Evidence map›Paper›PMID 34080889›Full record

ReviewThe American journal of psychiatry2021

Evolution, Emotion, and Episodic Engagement.

Daniel S Pine, Steven P Wise, Elisabeth A Murray

Open access · greenAbstract readReview
In one paragraph

Review in The American journal of psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.5field-weighted citation impact, top 5% 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

27 citing papers in PubMed, 46 citations in OpenAlex.

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  20. Social feedback biases emerge during recall but not prediction and shift across the development of social anxiety.Proceedings of the National Academy of Sciences of the United States of America · 2023
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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

3 authors.

Daniel S PineSection on Development and Affective Neuroscience, Emotion and Development Branch (Pine), and Section on the Neurobiology of Learning and Memory, Laboratory of Neuropsychology (Murray), NIMH, Bethesda, Md.; Olschefskie Institute for the Neurobiology of Knowledge, Bethesda, Md. (Wise).
Steven P WiseSection on Development and Affective Neuroscience, Emotion and Development Branch (Pine), and Section on the Neurobiology of Learning and Memory, Laboratory of Neuropsychology (Murray), NIMH, Bethesda, Md.; Olschefskie Institute for the Neurobiology of Knowledge, Bethesda, Md. (Wise).
Elisabeth A MurraySection on Development and Affective Neuroscience, Emotion and Development Branch (Pine), and Section on the Neurobiology of Learning and Memory, Laboratory of Neuropsychology (Murray), NIMH, Bethesda, Md.; Olschefskie Institute for the Neurobiology of Knowledge, Bethesda, Md. (Wise).

Funding

fMRI Studies Of Pediatric Mood And Anxiety DisordersZIAMH002781 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI PINE, DANIEL · 2009 to 2025
$41.5M
Mapping the Human Connectome: Structure, Function, and HeritabilityU54MH091657 · NIMH · WASHINGTON UNIVERSITY · PI UGURBIL, KAMIL, VAN ESSEN, DAVID C · 2010 to 2014
$34.7M
Fmri Studies Of Risk For Mood And Anxiety Disorders In ChildrenZIAMH002782 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI PINE, DANIEL · 2009 to 2025
$28.3M
Neural Substrates of Reward Processing and EmotionZIAMH002887 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI MURRAY, ELISABETH A · 2009 to 2025
$26.0M
Fmri Studies Of Pediatric Mood And Anxiety DisordersZ01MH002781 · NIMH · NATIONAL INSTITUTE OF MENTAL HEALTH · PI PINE, DANIEL · 2002 to 2008
$1.5M
Intramural NIH HHS Z01 MH002781NIMH NIH HHS U54 MH091657
6 · The paper itself

Abstract

Although rodent research provides important insights into neural correlates of human psychology, new cortical areas, connections, and cognitive abilities emerged during primate evolution, including human evolution. Comparison of human brains with those of nonhuman primates reveals two aspects of human brain evolution particularly relevant to emotional disorders: expansion of homotypical association areas and expansion of the hippocampus. Two uniquely human cognitive capacities link these phylogenetic developments with emotion: a subjective sense of participating in and reexperiencing remembered events and a limitless capacity to imagine details of future events. These abilities provided evolving humans with selective advantages, but they also created proclivities for emotional problems. The first capacity evokes the "reliving" of past events in the "here-and-now," accompanied by emotional responses that occurred during memory encoding. It contributes to risk for stress-related syndromes, such as posttraumatic stress disorder. The second capacity, an ability to imagine future events without temporal limitations, facilitates flexible, goal-related behavior by drawing on and creating a uniquely rich array of mental representations. It promotes goal achievement and reduces errors, but the mental construction of future events also contributes to developmental aspects of anxiety and mood disorders. With maturation of homotypical association areas, the concrete concerns of childhood expand to encompass the abstract apprehensions of adolescence and adulthood. These cognitive capacities and their dysfunction are amenable to a research agenda that melds experimental therapeutic interventions, cognitive neuropsychology, and developmental psychology in both humans and nonhuman primates.

Indexed as

Biological EvolutionCognitionEmotionsAnimalsBrainHumansMental DisordersPhylogenyPrimatesAmygdalaAnxietyBrain EvolutionEpisodic MemoryHippocampusPrefrontal Cortex

Identifiers

PMID34080889
PMCPMC8378585
OpenAlexW3164334017

What OpenQuestion holds

Textmetadata
LicenceTDM
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.