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Artificial Intelligence-Driven Algorithm for Drug Effect Prediction on Atrial Fibrillation: An in silico Population of Models Approach.

ABSTRACT: Background: Antiarrhythmic drugs are the first-line treatment for atrial fibrillation (AF), but their effect is highly dependent on the characteristics of the patient. Moreover, anatomical variability, and specifically atrial size, have also a strong influence on AF recurrence. Objective: We performed a proof-of-concept study using artificial intelligence (AI) that enabled us to identify proarrhythmic profiles based on pattern identification from in silico simulations. Methods: A population of models consisting of 127 electrophysiological profiles with a variation of nine electrophysiological variables (G _Na , I _NaK , G _K1, G _CaL , G _Kur , I _KCa , [Na] _ext , and [K] _ext and diffusion) was simulated using the Koivumaki atrial model on square planes corresponding to a normal (16 cm²) and dilated (22.5 cm²) atrium. The simple pore channel equation was used for drug implementation including three drugs (isoproterenol, flecainide, and verapamil). We analyzed the effect of every ionic channel combination to evaluate arrhythmia induction. A Random Forest algorithm was trained using the population of models and AF inducibility as input and output, respectively. The algorithm was trained with 80% of the data (N = 832) and 20% of the data was used for testing with a k-fold cross-validation (k = 5). Results: We found two electrophysiological patterns derived from the AI algorithm that was associated with proarrhythmic behavior in most of the profiles, where G _K1 was identified as the most important current for classifying the proarrhythmicity of a given profile. Additionally, we found different effects of the drugs depending on the electrophysiological profile and a higher tendency of the dilated tissue to fibrillate (Small tissue: 80 profiles vs Dilated tissue: 87 profiles). Conclusion: Artificial intelligence algorithms appear as a novel tool for electrophysiological pattern identification and analysis of the effect of antiarrhythmic drugs on a heterogeneous population of patients with AF.

SUBMITTER: Sanchez de la Nava AM

PROVIDER: S-EPMC8685526 | biostudies-literature | 2021

REPOSITORIES: biostudies-literature

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Artificial Intelligence-Driven Algorithm for Drug Effect Prediction on Atrial Fibrillation: An in silico Population of Models Approach.

Sanchez de la Nava Ana Maria AM Arenal Ángel Á Fernández-Avilés Francisco F Atienza Felipe F

Frontiers in physiology 20211206

Background: Antiarrhythmic drugs are the first-line treatment for atrial fibrillation (AF), but their effect is highly dependent on the characteristics of the patient. Moreover, anatomical variability, and specifically atrial size, have also a strong influence on AF recurrence. Objective: We performed a proof-of-concept study using artificial intelligence (AI) that enabled us to identify proarrhythmic profiles based on pattern identification from in silico simulations. Me ...[more]

PMID: 34938202

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Project description:BackgroundIn the context of atrial fibrillation (AF), traditional clinical practices have thus fallen short in several domains, such as identifying patients at risk of incident AF or patients with concomitant undetected paroxysmal AF. Novel approaches leveraging artificial intelligence have the potential to provide new tools to deal with some of these old problems.AimsTo discuss the roles of artificial intelligence (AI)-enabled electrocardiogram (ECG) pertaining to AF, potential roles of deep learning (DL) models in the context of current knowledge gaps, as well as limitations of these models.Materials & methodsAn extensive search and review of the currently available literature on the topics.ResultsOne key area where DL models can translate to better patient outcomes is through automated ECG interpretation. Challenges with regards to the benefits and harms of AF screening remain. In this context, a unique model was developed to detect underlying hidden AF from sinus rhythm.DiscussionKnowledge gaps remain regarding the best ways to monitor patients with embolic stroke of undetermined source (ESUS) and identifying those who would benefit most from oral anticoagulation. The AI-enabled AF model is one potential way to tackle this complex problem as it could be used to identify a subset of high-risk ESUS patients likely to benefit from empirical oral anticoagulation. The role of DL models assessing AF burden from long-duration ECG data is also discussed as a way of guiding management. There is a trend towards the use of consumer-grade wristbands and watches to detect AF from photoplethysmography data. However, ECG currently remains the gold standard to detect arrythmias including AF. Lastly, the role of adequate external validation of the models and clinical trials to study true performance is discussed.ConclusionAlgorithms using AI to interpret ECGs in various new ways have been developed. While still, much work needs to be done, these technologies have shown enormous potential in a short span of time. With further advancements and continuous research, these novel ways of interpretation may well become part of everyday clinical workflow.

