Evidence map›Paper›PMID 34369386›Full record

ArticleJCI insight2021

The influence of ApoE4 on the clinical outcomes and pathophysiology of degenerative cervical myelopathy.

Alexa Desimone, James Hong, Sydney T Brockie, Wenru Yu, Alex M Laliberte, Michael G Fehlings

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2021. 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
4.0field-weighted citation impact, top 5% 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, 24 citations in OpenAlex.

  1. Article
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  3. Letter to the editor concerning "CALM1 polymorphism in degenerative cervical myelopathy of the Indian cohort" by S. Maheshwari, et al. (Eur spine J [2025]; doi: 10.1007/s00586-025-09090-7).European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2025
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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

6 authors at 4 institutions in 2 countries.

Alexa DesimoneDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
James HongDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
Sydney T BrockieDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
Wenru YuDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
Alex M LaliberteDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
Michael G FehlingsDivision of Genetics and Development, Krembil Research Institute, University Health Network, Toronto, Ontario, Canada.
University Health Network · CAInstitute of Medical Sciences · INKrembil Research InstituteUniversity of Toronto · CA

Funding

CIHR
6 · The paper itself

Abstract

Degenerative cervical myelopathy (DCM) is the most common cause of nontraumatic spinal cord injury in adults worldwide. Surgical decompression is generally effective in improving neurological outcomes and halting progression of myelopathic deterioration. However, a subset of patients experience suboptimal neurological outcomes. Given the emerging evidence that apolipoprotein E4 (ApoE4) allelic status influences neurodegenerative conditions, we examined whether the presence of the ApoE4 allele may account for the clinical heterogeneity of treatment outcomes in patients with DCM. Our results demonstrate that human ApoE4+ DCM patients have a significantly lower extent of improvement after decompression surgery. Functional analysis of our DCM mouse model in targeted-replacement mice expressing human ApoE4 revealed delayed gait recovery, forelimb grip strength, and hind limb mechanical sensitivity after decompression surgery, compared with their ApoE3 counterparts. This was accompanied by an exacerbated proinflammatory response resulting in higher concentrations of TNF-α, IL-6, CCL3, and CXCL9. At the site of injury, there was a significant decrease in gray matter area, an increase in the activation of microglia/macrophages, and increased astrogliosis after decompression surgery in the ApoE4 mice. Our study is the first to our knowledge to investigate the pathophysiological underpinnings of ApoE4 in DCM, which suggests a possible personalized medicine approach for the treatment of DCM in ApoE4 carriers.

Indexed as

Cervical CordNeurodegenerative DiseasesPostoperative ComplicationsAllelesAnimalsApolipoprotein E4Decompression, SurgicalDisease Models, AnimalDisease ProgressionFemaleGenetic VariationHumansMaleMiceMiddle AgedModels, NeurologicalApolipoprotein E4AgingMouse modelsNeuroscienceSurgery

Identifiers

PMID34369386
PMCPMC8410082
OpenAlexW3188757778

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.