Affiliations: [a] Institute of Neuroscience and Physiology, Sahlgrenska Academy, Gothenburg University, Sweden | [b] Department of Psychology, Gothenburg University, Sweden
Correspondence:
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Correspondence to: Sindre Rolstad, Institute for Neuroscience and Physiology, Department of Psychiatry and Neurochemistry, The Sahlgrenska Academy at Gothenburg University, Blå stråket 15, plan 3, SE-413 45 Gothenburg, Sweden. Tel.: +46 766 186 122; Fax: +46 31 342 1533; E-mail: [email protected].
Abstract: The neurofilament light (NF-L) subunit is mainly expressed in large-caliber myelinated axons, and elevated concentrations in the cerebrospinal fluid (CSF) are correlated with damage to white matter and subcortical regions. Because the correlation between NF-L and cognition and functional impairment is largely unknown, we investigated associations in patients (n = 622) with (n = 199) and without (n = 423) vascular burden in subjective cognitive impairment (SCI, n = 168), mild cognitive impairment (MCI, n = 261), and dementia (n = 193). Patients were staged according to disease severity and the presence/absence of cerebrovascular disease. CSF amyloid-β1–42 (Aβ1–42) was included in all models due to its concomitant influence on vascular and primary etiology. Linear regression was used to assess associations between NF-L and Aβ1–42 and five cognitive domains of a comprehensive neuropsychological battery as well as with functional impairment using the Clinical Dementia Rating. Changes in these outcomes at the 2-year follow-up were also evaluated. In SCI and MCI patients with vascular burden, higher NF-L concentrations were associated with baseline cognitive performance (β = −0.38 to –0.58) and executive decline (β = −0.44). Lower Aβ1–42 levels were associated with worse cognitive performance in dementia (β = 0.46 to 0.51). In MCI and dementia patients without vascular burden, higher NF-L (β = −0.30 to −0.34) and lower Aβ1–42 concentrations (β = 0.30) were associated with reduced cognitive performance. Higher NF-L concentrations (β = −0.26) were associated with functional decline in patients with vascular burden. CSF NF-L is associated with cognition in patients with and without vascular etiology. These associations were greater in pre-dementia phases in those with vascular etiology and vice versa in those without vascular burden.
