Plasma Cystatin C Correlates with Plasma NfL Levels and Predicts Disease Progression in Parkinson’s Disease

Author:

Imarisio AlbertoORCID,Pilotto Andrea,Garrafa EmirenaORCID,Conforti Francesca,Masciocchi Stefano,Turrone Rosanna,Gipponi Stefano,Cottini Elisabetta,Rizzetti Maria Cristina,Porrini VanessaORCID,Gussago CristinaORCID,Pizzi Marina,Guadagni Fiorella,Zetterberg HenrikORCID,Ashton Nicholas J.,Hye AbdulORCID,Padovani Alessandro

Abstract

<b><i>Introduction:</i></b> Previous studies reported increased plasma levels of cystatin C (Cys-C) in Parkinson’s disease (PD) and claimed for a possible association with disease severity and progression. The aim of this study was to evaluate plasma Cys-C in PD and healthy controls (HC) and test its association with markers of peripheral inflammation, neurodegeneration, and clinical progression in a longitudinal study. <b><i>Methods:</i></b> Plasma Cys-C, high-sensitive C-reactive protein, interleukin 6, and neurofilament light chain (NfL) were assessed at the baseline in 71 consecutive non-demented PD and 69 HC. PD patients underwent an extensive motor and cognitive assessment at baseline and after 2 years of follow-up. The association of Cys-C with disease severity was evaluated in a multilinear model adjusted for the effect of age, sex, disease duration, and peripheral inflammation. <b><i>Results:</i></b> Cys-C levels appeared to be higher in PD compared to controls and correlated with the plasma neuronal marker NfL (<i>r</i> = 0.204, <i>p</i> = 0.046). In longitudinal analyses, PD patients with higher Cys-C levels exhibited faster motor progression at 2 years of follow-up independently from the peripheral inflammatory profile. <b><i>Conclusions:</i></b> Cys-C was associated with higher NfL levels and a remarkably faster motor progression in PD independently from peripheral inflammation. Further studies are needed in order to understand the mechanisms underpinning the association of Cys-C with higher neuronal damage markers in neurodegenerative diseases.

Publisher

S. Karger AG

Subject

Neurology (clinical),Neurology

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