Evidence map›Paper›PMID 36768415›Full record

ReviewInternational journal of molecular sciences2023

Alterations in Lymphocytic Metabolism-An Emerging Hallmark of MS Pathophysiology?

Viktoria B Greeck, Sarah K Williams, Jürgen Haas, Brigitte Wildemann, Richard Fairless

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
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

5 authors.

Viktoria B GreeckDepartment of Neurology, University Clinic Heidelberg, 69120 Heidelberg, Germany.
Sarah K WilliamsDepartment of Neurology, University Clinic Heidelberg, 69120 Heidelberg, Germany.
Jürgen HaasDepartment of Neurology, University Clinic Heidelberg, 69120 Heidelberg, Germany.
Brigitte WildemannDepartment of Neurology, University Clinic Heidelberg, 69120 Heidelberg, Germany.
Richard FairlessDepartment of Neurology, University Clinic Heidelberg, 69120 Heidelberg, Germany.ORCID 0000-0002-6817-9671

Funding

Deutsche Forschungsgemeinschaft FOR2289
6 · The paper itself

Abstract

Multiple sclerosis (MS) is a chronic autoimmune disease of the central nervous system (CNS) characterised by acute inflammation and subsequent neuro-axonal degeneration resulting in progressive neurological impairment. Aberrant immune system activation in the periphery and subsequent lymphocyte migration to the CNS contribute to the pathophysiology. Recent research has identified metabolic dysfunction as an additional feature of MS. It is already well known that energy deficiency in neurons caused by impaired mitochondrial oxidative phosphorylation results in ionic imbalances that trigger degenerative pathways contributing to white and grey matter atrophy. However, metabolic dysfunction in MS appears to be more widespread than the CNS. This review focuses on recent research assessing the metabolism and mitochondrial function in peripheral immune cells of MS patients and lymphocytes isolated from murine models of MS. Emerging evidence suggests that pharmacological modulation of lymphocytic metabolism may regulate their subtype differentiation and rebalance pro- and anti-inflammatory functions. As such, further understanding of MS immunometabolism may aid the identification of novel treatments to specifically target proinflammatory immune responses.

Indexed as

Multiple SclerosisAnimalsAnti-Inflammatory AgentsChronic DiseaseHumansLymphocytesMiceMitochondriaNeuronsAnti-Inflammatory Agentsautoimmunityglycolysislymphocytesmetabolismmitochondriamultiple sclerosisoxidative stressperipheral blood mononuclear cells

Identifiers

PMID36768415
PMCPMC9917089

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.