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Published on: May 8, 2016
CSF Leukocytes Transiently Increase Before Onset of Huntington Disease in Association With a Stage-Specific CSF
Yu Gao1, Birna Ásbjörnsdóttir2, Tua Vinther-Jensen2
1Department of Neurology, Ulm University Hospital, Germany.
Insights
Cerebrospinal fluid (CSF) leukocytes peak in late premanifest Huntington disease (HD), correlating with neurofilament light chain (NFL) levels. These findings reveal a dynamic inflammatory signaling network in HD progression.
Area of Science:
- Neuroscience
- Immunology
- Genetics
Background:
- Huntington disease (HD) is a neurodegenerative disorder caused by CAG-triplet expansion.
- CSF inflammatory biomarkers typically increase with HD progression.
- CSF leukocytes have not been previously explored as an inflammatory marker in HD.
Purpose of the Study:
- To investigate high-precision CSF-leukocyte counts across different stages of HD.
- To examine the association of CSF leukocytes with CSF neurofilament light chain (NFL) and cytokine/chemokine patterns.
- To understand the inflammatory signaling network in HD progression.
Main Methods:
- A cross-sectional case-control study involving 94 controls and 335 individuals with HD (presymptomatic and motor manifest stages).
- CSF leukocyte counts were analyzed and categorized based on disease burden score (DBS) and total functional capacity (TFC).
- CSF-NFL levels and 18 CSF cytokines/chemokines were analyzed in relation to HD stage.
Main Results:
- CSF leukocytes peaked in late premanifest HD (DBS ≥ 250) compared to early premanifest and manifest HD stages.
- Higher CSF leukocytes in late premanifest HD were associated with increased CSF-NFL levels.
- Specific cytokine/chemokine patterns (e.g., VEGF, IL-6, CCL22) differentiated HD stages and identified late premanifest HD with 75% sensitivity and 90% specificity.
Conclusions:
- CSF leukocyte counts peak in late premanifest HD, suggesting a critical inflammatory phase.
- The association with CSF-NFL and stage-specific chemokine/cytokine changes indicates a dynamic, neurotoxic inflammatory network in HD.
- These findings highlight the potential of CSF leukocytes and inflammatory markers for monitoring HD progression.
Background And Objectives:
CSF inflammatory biomarkers in Huntington disease (HD), a neurodegenerative CAG-triplet expansion disorder, usually increase with disease progression. CSF leukocytes as an inflammatory marker have not been explored in HD. We explored high-precision CSF-leukocyte counts across different HD stages in the multicenter prospective biosample HD study HDClarity and their association with CSF neurofilament light chain (NFL) and cytokine and chemokine patterns.
Methods:
A cross-sectional case-control study of the first average CSF leukocyte count of HDClarity study control participants (N = 94) and those carrying a repeat-expanded Huntingtin (HTT) allele (N = 335) categorized as having successive stages of presymptomatic and motor manifest HD as predefined by the HDClarity protocol (early presymptomatic [N = 48]: disease burden score [DBS] <250; late presymptomatic [N = 93]: DBS ≥ 250; early manifest HD [N = 171]: total functional capacity [TFC] 7-11; and late motor manifest HD [N = 23]: TFC < 11) was performed. CSF-NFL was available in 165. Results were juxtaposed with an independent single-center data set of 18 CSF cytokines and chemokines (57 CSFs, 19 control, 6 early and 8 late presymptomatic HD CSFs, and 19 manifest HD CSFs).
Results:
CSF leukocytes peaked in late premanifest (median, interquartile range: 1.0/µL, 0.33-1.33/µL) when compared with early premanifest (0.0/µL, 0.0-1.0/µL) but also early (0.33/µL, 0.0-1.0/µL) and late manifest HD (0.0/µL, 0.0-0.67/µL). CSF leukocytes in late premanifest HD were higher than in controls (0.0/µL, 0.0-1.0/µL). A CSF-leukocyte peak at a DBS between 256 and 344 closely corresponded to the late premanifest HD peak. Higher CSF leukocytes in late premanifest HD were associated with higher CSF-NFL levels. Exploratory analysis of CSF cytokine and chemokine levels revealed that low interleukin (IL)-7 but high vascular endothelial growth factor (VEGF) and C-C motif chemokine ligand (CCL)22 levels may distinguish HD from control CSF; high VEGF, IL-6, and IL-15 early from late premanifest HD CSF; and low CCL2, CCL17, and IL-8 late premanifest from manifest HD CSF. When consecutively applied, these patterns identified late premanifest HD participants with a 75% sensitivity (95% CI 41%-96%) and 90% specificity (78%-96%).
Discussion:
CSF leukocytes peaking in late premanifest HD, their association with increased CSF-NFL, and the corresponding stage-specific chemokine/cytokine changes indicate a temporally dynamic, probably neurotoxic inflammatory signaling network in HD.
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