Petra Schwingenschuh

Background and purpose Quantification of neurofilament light chain protein in serum (sNfL) enables the neuro‐axonal damage in peripheral blood to be reliably assessed and monitored. There is a long‐standing debate whether essential tremor represents a ‘benign’ tremor syndrome or whether it is linked to neurodegeneration. This study aims to investigate sNfL concentrations in essential tremor compared to healthy controls (cross‐sectionally and longitudinally) and to assess whether sNfL is associated with motor and nonmotor markers of disease progression. Methods Data of patients with essential tremor from our prospective registry on movement disorders (PROMOVE) were retrospectively analysed. Age‐, sex‐ and body‐mass‐index‐matched healthy controls were recruited from an ongoing community‐dwelling aging cohort. sNfL was quantified by an ultra‐sensitive single molecule array (Simoa). All participants underwent detailed clinical examination at baseline and after approximately 5 years of follow‐up. Results Thirty‐seven patients with clinically diagnosed essential tremor were included and 37 controls. The essential tremor group showed significantly higher sNfL levels compared to healthy controls at baseline and follow‐up. sNfL levels increased over time in both groups, and the slope of sNfL increase was similar in the essential tremor and healthy control groups. Comparing patients with a disease duration under 5 years to those with a longer disease duration, the former group had a significantly greater increase of sNfL over time, which strongly correlated to worsening of tremor and cognition. Conclusion Our findings indicate that neurodegeneration, possibly happening at an early disease stage, might play a role in the pathophysiology of essential tremor.