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Plasma neurofilament light-chain and phosphorylated tau as biomarkers of disease severity in Huntington's disease: Korean cohort data

  • Yun Su Hwang
  • , Eungseok Oh
  • , Manho Kim
  • , Chan Young Lee
  • , Hyun Sook Kim
  • , Sun Ju Chung
  • , Young Hee Sung
  • , Won Tae Yoon
  • , Jin Hwan Cho
  • , Jae Hyeok Lee
  • , Han Joon Kim
  • , Hee Jin Chang
  • , Beomseok Jeon
  • , Kyung Ah Woo
  • , Seong Beom Ko
  • , Kyum Yil Kwon
  • , Jangsup Moon
  • , Chaewon Shin
  • , Young Eun Kim
  • , Jee Young Lee*
  • *Corresponding author for this work
  • Chungnam National University
  • Seoul National University
  • Ewha Womans University
  • CHA University
  • University of Ulsan
  • Gachon University
  • Kangbuk Samsung Hospital
  • Samsung Medical Center, Sungkyunkwan university
  • Pusan National University
  • SMG-SNU Seoul Boramae Medical Center
  • Korea University
  • Soonchunhyang University
  • Hallym University

Research output: Contribution to journalJournal articlepeer-review

Abstract

Objective: To investigate neurofilament light chain (NfL), phosphorylated tau (p-Tau) and total tau (t-Tau) as plasma markers for clinical severity in Korean Huntington's disease (HD) cohort. Methods: Genetically-confirmed 67 HD patients participated from 13 referral hospitals in South Korea. The subjects were evaluated with the Unified Huntington's Disease Rating Scale (UHDRS), total motor score (TMS) and total functional capacity (TFC), Mini-Mental Status Examination (K-MMSE), Montreal Cognitive Assessment (MoCA-K), and Beck's depression inventory (K-BDI). We measured plasma NfL, p-Tau and t-Tau concentrations using single-molecule array (SIMOA) assays. Stages of HD were classified based on UHDRS-TFC score and plasma markers were analyzed for correlation with clinical severity scales. Results: Plasma NfL was elevated in both 6 premanifest and 61 full manifest HD patients compared to the reference value, which increased further from premanifest to manifest HD groups. The NfL level was not significantly correlated with UHDRS TMS or TFC scores in manifest HD patients. Plasma p-Tau was also elevated in HD patients (p = 0.038). The level was the highest in stage III-V HD (n = 30) group (post-hoc p < 0.05). The p-Tau was correlated with UHDRS TFC scores (adjusted p = 0.002). Plasma t-Tau neither differed among the groups nor associated with any clinical variables. Conclusions: This study supports plasma NfL being a biomarker for initial HD manifestation in Korean cohort, and a novel suggestion of plasma p-Tau as a potential biomarker reflecting the clinical severity in full-manifest HD.

Original languageEnglish
Article number120744
JournalJournal of the Neurological Sciences
Volume452
DOIs
StatePublished - 2023.09.15

Keywords

  • Biomarker
  • Huntingtin's disease
  • Neurofilament light chain
  • Phosphorylated tau
  • Plasma

Quacquarelli Symonds(QS) Subject Topics

  • Medicine

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