Chitotriosidase (CHIT1) is increased in microglia and macrophages in spinal cord of amyotrophic lateral sclerosis and cerebrospinal fluid levels correlate with disease severity and progression. Issue 3 (15th November 2017)
- Record Type:
- Journal Article
- Title:
- Chitotriosidase (CHIT1) is increased in microglia and macrophages in spinal cord of amyotrophic lateral sclerosis and cerebrospinal fluid levels correlate with disease severity and progression. Issue 3 (15th November 2017)
- Main Title:
- Chitotriosidase (CHIT1) is increased in microglia and macrophages in spinal cord of amyotrophic lateral sclerosis and cerebrospinal fluid levels correlate with disease severity and progression
- Authors:
- Steinacker, Petra
Verde, Federico
Fang, Lubin
Feneberg, Emily
Oeckl, Patrick
Roeber, Sigrun
Anderl-Straub, Sarah
Danek, Adrian
Diehl-Schmid, Janine
Fassbender, Klaus
Fliessbach, Klaus
Foerstl, Hans
Giese, Armin
Jahn, Holger
Kassubek, Jan
Kornhuber, Johannes
Landwehrmeyer, G Bernhard
Lauer, Martin
Pinkhardt, Elmar Hans
Prudlo, Johannes
Rosenbohm, Angela
Schneider, Anja
Schroeter, Matthias L
Tumani, Hayrettin
von Arnim, Christine A F
Weishaupt, Jochen
Weydt, Patrick
Ludolph, Albert C
Yilmazer Hanke, Deniz
Otto, Markus - Other Names:
- author non-byline.
Ackl Nibal author non-byline.
Arlt Sönke author non-byline.
Albrecht Franziska author non-byline.
Bisenius Sandrine author non-byline.
Gehlhaar Svenja author non-byline.
Gleiss Jakob author non-byline.
Halder Theresa author non-byline.
Lehmbeck Jan author non-byline.
Lampe Leonie author non-byline.
Levin Johannes author non-byline.
Maler Manuel author non-byline.
Oberhauser Felix author non-byline.
Oberstein Timo author non-byline.
Prix Catharina author non-byline.
Raiser Theresa author non-byline.
Richter-Schmiedinger Tanja author non-byline.
Saur Dorothee author non-byline.
Schachner Lisa author non-byline.
Schönecker Sonja author non-byline.
Schuemberg Katharina author non-byline.
Stenglein-Krapf Gisela author non-byline.
Wlasich Elisabeth author non-byline. - Abstract:
- Abstract : Objectives: Neurochemical markers of amyotrophic lateral sclerosis (ALS) that reflect underlying disease mechanisms might help in diagnosis, staging and prediction of outcome. We aimed at determining the origin and differential diagnostic and prognostic potential of the putative marker of microglial activation chitotriosidase (CHIT1). Methods: Altogether 316 patients were included, comprising patients with sporadic ALS, ALS mimics (disease controls (DCo)), frontotemporal lobar degeneration (FTLD), Creutzfeldt-Jakob disease (CJD), Alzheimer's disease (AD), Parkinson's disease (PD) and healthy controls (Con). CHIT1 and neurofilament levels were determined in cerebrospinal fluid (CSF) and blood and analysed with regard to diagnostic sensitivity and specificity and prognostic performance. Additionally, postmortem tissue was analysed for CHIT1 expression. Results: In ALS, CHIT1 CSF levels were higher compared with Con (p<0.0001), DCo (p<0.05) and neurodegenerative diseases (AD p<0.05, PD p<0.01, FTLD p<0.0001) except CJD. CHIT1 concentrations were correlated with ALS disease progression and severity but not with the survival time, as did neurofilaments. Serum CHIT1 levels were not different in ALS compared with any other study group. In the spinal cord of patients with ALS, but not Con, AD or CJD cases, CHIT1 was expressed in the corticospinal tract and CHIT1 staining colocalised with markers of microglia (IBA1) and macrophages (CD68). Conclusions: CHIT1 concentrationsAbstract : Objectives: Neurochemical markers of amyotrophic lateral sclerosis (ALS) that reflect underlying disease mechanisms might help in diagnosis, staging and prediction of outcome. We aimed at determining the origin and differential diagnostic and prognostic potential of the putative marker of microglial activation chitotriosidase (CHIT1). Methods: Altogether 316 patients were included, comprising patients with sporadic ALS, ALS mimics (disease controls (DCo)), frontotemporal lobar degeneration (FTLD), Creutzfeldt-Jakob disease (CJD), Alzheimer's disease (AD), Parkinson's disease (PD) and healthy controls (Con). CHIT1 and neurofilament levels were determined in cerebrospinal fluid (CSF) and blood and analysed with regard to diagnostic sensitivity and specificity and prognostic performance. Additionally, postmortem tissue was analysed for CHIT1 expression. Results: In ALS, CHIT1 CSF levels were higher compared with Con (p<0.0001), DCo (p<0.05) and neurodegenerative diseases (AD p<0.05, PD p<0.01, FTLD p<0.0001) except CJD. CHIT1 concentrations were correlated with ALS disease progression and severity but not with the survival time, as did neurofilaments. Serum CHIT1 levels were not different in ALS compared with any other study group. In the spinal cord of patients with ALS, but not Con, AD or CJD cases, CHIT1 was expressed in the corticospinal tract and CHIT1 staining colocalised with markers of microglia (IBA1) and macrophages (CD68). Conclusions: CHIT1 concentrations in the CSF of patients with ALS may reflect the extent of microglia/macrophage activation in the white matter of the spinal cord. CHIT1 could be a potentially useful marker for differential diagnosis and prediction of disease progression in ALS and, therefore, seems suitable as a supplemental marker for patient stratification in therapeutic trials. … (more)
- Is Part Of:
- Journal of neurology, neurosurgery and psychiatry. Volume 89:Issue 3(2018)
- Journal:
- Journal of neurology, neurosurgery and psychiatry
- Issue:
- Volume 89:Issue 3(2018)
- Issue Display:
- Volume 89, Issue 3 (2018)
- Year:
- 2018
- Volume:
- 89
- Issue:
- 3
- Issue Sort Value:
- 2018-0089-0003-0000
- Page Start:
- 239
- Page End:
- 247
- Publication Date:
- 2017-11-15
- Subjects:
- Neurology -- Periodicals
Nervous system -- Surgery -- Periodicals
Psychiatry -- Periodicals
616.8 - Journal URLs:
- http://jnnp.bmjjournals.com/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?action=archive&journal=192 ↗
http://www.bmj.com/archive ↗ - DOI:
- 10.1136/jnnp-2017-317138 ↗
- Languages:
- English
- ISSNs:
- 0022-3050
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 18218.xml