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Negative Affect and Risk of Atrial Fibrillation: MESA
BACKGROUND: Current literature examining the prospective relationship between depression and other measures of negative affect with atrial fibrillation (AF) are limited. We determined the relationships of depression, anger, anxiety, and chronic stress with incident AF in a multiethnic cohort of midd...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405728/ https://www.ncbi.nlm.nih.gov/pubmed/30563392 http://dx.doi.org/10.1161/JAHA.118.010603 |
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author | Garg, Parveen K. O'Neal, Wesley T. Diez‐Roux, Ana V. Alonso, Alvaro Soliman, Elsayed Z. Heckbert, Susan |
author_facet | Garg, Parveen K. O'Neal, Wesley T. Diez‐Roux, Ana V. Alonso, Alvaro Soliman, Elsayed Z. Heckbert, Susan |
author_sort | Garg, Parveen K. |
collection | PubMed |
description | BACKGROUND: Current literature examining the prospective relationship between depression and other measures of negative affect with atrial fibrillation (AF) are limited. We determined the relationships of depression, anger, anxiety, and chronic stress with incident AF in a multiethnic cohort of middle‐ and older‐aged adults. METHODS AND RESULTS: This analysis included 6644 MESA (Multi‐Ethnic Study of Atherosclerosis) study participants who were free of AF at baseline. Depressive symptoms were assessed at baseline and defined as either a 20‐item Center for Epidemiologic Studies Depression Scale score ≥16 or use of antidepressant medications. The Spielberger Trait Anger Scale, Spielberger Trait Anxiety Scale, and Chronic Burden Scale were also administered at baseline to assess anger, anxiety, and chronic stress, respectively. The primary outcome was incident AF, identified by follow‐up study visit ECGs, hospital discharge diagnoses, or Medicare claims data. A total of 875 (13%) incident AF cases were detected over a median follow‐up of nearly 13 years. A Center for Epidemiologic Studies Depression Scale score ≥16 (referent, Center for Epidemiologic Studies Depression Scale score <2) and antidepressant use were associated with a 34% and 36% higher risk of AF, respectively, in separate adjusted Cox proportional hazards analyses (hazard ratio, 1.34; 95% CI 1.04–1.74 for Center for Epidemiologic Studies Depression Scale ≥16; hazard ratio, 1.36; 95% CI, 1.04–1.77 for antidepressant use). No significant associations were observed for anger, anxiety, or chronic stress with development of AF. CONCLUSIONS: Depressive symptoms are associated with an increased risk of incident AF. Further study into whether improving depressive symptoms reduces AF incidence is important. |
format | Online Article Text |
id | pubmed-6405728 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-64057282019-03-21 Negative Affect and Risk of Atrial Fibrillation: MESA Garg, Parveen K. O'Neal, Wesley T. Diez‐Roux, Ana V. Alonso, Alvaro Soliman, Elsayed Z. Heckbert, Susan J Am Heart Assoc Original Research BACKGROUND: Current literature examining the prospective relationship between depression and other measures of negative affect with atrial fibrillation (AF) are limited. We determined the relationships of depression, anger, anxiety, and chronic stress with incident AF in a multiethnic cohort of middle‐ and older‐aged adults. METHODS AND RESULTS: This analysis included 6644 MESA (Multi‐Ethnic Study of Atherosclerosis) study participants who were free of AF at baseline. Depressive symptoms were assessed at baseline and defined as either a 20‐item Center for Epidemiologic Studies Depression Scale score ≥16 or use of antidepressant medications. The Spielberger Trait Anger Scale, Spielberger Trait Anxiety Scale, and Chronic Burden Scale were also administered at baseline to assess anger, anxiety, and chronic stress, respectively. The primary outcome was incident AF, identified by follow‐up study visit ECGs, hospital discharge diagnoses, or Medicare claims data. A total of 875 (13%) incident AF cases were detected over a median follow‐up of nearly 13 years. A Center for Epidemiologic Studies Depression Scale score ≥16 (referent, Center for Epidemiologic Studies Depression Scale score <2) and antidepressant use were associated with a 34% and 36% higher risk of AF, respectively, in separate adjusted Cox proportional hazards analyses (hazard ratio, 1.34; 95% CI 1.04–1.74 for Center for Epidemiologic Studies Depression Scale ≥16; hazard ratio, 1.36; 95% CI, 1.04–1.77 for antidepressant use). No significant associations were observed for anger, anxiety, or chronic stress with development of AF. CONCLUSIONS: Depressive symptoms are associated with an increased risk of incident AF. Further study into whether improving depressive symptoms reduces AF incidence is important. John Wiley and Sons Inc. 2018-12-19 /pmc/articles/PMC6405728/ /pubmed/30563392 http://dx.doi.org/10.1161/JAHA.118.010603 Text en © 2018 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Original Research Garg, Parveen K. O'Neal, Wesley T. Diez‐Roux, Ana V. Alonso, Alvaro Soliman, Elsayed Z. Heckbert, Susan Negative Affect and Risk of Atrial Fibrillation: MESA |
title | Negative Affect and Risk of Atrial Fibrillation: MESA |
title_full | Negative Affect and Risk of Atrial Fibrillation: MESA |
title_fullStr | Negative Affect and Risk of Atrial Fibrillation: MESA |
title_full_unstemmed | Negative Affect and Risk of Atrial Fibrillation: MESA |
title_short | Negative Affect and Risk of Atrial Fibrillation: MESA |
title_sort | negative affect and risk of atrial fibrillation: mesa |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6405728/ https://www.ncbi.nlm.nih.gov/pubmed/30563392 http://dx.doi.org/10.1161/JAHA.118.010603 |
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