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Plasma biomarkers and their correlation in adult children of parents with Alzheimer’s disease
Family history (FH) of late-onset Alzheimer’s disease (AD) is associated with changes in several cerebrospinal fluid (CSF) biomarkers in cognitively normal individuals. However, potential changes in plasma biomarkers remain unknown. This study aimed to evaluate potential plasma biomarkers and their...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468332/ https://www.ncbi.nlm.nih.gov/pubmed/36110426 http://dx.doi.org/10.3389/fnagi.2022.977515 |
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author | Huang, Ling-Chun Chen, Ming-Hui Chuu, Chih-Pin Li, Kuan-Ying Hour, Tzyh-Chyuan Yang, Yuan-Han |
author_facet | Huang, Ling-Chun Chen, Ming-Hui Chuu, Chih-Pin Li, Kuan-Ying Hour, Tzyh-Chyuan Yang, Yuan-Han |
author_sort | Huang, Ling-Chun |
collection | PubMed |
description | Family history (FH) of late-onset Alzheimer’s disease (AD) is associated with changes in several cerebrospinal fluid (CSF) biomarkers in cognitively normal individuals. However, potential changes in plasma biomarkers remain unknown. This study aimed to evaluate potential plasma biomarkers and their correlation in cognitively normal adult children (AC) and to compare this data with their AD parents and unrelated non-demented controls (NC). Participants with dementia due to AD, their AC and NC were recruited. Plasma samples were assessed for amyloid beta (Aβ)(1–42), Aβ(1–40), total tau (T-tau) and phosphorylated tau (P-tau). Kruskal–Wallis test was used for the comparison of this data between the three groups. Spearman rank correlation was used for evaluation of the correlations between Aβ(1–40) and Aβ(1–42), and T-tau and P-tau in the AD and AC groups. A total of 99 subjects completed the assessment (30 had AD; 38 were AC group; and 31 were NC). Compared with the NC group, there were significantly higher levels of Aβ(1–40), P-tau, and P-tau/T-tau ratio, and lower levels of Aβ(1–42) and Aβ(1–42)/Aβ(1–40) ratio in the AD and AC groups. The correlation between the level of Aβ(1–42) and Aβ(1–40) and level of T-tau and P-tau was only observed in the AC but not in the AD group. AC of AD parents demonstrate some indicators of AD like their parents. Disruption to the correlation between Aβ and tau in AD may be a biomarker for the development of AD in AC, which should be examined in a longitudinal cohort. |
format | Online Article Text |
id | pubmed-9468332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-94683322022-09-14 Plasma biomarkers and their correlation in adult children of parents with Alzheimer’s disease Huang, Ling-Chun Chen, Ming-Hui Chuu, Chih-Pin Li, Kuan-Ying Hour, Tzyh-Chyuan Yang, Yuan-Han Front Aging Neurosci Neuroscience Family history (FH) of late-onset Alzheimer’s disease (AD) is associated with changes in several cerebrospinal fluid (CSF) biomarkers in cognitively normal individuals. However, potential changes in plasma biomarkers remain unknown. This study aimed to evaluate potential plasma biomarkers and their correlation in cognitively normal adult children (AC) and to compare this data with their AD parents and unrelated non-demented controls (NC). Participants with dementia due to AD, their AC and NC were recruited. Plasma samples were assessed for amyloid beta (Aβ)(1–42), Aβ(1–40), total tau (T-tau) and phosphorylated tau (P-tau). Kruskal–Wallis test was used for the comparison of this data between the three groups. Spearman rank correlation was used for evaluation of the correlations between Aβ(1–40) and Aβ(1–42), and T-tau and P-tau in the AD and AC groups. A total of 99 subjects completed the assessment (30 had AD; 38 were AC group; and 31 were NC). Compared with the NC group, there were significantly higher levels of Aβ(1–40), P-tau, and P-tau/T-tau ratio, and lower levels of Aβ(1–42) and Aβ(1–42)/Aβ(1–40) ratio in the AD and AC groups. The correlation between the level of Aβ(1–42) and Aβ(1–40) and level of T-tau and P-tau was only observed in the AC but not in the AD group. AC of AD parents demonstrate some indicators of AD like their parents. Disruption to the correlation between Aβ and tau in AD may be a biomarker for the development of AD in AC, which should be examined in a longitudinal cohort. Frontiers Media S.A. 2022-08-30 /pmc/articles/PMC9468332/ /pubmed/36110426 http://dx.doi.org/10.3389/fnagi.2022.977515 Text en Copyright © 2022 Huang, Chen, Chuu, Li, Hour and Yang. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Huang, Ling-Chun Chen, Ming-Hui Chuu, Chih-Pin Li, Kuan-Ying Hour, Tzyh-Chyuan Yang, Yuan-Han Plasma biomarkers and their correlation in adult children of parents with Alzheimer’s disease |
title | Plasma biomarkers and their correlation in adult children of parents with Alzheimer’s disease |
title_full | Plasma biomarkers and their correlation in adult children of parents with Alzheimer’s disease |
title_fullStr | Plasma biomarkers and their correlation in adult children of parents with Alzheimer’s disease |
title_full_unstemmed | Plasma biomarkers and their correlation in adult children of parents with Alzheimer’s disease |
title_short | Plasma biomarkers and their correlation in adult children of parents with Alzheimer’s disease |
title_sort | plasma biomarkers and their correlation in adult children of parents with alzheimer’s disease |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9468332/ https://www.ncbi.nlm.nih.gov/pubmed/36110426 http://dx.doi.org/10.3389/fnagi.2022.977515 |
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