Evidence map›Paper›PMID 27259817›Full record

ArticleBiological psychiatry2017

Decreased Numbers of Somatostatin-Expressing Neurons in the Amygdala of Subjects With Bipolar Disorder or Schizophrenia: Relationship to Circadian Rhythms.

Harry Pantazopoulos, Jason T Wiseman, Matej Markota, Lucy Ehrenfeld, Sabina Berretta

Abstract read
In one paragraph

Article in Biological psychiatry, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed, 1 pooled it
2.2field-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

45 citing papers in PubMed, 1 synthesis or guideline pooled it, 70 citations in OpenAlex.

  1. Pooled it
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  15. Single-cell genomics and regulatory networks for 388 human brains.bioRxiv : the preprint server for biology · 2024
    Article
  16. Article
  17. Article
  18. Growth Hormone Action in Somatostatin Neurons Regulates Anxiety and Fear Memory.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  19. Review
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 1 country.

Harry PantazopoulosTranslational Neuroscience Laboratory, Mclean Hospital, Belmont; Department of Psychiatry, Harvard Medical School, Boston, Massachusetts. Electronic address: hpantazo@mclean.harvard.edu.
Jason T WisemanTranslational Neuroscience Laboratory, Mclean Hospital, Belmont.
Matej MarkotaTranslational Neuroscience Laboratory, Mclean Hospital, Belmont; Department of Psychiatry and Psychology, Mayo Clinic, Rochester, Minnesota.
Lucy EhrenfeldTranslational Neuroscience Laboratory, Mclean Hospital, Belmont.
Sabina BerrettaTranslational Neuroscience Laboratory, Mclean Hospital, Belmont; Department of Psychiatry, Harvard Medical School, Boston, Massachusetts; Program in Neuroscience, Harvard Medical School, Boston, Massachusetts.
McLean Hospital · USHarvard University · US

Funding

Disruption of Extracellular Matrix-Glial Interactions in SchizophreniaR01MH086522 · NIMH · MCLEAN HOSPITAL · PI BERRETTA, SABINA · 2011 to 2015
$2.0M
Supplement/'Partial' Rodent Model for GABA Defect in Schizophrenia/MH 066280R01MH066280 · NIMH · MC LEAN HOSPITAL (BELMONT, MA) · PI BERRETTA, SABINA · 2004 to 2008
$1.1M
NIMH NIH HHS R01 MH066280NIMH NIH HHS R01 MH086522
6 · The paper itself

Abstract

backgroundGrowing evidence points to a key role for somatostatin (SST) in schizophrenia (SZ) and bipolar disorder (BD). In the amygdala, neurons expressing SST play an important role in the regulation of anxiety, which is often comorbid in these disorders. We tested the hypothesis that SST-immunoreactive (IR) neurons are decreased in the amygdala of subjects with SZ and BD. Evidence for circadian SST expression in the amygdala and disrupted circadian rhythms and rhythmic peaks of anxiety in BD suggest a disruption of rhythmic expression of SST in this disorder.

methodsAmygdala sections from 12 SZ, 15 BD, and 15 control subjects were processed for immunocytochemistry for SST and neuropeptide Y, a neuropeptide partially coexpressed in SST-IR neurons. Total numbers (N

resultsSST-IR neurons were decreased in the lateral amygdala nucleus in BD (N

conclusionsDecreased SST-IR neurons in the amygdala of patients with SZ and BD, interpreted here as decreased SST expression, may disrupt responses to fear and anxiety regulation in these individuals. In BD, our findings raise the possibility that morning peaks of anxiety depend on a disruption of circadian regulation of SST expression in the amygdala.

Indexed as

Circadian RhythmAmygdalaBipolar DisorderFemaleHumansMaleNeuronsNeuropeptide YSchizophreniaSomatostatinNeuropeptide YSomatostatinAnxietyCircadianGamma-aminobutyric acidInterneuronMood disorderStress

Identifiers

PMID27259817
PMCPMC5065936
OpenAlexW2339291501

What OpenQuestion holds

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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.