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...

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Veröffentlicht in:Frontiers in aging neuroscience 2022-08, Vol.14, p.977515-977515
Hauptverfasser: Huang, Ling-Chun, Chen, Ming-Hui, Chuu, Chih-Pin, Li, Kuan-Ying, Hour, Tzyh-Chyuan, Yang, Yuan-Han
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Sprache:eng
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Zusammenfassung: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.
ISSN:1663-4365
1663-4365
DOI:10.3389/fnagi.2022.977515