Plasma neurofilament light chain is not elevated in people with first-episode psychosis or those at ultra-high risk for psychosis

Matthew J Y Kang; Dhamidhu Eratne; Cassandra Wannan; Alexander F Santillo; Dennis Velakoulis; Christos Pantelis; Vanessa Cropley

doi:10.1016/j.schres.2024.04.003

Plasma neurofilament light chain is not elevated in people with first-episode psychosis or those at ultra-high risk for psychosis

Schizophr Res. 2024 Apr 5:267:269-272. doi: 10.1016/j.schres.2024.04.003. Online ahead of print.

Authors

Matthew J Y Kang¹, Dhamidhu Eratne², Cassandra Wannan³, Alexander F Santillo⁴, Dennis Velakoulis⁵, Christos Pantelis⁶, Vanessa Cropley⁷

Affiliations

¹ Neuropsychiatry Centre, Royal Melbourne Hospital, Australia; Melbourne Neuropsychiatry Centre & Department of Psychiatry, University of Melbourne, Australia. Electronic address: matthew.kang1@unimelb.edu.au.
² Neuropsychiatry Centre, Royal Melbourne Hospital, Australia; Melbourne Neuropsychiatry Centre & Department of Psychiatry, University of Melbourne, Australia. Electronic address: deratne@unimelb.edu.au.
³ Melbourne Neuropsychiatry Centre & Department of Psychiatry, University of Melbourne, Australia; Orygen, Parkville, Victoria, Australia; Centre for Youth Mental Health, The University of Melbourne, Parkville, Victoria, Australia. Electronic address: Wannanc@unimelb.edu.au.
⁴ Clinical Memory Research Unit, Lund University, Sweden. Electronic address: alexander.frizell_santillo@med.lu.se.
⁵ Neuropsychiatry Centre, Royal Melbourne Hospital, Australia; Melbourne Neuropsychiatry Centre & Department of Psychiatry, University of Melbourne, Australia. Electronic address: Dennis.Velakoulis@mh.org.au.
⁶ Melbourne Neuropsychiatry Centre & Department of Psychiatry, University of Melbourne, Australia. Electronic address: cpant@unimelb.edu.au.
⁷ Melbourne Neuropsychiatry Centre & Department of Psychiatry, University of Melbourne, Australia; Orygen, Parkville, Victoria, Australia; Centre for Youth Mental Health, The University of Melbourne, Parkville, Victoria, Australia. Electronic address: vcropley@unimelb.edu.au.

PMID: 38581830
DOI: 10.1016/j.schres.2024.04.003

Abstract

Introduction: Neurofilament light chain (NfL), a blood biomarker of neuronal injury, shows promise in distinguishing neurodegenerative disorders from psychiatric conditions. This is especially relevant in psychosis, given neurological conditions such as autoimmune encephalitis and Niemann Pick Type C disease (NPC) may initially present with psychotic symptoms. Whilst NfL levels have been studied in established schizophrenia cases, their levels in first-episode psychosis (FEP) and ultra-high risk (UHR) for psychosis individuals remain largely unexplored. This study aimed to compare plasma NfL in people with FEP or UHR with healthy controls, as well as explore its associations with clinical data.

Method: We retrospectively analysed plasma NfL in 63 participants, consisting of 29 individuals with FEP, 10 individuals with UHR, and 24 healthy controls. We used general linear models (GLM), which were bootstrapped, to compute bias-corrected and accelerated (BCa) 95 % confidence intervals (CIs).

Results: Mean NfL levels were 5.2 pg/mL in FEP, 4.9 pg/mL in UHR, and 5.9 pg/mL in healthy controls. Compared to healthy controls, there were no significant differences in NfL levels in the FEP group (β = -0.22, 95 % CI [-0.86, 0.39], p = 0.516) nor UHR group (β = -0.37, 95 % CI [-0.90, 0.19], p = 0.182). There were no significant associations between NfL levels and clinical variables in the FEP group.

Discussion: Our study is the first to demonstrate that plasma NfL levels are not significantly elevated in individuals at UHR for psychosis compared to healthy controls, a finding also observed in the FEP cohort. These findings bolster the potential diagnostic utility of NfL in differentiating between psychiatric and neurodegenerative disorders.

Keywords: Biomarker; Neurofilament light chain; Psychosis.