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Changes in metabolic risk factors over 10 years and their associations with late-life cognitive performance: The Multi-Ethnic Study of Atherosclerosis
BACKGROUND: We examined whether changes in metabolic factors over 10 years were associated with cognitive performance. METHODS: Participants from the Multi-Ethnic Study of Atherosclerosis were followed since baseline (2000–2002) with five clinical examinations. At exam 5 (2010–2012), they received a...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390661/ https://www.ncbi.nlm.nih.gov/pubmed/28435852 http://dx.doi.org/10.1016/j.dadm.2017.03.003 |
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author | Hughes, Timothy M. Craft, Suzanne Baker, Laura D. Espeland, Mark A. Rapp, Stephen R. Sink, Kaycee M. Bertoni, Alain G. Burke, Gregory L. Gottesman, Rebecca F. Michos, Erin D. Luchsinger, José A. Fitzpatrick, Annette L. Hayden, Kathleen M. |
author_facet | Hughes, Timothy M. Craft, Suzanne Baker, Laura D. Espeland, Mark A. Rapp, Stephen R. Sink, Kaycee M. Bertoni, Alain G. Burke, Gregory L. Gottesman, Rebecca F. Michos, Erin D. Luchsinger, José A. Fitzpatrick, Annette L. Hayden, Kathleen M. |
author_sort | Hughes, Timothy M. |
collection | PubMed |
description | BACKGROUND: We examined whether changes in metabolic factors over 10 years were associated with cognitive performance. METHODS: Participants from the Multi-Ethnic Study of Atherosclerosis were followed since baseline (2000–2002) with five clinical examinations. At exam 5 (2010–2012), they received a short cognitive battery (Cognitive Abilities Screening Instrument [CASI], Digit Symbol Coding [DSC], and Digit Span [DS]). We examined associations between baseline metabolic factors and their changes over time before cognitive testing. RESULTS: Among 4392 participants, baseline metabolic disorders (fasting glucose, systolic and diastolic blood pressures) were significantly associated with poorer CASI, DSC, and DS scores measured 10 years later. Increases in blood pressure were associated with lower cognitive performance. Results did not differ by race/ethnicity and were stronger among those without the APOE ε4 allele. CONCLUSIONS: Cognitive performance was associated with antecedent abnormalities in glucose metabolism and blood pressure increases. Findings appeared stronger among APOE ε4-negative participants. |
format | Online Article Text |
id | pubmed-5390661 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-53906612017-04-21 Changes in metabolic risk factors over 10 years and their associations with late-life cognitive performance: The Multi-Ethnic Study of Atherosclerosis Hughes, Timothy M. Craft, Suzanne Baker, Laura D. Espeland, Mark A. Rapp, Stephen R. Sink, Kaycee M. Bertoni, Alain G. Burke, Gregory L. Gottesman, Rebecca F. Michos, Erin D. Luchsinger, José A. Fitzpatrick, Annette L. Hayden, Kathleen M. Alzheimers Dement (Amst) Diagnostic Assessment & Prognosis BACKGROUND: We examined whether changes in metabolic factors over 10 years were associated with cognitive performance. METHODS: Participants from the Multi-Ethnic Study of Atherosclerosis were followed since baseline (2000–2002) with five clinical examinations. At exam 5 (2010–2012), they received a short cognitive battery (Cognitive Abilities Screening Instrument [CASI], Digit Symbol Coding [DSC], and Digit Span [DS]). We examined associations between baseline metabolic factors and their changes over time before cognitive testing. RESULTS: Among 4392 participants, baseline metabolic disorders (fasting glucose, systolic and diastolic blood pressures) were significantly associated with poorer CASI, DSC, and DS scores measured 10 years later. Increases in blood pressure were associated with lower cognitive performance. Results did not differ by race/ethnicity and were stronger among those without the APOE ε4 allele. CONCLUSIONS: Cognitive performance was associated with antecedent abnormalities in glucose metabolism and blood pressure increases. Findings appeared stronger among APOE ε4-negative participants. Elsevier 2017-03-31 /pmc/articles/PMC5390661/ /pubmed/28435852 http://dx.doi.org/10.1016/j.dadm.2017.03.003 Text en © 2017 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Diagnostic Assessment & Prognosis Hughes, Timothy M. Craft, Suzanne Baker, Laura D. Espeland, Mark A. Rapp, Stephen R. Sink, Kaycee M. Bertoni, Alain G. Burke, Gregory L. Gottesman, Rebecca F. Michos, Erin D. Luchsinger, José A. Fitzpatrick, Annette L. Hayden, Kathleen M. Changes in metabolic risk factors over 10 years and their associations with late-life cognitive performance: The Multi-Ethnic Study of Atherosclerosis |
title | Changes in metabolic risk factors over 10 years and their associations with late-life cognitive performance: The Multi-Ethnic Study of Atherosclerosis |
title_full | Changes in metabolic risk factors over 10 years and their associations with late-life cognitive performance: The Multi-Ethnic Study of Atherosclerosis |
title_fullStr | Changes in metabolic risk factors over 10 years and their associations with late-life cognitive performance: The Multi-Ethnic Study of Atherosclerosis |
title_full_unstemmed | Changes in metabolic risk factors over 10 years and their associations with late-life cognitive performance: The Multi-Ethnic Study of Atherosclerosis |
title_short | Changes in metabolic risk factors over 10 years and their associations with late-life cognitive performance: The Multi-Ethnic Study of Atherosclerosis |
title_sort | changes in metabolic risk factors over 10 years and their associations with late-life cognitive performance: the multi-ethnic study of atherosclerosis |
topic | Diagnostic Assessment & Prognosis |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5390661/ https://www.ncbi.nlm.nih.gov/pubmed/28435852 http://dx.doi.org/10.1016/j.dadm.2017.03.003 |
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