Evidence map›Paper›PMID 35533827›Full record

ArticleNeuroImage2022

Graph theory analysis identified two hubs that connect sensorimotor and cognitive and cortical and subcortical nociceptive networks in the non-human primate.

Ruiqi Wu, Feng Wang, Pai-Feng Yang, John C Gore, Li Min Chen

Open access · goldAbstract read
In one paragraph

Article in NeuroImage, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

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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

5 authors at 3 institutions in 2 countries.

Ruiqi WuInstitute of Imaging Science, Vanderbilt University Medical Center, Nashville, TN 37232, United States; Department of Radiology and Radiological Sciences, Institute of Imaging Science, Vanderbilt University Medical Center, 1161 21st Ave. S. AA 1105 MCN, Nashville, TN 37232-2310, United States; State Key Laboratory of Medical Neurobiology and MOE Frontiers Center for Brain Science, Institutes of Brain Science, Fudan University, Shanghai 200032, China.
Feng WangInstitute of Imaging Science, Vanderbilt University Medical Center, Nashville, TN 37232, United States; Department of Radiology and Radiological Sciences, Institute of Imaging Science, Vanderbilt University Medical Center, 1161 21st Ave. S. AA 1105 MCN, Nashville, TN 37232-2310, United States.
Pai-Feng YangInstitute of Imaging Science, Vanderbilt University Medical Center, Nashville, TN 37232, United States; Department of Radiology and Radiological Sciences, Institute of Imaging Science, Vanderbilt University Medical Center, 1161 21st Ave. S. AA 1105 MCN, Nashville, TN 37232-2310, United States.
John C GoreInstitute of Imaging Science, Vanderbilt University Medical Center, Nashville, TN 37232, United States; Department of Radiology and Radiological Sciences, Institute of Imaging Science, Vanderbilt University Medical Center, 1161 21st Ave. S. AA 1105 MCN, Nashville, TN 37232-2310, United States; Department of Biomedical Engineering, Vanderbilt University, Nashville, TN 37232, United States.
Li Min ChenInstitute of Imaging Science, Vanderbilt University Medical Center, Nashville, TN 37232, United States; Department of Radiology and Radiological Sciences, Institute of Imaging Science, Vanderbilt University Medical Center, 1161 21st Ave. S. AA 1105 MCN, Nashville, TN 37232-2310, United States; Department of Psychology, Vanderbilt University, Nashville, TN 37232, United States. Electronic address: limin.chen@vanderbilt.edu.
Vanderbilt University · USVanderbilt University Medical Center · USFudan University · CN

Funding

Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Jeffrey L Neul · 2020 to 2026
$10.3M
Biophysical Basis of Functional Connectivity by MRIR01NS078680 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Li Min Chen, John C Gore · 2012 to 2026
$7.6M
Representation of Nociception in SII and Thalamus of PrimatesR01NS069909 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI CHEN, LI MIN · 2012 to 2016
$1.7M
NICHD NIH HHS P50 HD103537NINDS NIH HHS R01 NS069909NINDS NIH HHS R01 NS078680
6 · The paper itself

Abstract

Pain perception involves multiple brain regions and networks. Understanding how these brain networks work together is fundamental for appreciating network-wise changes reported in patients with chronic pain disorders. Parcellating pain related networks and understanding their causal relationships is the first step to understand how painful information is processed, integrated, and modulated, and it requires direct manipulation of specific brain regions. Nonhuman primates (NHP) offer an ideal model system to achieve these goals because cortical and subcortical regions in the NHP brain are established based on a variety of different types of data collected in a way that is not feasible or, at least, extremely difficult in humans (i.e., histology data, tract-tracing, intracerebral recordings). In addition, different methodological techniques can also help characterize and further understand these brain cortical and subcortical regions over the course of development. Here we used a heat nociceptive stimulation that is proven to elicit activity of nociceptive neurons in the cortex to refine and parcellate the whole brain nociceptive functional networks, to identify key network hubs, and to characterize network-wise temporal dynamic signatures using high-resolution fMRI. We first functionally localized 24 cortical and subcortical regions that responded to heat nociceptive stimuli (somatosensory area 1/2, area 3a/3b, S2, posterior insula (pIns), anterior insula, area 7b, posterior parietal cortex, anterior cingulate cortex (ACC), prefrontal cortex, caudate, and mediodorsal (MD) and ventral posterior lateral (VPL) thalamic nuclei) and used them as seeds in resting state fMRI (rsfMRI) data analysis. We applied both hierarchical clustering and graph-theory analyses of the pairwise rsfMRI correlation metrics and identified five cortical and one subcortical sub-networks: strong resting state functional connectivity (rsFC) between ACC and prefrontal regions, parietal cortex and area 7b, S2 and posterior insula, areas 3a/3b and 1/2 within the S1 cortex, and thalamic MD and caudate nuclei. The rsFC strengths between cortical areas within each subnetwork were significantly stronger than those between subcortical regions. Regions within each sub-network also exhibited highly correlated temporal dynamics at rest, but the overall dynamic patterns varied drastically across sub-networks. Graph-theory analysis identified the MD nucleus as a hub that connects subcortical and cortical nociceptive sub-networks. The S2-pIns connection joins the sensory and affective/cognitive sub-networks.

Indexed as

Brain MappingNociceptionAnimalsCognitionHumansMagnetic Resonance ImagingNeural PathwaysPainPrimatesBrain networkGraph theoryNon-human primatePainResting-state functional connectivityWhole brain

Identifiers

PMID35533827
PMCPMC9306334
OpenAlexW4229028765

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.