Evidence map›Paper›PMID 21894153›Full record

ReviewMolecular psychiatry2012

Pharmacogenetics of antipsychotic-induced weight gain: review and clinical implications.

T A P Lett, T J M Wallace, N I Chowdhury, A K Tiwari, J L Kennedy, D J Müller

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in Molecular psychiatry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04923204 (Genetic Variations Associated With the Therapeutic Response and Profile of Adverse Effects in the Treatment of Bipolar Depression), which is not on this map. Cited by 103 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
103citing papers in PubMed, 4 pooled it
11.6field-weighted citation impact, top 1% 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.

NCT04923204 completednot on this mapstarted 2016, after this paper: background citation

Genetic Variations Associated With the Therapeutic Response and Profile of Adverse Effects in the Treatment of Bipolar Depression

TypeobservationalSponsorAB Biotics, SARan2016 to 2019Enrolled76ConditionsBipolar DisorderArmsPharmacogenomic-testing with NEUROPHARMAGEN
3 · Its place in the literature

Who cites it

103 citing papers in PubMed, 4 syntheses or guidelines pooled it, 258 citations in OpenAlex.

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43 more citing papers are in PubMed but not listed here.

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 1 institution in 1 country.

T A P LettNeurogenetics Section, Centre for Addiction and Mental Health, Toronto, ON, Canada.
T J M Wallace
N I Chowdhury
A K Tiwari
J L Kennedy
D J Müller
Centre for Addiction and Mental Health · CA

Funding

Canadian Institutes of Health Research MOP 89853
6 · The paper itself

Abstract

Second-generation antipsychotics (SGAs), such as risperidone, clozapine and olanzapine, are the most common drug treatments for schizophrenia. SGAs presented an advantage over first-generation antipsychotics (FGAs), particularly regarding avoidance of extrapyramidal symptoms. However, most SGAs, and to a lesser degree FGAs, are linked to substantial weight gain. This substantial weight gain is a leading factor in patient non-compliance and poses significant risk of diabetes, lipid abnormalities (that is, metabolic syndrome) and cardiovascular events including sudden death. The purpose of this article is to review the advances made in the field of pharmacogenetics of antipsychotic-induced weight gain (AIWG). We included all published association studies in AIWG from December 2006 to date using the Medline and ISI web of knowledge databases. There has been considerable progress reaffirming previous findings and discovery of novel genetic factors. The HTR2C and leptin genes are among the most promising, and new evidence suggests that the DRD2, TNF, SNAP-25 and MC4R genes are also prominent risk factors. Further promising findings have been reported in novel susceptibility genes, such as CNR1, MDR1, ADRA1A and INSIG2. More research is required before genetically informed, personalized medicine can be applied to antipsychotic treatment; nevertheless, inroads have been made towards assessing genetic liability and plausible clinical application.

Indexed as

Antipsychotic AgentsAppetiteBiogenic MonoaminesBiological TransportBiotransformationCardiovascular DiseasesEpigenesis, GeneticGenetic Association StudiesGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLipid MetabolismMeta-Analysis as TopicMetabolic SyndromeNeurotransmitter AgentsObesityAntipsychotic AgentsBiogenic MonoaminesNeurotransmitter AgentsReceptors, Neurotransmitter

Identifiers

PMID21894153
OpenAlexW2061767937

What OpenQuestion holds

Textmetadata
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.