Evidence map›Paper›PMID 23576128›Full record

Trial reportBrain : a journal of neurology2013

The salience network causally influences default mode network activity during moral reasoning.

Winston Chiong, Stephen M Wilson, Mark D'Esposito, Andrew S Kayser, Scott N Grossman, Pardis Poorzand, William W Seeley, Bruce L Miller, Katherine P Rankin

Open access · bronzeAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Brain : a journal of neurology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 128 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
128citing papers in PubMed, 5 pooled it
11.0field-weighted citation impact, top 1% 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

128 citing papers in PubMed, 5 syntheses or guidelines pooled it, 232 citations in OpenAlex.

  1. Pooled it
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  4. Functional Segregation of the Human Dorsomedial Prefrontal Cortex.Cerebral cortex (New York, N.Y. : 1991) · 2016
    Pooled it
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  6. Facial Emotion Recognition Ability May Improve in Alzheimer Disease: A Pilot Study.Cognitive and behavioral neurology : official journal of the Society for Behavioral and Cognitive Neurology · 2026
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68 more citing papers are in PubMed but not listed here.

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

9 authors at 3 institutions in 1 country.

Winston ChiongMemory and Ageing Centre, Department of Neurology, University of California, San Francisco, CA 94158, USA. winston.chiong@ucsf.edu
Stephen M Wilson
Mark D'Esposito
Andrew S Kayser
Scott N Grossman
Pardis Poorzand
William W Seeley
Bruce L Miller
Katherine P Rankin
University Memory and Aging Center · USUniversity of California, San Francisco · USUniversity of California, Berkeley · US

Funding

TDP-43 Loss-of-Function: Biology to BiomarkersP01AG019724 · NIA · UNIVERSITY OF PENNSYLVANIA · PI Jennifer Merrilees · 2002 to 2026
$67.2M
Transgenic Mouse Models of Tau PathologiesP01AG017586 · NIA · UNIVERSITY OF PENNSYLVANIA · PI LEE, VIRGINIA M · 2000 to 2021
$37.3M
MEMORYP01NS040813 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI D'ESPOSITO, MARK · 2002 to 2012
$12.9M
Working Memory and Prefrontal CortexR01MH063901 · NIMH · UNIVERSITY OF CALIFORNIA BERKELEY · PI D'ESPOSITO, MARK · 2001 to 2022
$7.6M
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
NIA NIH HHS P01 AG017586NIA NIH HHS P01 AG019724NIA NIH HHS P01-AG019724NIA NIH HHS R01 AG029577NIA NIH HHS R01-AG029577-01NIA NIH HHS RF1 AG029577NIMH NIH HHS MH 63901NIMH NIH HHS R01 MH063901NINDS NIH HHS NS40813NINDS NIH HHS P01 NS040813
6 · The paper itself

Abstract

Large-scale brain networks are integral to the coordination of human behaviour, and their anatomy provides insights into the clinical presentation and progression of neurodegenerative illnesses such as Alzheimer's disease, which targets the default mode network, and behavioural variant frontotemporal dementia, which targets a more anterior salience network. Although the default mode network is recruited when healthy subjects deliberate about 'personal' moral dilemmas, patients with Alzheimer's disease give normal responses to these dilemmas whereas patients with behavioural variant frontotemporal dementia give abnormal responses to these dilemmas. We hypothesized that this apparent discrepancy between activation- and patient-based studies of moral reasoning might reflect a modulatory role for the salience network in regulating default mode network activation. Using functional magnetic resonance imaging to characterize network activity of patients with behavioural variant frontotemporal dementia and healthy control subjects, we present four converging lines of evidence supporting a causal influence from the salience network to the default mode network during moral reasoning. First, as previously reported, the default mode network is recruited when healthy subjects deliberate about 'personal' moral dilemmas, but patients with behavioural variant frontotemporal dementia producing atrophy in the salience network give abnormally utilitarian responses to these dilemmas. Second, patients with behavioural variant frontotemporal dementia have reduced recruitment of the default mode network compared with healthy control subjects when deliberating about these dilemmas. Third, a Granger causality analysis of functional neuroimaging data from healthy control subjects demonstrates directed functional connectivity from nodes of the salience network to nodes of the default mode network during moral reasoning. Fourth, this Granger causal influence is diminished in patients with behavioural variant frontotemporal dementia. These findings are consistent with a broader model in which the salience network modulates the activity of other large-scale networks, and suggest a revision to a previously proposed 'dual-process' account of moral reasoning. These findings also characterize network interactions underlying abnormal moral reasoning in frontotemporal dementia, which may serve as a model for the aberrant judgement and interpersonal behaviour observed in this disease and in other disorders of social function. More broadly, these findings link recent work on the dynamic interrelationships between large-scale brain networks to observable impairments in dementia syndromes, which may shed light on how diseases that target one network also alter the function of interrelated networks.

Indexed as

MoralsAgedBrainCohort StudiesFemaleFrontotemporal DementiaHumansMaleMiddle AgedNerve NetPhotic StimulationThinkingdefault mode networkfrontotemporal dementiafunctional neuroimagingmoral reasoningsalience network

Identifiers

PMID23576128
PMCPMC3673466
OpenAlexW2030761935

What OpenQuestion holds

Textmetadata
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.