Evidence map›Paper›PMID 25903154›Full record

ArticleBMC medicine2015

A genetic risk score combining 32 SNPs is associated with body mass index and improves obesity prediction in people with major depressive disorder.

Chi-Fa Hung, Gerome Breen, Darina Czamara, Tanguy Corre, Christiane Wolf, Stefan Kloiber, Sven Bergmann, Nick Craddock, Michael Gill, Florian Holsboer and 20 more

Open access · goldAbstract read
In one paragraph

Article in BMC medicine, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
10.6field-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.

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

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 72 citations in OpenAlex.

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  10. Evaluation of polygenic risk score for risk prediction of gastric cancer.World journal of gastrointestinal oncology · 2023
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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

30 authors at 18 institutions in 9 countries.

Chi-Fa HungMRC SGDP Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, Box PO82, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK. chifa.hung@gmail.com.
Gerome BreenMRC SGDP Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, Box PO82, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK. gerome.breen@gmail.com.
Darina CzamaraMax-Planck-Institute of Psychiatry, Kraepelinstraße 2, 80804, Munich, Germany. darina@mpipsykl.mpg.de.
Tanguy CorreInstitute of Social and Preventive Medicine (IUMSP), Centre Hospitalier, Universitaire Vaudois (CHUV), 1010, Lausanne, Switzerland. tanguy.corre@unil.ch.
Christiane WolfMax-Planck-Institute of Psychiatry, Kraepelinstraße 2, 80804, Munich, Germany. cwolf@mpipsykl.mpg.de.
Stefan KloiberMax-Planck-Institute of Psychiatry, Kraepelinstraße 2, 80804, Munich, Germany. stkloiber@mpipsykl.mpg.de.
Sven BergmannInstitute of Social and Preventive Medicine (IUMSP), Centre Hospitalier, Universitaire Vaudois (CHUV), 1010, Lausanne, Switzerland. sven.bergmann@unil.ch.
Nick CraddockMRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK. craddockn@Cardiff.ac.uk.
Michael GillDepartment of Psychiatry, Trinity Centre for Health Sciences, Dublin 8, Ireland. mgill@tcd.ie.
Florian HolsboerMax-Planck-Institute of Psychiatry, Kraepelinstraße 2, 80804, Munich, Germany. holsboer@mpipsykl.mpg.de.
Lisa JonesDepartment of Psychiatry, School of Clinical and Experimental Medicine, University of Birmingham, Birmingham, B15 2TT, UK. l.a.jones@bham.ac.uk.
Ian JonesMRC Centre for Neuropsychiatric Genetics and Genomics, Cardiff University, Hadyn Ellis Building, Maindy Road, Cardiff, CF24 4HQ, UK. jonesir1@cf.ac.uk.
Ania KorszunBarts and The London School of Medicine and Dentistry, Queen Mary's University of London, London, E1 2AD, UK. a.korszun@qmul.ac.uk.
Zoltan KutalikInstitute of Social and Preventive Medicine (IUMSP), Centre Hospitalier, Universitaire Vaudois (CHUV), 1010, Lausanne, Switzerland. zoltan.kutalik@unil.ch.
Susanne LucaeMax-Planck-Institute of Psychiatry, Kraepelinstraße 2, 80804, Munich, Germany. lucae@mpipsykl.mpg.de.
Wolfgang MaierDepartment of Psychiatry, University of Bonn, 53127, Bonn, Germany. wolfgang.maier@ukb.uni-bonn.de.
Ole MorsResearch Department P, Aarhus University Hospital, Skovagervej 2, DK-8240, Risskov, Denmark. nielmors@rm.dk.
Michael J OwenMRC Centre for Neuropsychiatric Genetics and Genomics, Department of Psychological Medicine and Neurology, School of Medicine, Cardiff University, Henry Wellcome Building, Heath Park, Cardiff, CF14 4XN, UK. owenmj@cardiff.ac.uk.
John RiceDepartment of Psychiatry, Washington University School of Medicine, St Louis, MO, 63130, USA. jrice@wustl.edu.
Marcella RietschelCentral Institute of Mental Health, 68159, Mannheim, Germany. marcella.rietschel@zi-mannheim.de.
Rudolf UherMRC SGDP Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, Box PO82, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK. rudolf.uher@cdha.nshealth.ca.
Peter VollenweiderDivision of Internal Medicine, CHUV, Rue du Bugnon 21, 1011, Lausanne, Switzerland. peter.vollenweider@chuv.ch.
Gerard WaeberDivision of Internal Medicine, CHUV, Rue du Bugnon 21, 1011, Lausanne, Switzerland. gerard.waeber@chuv.hospvd.ch.
Ian W CraigMRC SGDP Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, Box PO82, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK. ian.craig@kcl.ac.uk.
Anne E FarmerMRC SGDP Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, Box PO82, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK. anne.farmer@kcl.ac.uk.
Cathryn M LewisMRC SGDP Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, Box PO82, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK. cathryn.lewis@kcl.ac.uk.
Bertram Müller-MyhsokMax-Planck-Institute of Psychiatry, Kraepelinstraße 2, 80804, Munich, Germany. bmm@mpipsykl.mpg.de.
Martin PreisigDepartment of Psychiatry, Lausanne University Hospital, 1008, Prilly-Lausanne, Switzerland. martin.preisig@chuv.ch.
Peter McGuffinMRC SGDP Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, Box PO82, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK. peter.mcguffin@kcl.ac.uk.
Margarita RiveraMRC SGDP Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, Box PO82, De Crespigny Park, Denmark Hill, London, SE5 8AF, UK. margarita.rivera_sanchez@kcl.ac.uk.
Max Planck Institute of Psychiatry · DEKing's College London · GBCardiff University · GBSIB Swiss Institute of Bioinformatics · CHAarhus University Hospital · DKCentral Institute of Mental Health · DEChang Gung University · TWDalhousie University · CAGuy's Hospital · GBHôpital Orthopédique de la Suisse Romande · CHQueen Mary University of London · GBTrinity College Dublin · IEUniversidad de Granada · ESUniversity Hospital of Lausanne · CHUniversity of Birmingham · GBUniversity of Bonn · DEUniversity of Lausanne · CHWashington University in St. Louis · US

