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Association of Abnormal P‐Wave Indices With Dementia and Cognitive Decline Over 25 Years: ARIC‐NCS (The Atherosclerosis Risk in Communities Neurocognitive Study)
BACKGROUND: Abnormal P‐wave indices (PWIs)—reflecting underlying left atrial abnormality—are associated with increased risk of stroke independent of atrial fibrillation. We assessed whether abnormal PWIs are associated with incident dementia and greater cognitive decline, independent of atrial fibri...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6951047/ https://www.ncbi.nlm.nih.gov/pubmed/31830872 http://dx.doi.org/10.1161/JAHA.119.014553 |
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author | Gutierrez, Alejandra Norby, Faye L. Maheshwari, Ankit Rooney, Mary R. Gottesman, Rebecca F. Mosley, Thomas H. Lutsey, Pamela L. Oldenburg, Niki Soliman, Elsayed Z. Alonso, Alvaro Chen, Lin Y. |
author_facet | Gutierrez, Alejandra Norby, Faye L. Maheshwari, Ankit Rooney, Mary R. Gottesman, Rebecca F. Mosley, Thomas H. Lutsey, Pamela L. Oldenburg, Niki Soliman, Elsayed Z. Alonso, Alvaro Chen, Lin Y. |
author_sort | Gutierrez, Alejandra |
collection | PubMed |
description | BACKGROUND: Abnormal P‐wave indices (PWIs)—reflecting underlying left atrial abnormality—are associated with increased risk of stroke independent of atrial fibrillation. We assessed whether abnormal PWIs are associated with incident dementia and greater cognitive decline, independent of atrial fibrillation and ischemic stroke. METHODS AND RESULTS: We included 13 714 participants (mean age, 57±6 years; 56% women; 23% black) who were followed for dementia through the end of 2015. (Abnormal P‐wave terminal force in lead V1, ≥4000 μV×ms), abnormal P‐wave axis (>75° or <0°), prolonged P‐wave duration (>120 ms), and advanced interatrial block were determined from ECGs at visits 2 to 4. Dementia was adjudicated by an expert panel using data from cognitive tests and hospitalization International Classification of Diseases codes. Cognitive function was measured longitudinally using 3 neuropsychological tests. Cox proportional hazards models were used to assess the association between time‐dependent abnormal PWIs with incident dementia. Linear regression models were used to evaluate PWIs with cognitive function over time. At the conclusion of the study, 19%, 16%, 28%, and 1.9% of participants had abnormal P‐wave terminal force in lead V1, abnormal P‐wave axis, prolonged P‐wave duration, and advanced interatrial block, respectively. During mean follow‐up of 18 years, there were 1390 (10%) dementia cases. All abnormal PWIs except advanced interatrial block were associated with an increased risk of dementia even after adjustment for incident atrial fibrillation and stroke: multivariable hazard ratio of abnormal P wave terminal force in lead V1=1.60, 95% CI, 1.41 to 2.83; abnormal P‐wave axis, hazard ratio =1.36, 95% CI, 1.17 to 2.57; prolonged P‐wave duration, hazard ratio=1.60, 95% CI, 1.42 to 1.80. Only abnormal P‐wave terminal force in lead V1 was associated with greater decline in global cognition. CONCLUSIONS: Abnormal PWIs are independently associated with an increased risk of dementia. This novel finding should be replicated in other cohorts and the underlying mechanisms should be evaluated. |
format | Online Article Text |
