Evidence map›Paper›PMID 23681979›Full record

ReviewCNS drugs2013

Blocking LINGO-1 as a therapy to promote CNS repair: from concept to the clinic.

Sha Mi, R Blake Pepinsky, Diego Cadavid

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in CNS drugs, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02493049 (Randomized, Controlled Pilot Trial of Domperidone in Relapsing-Remitting Multiple Sclerosis), which is not on this map. Cited by 84 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed, 1 pooled it
8.5field-weighted citation impact, top 2% 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.

NCT02493049 phase2completednot on this mapstarted 2015, after this paper: background citation

Randomized, Controlled Pilot Trial of Domperidone in Relapsing-Remitting Multiple Sclerosis

TypeinterventionalSponsorUniversity of CalgaryRan2015 to 2019Enrolled17ConditionsMultiple Sclerosis, Relapsing-RemittingArmsDomperidone
3 · Its place in the literature

Who cites it

84 citing papers in PubMed, 1 synthesis or guideline pooled it, 161 citations in OpenAlex.

  1. Pooled it
  2. Initial Impairment and Recovery of Vision-Related Functioning in Participants With Acute Optic Neuritis From the RENEW Trial of Opicinumab.Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society · 2019
    Trial
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Effect of retinoic acid on delayed encephalopathy after acute carbon monoxide poisoning: Role of the lncRNAZhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Article
  9. Review
  10. Review
  11. Article
  12. Article
  13. Review
  14. Article
  15. Developing drugs that promote remyelination: Is our in vitro screening approach too simplistic?Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2024
    Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article

24 more citing papers are in PubMed but not listed here.

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

3 authors at 1 institution in 1 country.

Sha MiDepartment of Discovery Neurobiology, Biogen Idec Inc., 14 Cambridge Center, Cambridge, MA 02142, USA. sha.mi@biogenidec.com
R Blake Pepinsky
Diego Cadavid
Biogen (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

LINGO-1 is a leucine-rich repeat and Ig domain-containing, Nogo receptor interacting protein, selectively expressed in the CNS on both oligodendrocytes and neurons. Its expression is developmentally regulated, and is upregulated in CNS diseases and injury. In animal models, LINGO-1 expression is upregulated in rat spinal cord injury, experimental autoimmune encephalomyelitis, 6-hydroxydopamine neurotoxic lesions and glaucoma models. In humans, LINGO-1 expression is increased in oligodendrocyte progenitor cells from demyelinated white matter of multiple sclerosis post-mortem samples, and in dopaminergic neurons from Parkinson's disease brains. LINGO-1 negatively regulates oligodendrocyte differentiation and myelination, neuronal survival and axonal regeneration by activating ras homolog gene family member A (RhoA) and inhibiting protein kinase B (Akt) phosphorylation signalling pathways. Across diverse animal CNS disease models, targeted LINGO-1 inhibition promotes neuron and oligodendrocyte survival, axon regeneration, oligodendrocyte differentiation, remyelination and functional recovery. The targeted inhibition of LINGO-1 function presents a novel therapeutic approach for the treatment of CNS diseases.

Indexed as

AgingAnimalsAntibodies, MonoclonalCell SurvivalCentral Nervous System DiseasesClinical Trials as TopicHumansMembrane ProteinsNerve Tissue ProteinsNeuronsOligodendrogliaSignal TransductionAntibodies, MonoclonalLINGO1 protein, humanMembrane ProteinsNerve Tissue Proteins

Identifiers

PMID23681979
OpenAlexW1975823659

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.