CSF IL-6, GDF-15, GFAP and NfL levels in early Alzheimer disease: a pilot study

早期阿尔茨海默病患者的脑脊液 IL-6、GDF-15、GFAP 和 NfL 水平:一项初步研究

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作者:Domenico Plantone, Matteo Pardini, Carlo Manco, Delia Righi, Paolo Alessandro Alì, Dario Arnaldi, Virginia Pelagotti, Federico Massa, Miriana d'Alessandro, Elena Bargagli, Nicola De Stefano

Background

Despite their potential usefulness as biomarkers, no study has investigated the interactions between cerebrospinal fluid (CSF) changes of neurofilament light chain (NfL), glial fibrillary acidic protein (GFAP), growth differentiation factor 15 (GDF-15), transactive response DNA binding protein (TDP-43) and interleukin-6 (IL-6) and the core AD CSF biomarkers in the same cohort of AD patients. Objectives: The

Conclusion

Our findings highlight that CSF IL-6 levels correlate positively with markers of neuronal damage. CSF TDP-43 levels significantly correlated with GFAP, suggesting a potential link with reactive gliosis and astrocyte activation. In addition, while CSF GDF-15 levels negatively correlate with MMSE scores, mediation analysis revealed that this association is primarily indirect and mediated through Aβ 1-42 levels.

Methods

We assessed the levels of NfL, GFAP, GDF-15, TDP-43 and IL-6 in the CSF samples of 52 early AD patients and evaluated their partial reciprocal correlations and those with Abeta42, p-Tau, t-Tau and Mini-Mental State Examination (MMSE), always adding age, sex and educational level as covariates.

Results

MMSE score showed a positive correlation with the Aβ 1-42 concentrations (r = 0.485; p < 0.001), and a negative correlation with GDF-15 concentrations (r = -0.418; p = 0.002). IL-6 concentrations showed a positive correlation with NfL concentrations (r = 0.312; p = 0.026) and a negative correlation with TDP-43 concentrations (r = -0.322; p = 0.021). TDP-43 concentrations showed a positive correlation with GFAP (r = 0.33, p = 0.018). The mediation analysis suggests that the association between GDF-15 and MMSE is primarily mediated by Aβ 1-42. CSF GDF-15 concentrations were higher in AD patients with low Aβ 1-42 concentrations than those with high Aβ 1-42 concentrations (p < 0.001).

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