Serum NfL in Alzheimer Dementia: Results of the Prospective Dementia Registry Austria.
Daniela KernMicheal KhalilLukas PirpamerArabella BuchmannEdith HoferPeter Dal-BiancoElisabeth StögmannChristoph ScherflerThomas BenkeGerhard RansmayrReinhold SchmidtPublished in: Medicina (Kaunas, Lithuania) (2022)
Background and Objectives : The neurofilament light chain (NfL) is a biomarker for neuro-axonal injury in various acute and chronic neurological disorders, including Alzheimer's disease (AD). We here investigated the cross-sectional and longitudinal associations between baseline serum NfL (sNfL) levels and cognitive, behavioural as well as MR volumetric findings in the Prospective Dementia Registry Austria (PRODEM-Austria). Materials and Methods : All participants were clinically diagnosed with AD according to NINCDS-ADRDA criteria and underwent a detailed clinical assessment, cognitive testing (including the Mini Mental State Examination (MMSE) and the Consortium to Establish a Registry for Alzheimer's Disease (CERAD)), the neuropsychiatric inventory (NPI) and laboratory evaluation. A total of 237 patients were included in the study. Follow-up examinations were done at 6 months, 1 year and 2 years with 93.3% of patients undergoing at least one follow-up. We quantified sNfL by a single molecule array (Simoa). In a subgroup of 125 subjects, brain imaging data (1.5 or 3T MRI, with 1 mm isotropic resolution) were available. Brain volumetry was assessed using the FreeSurfer image analysis suite (v6.0). Results : Higher sNfL concentrations were associated with worse performance in cognitive tests at baseline, including CERAD (B = -10.084, SE = 2.999, p < 0.001) and MMSE (B = -3.014, SE = 1.293, p = 0.021). The sNfL levels also correlated with the presence of neuropsychiatric symptoms (NPI total score: r = 0.138, p = 0.041) and with smaller volumes of the temporal lobe (B = -0.012, SE = 0.003, p = 0.001), the hippocampus (B = -0.001, SE = 0.000201, p = 0.013), the entorhinal (B = -0.000308, SE = 0.000124, p = 0.014), and the parahippocampal cortex (B = -0.000316, SE = 0.000113, p = 0.006). The sNfL values predicted more pronounced cognitive decline over the mean follow-up period of 22 months, but there were no significant associations with respect to change in neuropsychiatric symptoms and brain volumetric measures. Conclusions : the sNfL levels relate to cognitive, behavioural, and imaging hallmarks of AD and predicts short term cognitive decline.
Keyphrases
- cognitive decline
- mild cognitive impairment
- single molecule
- high resolution
- cross sectional
- patients undergoing
- white matter
- cerebral ischemia
- resting state
- atomic force microscopy
- cognitive impairment
- contrast enhanced
- newly diagnosed
- magnetic resonance imaging
- end stage renal disease
- ejection fraction
- liver failure
- computed tomography
- big data
- intensive care unit
- brain injury
- living cells
- blood brain barrier
- clinical trial
- cerebrospinal fluid
- optical coherence tomography
- optic nerve