Cerebrospinal fluid lipocalin 2 as a novel biomarker for the differential diagnosis of vascular dementia

Franc Llorens(Bellvitge University Hospital), Péter Hermann(Universitätsmedizin Göttingen), Anna Villar‐Piqué(Universitätsmedizin Göttingen), Daniela Díaz‐Lucena(Biomedical Research Networking Center on Neurodegenerative Diseases), Katarina Nägga(Linköping University), Oskar Hansson(Lund University), Isabel Santana(Hospitais da Universidade de Coimbra), Matthias Schmitz(German Center for Neurodegenerative Diseases), Christian Schmidt(Universitätsmedizin Göttingen), Daniela Varges(Universitätsmedizin Göttingen), Stefan Goebel(Universitätsmedizin Göttingen), Julien Dumurgier(Inserm), Henrik Zetterberg(Sahlgrenska University Hospital), Kaj Blennow(Sahlgrenska University Hospital), Claire Paquet(Inserm), Inês Baldeiras(Hospitais da Universidade de Coimbra), Isidró Ferrer(Biomedical Research Networking Center on Neurodegenerative Diseases), Inga Zerr(German Center for Neurodegenerative Diseases)
Nature Communications
January 30, 2020
Cited by 118Open Access
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Abstract

The clinical diagnosis of vascular dementia (VaD) is based on imaging criteria, and specific biochemical markers are not available. Here, we investigated the potential of cerebrospinal fluid (CSF) lipocalin 2 (LCN2), a secreted glycoprotein that has been suggested as mediating neuronal damage in vascular brain injuries. The study included four independent cohorts with a total n = 472 samples. LCN2 was significantly elevated in VaD compared to controls, Alzheimer's disease (AD), other neurodegenerative dementias, and cognitively unimpaired patients with cerebrovascular disease. LCN2 discriminated VaD from AD without coexisting VaD with high accuracy. The main findings were consistent over all cohorts. Neuropathology disclosed a high percentage of macrophages linked to subacute infarcts, reactive astrocytes, and damaged blood vessels in multi-infarct dementia when compared to AD. We conclude that CSF LCN2 is a promising candidate biochemical marker in the differential diagnosis of VaD and neurodegenerative dementias.


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