Evidence map›Paper›PMID 36523131›Full record

ArticleJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism2023

Red blood cells as glucose carriers to the human brain: Modulation of cerebral activity by erythrocyte exchange transfusion in Glut1 deficiency (G1D).

Richard C Wang, Eunice E Lee, Nicole De Simone, Gauri Kathote, Sharon Primeaux, Adrian Avila, Dong-Min Yu, Mark Johnson, Levi B Good, Vikram Jakkamsetti and 3 more

Open access · greenAbstract read
In one paragraph

Article in Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.9field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 16 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Richard C WangDepartment of Dermatology, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Eunice E LeeDepartment of Dermatology, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Nicole De SimoneDepartment of Pathology, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Gauri KathoteRare Brain Disorders Program, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Sharon PrimeauxRare Brain Disorders Program, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Adrian AvilaRare Brain Disorders Program, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Dong-Min YuDepartment of Dermatology, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Mark JohnsonDepartment of Neurology, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Levi B GoodRare Brain Disorders Program, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Vikram JakkamsettiRare Brain Disorders Program, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Ravi SarodeDepartments of Pathology and Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Alice Ann HollandDepartment of Psychiatry, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Juan M PascualRare Brain Disorders Program, The University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID 0000-0002-0843-8221
The University of Texas Southwestern Medical Center · USCenter for Human Genetics · US

Funding

Mechanisms of Glucose Dependence in Proliferating CellsR01AR072655 · NIAMS · UT SOUTHWESTERN MEDICAL CENTER · PI WANG, RICHARD C · 2018 to 2022
$1.7M
NIAMS NIH HHS R01 AR072655
6 · The paper itself

Abstract

Red blood cells circulating through the brain are briefly but closely apposed to the capillary endothelium. We hypothesized that this contact provides a nearly direct pathway for metabolic substrate transfer to neural cells that complements the better characterized plasma to endothelium transfer. While brain function is considered independent of normal fluctuations in blood glucose concentration, this is not borne out by persons with glucose transporter I (GLUT1) deficiency (G1D). In them, encephalopathy is often ameliorated by meal or carbohydrate administration, and this enabled us to test our hypothesis: Since red blood cells contain glucose, and since the red cells of G1D individuals are also deficient in GLUT1, replacing them with normal donor cells via exchange transfusion could augment erythrocyte to neural cell glucose transport via mass action in the setting of unaltered erythrocyte count or plasma glucose abundance. This motivated us to perform red blood cell exchange in 3 G1D persons. There were rapid, favorable and unprecedented changes in cognitive, electroencephalographic and quality-of-life measures. The hypothesized transfer mechanism was further substantiated by

Indexed as

BrainCarbohydrate Metabolism, Inborn ErrorsErythrocytesGlucoseAdultGlucose Transporter Type 1HumansMonosaccharide Transport ProteinsGlucoseGlucose Transporter Type 1Monosaccharide Transport Proteinselectroencephalographyerythrocyteexchange transfusionfluxGlucose

Identifiers

PMID36523131
PMCPMC9941860
OpenAlexW4311663353

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.