Evidence map›Paper›PMID 26965745›Full record

ArticleSchizophrenia research2016

Hyperactivity of caudate, parahippocampal, and prefrontal regions during working memory in never-medicated persons at clinical high-risk for psychosis.

Heidi W Thermenos, Richard J Juelich, Samantha R DiChiara, Raquelle I Mesholam-Gately, Kristen A Woodberry, Joanne Wojcik, Nikos Makris, Matcheri S Keshavan, Susan Whitfield-Gabrieli, Tsung-Ung W Woo and 5 more

Open access · greenAbstract read
In one paragraph

Article in Schizophrenia research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Associations of psychotic-like experiences, related symptoms, and working memory with functioning.European psychiatry : the journal of the Association of European Psychiatrists · 2020
    Article
  7. Article
  8. Article
  9. Using Cognitive Neuroscience to Improve Mental Health Treatment: A Comprehensive Review.Journal of the Society for Social Work and Research · 2018
    Article
  10. 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

15 authors at 8 institutions in 1 country.

Heidi W ThermenosHarvard Medical School, Boston, MA, USA; Massachusetts Mental Health Center Division of Public Psychiatry, Beth Israel Deaconess Medical Center, Boston, MA, USA; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA. Electronic address: hthermen@bidmc.harvard.edu.
Richard J JuelichHarvard Medical School, Boston, MA, USA; Department of Psychiatry, McLean Hospital, Belmont, MA, USA.
Samantha R DiChiaraHarvard Medical School, Boston, MA, USA; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.
Raquelle I Mesholam-GatelyHarvard Medical School, Boston, MA, USA; Massachusetts Mental Health Center Division of Public Psychiatry, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Kristen A WoodberryHarvard Medical School, Boston, MA, USA; Massachusetts Mental Health Center Division of Public Psychiatry, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Joanne WojcikHarvard Medical School, Boston, MA, USA; Massachusetts Mental Health Center Division of Public Psychiatry, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Nikos MakrisDepartment of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.
Matcheri S KeshavanHarvard Medical School, Boston, MA, USA; Massachusetts Mental Health Center Division of Public Psychiatry, Beth Israel Deaconess Medical Center, Boston, MA, USA.
Susan Whitfield-GabrieliMcGovern Institute for Brain Research, Poitras Center for Affective Disorders Research, Massachusetts Institute of Technology, Cambridge, MA, USA.
Tsung-Ung W WooHarvard Medical School, Boston, MA, USA; Massachusetts Mental Health Center Division of Public Psychiatry, Beth Israel Deaconess Medical Center, Boston, MA, USA; Laboratory of Cellular Neuropathology, McLean Hospital, Belmont, MA, USA.
Tracey L PetryshenHarvard Medical School, Boston, MA, USA; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.
Jill M GoldsteinHarvard Medical School, Boston, MA, USA; Department of Medicine, Division of Women's Health, Connor's Center for Women's Health & Gender Biology, Department of Psychiatry, Brigham and Women's Hospital, Boston, MA, USA.
Martha E ShentonHarvard Medical School, Boston, MA, USA; Psychiatry Neuroimaging Laboratory, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA; VA Boston Healthcare System, Brockton, MA, USA.
Robert W McCarleyHarvard Medical School, Boston, MA, USA; Psychiatry Neuroimaging Laboratory, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA; VA Boston Healthcare System, Brockton, MA, USA.
Larry J SeidmanHarvard Medical School, Boston, MA, USA; Massachusetts Mental Health Center Division of Public Psychiatry, Beth Israel Deaconess Medical Center, Boston, MA, USA; Department of Psychiatry, Massachusetts General Hospital, Boston, MA, USA.
Beth Israel Deaconess Medical Center · USMassachusetts General Hospital · USHarvard University · USMassachusetts Mental Health Center · USBrigham and Women's Hospital · USMassachusetts Institute of Technology · USMcLean Hospital · USVA Boston Healthcare System · US

