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000138738 0247_ $$2doi$$a10.1016/j.neuron.2016.05.018
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000138738 041__ $$aEnglish
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000138738 1001_ $$0P:(DE-2719)2810940$$aBacioglu, Mehtap$$b0$$eFirst author$$udzne
000138738 245__ $$aNeurofilament Light Chain in Blood and CSF as Marker of Disease Progression in Mouse Models and in Neurodegenerative Diseases.
000138738 260__ $$aNew York, NY$$bElsevier$$c2016
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000138738 520__ $$aA majority of current disease-modifying therapeutic approaches for age-related neurodegenerative diseases target their characteristic proteopathic lesions (α-synuclein, Tau, Aβ). To monitor such treatments, fluid biomarkers reflecting the underlying disease process are crucial. We found robust increases of neurofilament light chain (NfL) in CSF and blood in murine models of α-synucleinopathies, tauopathy, and β-amyloidosis. Blood and CSF NfL levels were strongly correlated, and NfL increases coincided with the onset and progression of the corresponding proteopathic lesions in brain. Experimental induction of α-synuclein lesions increased CSF and blood NfL levels, while blocking Aβ lesions attenuated the NfL increase. Consistently, we also found NfL increases in CSF and blood of human α-synucleinopathies, tauopathies, and Alzheimer's disease. Our results suggest that CSF and particularly blood NfL can serve as a reliable and easily accessible biomarker to monitor disease progression and treatment response in mouse models and potentially in human proteopathic neurodegenerative diseases.
000138738 536__ $$0G:(DE-HGF)POF3-342$$a342 - Disease Mechanisms and Model Systems (POF3-342)$$cPOF3-342$$fPOF III$$x0
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000138738 542__ $$2Crossref$$i2016-07-01$$uhttps://www.elsevier.com/tdm/userlicense/1.0/
000138738 542__ $$2Crossref$$i2017-07-06$$uhttps://www.elsevier.com/open-access/userlicense/1.0/
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000138738 650_7 $$2NLM Chemicals$$aBiomarkers
000138738 650_7 $$2NLM Chemicals$$aNeurofilament Proteins
000138738 650_7 $$2NLM Chemicals$$aalpha-Synuclein
000138738 650_2 $$2MeSH$$aAnimals
000138738 650_2 $$2MeSH$$aAxons: metabolism
000138738 650_2 $$2MeSH$$aBiomarkers: blood
000138738 650_2 $$2MeSH$$aBiomarkers: cerebrospinal fluid
000138738 650_2 $$2MeSH$$aBrain: metabolism
000138738 650_2 $$2MeSH$$aBrain: pathology
000138738 650_2 $$2MeSH$$aDisease Progression
000138738 650_2 $$2MeSH$$aIntermediate Filaments: metabolism
000138738 650_2 $$2MeSH$$aMice, Inbred C57BL
000138738 650_2 $$2MeSH$$aMice, Transgenic
000138738 650_2 $$2MeSH$$aNeurodegenerative Diseases: diagnosis
000138738 650_2 $$2MeSH$$aNeurodegenerative Diseases: metabolism
000138738 650_2 $$2MeSH$$aNeurodegenerative Diseases: pathology
000138738 650_2 $$2MeSH$$aNeurofilament Proteins: blood
000138738 650_2 $$2MeSH$$aNeurofilament Proteins: cerebrospinal fluid
000138738 650_2 $$2MeSH$$aalpha-Synuclein: metabolism
000138738 7001_ $$0P:(DE-2719)9000196$$aMaia, Luis F$$b1$$udzne
000138738 7001_ $$0P:(DE-2719)2811828$$aPreische, Oliver$$b2$$udzne
000138738 7001_ $$0P:(DE-2719)2811018$$aSchelle, Juliane$$b3$$udzne
000138738 7001_ $$0P:(DE-2719)2812177$$aApel, Anja$$b4$$udzne
000138738 7001_ $$0P:(DE-2719)9000387$$aKaeser, Stephan A$$b5$$udzne
000138738 7001_ $$0P:(DE-2719)9000294$$aSchweighauser, Manuel$$b6$$udzne
000138738 7001_ $$0P:(DE-2719)2811141$$aEninger, Timo$$b7$$udzne
000138738 7001_ $$0P:(DE-2719)2810762$$aLambert, Marius$$b8$$udzne
000138738 7001_ $$0P:(DE-2719)9000943$$aPilotto, Andrea$$b9$$udzne
000138738 7001_ $$0P:(DE-HGF)0$$aShimshek, Derya R$$b10
000138738 7001_ $$0P:(DE-HGF)0$$aNeumann, Ulf$$b11
000138738 7001_ $$0P:(DE-2719)2810803$$aKahle, Philipp J$$b12$$udzne
000138738 7001_ $$0P:(DE-2719)9000301$$aStaufenbiel, Matthias$$b13$$udzne
000138738 7001_ $$0P:(DE-2719)2810592$$aNeumann, Manuela$$b14$$udzne
000138738 7001_ $$0P:(DE-2719)2810915$$aMaetzler, Walter$$b15$$udzne
000138738 7001_ $$0P:(DE-HGF)0$$aKuhle, Jens$$b16$$eCorresponding author
000138738 7001_ $$0P:(DE-2719)2000010$$aJucker, Mathias$$b17$$eLast author$$udzne
000138738 77318 $$2Crossref$$3journal-article$$a10.1016/j.neuron.2016.05.018$$b : Elsevier BV, 2016-07-01$$n1$$p56-66$$tNeuron$$v91$$x0896-6273$$y2016
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