·001) or MACE (12·6 [8·5–18·6], p<0·001) comparing three vessels with an FAI Score in the top versus bottom quartile for each artery. FAI Score in any coronary artery predicted cardiac mortality and MACE independently from cardiovascular risk factors and the presence or extent of CAD. The AI-Risk classification was positively associated with cardiac mortality (6·75 [5·17–8·82], p<0·001, for very high risk vs low or medium risk) and MACE (4·68 [3·93–5·57], p<0·001 for very high risk vs low or medium risk). Finally, the AI-Risk model was well calibrated against true events. Interpretation The FAI Score captures inflammatory risk beyond the current clinical risk stratification and CCTA interpretation, particularly among patients without obstructive CAD. The AI-Risk integrates this information in a prognostic algorithm, which could be used as an alternative to traditional risk factor-based risk calculators. Funding British Heart Foundation, NHS-AI award, Innovate UK, National Institute for Health and Care Research, and the Oxford Biomedical Research Centre.en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/97228
dc.description.abstractBACKGROUND: Coronary computed tomography angiography (CCTA) is the first line investigation for chest pain, and it is used to guide revascularisation. However, the widespread adoption of CCTA has revealed a large group of individuals without obstructive coronary artery disease (CAD), with unclear prognosis and management. Measurement of coronary inflammation from CCTA using the perivascular fat attenuation index (FAI) Score could enable cardiovascular risk prediction and guide the management of individuals without obstructive CAD. The Oxford Risk Factors And Non-invasive imaging (ORFAN) study aimed to evaluate the risk profile and event rates among patients undergoing CCTA as part of routine clinical care in the UK National Health Service (NHS); to test the hypothesis that coronary arterial inflammation drives cardiac mortality or major adverse cardiac events (MACE) in patients with or without CAD; and to externally validate the performance of the previously trained artificial intelligence (AI)-Risk prognostic algorithm and the related AI-Risk classification system in a UK population. METHODS: This multicentre, longitudinal cohort study included 40 091 consecutive patients undergoing clinically indicated CCTA in eight UK hospitals, who were followed up for MACE (ie, myocardial infarction, new onset heart failure, or cardiac death) for a median of 2·7 years (IQR 1·4-5·3). The prognostic value of FAI Score in the presence and absence of obstructive CAD was evaluated in 3393 consecutive patients from the two hospitals with the longest follow-up (7·7 years [6·4-9·1]). An AI-enhanced cardiac risk prediction algorithm, which integrates FAI Score, coronary plaque metrics, and clinical risk factors, was then evaluated in this population. FINDINGS: In the 2·7 year median follow-up period, patients without obstructive CAD (32 533 [81·1%] of 40 091) accounted for 2857 (66·3%) of the 4307 total MACE and 1118 (63·7%) of the 1754 total cardiac deaths in the whole of Cohort A. Increased FAI Score in all the three coronary arteries had an additive impact on the risk for cardiac mortality (hazard ratio [HR] 29·8 [95% CI 13·9-63·9], p<0·001) or MACE (12·6 [8·5-18·6], p<0·001) comparing three vessels with an FAI Score in the top versus bottom quartile for each artery. FAI Score in any coronary artery predicted cardiac mortality and MACE independently from cardiovascular risk factors and the presence or extent of CAD. The AI-Risk classification was positively associated with cardiac mortality (6·75 [5·17-8·82], p<0·001, for very high risk vs low or medium risk) and MACE (4·68 [3·93-5·57], p<0·001 for very high risk vs low or medium risk). Finally, the AI-Risk model was well calibrated against true events. INTERPRETATION: The FAI Score captures inflammatory risk beyond the current clinical risk stratification and CCTA interpretation, particularly among patients without obstructive CAD. The AI-Risk integrates this information in a prognostic algorithm, which could be used as an alternative to traditional risk factor-based risk calculators. FUNDING: British Heart Foundation, NHS-AI award, Innovate UK, National Institute for Health and Care Research, and the Oxford Biomedical Research Centre.en_US
dc.languageeng
dc.publisherElsevieren_US
dc.relation.ispartofLancet
dc.rightsThis is an Open Access article under the CC BY 4.0 license.
dc.titleInflammatory risk and cardiovascular events in patients without obstructive coronary artery disease: the ORFAN multicentre, longitudinal cohort study.en_US
dc.typeArticleen_US
dc.rights.holder© 2024 The Author(s). Published by Elsevier Ltd.
dc.identifier.doi10.1016/S0140-6736(24)00596-8
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/38823406en_US
pubs.notesNot knownen_US
pubs.publication-statusPublished onlineen_US
dcterms.dateAccepted2024-03-22
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US


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