Evidence map›Paper›PMID 18206351›Full record

ReviewSchizophrenia research2008

Impact of atypical antipsychotic therapy on leptin, ghrelin, and adiponectin.

Hua Jin, Jonathan M Meyer, Sunder Mudaliar, Dilip V Jeste

Open access · greenAbstract readComparative StudyReview
In one paragraph

Review in Schizophrenia research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed, 3 pooled it
4.5field-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.

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

52 citing papers in PubMed, 3 syntheses or guidelines pooled it, 147 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Antipsychotic-induced changes in blood levels of leptin in schizophrenia: a meta-analysis.Canadian journal of psychiatry. Revue canadienne de psychiatrie · 2015
    Pooled it
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Review
  10. Review
  11. Article
  12. Review
  13. Mechanism and treatments of antipsychotic-induced weight gain.International journal of obesity (2005) · 2023
    Review
  14. Selective 5-HTPharmaceuticals (Basel, Switzerland) · 2023
    Article
  15. Article
  16. Article
  17. Ghrelin mediated regulation of neurosynaptic transmitters in depressive disorders.Current research in pharmacology and drug discovery · 2022
    Review
  18. Review
  19. Review
  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

4 authors at 2 institutions in 1 country.

Hua JinDepartment of Psychiatry, University of California at San Diego, USA. hjin@ucsd.edu
Jonathan M Meyer
Sunder Mudaliar
Dilip V Jeste
University of California, San Diego · USVA San Diego Healthcare System · US

Funding

Research Methods CoreP30MH080002 · NIMH · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JESTE, DILIP V. · 2007 to 2011
$9.6M
Metabolic Effects of Newer Antipsychotics in Older PtsR01MH071536 · NIMH · VETERANS MEDICAL RESEARCH FDN/SAN DIEGO · PI JESTE, DILIP V. · 2005 to 2009
$4.8M
NIMH NIH HHS MH071536NIMH NIH HHS P30 MH080002NIMH NIH HHS R01 MH071536
6 · The paper itself

Abstract

backgroundMany adverse effects of atypical antipsychotic treatment are associated with antagonism of monoamine receptors; however, data indicate that important metabolic effects, such as hypertriglyceridemia and impairment in glucose/insulin homeostasis, may not be related to these mechanisms, leading investigators to explore alternative hypotheses. Promising candidates include a possible impact of antipsychotics on peptide hormonal regulators of metabolic control such as leptin, ghrelin, and adiponectin. The purpose of this review is to summarize recent data on changes in these hormones during atypical antipsychotic treatment.

methodsA Medline search was performed for papers published from January 1999 to January 2007 using key words antipsychotic, atypical antipsychotic, and individual atypical antipsychotic drug names cross-referenced with leptin, ghrelin, and adiponectin.

resultsThe bulk of the published work focused on changes in body weight and serum leptin, with far less data on ghrelin, and adiponectin, and nonweight metabolic changes. Leptin changes were directly related to a medication's weight gain liability, with no added antipsychotic effects on leptin signaling. Conflicting results emerged for the other markers, but all three long-term studies on ghrelin showed increased levels in patients on atypical antipsychotics with weight gain liabilities.

conclusionsLeptin increases during antipsychotic treatment are a result of weight gain rather than a direct impact of atypical antipsychotics on leptin physiology. Preliminary long-term data show increased ghrelin levels, but this finding must be replicated. The association with antipsychotic effects on glucose and lipid metabolism and these hormones remains virtually unstudied. Future research should indicate whether ghrelin and other peptide hormones may be useful predictors of weight gain or metabolic changes in patients on antipsychotics.

Indexed as

AdiponectinAdultAnimalsAntipsychotic AgentsBody Mass IndexBody WeightCross-Sectional StudiesFemaleGhrelinHumansIn Vitro TechniquesLeptinMaleMetabolic SyndromeObesityPharmacogeneticsAdiponectinAntipsychotic AgentsGhrelinLeptin

Identifiers

PMID18206351
PMCPMC2699769
OpenAlexW2046206286

What OpenQuestion holds

Textmetadata
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.