Project description:BackgroundThe identification of latent atrial fibrillation (AF) in patients with ischemic stroke (IS) attributed to noncardioembolic etiology may have therapeutic implications. An artificial intelligence (AI) model identifying the electrocardiographic signature of AF present during normal sinus rhythm (NSR; AI-ECG-AF) can identify individuals with a high likelihood of paroxysmal AF (PAF) with NSR electrocardiogram (ECG).ObjectivesUsing AI-ECG-AF, we aimed to compare the PAF risk between noncardioembolic IS subgroups and general patients of a university hospital after controlling for confounders. Further, we sought to compare the risk of PAF among noncardioembolic IS subgroups.MethodsAfter training AI-ECG-AF with ECG data of university hospital patients, model inference outputs were obtained for the control group (i.e., general patient population) and NSRs of noncardioembolic IS patients. We conducted multiple linear regression (MLiR) and multiple logistic regression (MLoR) analyses with inference outputs (for MLiR) or their binary form (set at threshold = 0.5 for MLoR) used as dependent variables and patient subgroups and potential confounders (age and sex) set as independent variables.ResultsThe number of NSRs inferenced for the control group, cryptogenic, large artery atherosclerosis (LAA), and small artery occlusion (SAO) strokes were 133,340, 133, 276, and 290, respectively. The regression analyses indicated that patients with noncardioembolic IS had a higher PAF risk based on AI-ECG-AF relative to the control group, after controlling for confounders with the "cryptogenic" subgroup having the highest risk (odds ratio [OR] = 1.974, 95% confidence interval [CI]: 1.371-2.863) followed by the "LAA" (OR = 1.592, 95% CI: 1.238-2.056) and "SAO" subgroups (OR = 1.400, 95% CI: 1.101-1.782). Subsequent regression analyses failed to illustrate the differences in PAF risk based on AI-ECG-AF among noncardioembolic IS subgroups.ConclusionUsing AI-ECG-AF, we found that noncardioembolic IS patients had a higher PAF risk relative to the general patient population. The results from our study imply the need for more vigorous cardiac monitoring in noncardioembolic IS patients. AI-ECG-AF can be a cost-effective screening tool to identify high-risk noncardioembolic IS patients of PAF on-the-spot to be candidates for receiving additional prolonged cardiac monitoring. Our study highlights the potential of AI in clinical practice.

Project description:Atrial stretch may contribute to the mechanism of atrial fibrillation (AF) recurrence after atrial fibrillation catheter ablation (AFCA). We tested whether the left atrial (LA) wall stress (LAW-stress[measured]) could be predicted by artificial intelligence (AI) using non-invasive parameters (LAW-stress[AI]) and whether rhythm outcome after AFCA could be predicted by LAW-stress[AI] in an independent cohort. Cohort 1 included 2223 patients, and cohort 2 included 658 patients who underwent AFCA. LAW-stress[measured] was calculated using the Law of Laplace using LA diameter by echocardiography, peak LA pressure measured during procedure, and LA wall thickness measured by customized software (AMBER) using computed tomography. The highest quartile (Q4) LAW-stress[measured] was predicted and validated by AI using non-invasive clinical parameters, including non-paroxysmal type of AF, age, presence of hypertension, diabetes, vascular disease, and heart failure, left ventricular ejection fraction, and the ratio of the peak mitral flow velocity of the early rapid filling to the early diastolic velocity of the mitral annulus (E/Em). We tested the AF/atrial tachycardia recurrence 3 months after the blanking period after AFCA using the LAW-stress[measured] and LAW-stress[AI] in cohort 1 and LAW-stress[AI] in cohort 2. LAW-stress[measured] was independently associated with non-paroxysmal AF (p < 0.001), diabetes (p = 0.012), vascular disease (p = 0.002), body mass index (p < 0.001), E/Em (p < 0.001), and mean LA voltage measured by electrogram voltage mapping (p < 0.001). The best-performing AI model had acceptable prediction power for predicting Q4-LAW-stress[measured] (area under the receiver operating characteristic curve 0.734). During 26.0 (12.0-52.0) months of follow-up, AF recurrence was significantly higher in the Q4-LAW-stress[measured] group [log-rank p = 0.001, hazard ratio 2.43 (1.21-4.90), p = 0.013] and Q4-LAW-stress[AI] group (log-rank p = 0.039) in cohort 1. In cohort 2, the Q4-LAW-stress[AI] group consistently showed worse rhythm outcomes (log-rank p < 0.001). A higher LAW-stress was associated with poorer rhythm outcomes after AFCA. AI was able to predict this complex but useful prognostic parameter using non-invasive parameters with moderate accuracy.

Dataset Information

Artificial Intelligence-Driven Algorithm for Drug Effect Prediction on Atrial Fibrillation: An in silico Population of Models Approach.

Publications

Artificial Intelligence-Driven Algorithm for Drug Effect Prediction on Atrial Fibrillation: An <i>in silico</i> Population of Models Approach.

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