TNF receptors are associated with tau pathology and conversion to Alzheimer’s dementia in subjects with mild cognitive impairment

•higher CSF levels of TNF-α related inflammatory proteins in the MCI and AD patients with positive tau pathology.•TNF receptors were associated with t-tau and p-tau, other than Aβ1-42, in HC, MCI and AD subjects.•TNF receptors are potential early predictors for the MCI-to-AD conversion. Tumor necros...

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Veröffentlicht in:Neuroscience letters 2020-11, Vol.738, p.135392-135392, Article 135392
Hauptverfasser: Zhao, Aonan, Li, Yuanyuan, Deng, Yulei
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Sprache:eng
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Zusammenfassung:•higher CSF levels of TNF-α related inflammatory proteins in the MCI and AD patients with positive tau pathology.•TNF receptors were associated with t-tau and p-tau, other than Aβ1-42, in HC, MCI and AD subjects.•TNF receptors are potential early predictors for the MCI-to-AD conversion. Tumor necrosis factor-a (TNF-α) signaling pathway plays a significant role in Alzheimer’s disease (AD). This study aimed to explore the relationship between TNF-α related inflammatory proteins and pathological markers of AD, and examine their possibility as a predictor of the conversion of mild cognitive impairment (MCI) to AD. This study included both cross-sectional and longitudinal designs. The levels of TNF-α related inflammatory proteins, Aβ1-42, total-tau(t-tau), phosphorylated tau (p-tau) from cerebrospinal fluid (CSF) were analyzed in healthy controls (HC, n = 90), MCI (n = 116), and AD participants (n = 75) from the Alzheimer’s Disease Neuroimaging Initiative (ADNI). Kaplan-Meier analyses were used to evaluate the predictive value of the examined putative AD markers after follow-up visits. In the cross-sectional cohort, we observed higher CSF levels of TNF-α related inflammatory proteins in the MCI and AD patients with positive tau pathology. TNF receptors (TNFR) were more closely associated with t-tau and p-tau than Aβ1-42, in HC, MCI and AD subjects. In the longitudinal cohort with a mean follow-up of 30.2 months, MCI patients with high levels of CSF TNFR1 (p = 0.001) and low levels of TNFR2 (p 
ISSN:0304-3940
1872-7972
DOI:10.1016/j.neulet.2020.135392