Evidence map›Paper›PMID 28928638›Full record

ArticleFrontiers in neuroanatomy2017

Affective Circuitry Alterations in Patients with Trigeminal Neuralgia.

Dave J Hayes, David Q Chen, Jidan Zhong, Ariel Lin, Brendan Behan, Matthew Walker, Mojgan Hodaie

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neuroanatomy, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 3 pooled it
3.5field-weighted citation impact, top 7% 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

31 citing papers in PubMed, 3 syntheses or guidelines pooled it, 48 citations in OpenAlex.

  1. Neuromodulation of the central nervous system for facial pain.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
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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

7 authors at 3 institutions in 2 countries.

Dave J HayesPsychology Department and Neuroscience Program, Union CollegeSchenectady, NY, United States.
David Q ChenDivision of Brain, Imaging and Behaviour Systems Neuroscience and Division of Neurosurgery, Department of Surgery, Toronto Western Hospital, Krembil Research Institute, University Health Network, University of TorontoToronto, ON, Canada.
Jidan ZhongDivision of Brain, Imaging and Behaviour Systems Neuroscience and Division of Neurosurgery, Department of Surgery, Toronto Western Hospital, Krembil Research Institute, University Health Network, University of TorontoToronto, ON, Canada.
Ariel LinPsychology Department and Neuroscience Program, Union CollegeSchenectady, NY, United States.
Brendan BehanDivision of Brain, Imaging and Behaviour Systems Neuroscience and Division of Neurosurgery, Department of Surgery, Toronto Western Hospital, Krembil Research Institute, University Health Network, University of TorontoToronto, ON, Canada.
Matthew WalkerDivision of Brain, Imaging and Behaviour Systems Neuroscience and Division of Neurosurgery, Department of Surgery, Toronto Western Hospital, Krembil Research Institute, University Health Network, University of TorontoToronto, ON, Canada.
Mojgan HodaieDivision of Brain, Imaging and Behaviour Systems Neuroscience and Division of Neurosurgery, Department of Surgery, Toronto Western Hospital, Krembil Research Institute, University Health Network, University of TorontoToronto, ON, Canada.
University of Toronto · CAKrembil Research InstituteUnion College · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Trigeminal neuralgia (TN) is a severe chronic neuropathic facial pain disorder. Affect-related behavioral and structural brain changes have been noted across chronic pain disorders, but have not been well-studied in TN. We examined the potential impact of TN (37 patients: 23 with right-sided TN, 14 with left-sided TN), compared to age- and sex-matched healthy controls, on three major white matter tracts responsible for carrying affect-related signals-i.e., cingulum, fornix, and medial forebrain bundle. Diffusion magnetic resonance imaging (dMRI), deterministic multi-tensor tractography for tract modeling, and a model-driven region-of-interest approach was used. We also used volumetric gray matter analysis on key targets of these pathways (i.e., hippocampus, cingulate cortex subregions, nucleus accumbens, and ventral diencephalon). Hypotheses included: (1) successful modeling of tracts; (2) altered white matter microstructure of the cingulum and medial forebrain bundle (via changes in dMRI metrics such as fractional anisotropy, and mean, axial, and radial diffusivities) compared to controls; (3) no alterations in the control region of the fornix; (4) corresponding decreases in gray matter volumes. Results showed (1) all 325 tracts were successfully modeled, although 11 were partially complete; (2) The cingulum and medial forebrain bundle (MFB) were altered in those with TN, with dMRI metric changes in the middle (

Indexed as

chronic neuropathic paindiffusion magnetic resonancedMRIDTIemotiongray matterMRIstructural neuroimaging

Identifiers

PMID28928638
PMCPMC5591854
OpenAlexW2753443932

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.