Evidence map›Paper›PMID 34981605›Full record

ArticleHuman brain mapping2022

Influence of periaqueductal gray on other salience network nodes predicts social sensitivity.

Myrthe G Rijpma, Winson F Z Yang, Gianina Toller, Giovanni Battistella, Arseny A Sokolov, Virginia E Sturm, William W Seeley, Joel H Kramer, Bruce L Miller, Katherine P Rankin

Open access · goldAbstract read
In one paragraph

Article in Human brain mapping, 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
2.1field-weighted citation impact, top 14% 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, 11 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. The effect of acupuncture at theFrontiers in integrative neuroscience · 2023
    Article
  6. Review
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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

10 authors at 3 institutions in 3 countries.

Myrthe G RijpmaDepartment of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, California, USA.ORCID 0000-0001-7276-9175
Winson F Z YangDepartment of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, California, USA.
Gianina TollerDepartment of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, California, USA.
Giovanni BattistellaDepartment of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, California, USA.
Arseny A SokolovDépartement des Neurosciences Cliniques, Neuroscape@NeuroTech Platform, Service de Neuropsychologie et de Neuroréhabilitation, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.
Virginia E SturmDepartment of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, California, USA.
William W SeeleyDepartment of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, California, USA.
Joel H KramerDepartment of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, California, USA.
Bruce L MillerDepartment of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, California, USA.
Katherine P RankinDepartment of Neurology, Memory and Aging Center, University of California San Francisco, San Francisco, California, USA.
University of California, San Francisco · USTexas Tech University · USWellcome Centre for Human Neuroimaging · GB

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Merrilees · 2002 to 2026
$67.2M
Research Education ComponentP30AG062422 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Gil Dan Rabinovici · 2019 to 2026
$36.9M
PrPSc SPECIFIC INTERACTION WITH NOVEL PrP-Fc FUSION PROTEINSP50AG023501 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI HUANG, YADONG · 2004 to 2018
$27.1M
Emotion network dysfunction and decline in early frontotemporal dementiaR01AG052496 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Virginia Emily Sturm · 2017 to 2026
$6.9M
Attention and Semantic Evaluation as Predictors of Empathy in Healthy Aging and Frontotemporal DementiaRF1AG029577 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RANKIN, KATHERINE P · 2019 to 2019
$4.0M
Measuring Altered Social Behavior in Neurodegenerative DiseaseR01AG029577 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RANKIN, KATHERINE P · 2008 to 2018
$3.6M
Neuroanatomy of social Function in FTDK23AG021606 · NIA · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI RANKIN, KATHERINE P · 2003 to 2005
$204k
NIA NIH HHS P01 AG019724NIA NIH HHS P30 AG062422NIA NIH HHS R01 AG029577NIA NIH HHS R01 AG052496NIA NIH HHS RF1 AG029577NIH HHS K23-AG021606NIH HHS P50AG023501
6 · The paper itself

Abstract

The intrinsic connectivity of the salience network (SN) plays an important role in social behavior, however the directional influence that individual nodes have on each other has not yet been fully determined. In this study, we used spectral dynamic causal modeling to characterize the effective connectivity patterns in the SN for 44 healthy older adults and for 44 patients with behavioral variant frontotemporal dementia (bvFTD) who have focal SN dysfunction. We examined the relationship of SN effective connections with individuals' socioemotional sensitivity, using the revised self-monitoring scale, an informant-facing questionnaire that assesses sensitivity to expressive behavior. Overall, average SN effective connectivity for bvFTD patients differs from healthy older adults in cortical, hypothalamic, and thalamic nodes. For the majority of healthy individuals, strong periaqueductal gray (PAG) output to right cortical (p < .01) and thalamic nodes (p < .05), but not PAG output to other central pattern generators contributed to sensitivity to socioemotional cues. This effect did not exist for the majority of bvFTD patients; PAG output toward other SN nodes was weak, and this lack of output negatively influenced socioemotional sensitivity. Instead, input to the left vAI from other SN nodes supported patients' sensitivity to others' socioemotional behavior (p < .05), though less effectively. The key role of PAG output to cortical and thalamic nodes for socioemotional sensitivity suggests that its core functions, that is, generating autonomic changes in the body, and moreover representing the internal state of the body, is necessary for optimal social responsiveness, and its breakdown is central to bvFTD patients' social behavior deficits.

Indexed as

Frontotemporal DementiaPeriaqueductal GrayAgedCerebral CortexCuesHumansMagnetic Resonance Imagingbehavioral variant frontotemporal dementiadynamic causal modelingperiaqueductal graysalience networksocioemotional sensitivity

Identifiers

PMID34981605
PMCPMC8886662
OpenAlexW4205728961

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.