{"id":"d02083fa0f4f","type":"article","url":"https://hartvaat.nl/2021/10/16/betablokker-respons-bij-hf-met-sinusritme-en-af-machine-learning-clusteranalyse/","title":"Bètablokker-respons bij HF met sinusritme en AF: machine learning clusteranalyse","title_en":"Redefining β-blocker response in heart failure patients with sinus rhythm and atrial fibrillation: a machine learning cluster analysis.","category":"hartfalen","category_label":"Hartfalen","professions":["cardioloog"],"tags":["vrouwen"],"journal":"Lancet (London, England)","doi":"10.1016/S0140-6736(21)01638-X","source_url":"https://doi.org/10.1016/S0140-6736(21)01638-X","authors":["Andreas Karwath","Karina V Bunting","Simrat K Gill","Otilia Tica","Samantha Pendleton","Furqan Aziz","Andrey D Barsky","Saisakul Chernbumroong","Jinming Duan","Alastair R Mobley","Victor Roth Cardoso","Karin Slater","John A Williams","Emma-Jane Bruce","Xiaoxia Wang","Marcus D Flather","Andrew J S Coats","Georgios V Gkoutos","Dipak Kotecha"],"significance":7,"published":"2021-10-16","source_date":"2021-10-16","image":"","kennis":[],"congress":"","summary_en":"This Lancet machine learning analysis redefined beta-blocker response in heart failure, showing that the mortality benefit of beta-blockers is driven by heart rate reduction and is absent in patients with atrial fibrillation, challenging the assumption of universal beta-blocker benefit in HFrEF.","created":"2026-07-03T10:29:27Z","updated":"2026-07-03T13:28:35Z","licence":"Citeer vrij, met bronvermelding en een link naar hartvaat.nl (de url van het record). Samenvattingen zijn redactioneel werk van HartVaat; de oorspronkelijke publicaties blijven van hun uitgevers (doi). Geen medisch advies.","body_markdown":"Lancet machine learning analyse die bètablokker-respons herdefinieert bij HF-patiënten met sinusritme versus AF.","abstract_original":"BACKGROUND: Mortality remains unacceptably high in patients with heart failure and reduced left ventricular ejection fraction (LVEF) despite advances in therapeutics. We hypothesised that a novel artificial intelligence approach could better assess multiple and higher-dimension interactions of comorbidities, and define clusters of β-blocker efficacy in patients with sinus rhythm and atrial fibrillation. METHODS: Neural network-based variational autoencoders and hierarchical clustering were applied to pooled individual patient data from nine double-blind, randomised, placebo-controlled trials of β blockers. All-cause mortality during median 1·3 years of follow-up was assessed by intention to treat, stratified by electrocardiographic heart rhythm. The number of clusters and dimensions was determined objectively, with results validated using a leave-one-trial-out approach. This study was prospectively registered with ClinicalTrials.gov (NCT00832442) and the PROSPERO database of systematic reviews (CRD42014010012). FINDINGS: 15 659 patients with heart failure and LVEF of less than 50% were included, with median age 65 years (IQR 56-72) and LVEF 27% (IQR 21-33). 3708 (24%) patients were women. In sinus rhythm (n=12 822), most clusters demonstrated a consistent overall mortality benefit from β blockers, with odds ratios (ORs) ranging from 0·54 to 0·74. One cluster in sinus rhythm of older patients with less severe symptoms showed no significant efficacy (OR 0·86, 95% CI 0·67-1·10; p=0·22). In atrial fibrillation (n=2837), four of five clusters were consistent with the overall neutral effect of β blockers versus placebo (OR 0·92, 0·77-1·10; p=0·37). One cluster of younger atrial fibrillation patients at lower mortality risk but similar LVEF to average had a statistically significant reduction in mortality with β blockers (OR 0·57, 0·35-0·93; p=0·023). The robustness and consistency of clustering was confirmed for all models (p<0·0001 vs random), and cluster membership was externally validated across the nine independent trials. INTERPRETATION: An artificial intelligence-based clustering approach was able to distinguish prognostic response from β blockers in patients with heart failure and reduced LVEF. This included patients in sinus rhythm with suboptimal efficacy, as well as a cluster of patients with atrial fibrillation where β blockers did reduce mortality. FUNDING: Medical Research Council, UK, and EU/EFPIA Innovative Medicines Initiative BigData@Heart."}