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A latent class analysis of cognitive decline in US adults, BRFSS 2015-2020

BACKGROUND: Cognitive decline can be an early indicator for dementia. Using quantitative methods and national representative survey data, we can monitor the potential burden of disease at the population-level. METHODS: BRFSS is an annual, nationally representative questionnaire in the United States....

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Autores principales: Snead, Ryan, Dumenci, Levent, Jones, Resa M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380313/
https://www.ncbi.nlm.nih.gov/pubmed/35974367
http://dx.doi.org/10.1186/s12889-022-14001-2
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author Snead, Ryan
Dumenci, Levent
Jones, Resa M.
author_facet Snead, Ryan
Dumenci, Levent
Jones, Resa M.
author_sort Snead, Ryan
collection PubMed
description BACKGROUND: Cognitive decline can be an early indicator for dementia. Using quantitative methods and national representative survey data, we can monitor the potential burden of disease at the population-level. METHODS: BRFSS is an annual, nationally representative questionnaire in the United States. The optional cognitive decline module is a six-item self-reported scale pertaining to challenges in daily life due to memory loss and growing confusion over the past twelve months. Respondents are 45+, pooled from 2015-2020. Latent class analysis was used to determine unobserved subgroups of subjective cognitive decline (SCD) based on item response patterns. Multinomial logistic regression predicted latent class membership from socio-demographic covariates. RESULTS: A total of 54,771 reported experiencing SCD. The optimal number of latent classes was three, labeled as Mild, Moderate, and Severe SCD. Thirty-five percent of the sample belonged to the Severe group. Members of this subgroup were significantly less likely to be older (65+ vs. 45-54 OR = 0.29, 95% CI: 0.23-0.35) and more likely to be non-Hispanic Black (OR = 1.80, 95% CI: 1.53-2.11), have not graduated high school (OR = 1.60, 95% CI: 1.34-1.91), or earned <$15K a year (OR = 3.03, 95% CI: 2.43-3.77). CONCLUSIONS: This study determined three latent subgroups indicating severity of SCD and identified socio-demographic predictors. Using a single categorical indicator of SCD severity instead of six separate items improves the versatility of population-level surveillance.
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spelling pubmed-93803132022-08-17 A latent class analysis of cognitive decline in US adults, BRFSS 2015-2020 Snead, Ryan Dumenci, Levent Jones, Resa M. BMC Public Health Research BACKGROUND: Cognitive decline can be an early indicator for dementia. Using quantitative methods and national representative survey data, we can monitor the potential burden of disease at the population-level. METHODS: BRFSS is an annual, nationally representative questionnaire in the United States. The optional cognitive decline module is a six-item self-reported scale pertaining to challenges in daily life due to memory loss and growing confusion over the past twelve months. Respondents are 45+, pooled from 2015-2020. Latent class analysis was used to determine unobserved subgroups of subjective cognitive decline (SCD) based on item response patterns. Multinomial logistic regression predicted latent class membership from socio-demographic covariates. RESULTS: A total of 54,771 reported experiencing SCD. The optimal number of latent classes was three, labeled as Mild, Moderate, and Severe SCD. Thirty-five percent of the sample belonged to the Severe group. Members of this subgroup were significantly less likely to be older (65+ vs. 45-54 OR = 0.29, 95% CI: 0.23-0.35) and more likely to be non-Hispanic Black (OR = 1.80, 95% CI: 1.53-2.11), have not graduated high school (OR = 1.60, 95% CI: 1.34-1.91), or earned <$15K a year (OR = 3.03, 95% CI: 2.43-3.77). CONCLUSIONS: This study determined three latent subgroups indicating severity of SCD and identified socio-demographic predictors. Using a single categorical indicator of SCD severity instead of six separate items improves the versatility of population-level surveillance. BioMed Central 2022-08-16 /pmc/articles/PMC9380313/ /pubmed/35974367 http://dx.doi.org/10.1186/s12889-022-14001-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Snead, Ryan
Dumenci, Levent
Jones, Resa M.
A latent class analysis of cognitive decline in US adults, BRFSS 2015-2020
title A latent class analysis of cognitive decline in US adults, BRFSS 2015-2020
title_full A latent class analysis of cognitive decline in US adults, BRFSS 2015-2020
title_fullStr A latent class analysis of cognitive decline in US adults, BRFSS 2015-2020
title_full_unstemmed A latent class analysis of cognitive decline in US adults, BRFSS 2015-2020
title_short A latent class analysis of cognitive decline in US adults, BRFSS 2015-2020
title_sort latent class analysis of cognitive decline in us adults, brfss 2015-2020
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9380313/
https://www.ncbi.nlm.nih.gov/pubmed/35974367
http://dx.doi.org/10.1186/s12889-022-14001-2
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