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Plasma and CSF Autoimmune Markers in Orthostatic Tremor Insights from a Prospective Tertiary Centre Cohort

P. Becker, M. Silsby, A. Martin, L. Williams, S. Nagaratnam, J. Qiu, D. Wilson, S. Xi, M. Georgiades, N. Jeyakumar, M. Lin, D. Brown, V. Fung (Sydney, Australia)

Meeting: 2026 International Congress

Keywords: Orthostatic tremor (also see Tremors)

Category: Tremor

Objective: To investigate markers of autoimmunity in plasma and cerebrospinal fluid (CSF) in a prospective cohort of patients with OT evaluated at a tertiary movement disorders centre.

Background: Orthostatic tremor (OT) is a rare and likely underdiagnosed movement disorder characterised by a high-frequency tremor of the lower limbs that emerges during standing or weight-bearing and improves when sitting or walking (1). The pathophysiology remains uncertain, with current hypotheses suggesting dysfunction of a central oscillator or disruption of the cerebello-brainstem-thalamo-cortical network involved in postural control. Immune mechanisms have been proposed as a potential contributor in some cases, supported by reports of OT associated with paraproteinaemia and inflammatory CSF findings, making the evaluation of autoimmune markers clinically relevant.

Method: We analysed a prospective cohort of 21 patients with OT. Diagnosis was based on clinical symptoms and examination findings and confirmed in all patients by electrophysiological studies demonstrating high-frequency OT. Paired plasma and CSF samples were collected and analysed for markers of autoimmunity.

Results: Twenty-one patients were included. Mean age was 65.6 ± 8.7 years (range 51–80), with a female predominance (17/21, 81%). Serum immunoelectrophoresis identified monoclonal paraproteins in three patients (3/21, 14%), higher than the approximately 4–5% prevalence reported in age-matched populations (3). CSF abnormalities were observed in a subset of patients, including pleocytosis in three (14%), elevated protein in four (19%; up to 0.79 g/L), and oligoclonal band abnormalities in two (9.5%).

Conclusion: This prospective cohort represents one of the largest OT series in which serum and CSF autoimmune markers were systematically evaluated. Although most tests were negative, isolated abnormalities were detected. As a descriptive case series, these findings are hypothesis-generating but suggest that immune mechanisms may contribute to OT in a subset of patients and justify further investigation in larger cohorts.

References: Af Edholm, K., Uribarri, G., Sundgren, M., Svenningsson, A., Fransén, E., 2026. Orthostatic Tremor Is Evoked by Muscle Load Without the Need for Orthostatic Position. Movement Disord Clin Pract 13, 208–215. https://doi.org/10.1002/mdc3.70270

Phipps, C.J., Whitney, D., Shou, J., Torres-Russotto, D., Warren, D.E., 2024. Measurement of Functional Brain Network Connectivity in People with Orthostatic Tremor. Brain Sciences 14, 219. https://doi.org/10.3390/brainsci14030219

Rajkumar, S.V., Kumar, S., 2025. Monoclonal Gammopathy of Undetermined Significance. N Engl J Med 393, 1315–1326. https://doi.org/10.1056/NEJMra2412716

To cite this abstract in AMA style:

P. Becker, M. Silsby, A. Martin, L. Williams, S. Nagaratnam, J. Qiu, D. Wilson, S. Xi, M. Georgiades, N. Jeyakumar, M. Lin, D. Brown, V. Fung. Plasma and CSF Autoimmune Markers in Orthostatic Tremor Insights from a Prospective Tertiary Centre Cohort [abstract]. Mov Disord. 2026; 41 (suppl 1). https://www.mdsabstracts.org/abstract/plasma-and-csf-autoimmune-markers-in-orthostatic-tremor-insights-from-a-prospective-tertiary-centre-cohort/. Accessed October 1, 2026.
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