Evidence map›Paper›PMID 39714123›Full record

ArticleAnnals of neurology2025

Increased White Matter Aerobic Glycolysis in Multiple Sclerosis.

Matthew R Brier, Bradley Judge, Chunwei Ying, Amber Salter, Hongyu An, Aakash Patel, Qing Wang, Yong Wang, Anne H Cross, Robert T Naismith and 2 more

Abstract read
In one paragraph

Article in Annals of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. White matter hyperintensities are associated with locus coeruleus atrophy and astrocytic βAlzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  2. Review
  3. Review
  4. Review
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

12 authors.

Matthew R BrierDepartment of Neurology, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0001-5987-8705
Bradley JudgeDepartment of Neurology, Washington University School of Medicine, St. Louis, MO.
Chunwei YingMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Amber SalterDepartment of Neurology, University of Texas Southwestern Medical Center, Dallas, TX.ORCID 0000-0002-1088-110X
Hongyu AnMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Aakash PatelDepartment of Psychiatry, Washington University School of Medicine, St. Louis, MO.
Qing WangMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Yong WangMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Anne H CrossDepartment of Neurology, Washington University School of Medicine, St. Louis, MO.ORCID 0000-0003-0829-7569
Robert T NaismithDepartment of Neurology, Washington University School of Medicine, St. Louis, MO.
Tammie Ls BenzingerMallinckrodt Institute of Radiology, Washington University School of Medicine, St. Louis, MO.
Manu S GoyalDepartment of Neurology, Washington University School of Medicine, St. Louis, MO.

Funding

WU INSTITUTE OF CLINICAL AND TRANSLATIONAL SCIENCESUL1TR002345 · NCATS · WASHINGTON UNIVERSITY · PI William G. Powderly · 2017 to 2026
$97.8M
Washington University Institute of Clinical and Translational Sciences (KL2) KL2TR002346 · NCATS · WASHINGTON UNIVERSITY · PI Dominic N Reeds · 2017 to 2026
$14.0M
PET SPHINGOSINE-1-PHOSPHATE RECEPTOR 1 (S1PR1) RADIOTRACERS FOR MULTIPLE SCLEROSISR01NS103988 · NINDS · WASHINGTON UNIVERSITY · PI Tammie Lee Smith Benzinger, Zhude Tu · 2017 to 2026
$5.3M
Quantitative Endogenous MRI Imaging of Neuroinflammation in ADR01AG074909 · NIA · WASHINGTON UNIVERSITY · PI QING WANG · 2022 to 2026
$3.7M
White Matter Metabolism in the Context of Aging, White Matter Hyperintensities and Alzheimer's DiseaseRF1AG073210 · NIA · WASHINGTON UNIVERSITY · PI GOYAL, MANU S, VLASSENKO, ANDREI G. · 2022 to 2022
$2.3M
PET and MRI Evaluation of Cerebral Inflammation and Metabolic Stress in Relapsing Multiple SclerosisK23NS128325 · NINDS · WASHINGTON UNIVERSITY · PI Matthew Ryan Brier · 2023 to 2026
$931k
Validation of Diffusion Basis Spectrum Imaging of Neuroinflammation in SchizophreniaR21MH131962 · NIMH · WASHINGTON UNIVERSITY · PI MAMAH, DANIEL, WANG, YONG · 2023 to 2024
$429k
National Center for Advancing Translational Sciences (NCATS) UL1TR002345National Multiple Sclerosis Society BI-2105-37656NCATS NIH HHS KL2 TR002346NCATS NIH HHS UL1 TR002345NIA NIH HHS R01 AG074909NIA NIH HHS RF1 AG073210NIMH NIH HHS R21 MH131962NINDS NIH HHS K23 NS128325NINDS NIH HHS KL2 TR002346NINDS NIH HHS R01 NS103988
6 · The paper itself

Abstract

objectiveDespite treatments which reduce relapses in multiple sclerosis (MS), many patients continue to experience progressive disability accumulation. MS is associated with metabolic disruptions and cerebral metabolic stress predisposes to tissue injury and possibly impaired remyelination. Additionally, myelin homeostasis is metabolically expensive and reliant on glycolysis. We investigated cerebral metabolic changes in MS and when in the disease course they occurred, and assessed their relationship with microstructural changes.

methodsThis study used combined fluorodeoxyglucose (FDG) positron emission tomography (PET) and magnetic resonance imaging (MRI) to measure cerebral metabolic rate of glucose and oxygen, thereby quantifying glycolysis. Twelve healthy controls, 20 patients with relapsing MS, and 13 patients with non-relapsing MS were studied. Relapsing patients with MS were treatment naïve and scanned pre- and post-initiation of high efficacy disease modifying therapy.

resultsIn normal appearing white matter, we observed increased glucose utilization and reduced oxygen utilization in newly diagnosed MS, consistent with increased glycolysis. Increased glycolysis was greater in patients with a longer disease duration course and higher disability. Among newly diagnosed patients, different treatments had differential impacts on glucose utilization. Last, whereas hypermetabolism within lesions was clearly associated with inflammation, no such relationship was found within normal appearing white matter.

interpretationIncreased white matter glycolysis is a prominent feature of cerebral metabolism in MS. It begins early in the disease course, increases with disease duration and is independent of microstructural evidence of inflammation in normal appearing white matter. Optimization of the metabolic environment may be an important component of therapies designed to reduce progressive disability. ANN NEUROL 2025;97:766-778.

Indexed as

GlycolysisMultiple SclerosisMultiple Sclerosis, Relapsing-RemittingWhite MatterAdultFemaleFluorodeoxyglucose F18GlucoseHumansMagnetic Resonance ImagingMaleMiddle AgedPositron-Emission TomographyFluorodeoxyglucose F18Glucose

Identifiers

PMID39714123
PMCPMC11890956

What OpenQuestion holds

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Registered trials

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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.