Predicting Silent Atrial Fibrillation in the Elderly: A Report from the NOMED-AF Cross-Sectional Study.

risk assessment risk factors silent atrial fibrillation

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
26 May 2021
Historique:
received: 29 04 2021
revised: 20 05 2021
accepted: 21 05 2021
entrez: 2 6 2021
pubmed: 3 6 2021
medline: 3 6 2021
Statut: epublish

Résumé

Silent atrial fibrillation (SAF) is common and is associated with poor outcomes. to study the risk factors for AF and SAF in the elderly (≥65 years) general population and to develop a risk stratification model for predicting SAF. Continuous ECG monitoring was performed for up to 30 days using a vest-based system in a cohort from NOMED-AF, a cross-sectional study based on a nationwide population sample. The independent risk factors for AF and SAF were determined using multiple logistic regression. ROC analysis was applied to validate the developed risk stratification score. From the total cohort of 3014 subjects, AF was diagnosed in 680 individuals (mean age, 77.5 ± 7.9; 50.1% men) with AF, and, of these, 41% had SAF. Independent associations with an increased risk of AF were age, male gender, coronary heart disease, thyroid diseases, prior ischemic stroke or transient ischemic attack (ICS/TIA), diabetes, heart failure, chronic kidney disease (CKD), obesity, and NT-proBNP >125 ng/mL. The risk factors for SAF were age, male gender, ICS/TIA, diabetes, heart failure, CKD, and NT-proBNP >125 ng/mL. We developed a clinical risk scale (MR-DASH score) that achieved a good level of prediction in the derivation cohort (AUC 0.726) and the validation cohort (AUC 0.730). SAF is associated with various clinical risk factors in a population sample of individuals ≥65 years. Stratifying individuals from the general population according to their risk for SAF may be possible using the MR-DASH score, facilitating targeted screening programs of individuals with a high risk of SAF.

Sections du résumé

BACKGROUND BACKGROUND
Silent atrial fibrillation (SAF) is common and is associated with poor outcomes.
AIMS OBJECTIVE
to study the risk factors for AF and SAF in the elderly (≥65 years) general population and to develop a risk stratification model for predicting SAF.
METHODS METHODS
Continuous ECG monitoring was performed for up to 30 days using a vest-based system in a cohort from NOMED-AF, a cross-sectional study based on a nationwide population sample. The independent risk factors for AF and SAF were determined using multiple logistic regression. ROC analysis was applied to validate the developed risk stratification score.
RESULTS RESULTS
From the total cohort of 3014 subjects, AF was diagnosed in 680 individuals (mean age, 77.5 ± 7.9; 50.1% men) with AF, and, of these, 41% had SAF. Independent associations with an increased risk of AF were age, male gender, coronary heart disease, thyroid diseases, prior ischemic stroke or transient ischemic attack (ICS/TIA), diabetes, heart failure, chronic kidney disease (CKD), obesity, and NT-proBNP >125 ng/mL. The risk factors for SAF were age, male gender, ICS/TIA, diabetes, heart failure, CKD, and NT-proBNP >125 ng/mL. We developed a clinical risk scale (MR-DASH score) that achieved a good level of prediction in the derivation cohort (AUC 0.726) and the validation cohort (AUC 0.730).
CONCLUSIONS CONCLUSIONS
SAF is associated with various clinical risk factors in a population sample of individuals ≥65 years. Stratifying individuals from the general population according to their risk for SAF may be possible using the MR-DASH score, facilitating targeted screening programs of individuals with a high risk of SAF.

Identifiants

pubmed: 34073411
pii: jcm10112321
doi: 10.3390/jcm10112321
pmc: PMC8199269
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Narodowe Centrum Badań i Rozwoju
ID : STRATEGMED2/269343/18/NCBR/2016

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Auteurs

Katarzyna Mitrega (K)

Department of Cardiology, Silesian Centre of Heart Diseases, 41-800 Zabrze, Poland.

Gregory Y H Lip (GYH)

Liverpool Centre for Cardiovascular Science, University of Liverpool and Liverpool Heart & Chest Hospital, Liverpool 14 3PE, UK.
Aalborg Thrombosis Research Unit, Department of Clinical Medicine, Aalborg University, DK-9100 Aalborg, Denmark.

Beata Sredniawa (B)

Department of Cardiology, Silesian Centre of Heart Diseases, 41-800 Zabrze, Poland.
Department of Cardiology, Medical University of Silesia, DMS in Zabrze, 40-055 Katowice, Poland.
Silesian Park of Medical Technology Kardio-Med Silesia in Zabrze, 41-800 Zabrze, Poland.

Adam Sokal (A)

Department of Cardiology, Silesian Centre of Heart Diseases, 41-800 Zabrze, Poland.

Witold Streb (W)

Department of Cardiology, Silesian Centre of Heart Diseases, 41-800 Zabrze, Poland.

Karol Przyludzki (K)

Department of Cardiology, Silesian Centre of Heart Diseases, 41-800 Zabrze, Poland.

Tomasz Zdrojewski (T)

Department of Preventive Medicine and Education, Medical University of Gdansk, 80-210 Gdansk, Poland.

Lukasz Wierucki (L)

Department of Preventive Medicine and Education, Medical University of Gdansk, 80-210 Gdansk, Poland.

Marcin Rutkowski (M)

Department of Preventive Medicine and Education, Medical University of Gdansk, 80-210 Gdansk, Poland.

Piotr Bandosz (P)

Department of Preventive Medicine and Education, Medical University of Gdansk, 80-210 Gdansk, Poland.

Jaroslaw Kazmierczak (J)

Department of Cardiology, Pomeranian Medical University, 70-204 Szczecin, Poland.

Tomasz Grodzicki (T)

Department of Internal Medicine and Gerontology, Jagiellonian University Medical College, 31-007 Krakow, Poland.

Grzegorz Opolski (G)

First Chair and Department of Cardiology, Medical University of Warsaw, 02-091 Warsaw, Poland.

Zbigniew Kalarus (Z)

Department of Cardiology, Silesian Centre of Heart Diseases, 41-800 Zabrze, Poland.
Department of Cardiology, Medical University of Silesia, DMS in Zabrze, 40-055 Katowice, Poland.
Silesian Park of Medical Technology Kardio-Med Silesia in Zabrze, 41-800 Zabrze, Poland.

Classifications MeSH