Publications by authors named "Aaron Mark Lee"

Aims: The importance of early life factors in determining health in later adulthood is increasingly recognized. This study evaluated the association of adverse childhood experiences (ACEs) with cardiovascular magnetic resonance (CMR) phenotypes.

Methods And Results: UK Biobank participants who had completed CMR and the self-reported questionnaire on traumatic childhood experiences were included.

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Article Synopsis
  • Explainable artificial intelligence (XAI) helps us understand how AI makes decisions, which is important for trusting its predictions.
  • A review of XAI used in heart-related AI shows only 37% of studies checked the quality of explanations, with many not evaluating them at all.
  • The goal is to encourage more research in healthcare to not just use XAI, but also assess its explanations to ensure the AI is safe and reliable.
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Article Synopsis
  • The study addresses the lack of population-specific cardiovascular magnetic resonance (CMR) reference ranges, which is important for clinical care.
  • It provides CMR reference ranges based on data from 9,088 healthy individuals, considering age, sex, and ethnicity, thus enhancing the understanding of heart metrics across diverse demographics.
  • The analysis involved advanced software and various imaging techniques, resulting in a comprehensive set of healthy CMR-derived volumetric reference ranges that can be applied in clinical settings.
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Background: Inherited cardiomyopathies present with broad variation of phenotype. Data are limited regarding genetic screening strategies and outcomes associated with predicted deleterious variants in cardiomyopathy-associated genes in the general population.

Objectives: The authors aimed to determine the risk of mortality and composite cardiomyopathy-related outcomes associated with predicted deleterious variants in cardiomyopathy-associated genes in the UK Biobank.

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Aims: To evaluate the relationship between neuroticism personality traits and cardiovascular magnetic resonance (CMR) measures of cardiac morphology and function, considering potential differential associations in men and women.

Methods And Results: The analysis includes 36 309 UK Biobank participants (average age = 63.9 ± 7.

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Artificial intelligence applications have shown success in different medical and health care domains, and cardiac imaging is no exception. However, some machine learning models, especially deep learning, are considered black box as they do not provide an explanation or rationale for model outcomes. Complexity and vagueness in these models necessitate a transition to explainable artificial intelligence (XAI) methods to ensure that model results are both transparent and understandable to end users.

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Objective: To examine association of COVID-19 with incident cardiovascular events in 17 871 UK Biobank cases between March 2020 and 2021.

Methods: COVID-19 cases were defined using health record linkage. Each case was propensity score-matched to two uninfected controls on age, sex, deprivation, body mass index, ethnicity, diabetes, prevalent ischaemic heart disease (IHD), smoking, hypertension and high cholesterol.

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Background: There is a paucity of data regarding the phenotype of dilated cardiomyopathy (DCM) gene variants in the general population. We aimed to determine the frequency and penetrance of DCM-associated putative pathogenic gene variants in a general adult population, with a focus on the expression of clinical and subclinical phenotype, including structural, functional, and arrhythmic disease features.

Methods: UK Biobank participants who had undergone whole exome sequencing, ECG, and cardiovascular magnetic resonance imaging were selected for study.

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Pericardial adipose tissue (PAT) may represent a novel risk marker for cardiovascular disease. However, absence of rapid radiation-free PAT quantification methods has precluded its examination in large cohorts. We developed a fully automated quality-controlled tool for cardiovascular magnetic resonance (CMR) PAT quantification in the UK Biobank (UKB).

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