Altered Cerebrospinal Fluid (CSF) in Children with Ataxia Telangiectasia.


Journal

Cerebellum (London, England)
ISSN: 1473-4230
Titre abrégé: Cerebellum
Pays: United States
ID NLM: 101089443

Informations de publication

Date de publication:
Feb 2021
Historique:
pubmed: 21 8 2020
medline: 26 10 2021
entrez: 21 8 2020
Statut: ppublish

Résumé

Ataxia telangiectasia (A-T) is a devastating multi-system disorder characterized by progressive cerebellar ataxia and immunodeficiency. The neurological decline may be caused by multiple factors of which ongoing inflammation and oxidative stress may play a dominant role. The objective of the present investigation was to determine cerebrospinal fluid (CSF) proteins and possible low-grade inflammation and its relation to age and neurological deterioration. In the present study, we investigated 15 patients with A-T from 2 to 16 years. Our investigation included blood and CSF tests, clinical neurological examination, A-T score, and MRI findings. The albumin ratio (AR) was analyzed to determine the blood-brain-barrier function. In addition, inflammatory cytokines (IL-1α, IL-6, IL-8, IL-12 p40, IL-17A, IFN-γ, TNF-α) were measured by the multiplex cytometric bead array. We compared the results with those from an age-matched control group. Three of the A-T patients were analyzed separately (one after resection of a cerebral meningioma, one after radiation and chemotherapy due to leukemia, one after stem cell transplantation). Patient had significantly more moderate and severe side effects due to CSF puncture (vomiting, headache, need for anti-emetic drugs) compared with healthy controls. Total protein, albumin, and the AR increased with age indicating a disturbed blood barrier function in older children. There were no differences for cytokines in serum and CSF with the exception of IL-2, which was significantly higher in controls in serum. The AR is significantly altered in A-T patients, but low-grade inflammation is not detectable in serum and CSF.

Identifiants

pubmed: 32815118
doi: 10.1007/s12311-020-01175-x
pii: 10.1007/s12311-020-01175-x
pmc: PMC7862200
doi:

Substances chimiques

Biomarkers 0
Cytokines 0
IL17A protein, human 0
IL2 protein, human 0
Interleukin-17 0
Interleukin-2 0
Serum Albumin 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

31-40

Subventions

Organisme : A-T Children's Project
ID : 2015

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Auteurs

S Woelke (S)

Department for Children and Adolescents, Division of Allergology, Pulmonology and Cystic Fibrosis, Goethe University, Theodor-Stern-Kai 7, 60590, Frankfurt/Main, Germany.

R Schrewe (R)

Department for Children and Adolescents, Division of Allergology, Pulmonology and Cystic Fibrosis, Goethe University, Theodor-Stern-Kai 7, 60590, Frankfurt/Main, Germany.

H Donath (H)

Department for Children and Adolescents, Division of Allergology, Pulmonology and Cystic Fibrosis, Goethe University, Theodor-Stern-Kai 7, 60590, Frankfurt/Main, Germany.

M Theis (M)

Department for Children and Adolescents, Division of Pediatric Neurology, Goethe University Hospital, Frankfurt, Germany.

M Kieslich (M)

Department for Children and Adolescents, Division of Pediatric Neurology, Goethe University Hospital, Frankfurt, Germany.

R Duecker (R)

Department for Children and Adolescents, Division of Allergology, Pulmonology and Cystic Fibrosis, Goethe University, Theodor-Stern-Kai 7, 60590, Frankfurt/Main, Germany.

G Auburger (G)

Experimental Neurology Medical Faculty, Goethe University, Frankfurt, Germany.

R Schubert (R)

Experimental Neurology Medical Faculty, Goethe University, Frankfurt, Germany.

S Zielen (S)

Department for Children and Adolescents, Division of Allergology, Pulmonology and Cystic Fibrosis, Goethe University, Theodor-Stern-Kai 7, 60590, Frankfurt/Main, Germany. Stefan.Zielen@kgu.de.

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Classifications MeSH