Funding

Medical Research Council G0701420Medical Research Council MR/L010305/1
6 · The paper itself

Abstract

backgroundObesity is strongly associated with major depressive disorder (MDD) and various other diseases. Genome-wide association studies have identified multiple risk loci robustly associated with body mass index (BMI). In this study, we aimed to investigate whether a genetic risk score (GRS) combining multiple BMI risk loci might have utility in prediction of obesity in patients with MDD.

methodsLinear and logistic regression models were conducted to predict BMI and obesity, respectively, in three independent large case-control studies of major depression (Radiant, GSK-Munich, PsyCoLaus). The analyses were first performed in the whole sample and then separately in depressed cases and controls. An unweighted GRS was calculated by summation of the number of risk alleles. A weighted GRS was calculated as the sum of risk alleles at each locus multiplied by their effect sizes. Receiver operating characteristic (ROC) analysis was used to compare the discriminatory ability of predictors of obesity.

resultsIn the discovery phase, a total of 2,521 participants (1,895 depressed patients and 626 controls) were included from the Radiant study. Both unweighted and weighted GRS were highly associated with BMI (P < 0.001) but explained only a modest amount of variance. Adding 'traditional' risk factors to GRS significantly improved the predictive ability with the area under the curve (AUC) in the ROC analysis, increasing from 0.58 to 0.66 (95% CI, 0.62-0.68; χ(2) = 27.68; P < 0.0001). Although there was no formal evidence of interaction between depression status and GRS, there was further improvement in AUC in the ROC analysis when depression status was added to the model (AUC = 0.71; 95% CI, 0.68-0.73; χ(2) = 28.64; P <0.0001). We further found that the GRS accounted for more variance of BMI in depressed patients than in healthy controls. Again, GRS discriminated obesity better in depressed patients compared to healthy controls. We later replicated these analyses in two independent samples (GSK-Munich and PsyCoLaus) and found similar results.

conclusionsA GRS proved to be a highly significant predictor of obesity in people with MDD but accounted for only modest amount of variance. Nevertheless, as more risk loci are identified, combining a GRS approach with information on non-genetic risk factors could become a useful strategy in identifying MDD patients at higher risk of developing obesity.

Indexed as

Body Mass IndexPolymorphism, Single NucleotideAdultAgedArea Under CurveCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLogistic ModelsMajor Depressive DisorderMaleMiddle AgedObesityRisk

Identifiers

PMID25903154
PMCPMC4407390
OpenAlexW2111126006

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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.