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Longitudinal Effects of Herpesviruses on Multiple Cognitive Outcomes in Healthy Elderly Adults

BACKGROUND: Herpesviruses have been proposed to be involved in Alzheimer’s disease development as potentially modifiable pathology triggers. OBJECTIVE: To investigate associations of serum antibodies for herpes simplex virus (HSV)-1 and cytomegalovirus (CMV) and anti-herpesvirus treatment with cogni...

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Autores principales: Weidung, Bodil, Josefsson, Maria, Lyttkens, Peter, Olsson, Jan, Elgh, Fredrik, Lind, Lars, Kilander, Lena, Lövheim, Hugo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357165/
https://www.ncbi.nlm.nih.gov/pubmed/37334589
http://dx.doi.org/10.3233/JAD-221116
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author Weidung, Bodil
Josefsson, Maria
Lyttkens, Peter
Olsson, Jan
Elgh, Fredrik
Lind, Lars
Kilander, Lena
Lövheim, Hugo
author_facet Weidung, Bodil
Josefsson, Maria
Lyttkens, Peter
Olsson, Jan
Elgh, Fredrik
Lind, Lars
Kilander, Lena
Lövheim, Hugo
author_sort Weidung, Bodil
collection PubMed
description BACKGROUND: Herpesviruses have been proposed to be involved in Alzheimer’s disease development as potentially modifiable pathology triggers. OBJECTIVE: To investigate associations of serum antibodies for herpes simplex virus (HSV)-1 and cytomegalovirus (CMV) and anti-herpesvirus treatment with cognitive outcomes in relation to interactions with APOE ɛ4. METHODS: The study included 849 participants in the population-based Prospective Investigation of the Vasculature in Uppsala Seniors study. Cognitive performance at the ages of 75 and 80 years was assessed using the Mini-Mental State Examination (MMSE), trail-making test (TMT) A and B, and 7-minute screening test (7MS). RESULTS: Anti– HSV-1 IgG positivity was associated cross-sectionally with worse performance on the MMSE, TMT-A, TMT-B, 7MS, enhanced free recall, and verbal fluency tests (p = 0.016, p = 0.016, p < 0.001, p = 0.001, p = 0.033, and p < 0.001, respectively), but not orientation or clock drawing. Cognitive scores did not decline over time and longitudinal changes did not differ according to HSV-1 positivity. Anti– CMV IgG positivity was not associated cross-sectionally with cognition, but TMT-B scores declined more in anti– CMV IgG carriers. Anti– HSV-1 IgG interacted with APOE ɛ4 in association with worse TMT-A and better enhanced cued recall. Anti– HSV IgM interacted with APOE ɛ4 and anti-herpesvirus treatment in association with worse TMT-A and clock drawing, respectively. CONCLUSION: These findings indicate that HSV-1 is linked to poorer cognition in cognitively healthy elderly adults, including impairments in executive function, memory, and expressive language. Cognitive performance did not decline over time, nor was longitudinal decline associated with HSV-1.
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spelling pubmed-103571652023-07-21 Longitudinal Effects of Herpesviruses on Multiple Cognitive Outcomes in Healthy Elderly Adults Weidung, Bodil Josefsson, Maria Lyttkens, Peter Olsson, Jan Elgh, Fredrik Lind, Lars Kilander, Lena Lövheim, Hugo J Alzheimers Dis Research Article BACKGROUND: Herpesviruses have been proposed to be involved in Alzheimer’s disease development as potentially modifiable pathology triggers. OBJECTIVE: To investigate associations of serum antibodies for herpes simplex virus (HSV)-1 and cytomegalovirus (CMV) and anti-herpesvirus treatment with cognitive outcomes in relation to interactions with APOE ɛ4. METHODS: The study included 849 participants in the population-based Prospective Investigation of the Vasculature in Uppsala Seniors study. Cognitive performance at the ages of 75 and 80 years was assessed using the Mini-Mental State Examination (MMSE), trail-making test (TMT) A and B, and 7-minute screening test (7MS). RESULTS: Anti– HSV-1 IgG positivity was associated cross-sectionally with worse performance on the MMSE, TMT-A, TMT-B, 7MS, enhanced free recall, and verbal fluency tests (p = 0.016, p = 0.016, p < 0.001, p = 0.001, p = 0.033, and p < 0.001, respectively), but not orientation or clock drawing. Cognitive scores did not decline over time and longitudinal changes did not differ according to HSV-1 positivity. Anti– CMV IgG positivity was not associated cross-sectionally with cognition, but TMT-B scores declined more in anti– CMV IgG carriers. Anti– HSV-1 IgG interacted with APOE ɛ4 in association with worse TMT-A and better enhanced cued recall. Anti– HSV IgM interacted with APOE ɛ4 and anti-herpesvirus treatment in association with worse TMT-A and clock drawing, respectively. CONCLUSION: These findings indicate that HSV-1 is linked to poorer cognition in cognitively healthy elderly adults, including impairments in executive function, memory, and expressive language. Cognitive performance did not decline over time, nor was longitudinal decline associated with HSV-1. IOS Press 2023-07-18 /pmc/articles/PMC10357165/ /pubmed/37334589 http://dx.doi.org/10.3233/JAD-221116 Text en © 2023 – The authors. Published by IOS Press https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY 4.0) License (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Weidung, Bodil
Josefsson, Maria
Lyttkens, Peter
Olsson, Jan
Elgh, Fredrik
Lind, Lars
Kilander, Lena
Lövheim, Hugo
Longitudinal Effects of Herpesviruses on Multiple Cognitive Outcomes in Healthy Elderly Adults
title Longitudinal Effects of Herpesviruses on Multiple Cognitive Outcomes in Healthy Elderly Adults
title_full Longitudinal Effects of Herpesviruses on Multiple Cognitive Outcomes in Healthy Elderly Adults
title_fullStr Longitudinal Effects of Herpesviruses on Multiple Cognitive Outcomes in Healthy Elderly Adults
title_full_unstemmed Longitudinal Effects of Herpesviruses on Multiple Cognitive Outcomes in Healthy Elderly Adults
title_short Longitudinal Effects of Herpesviruses on Multiple Cognitive Outcomes in Healthy Elderly Adults
title_sort longitudinal effects of herpesviruses on multiple cognitive outcomes in healthy elderly adults
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10357165/
https://www.ncbi.nlm.nih.gov/pubmed/37334589
http://dx.doi.org/10.3233/JAD-221116
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