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      Psychological aspects of atrial fibrillation: A systematic narrative review : Impact on incidence, cognition, prognosis, and symptom perception

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          Abstract

          Purpose of the review

          Atrial fibrillation (AF) is the most frequent arrhythmia in the general population. This review aims to provide a comprehensive overview of the psychological aspects of AF, compiling evidence from epidemiological, clinical, and basic research sources.

          Recent findings

          Findings from large-scale population-based and clinical longitudinal studies reveal an association between negative affectivity (e.g. depression) and the incidence and clinical prognosis of AF. Studies investigating the impact of work stress parameters on AF onset show conflicting results. Researchers have reported the impact of AF on cognitive decline and on health-related quality of life, and have highlighted the role of interoceptive cues in the development of AF symptom burden and gender differences in psychological covariates of AF. Among biological pathways linking psychosocial factors to AF, research on autonomic regulation has yielded the most evidence so far, showing that the onset of AF is associated with simultaneous sympatho-vagal activation rather than an increase in vagal or sympathetic drive alone. Thus, modulation of the autonomic nervous system is likely to be a promising strategy for protecting the myocardium from pro-arrhythmic autonomic influences.

          Summary

          In total, the findings show that AF is embedded as a disease condition in a psycho-societal context and is not an isolated medical problem per se. A broader perspective than a focus on the electrophysiology alone is urgently needed.

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          Most cited references73

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          Inflammation and the pathogenesis of atrial fibrillation.

          Atrial fibrillation (AF) is the most common cardiac arrhythmia. However, the development of preventative therapies for AF has been disappointing. The infiltration of immune cells and proteins that mediate the inflammatory response in cardiac tissue and circulatory processes is associated with AF. Furthermore, the presence of inflammation in the heart or systemic circulation can predict the onset of AF and recurrence in the general population, as well as in patients after cardiac surgery, cardioversion, and catheter ablation. Mediators of the inflammatory response can alter atrial electrophysiology and structural substrates, thereby leading to increased vulnerability to AF. Inflammation also modulates calcium homeostasis and connexins, which are associated with triggers of AF and heterogeneous atrial conduction. Myolysis, cardiomyocyte apoptosis, and the activation of fibrotic pathways via fibroblasts, transforming growth factor-β and matrix metalloproteases are also mediated by inflammatory pathways, which can all contribute to structural remodelling of the atria. The development of thromboembolism, a detrimental complication of AF, is also associated with inflammatory activity. Understanding the complex pathophysiological processes and dynamic changes of AF-associated inflammation might help to identify specific anti-inflammatory strategies for the prevention of AF.
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            Estimates of current and future incidence and prevalence of atrial fibrillation in the U.S. adult population.

            Estimates and projections of diagnosed incidence and prevalence of atrial fibrillation (AF) in the United States have been highly inconsistent across published studies. Although it is generally acknowledged that AF incidence and prevalence are increasing due to growing numbers of older people in the U.S. population, estimates of the rate of expected growth have varied widely. Reasons for these variations include differences in study design, covered time period, birth cohort, and temporal effects, as well as improvements in AF diagnosis due to increased use of diagnostic tools and health care awareness. The objective of this study was to estimate and project the incidence and prevalence of diagnosed AF in the United States out to 2030. A large health insurance claims database for the years 2001 to 2008, representing a geographically diverse 5% of the U.S. population, was used in this study. The trend and growth rate in AF incidence and prevalence was projected by a dynamic age-period cohort simulation progression model that included all diagnosed AF cases in future prevalence projections regardless of follow-up treatment, as well as those cases expected to be chronic in nature. Results from the model showed that AF incidence will double, from 1.2 million cases in 2010 to 2.6 million cases in 2030. Given this increase in incidence, AF prevalence is projected to increase from 5.2 million in 2010 to 12.1 million cases in 2030. The effect of uncertainty in model parameters was explored in deterministic and probabilistic sensitivity analyses. Variability in future trends in AF incidence and recurrence rates has the greatest impact on the projected estimates of chronic AF prevalence. It can be concluded that both incidence and prevalence of AF are likely to rise from 2010 to 2030, but there exists a wide range of uncertainty around the magnitude of future trends.
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              Detection, risk factors, and functional consequences of cerebral microinfarcts.

              Cerebral microinfarcts are small lesions that are presumed to be ischaemic. Despite the small size of these lesions, affected individuals can have hundreds to thousands of cerebral microinfarcts, which cause measurable disruption to structural brain connections, and are associated with dementia that is independent of Alzheimer's disease pathology or larger infarcts (ie, lacunar infarcts, and large cortical and non-lacunar subcortical infarcts). Substantial progress has been made with regard to understanding risk factors and functional consequences of cerebral microinfarcts, partly driven by new in-vivo detection methods and the development of animal models that closely mimic multiple aspects of cerebral microinfarcts in human beings. Evidence from these advances suggests that cerebral microinfarcts can be manifestations of both small vessel and large vessel disease, that cerebral microinfarcts are independently associated with cognitive impairment, and that these lesions are likely to cause damage to brain structure and function that extends beyond their actual lesion boundaries. Criteria for the identification of cerebral microinfarcts with in-vivo MRI are provided to support further studies of the association between these lesions and cerebrovascular disease and dementia.
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                Author and article information

                Contributors
                karl-heinz.ladwig@tum.de
                Andreas.Goette@vincenz.de
                seryan.atasoy@helmholtz-muenchen.de
                hamimatunnisa.johar@helmholtz-muenchen.de
                Journal
                Curr Cardiol Rep
                Curr Cardiol Rep
                Current Cardiology Reports
                Springer US (New York )
                1523-3782
                1534-3170
                10 September 2020
                10 September 2020
                2020
                : 22
                : 11
                : 137
                Affiliations
                [1 ]GRID grid.6936.a, ISNI 0000000123222966, Department of Psychosomatic Medicine and Psychotherapy, Klinikum rechts der Isar, , Technische Universität München (TUM), ; Langerstr. 3, 81675 Munich, Germany
                [2 ]GRID grid.4567.0, ISNI 0000 0004 0483 2525, Institute of Epidemiology, Mental Health Research Unit, German Research Center for Environmental Health, , Helmholtz Zentrum München, ; Neuherberg, Germany
                [3 ]GRID grid.452396.f, ISNI 0000 0004 5937 5237, German Centre for Cardiovascular Research (DZHK), , Partner site Munich Heart Alliance, ; Munich, Germany
                [4 ]St. Vincenz-Krankenhaus GmbH, Medizinischen Klinik II, Paderborn, Germany
                [5 ]GRID grid.411559.d, ISNI 0000 0000 9592 4695, Working Group on Molecular Electrophysiology, , University Hospital Magdeburg, ; Magdeburg, Germany
                [6 ]GRID grid.8664.c, ISNI 0000 0001 2165 8627, Department of Psychosomatic Medicine and Psychotherapy, , University of Gießen and Marburg, ; Marburg, Germany
                Author information
                http://orcid.org/0000-0003-0710-1720
                Article
                1396
                10.1007/s11886-020-01396-w
                7496063
                32910300
                89d71adb-8e78-4caa-b53d-5c654fddb918
                © The Author(s) 2020

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                Funding
                Funded by: Technische Universität München (1025)
                Categories
                Psychological Aspects of Cardiovascular Diseases (A Steptoe, Section Editor)
                Custom metadata
                © Springer Science+Business Media, LLC, part of Springer Nature 2020

                Cardiovascular Medicine
                atrial fibrillation,psychosocial stress,cognition,dementia,symptom perception,depression,anxiety,ptsd,autonomic regulation

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