Funding

HARVARD CLINICAL AND TRANSLATIONAL SCIENCE CENTER (UL1)UL1RR025758 · NCRR · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2008 to 2011
$91.4M
ZINC STATUS AND T CELL DISORDER IN MILD HUMAN ZINC DEFICIENCYM01RR001032 · NCRR · BETH ISRAEL DEACONESS MEDICAL CENTER · PI MANTZOROS, CHRISTOS S · 1985 to 2008
$32.3M
ULTRAHIGH FIELD TECHNOLOGY FOR FUNCTIONAL IMAGINGP41RR014075 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI HAMALAINEN, MATTI · 1999 to 2011
$16.4M
Vulnerability to Progression SchizophreniaP50MH080272 · NIMH · BETH ISRAEL DEACONESS MEDICAL CENTER · PI WOO, TSUNGUNG · 2007 to 2011
$9.9M
Project 4P41EB015896 · NIBIB · MASSACHUSETTS GENERAL HOSPITAL · PI ROSEN, BRUCE R · 2012 to 2018
$9.8M
Administrative Supplement Harmonization of At Risk Multisite Observational Networks for Youth(HARMONY)U01MH081928 · NIMH · BETH ISRAEL DEACONESS MEDICAL CENTER · PI STONE, WILLIAM SETH · 2008 to 2018
$7.1M
A Storage Area Network for Structural and Functional Image AnalysisS10RR023401 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI FISCHL, BRUCE · 2009 to 2009
$2.0M
SILICON GRAPHICS PRISM EXTREME 128P/1TBS10RR023043 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI SORENSEN, ALMA GREGORY · 2006 to 2006
$1.5M
Innovative Intervention for Reducing Stress Reactivity and Risk for PsychosisK23MH102358 · NIMH · MAINEHEALTH · PI WOODBERRY, KRISTEN ANNE · 2014 to 2017
$722k
A Siemens MAGNETOTOM Trio 3 Tesla MRI SystemS10RR021110 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI ROSEN, BRUCE R · 2006 to 2006
$500k
Computeserver Structural &Functional Image AnalysisS10RR019307 · NCRR · MASSACHUSETTS GENERAL HOSPITAL · PI FISCHL, BRUCE · 2004 to 2004
$496k
NCRR NIH HHS 1S10RR019307NCRR NIH HHS 1S10RR023043NCRR NIH HHS 1S10RR023401NCRR NIH HHS M01 RR001032NCRR NIH HHS M01RR01032NCRR NIH HHS P41 RR014075NCRR NIH HHS P41RR14075NCRR NIH HHS S10 RR019307NCRR NIH HHS S10 RR021110NCRR NIH HHS S10RR021110NCRR NIH HHS S10 RR023043NCRR NIH HHS S10 RR023401NCRR NIH HHS UL1 RR025758NCRR NIH HHS UL1RR025758NIBIB NIH HHS P41 EB015896NIBIB NIH HHS P41EB015896NIMH NIH HHS K23 MH102358NIMH NIH HHS P50 MH080272NIMH NIH HHS P50MH080272NIMH NIH HHS U01 MH081928NIMH NIH HHS UO1 MH081928
6 · The paper itself

Abstract

backgroundDeficits in working memory (WM) are a core feature of schizophrenia (SZ) and other psychotic disorders. We examined brain activity during WM in persons at clinical high risk (CHR) for psychosis.

methodsThirty-seven CHR and 34 healthy control participants underwent functional MRI (fMRI) on a 3.0T scanner while performing an N-back WM task. The sample included a sub-sample of CHR participants who had no lifetime history of treatment with psychotropic medications (n=11). Data were analyzed using SPM8 (2-back>0-back contrast). Pearson correlations between brain activity, symptoms, and WM performance were examined.

resultsThe total CHR group and medication-naive CHR sub-sample were comparable to controls in most demographic features and in N-back WM performance, but had significantly lower IQ. Relative to controls, medication-naïve CHR showed hyperactivity in the left parahippocampus (PHP) and the left caudate during performance of the N-back WM task. Relative to medication-exposed CHR, medication naïve CHR exhibited hyperactivity in the left caudate and the right dorsolateral prefrontal cortex (DLPFC). DLPFC activity was significantly negatively correlated with WM performance. PHP, caudate and DLPFC activity correlated strongly with symptoms, but results did not withstand FDR-correction for multiple comparisons. When all CHR participants were combined (regardless of medication status), only trend-level PHP hyperactivity was observed in CHR relative to controls.

conclusionsMedication-naïve CHR exhibit hyperactivity in regions that subserve WM. These regions are implicated in studies of schizophrenia and risk for psychosis. Results emphasize the importance of medication status in the interpretation of task - induced brain activity.

Indexed as

AdolescentAdultBrain MappingCase-Control StudiesCaudate NucleusCognition DisordersFemaleHumansImage Processing, Computer-AssistedMagnetic Resonance ImagingMaleMemory, Short-TermNeuropsychological TestsOxygenParahippocampal GyrusPrefrontal CortexOxygenClinical high riskfMRIProdromePsychosisWorking memory

Identifiers

PMID26965745
PMCPMC4836956
OpenAlexW2293122865

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Registered trials

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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.