Evidence map›Paper›PMID 32213216›Full record

ArticleActa neuropsychiatrica2020

Association between GLP-1 receptor gene polymorphisms with reward learning, anhedonia and depression diagnosis.

Hale Yapici-Eser, Vivek Appadurai, Candan Yasemin Eren, Dilek Yazici, Chia-Yen Chen, Dost Öngür, Diego A Pizzagalli, Thomas Werge, Mei-Hua Hall

Open access · greenAbstract read
In one paragraph

Article in Acta neuropsychiatrica, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 20 citations in OpenAlex.

  1. Pooled it
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  7. Variants inHeliyon · 2024
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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

9 authors at 4 institutions in 3 countries.

Hale Yapici-EserSchool of Medicine, Koç University, İstanbul, Turkey.ORCID https://orcid.org/0000-0003-0318-2770
Vivek AppaduraiThe Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, Denmark.
Candan Yasemin ErenResearch Center for Translational Medicine, Koç University,İstanbul, Turkey.
Dilek YaziciSchool of Medicine, Koç University, İstanbul, Turkey.
Chia-Yen ChenPsychiatric and Neurodevelopmental Genetics Unit and Analytic and Translational Genetics Unit, Massachusetts General Hospital, Boston, MA, USA.
Dost ÖngürDepartment of Psychiatry, Harvard Medical School, Boston, MA, USA.
Diego A PizzagalliDepartment of Psychiatry, Harvard Medical School, Boston, MA, USA.
Thomas WergeThe Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH, Aarhus, Denmark.
Mei-Hua HallDepartment of Psychiatry, Harvard Medical School, Boston, MA, USA.
Harvard University · USKoç University · TRMental Health Services · DKUniversity of Copenhagen · DK

Funding

Neuroimaging Studies of Reward Processing in DepressionR37MH068376 · NIMH · UNIVERSITY OF CALIFORNIA-IRVINE · PI Diego A Pizzagalli · 2016 to 2026
$7.4M
Neuroimaging Studies of Reward Processing in DepressionR01MH068376 · NIMH · MCLEAN HOSPITAL · PI PIZZAGALLI, DIEGO A · 2004 to 2014
$4.5M
Neurobiological Markers as Predictors of Later Functional Outcome in First Episode PsychosisR01MH109687 · NIMH · MCLEAN HOSPITAL · PI HALL, MEI-HUA · 2016 to 2021
$2.5M
Research and Mentoring on Brain and Peripheral Bioenergetics in SchizophreniaK24MH104449 · NIMH · MCLEAN HOSPITAL · PI ONGUR, DOST · 2015 to 2019
$749k
Genetic Basis of Reward Learning and Symptom, Smoking, and Neural Signature CorrelatesR03MH108850 · NIMH · MCLEAN HOSPITAL · PI HALL, MEI-HUA · 2016 to 2017
$163k
NIMH NIH HHS K24 MH104449NIMH NIH HHS R01 MH068376NIMH NIH HHS R01 MH109687NIMH NIH HHS R03 MH108850NIMH NIH HHS R37 MH068376
6 · The paper itself

Abstract

backgroundGlucagon-like peptide-1 receptors (GLP-1Rs) are widely expressed in the brain. Evidence suggests that they may play a role in reward responses and neuroprotection. However, the association of GLP-1R with anhedonia and depression diagnosis has not been studied. Here, we examined the association of GLP-1R polymorphisms with objective and subjective measures of anhedonia, as well as depression diagnosis.

methodsObjective [response bias assessed by the probabilistic reward task (PRT)] and subjective [Snaith-Hamilton Pleasure Scale (SHAPS)] measures of anhedonia, clinical variables and DNA samples were collected from 100 controls and 164 patients at McLean Hospital. An independent sample genotyped as part of the Psychiatric Genomics Consortium (PGC) was used to study the effect of putative GLP-1R polymorphisms linked to response bias in PRT on depression diagnosis.

resultsThe C allele in rs1042044 was significantly associated with increased PRT response bias, when controlling for age, sex, case-control status and PRT discriminability. AA genotype of rs1042044 showed higher anhedonia phenotype based on SHAPS scores. However, analysis of PGC major depressive disorder data showed no association between rs1042044 and depression diagnosis.

conclusionFindings suggest a possible association of rs1042044 with anhedonia but no association with depression diagnosis.

Indexed as

RewardAnhedoniaCase-Control StudiesCorrelation of DataDepressive DisorderGenotypeGlucagon-Like Peptide-1 ReceptorHumansLearningMajor Depressive DisorderPhenotypePolymorphism, GeneticGLP1R protein, humanGlucagon-Like Peptide-1 ReceptoranhedoniadepressionGLP-1polymorphismreward

Identifiers

PMID32213216
PMCPMC7351594
OpenAlexW3014044574

What OpenQuestion holds

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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.