Evidence for communication of peripheral iron status to cerebrospinal fluid: clinical implications for therapeutic strategy.


Journal

Fluids and barriers of the CNS
ISSN: 2045-8118
Titre abrégé: Fluids Barriers CNS
Pays: England
ID NLM: 101553157

Informations de publication

Date de publication:
16 Apr 2020
Historique:
received: 07 01 2020
accepted: 04 04 2020
entrez: 17 4 2020
pubmed: 17 4 2020
medline: 1 12 2020
Statut: epublish

Résumé

Iron is crucial for proper functioning of all organs including the brain. Deficiencies and excess of iron are common and contribute to substantial morbidity and mortality. Whereas iron's involvement in erythropoiesis drives clinical practice, the guidelines informing interventional strategies for iron repletion in neurological disorders are poorly defined. The objective of this study was to determine if peripheral iron status is communicated to the brain. We used a bi-chamber cell culture model of the blood-brain-barrier to determine transcytosis of iron delivered by transferrin as a metric of iron transport. In the apical chamber (representative of the blood) we placed transferrin complexed with iron We demonstrate that iron transport correlates positively with plasma hemoglobin concentrations but not serum ferritin levels. The clinical ramifications of these findings are several- fold. They suggest that erythropoietic demands for iron take precedence over brain requirements, and that the metric traditionally considered to be the most specific test reflecting total body iron stores and relied upon to inform treatment decisions-i.e., serum ferritin-may not be the preferred peripheral indicator when attempting to promote brain iron uptake. The future direction of this line of investigation is to identify the factor(s) in the CSF that influence iron transport at the level of the BBB.

Sections du résumé

BACKGROUND BACKGROUND
Iron is crucial for proper functioning of all organs including the brain. Deficiencies and excess of iron are common and contribute to substantial morbidity and mortality. Whereas iron's involvement in erythropoiesis drives clinical practice, the guidelines informing interventional strategies for iron repletion in neurological disorders are poorly defined. The objective of this study was to determine if peripheral iron status is communicated to the brain.
METHODS METHODS
We used a bi-chamber cell culture model of the blood-brain-barrier to determine transcytosis of iron delivered by transferrin as a metric of iron transport. In the apical chamber (representative of the blood) we placed transferrin complexed with iron
RESULTS RESULTS
We demonstrate that iron transport correlates positively with plasma hemoglobin concentrations but not serum ferritin levels.
CONCLUSIONS CONCLUSIONS
The clinical ramifications of these findings are several- fold. They suggest that erythropoietic demands for iron take precedence over brain requirements, and that the metric traditionally considered to be the most specific test reflecting total body iron stores and relied upon to inform treatment decisions-i.e., serum ferritin-may not be the preferred peripheral indicator when attempting to promote brain iron uptake. The future direction of this line of investigation is to identify the factor(s) in the CSF that influence iron transport at the level of the BBB.

Identifiants

pubmed: 32295615
doi: 10.1186/s12987-020-00190-8
pii: 10.1186/s12987-020-00190-8
pmc: PMC7161256
doi:

Substances chimiques

Hemoglobins 0
Transferrin 0
Ferritins 9007-73-2
Iron E1UOL152H7

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

28

Subventions

Organisme : NINDS NIH HHS
ID : R01 NS113912
Pays : United States
Organisme : Foundation for the National Institutes of Health
ID : 1R01NS089719
Organisme : NINDS NIH HHS
ID : 1R01NS113912
Pays : United States

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Auteurs

James R Connor (JR)

Department of Neurosurgery, Penn State Hershey Medical Center, University Dr (H110), 850, Hershey, PA, 17033, USA. jconnor@pennstatehealth.psu.edu.
Department of Neural and Behavioral Sciences, Penn State Hershey Medical Center, Hershey, PA, USA. jconnor@pennstatehealth.psu.edu.

Kari Duck (K)

Department of Neurosurgery, Penn State Hershey Medical Center, University Dr (H110), 850, Hershey, PA, 17033, USA.

Stephanie Patton (S)

Department of Neurosurgery, Penn State Hershey Medical Center, University Dr (H110), 850, Hershey, PA, 17033, USA.

Ian A Simpson (IA)

Department of Neural and Behavioral Sciences, Penn State Hershey Medical Center, Hershey, PA, USA.

Lynn Marie Trotti (LM)

Department of Neurology, Emory University, Atlanta, GA, USA.

Richard Allen (R)

Department of Neurology, Johns Hopkins University, Baltimore, MD, USA.

Christopher J Earley (CJ)

Department of Neurology, Johns Hopkins University, Baltimore, MD, USA.

David Rye (D)

Department of Neurology, Emory University, Atlanta, GA, USA.

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Classifications MeSH