id | pubmed-6951047 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69510472020-01-10 Association of Abnormal P‐Wave Indices With Dementia and Cognitive Decline Over 25 Years: ARIC‐NCS (The Atherosclerosis Risk in Communities Neurocognitive Study) Gutierrez, Alejandra Norby, Faye L. Maheshwari, Ankit Rooney, Mary R. Gottesman, Rebecca F. Mosley, Thomas H. Lutsey, Pamela L. Oldenburg, Niki Soliman, Elsayed Z. Alonso, Alvaro Chen, Lin Y. J Am Heart Assoc Original Research BACKGROUND: Abnormal P‐wave indices (PWIs)—reflecting underlying left atrial abnormality—are associated with increased risk of stroke independent of atrial fibrillation. We assessed whether abnormal PWIs are associated with incident dementia and greater cognitive decline, independent of atrial fibrillation and ischemic stroke. METHODS AND RESULTS: We included 13 714 participants (mean age, 57±6 years; 56% women; 23% black) who were followed for dementia through the end of 2015. (Abnormal P‐wave terminal force in lead V1, ≥4000 μV×ms), abnormal P‐wave axis (>75° or <0°), prolonged P‐wave duration (>120 ms), and advanced interatrial block were determined from ECGs at visits 2 to 4. Dementia was adjudicated by an expert panel using data from cognitive tests and hospitalization International Classification of Diseases codes. Cognitive function was measured longitudinally using 3 neuropsychological tests. Cox proportional hazards models were used to assess the association between time‐dependent abnormal PWIs with incident dementia. Linear regression models were used to evaluate PWIs with cognitive function over time. At the conclusion of the study, 19%, 16%, 28%, and 1.9% of participants had abnormal P‐wave terminal force in lead V1, abnormal P‐wave axis, prolonged P‐wave duration, and advanced interatrial block, respectively. During mean follow‐up of 18 years, there were 1390 (10%) dementia cases. All abnormal PWIs except advanced interatrial block were associated with an increased risk of dementia even after adjustment for incident atrial fibrillation and stroke: multivariable hazard ratio of abnormal P wave terminal force in lead V1=1.60, 95% CI, 1.41 to 2.83; abnormal P‐wave axis, hazard ratio =1.36, 95% CI, 1.17 to 2.57; prolonged P‐wave duration, hazard ratio=1.60, 95% CI, 1.42 to 1.80. Only abnormal P‐wave terminal force in lead V1 was associated with greater decline in global cognition. CONCLUSIONS: Abnormal PWIs are independently associated with an increased risk of dementia. This novel finding should be replicated in other cohorts and the underlying mechanisms should be evaluated. John Wiley and Sons Inc. 2019-12-13 /pmc/articles/PMC6951047/ /pubmed/31830872 http://dx.doi.org/10.1161/JAHA.119.014553 Text en © 2019 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 Gutierrez, Alejandra Norby, Faye L. Maheshwari, Ankit Rooney, Mary R. Gottesman, Rebecca F. Mosley, Thomas H. Lutsey, Pamela L. Oldenburg, Niki Soliman, Elsayed Z. Alonso, Alvaro Chen, Lin Y. Association of Abnormal P‐Wave Indices With Dementia and Cognitive Decline Over 25 Years: ARIC‐NCS (The Atherosclerosis Risk in Communities Neurocognitive Study) |
title | Association of Abnormal P‐Wave Indices With Dementia and Cognitive Decline Over 25 Years: ARIC‐NCS (The Atherosclerosis Risk in Communities Neurocognitive Study) |
title_full | Association of Abnormal P‐Wave Indices With Dementia and Cognitive Decline Over 25 Years: ARIC‐NCS (The Atherosclerosis Risk in Communities Neurocognitive Study) |
title_fullStr | Association of Abnormal P‐Wave Indices With Dementia and Cognitive Decline Over 25 Years: ARIC‐NCS (The Atherosclerosis Risk in Communities Neurocognitive Study) |
title_full_unstemmed | Association of Abnormal P‐Wave Indices With Dementia and Cognitive Decline Over 25 Years: ARIC‐NCS (The Atherosclerosis Risk in Communities Neurocognitive Study) |
title_short | Association of Abnormal P‐Wave Indices With Dementia and Cognitive Decline Over 25 Years: ARIC‐NCS (The Atherosclerosis Risk in Communities Neurocognitive Study) |
title_sort | association of abnormal p‐wave indices with dementia and cognitive decline over 25 years: aric‐ncs (the atherosclerosis risk in communities neurocognitive study) |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6951047/ https://www.ncbi.nlm.nih.gov/pubmed/31830872 http://dx.doi.org/10.1161/JAHA.119.014553 |
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