Evidence map›Paper›PMID 23768813›Full record

Trial reportSchizophrenia research2013

Targeting alpha-7 nicotinic neurotransmission in schizophrenia: a novel agonist strategy.

Stephen I Deutsch, Barbara L Schwartz, Nina R Schooler, Clayton H Brown, Richard B Rosse, Stephanie M Rosse

Open access · greenAbstract readMulticenter StudyRandomized Controlled Trial
In one paragraph

Trial report in Schizophrenia research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed, 3 pooled it
3.7field-weighted citation impact, top 6% 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

31 citing papers in PubMed, 3 syntheses or guidelines pooled it, 80 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Trial
  6. Trial
  7. Trial
  8. Trial
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Cognition and addiction
.Dialogues in clinical neuroscience · 2019
    Review
  15. Alpha7 Nicotinic Receptors as Therapeutic Targets in Schizophrenia.Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco · 2019
    Review
  16. Review
  17. Article
  18. Article
  19. Cognitive Functioning in Older Adults With Schizophrenia.Focus (American Psychiatric Publishing) · 2017
    Review
  20. Review
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

6 authors at 3 institutions in 1 country.

Stephen I DeutschDepartment of Psychiatry and Behavioral Sciences, Eastern Virginia Medical School, United States; Department of Psychiatry, Georgetown University School of Medicine, United States. Deutscsi@evms.edu
Barbara L Schwartz
Nina R Schooler
Clayton H Brown
Richard B Rosse
Stephanie M Rosse
Georgetown University · USEastern Virginia Medical School · USUniversity of Maryland, Baltimore · US

Funding

Interventions to Test the alpha 7 Nicotinic Receptor Model in SchizophreniaR34MH077849 · NIMH · GEORGETOWN UNIVERSITY · PI DEUTSCH, STEPHEN I · 2007 to 2009
$779k
NIMH NIH HHS R34 MH077849
6 · The paper itself

Abstract

Alpha7 nicotinic acetylcholine receptor (α7 nAChR) agonists may be valuable treatments for negative symptoms and cognitive impairment in schizophrenia. Unfortunately, chronic exposure to an agonist may reduce the receptor's sensitivity. Therefore, we combined CDP-choline, a dietary source of the direct agonist choline, with galantamine, a positive allosteric modulator (PAM) of nicotinic acetylcholine receptors, to improve the efficiency of transducing the choline signal and, possibly, preserve the receptor in a sensitive state. We conducted a single-site, double-blind randomized clinical trial comparing galantamine/CDP-choline to placebos in schizophrenia patients with negative symptoms who were receiving second generation antipsychotics. Forty-three subjects received galantamine and CDP-choline or matching placebos for 16weeks. The primary outcome measure was the 5-item Marder negative-symptoms factor of the Positive and Negative Syndrome Scale (PANSS). Cognition and functioning were also assessed. Trial completion was high; 79%. There was no significant treatment effect on negative symptoms, other PANSS symptom factors, or the MATRICS Cognitive Consensus Battery. There were significant treatment effects in overall functioning and a test of free verbal recall. Three subjects discontinued treatment in the active treatment group for gastro-intestinal adverse events (AE). The most common AE for galantamine/CDP-choline was abdominal pain; for placebo it was headache and sweating. Although there was no significant treatment effect on negative symptoms, the direction of effect mirrored the effects on a cognitive measure and overall functioning. Further study of α7 nAChR agonist/PAMs is warranted in larger studies that will have greater power.

Indexed as

AdultAgedalpha7 Nicotinic Acetylcholine ReceptorCognition DisordersCytidine Diphosphate CholineDouble-Blind MethodFemaleGalantamineHumansMaleMiddle AgedNeuropsychological TestsNootropic AgentsPsychiatric Status Rating ScalesPsychotic DisordersSchizophreniaalpha7 Nicotinic Acetylcholine ReceptorCytidine Diphosphate CholineGalantamineNootropic AgentsAcetylcholineAlpha7 nicotinic receptorNegative symptomsNeurocognitionPositive allosteric modulatorSchizophrenia

Identifiers

PMID23768813
PMCPMC3732552
OpenAlexW2155797616

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.