Evidence map›Paper›PMID 22845918›Full record

ArticleJournal of neurotrauma2012

Decreased spinothalamic and dorsal column medial lemniscus-mediated function is associated with neuropathic pain after spinal cord injury.

Yenisel Cruz-Almeida, Elizabeth R Felix, Alberto Martinez-Arizala, Eva G Widerström-Noga

Registry-linked trialAbstract read
In one paragraph

Article in Journal of neurotrauma, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00561782 (MR Spectroscopy), which is not on this map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.5field-weighted citation impact, top 18% 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.

NCT00561782 completednot on this map

MR Spectroscopy (MRS) as a Diagnostic and Outcome Measure in Pain and SCI

TypeobservationalSponsorUS Department of Veterans AffairsRan2007 to 2010Enrolled94ConditionsSpinal Cord Injury, Hyperalgesia, Secondary, Hyperalgesic Sensations
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 50 citations in OpenAlex.

  1. Article
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  4. Article
  5. Review
  6. Article
  7. Article
  8. Multidimensional pain phenotypes after Traumatic Brain Injury.Frontiers in pain research (Lausanne, Switzerland) · 2022
    Article
  9. Article
  10. Article
  11. Article
  12. Tissue bridges predict neuropathic pain emergence after spinal cord injury.Journal of neurology, neurosurgery, and psychiatry · 2020
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. 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

4 authors at 1 institution in 1 country.

Yenisel Cruz-AlmeidaResearch Service, Department of Veterans Affairs Medical Center, Miami, Florida, USA.
Elizabeth R Felix
Alberto Martinez-Arizala
Eva G Widerström-Noga
University of Miami · US

Funding

University of Florida Older Americans Independence Center (OAIC)P30AG028740 · NIA · UNIVERSITY OF FLORIDA · PI Peihua Qiu · 2007 to 2026
$22.8M
Comprehensive Training Program in Oral BiologyT90DE021990 · NIDCR · UNIVERSITY OF FLORIDA · PI Jose A Lemos · 2011 to 2026
$8.2M
Ethnic Differences in Responses to Painful StimuliR01AG033906 · NIA · UNIVERSITY OF FLORIDA · PI FILLINGIM, ROGER B · 2009 to 2013
$4.5M
The Effects of Aging on Experimental Models of Pain Inhibition and FacilitationR01AG039659 · NIA · UNIVERSITY OF FLORIDA · PI RILEY, JOSEPH L · 2011 to 2016
$3.0M
NIA NIH HHS L30 AG043172NIA NIH HHS P30 AG028740NIA NIH HHS R01 AG033906NIA NIH HHS R01 AG039659NIDCR NIH HHS T90 DE021990
6 · The paper itself

Abstract

Neuropathic pain (NP) after spinal cord injury (SCI) can significantly and negatively affect quality of life and is often refractory to currently available treatments. In order to find more effective therapeutic avenues, it would be helpful to identify the primary underlying pathophysiological mechanisms in each individual. The aim of the present study was to assess the relationship between the presence and severity of NP after SCI and measures of somatosensory function mediated via the dorsal column medial lemniscal (DCML) pathway and the spinothalamic tract (STT). Vibratory, mechanical, thermal, and pain thresholds measured in areas at and below the neurological level of injury (LOI) in persons with SCI and NP (SCI-NP, n=47) and in persons with SCI without NP (SCI-noNP, n=18) were normalized to data obtained from able-bodied pain-free control subjects (A-B, n=30). STT-mediated function at and below the LOI was significantly impaired in both SCI groups compared with A-B controls (p<0.001), but not significantly different between the two SCI groups (NP vs. no-NP). In contrast, the SCI-NP group had significantly greater impairment of DCML-mediated function at the LOI, as reflected by greater vibratory detection deficits (z=-3.89±0.5), compared with the SCI-noNP group (z=-1.95±0.7, p=0.034). Within the SCI-NP group, NP severity was significantly associated with increased thermal sensitivity below the LOI (r=0.50, p=0.038). Our results suggest that both impaired STT and DCML-mediated function are necessary for the development of NP after SCI. However, within the SCI-NP group, greater NP severity was associated with greater sensitivity to thermal stimuli below the LOI. This finding concurs with other studies suggesting that STT damage with some sparing is associated with NP.

Indexed as

AdultAnalysis of VarianceCold TemperatureData Interpretation, StatisticalDisability EvaluationFemaleHot TemperatureHumansMaleMediodorsal Thalamic NucleusMiddle AgedNeuralgiaPain MeasurementPhysical StimulationReference ValuesSensation

Identifiers

PMID22845918
PMCPMC3510448
OpenAlexW2027409384

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.