Evidence map›Paper›PMID 23882201›Full record

ArticleFrontiers in human neuroscience2013

Neural markers of errors as endophenotypes in neuropsychiatric disorders.

Dara S Manoach, Yigal Agam

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Frontiers in human neuroscience, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02801513 (Maintaining Mechanisms of Chronic Depression and Their Changeability), which is not on this map. Cited by 35 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 1 pooled it
5.0field-weighted citation impact, top 4% 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.

NCT02801513 nacompletednot on this map

Maintaining Mechanisms of Chronic Depression and Their Changeability: the Role of Discrepancy-based Processing

TypeinterventionalSponsorFreie Universität BerlinRan2013 to 2015Enrolled74ConditionsMajor Depressive DisorderArmsBrief Mindfulness Training, Resting Control Training
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 1 synthesis or guideline pooled it, 82 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Neural signature of error processing in major depression.European archives of psychiatry and clinical neuroscience · 2021
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Error-related neural activity and alcohol use disorder: Differences from risk to remission.Progress in neuro-psychopharmacology & biological psychiatry · 2019
    Article
  19. Article
  20. Article
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

2 authors at 2 institutions in 1 country.

Dara S ManoachDepartment of Psychiatry, Massachusetts General Hospital and Harvard Medical School Boston, MA, USA ; Athinoula A. Martinos Center for Biomedical Imaging Charlestown, MA, USA.
Yigal Agam
Harvard University · USMassachusetts General Hospital · US

Funding

Spatiotemporal dynamics of executive function in schizoR01MH067720 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI MANOACH, DARA S · 2004 to 2011
$3.1M
Multimodal Studies of Executive Function Deficits in Autism Spectrum DisordersF32MH088081 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI AGAM, YIGAL N · 2009 to 2012
$155k
NIMH NIH HHS F32 MH088081NIMH NIH HHS R01 MH067720
6 · The paper itself

Abstract

Learning from errors is fundamental to adaptive human behavior. It requires detecting errors, evaluating what went wrong, and adjusting behavior accordingly. These dynamic adjustments are at the heart of behavioral flexibility and accumulating evidence suggests that deficient error processing contributes to maladaptively rigid and repetitive behavior in a range of neuropsychiatric disorders. Neuroimaging and electrophysiological studies reveal highly reliable neural markers of error processing. In this review, we evaluate the evidence that abnormalities in these neural markers can serve as sensitive endophenotypes of neuropsychiatric disorders. We describe the behavioral and neural hallmarks of error processing, their mediation by common genetic polymorphisms, and impairments in schizophrenia, obsessive-compulsive disorder, and autism spectrum disorders. We conclude that neural markers of errors meet several important criteria as endophenotypes including heritability, established neuroanatomical and neurochemical substrates, association with neuropsychiatric disorders, presence in syndromally-unaffected family members, and evidence of genetic mediation. Understanding the mechanisms of error processing deficits in neuropsychiatric disorders may provide novel neural and behavioral targets for treatment and sensitive surrogate markers of treatment response. Treating error processing deficits may improve functional outcome since error signals provide crucial information for flexible adaptation to changing environments. Given the dearth of effective interventions for cognitive deficits in neuropsychiatric disorders, this represents a potentially promising approach.

Indexed as

anterior cingulateerror processingerror-related negativityimaging geneticsresponse monitoring

Identifiers

PMID23882201
PMCPMC3714549
OpenAlexW2143605825

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

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.