Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
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PMID
25150574
TITLE
Alleles that increase risk for type 2 diabetes mellitus are not associated with increased risk for Alzheimer's disease.
ABSTRACT
Although epidemiological studies suggest that type 2 diabetes mellitus (T2DM) increases the risk of late-onset Alzheimer's disease (LOAD), the biological basis of this relationship is not well understood. The aim of this study was to examine the genetic comorbidity between the 2 disorders and to investigate whether genetic liability to T2DM, estimated by a genotype risk scores based on T2DM associated loci, is associated with increased risk of LOAD. This study was performed in 2 stages. In stage 1, we combined genotypes for the top 15 T2DM-associated polymorphisms drawn from approximately 3000 individuals (1349 cases and 1351 control subjects) with extracted and/or imputed data from 6 genome-wide studies (>10,000 individuals; 4507 cases, 2183 controls, 4989 population controls) to form a genotype risk score and examined if this was associated with increased LOAD risk in a combined meta-analysis. In stage 2, we investigated the association of LOAD with an expanded T2DM score made of 45 well-established variants drawn from the 6 genome-wide studies. Results were combined in a meta-analysis. Both stage 1 and stage 2 T2DM risk scores were not associated with LOAD risk (odds ratio = 0.988; 95% confidence interval, 0.972-1.004; p = 0.144 and odds ratio = 0.993; 95% confidence interval, 0.983-1.003; p = 0.149 per allele, respectively). Contrary to expectation, genotype risk scores based on established T2DM candidates were not associated with increased risk of LOAD. The observed epidemiological associations between T2DM and LOAD could therefore be a consequence of secondary disease processes, pleiotropic mechanisms, and/or common environmental risk factors. Future work should focus on well-characterized longitudinal cohorts with extensive phenotypic and genetic data relevant to both LOAD and T2DM.
Copyright © 2014 Elsevier Inc. All rights reserved.
DATE PUBLISHED
2014 Dec
HISTORY
PUBSTATUS PUBSTATUSDATE
received 2014/07/15
accepted 2014/07/20
aheadofprint 2014/07/24
entrez 2014/08/25 06:00
pubmed 2014/08/26 06:00
medline 2015/11/10 06:00
AUTHORS
NAME COLLECTIVENAME LASTNAME FORENAME INITIALS AFFILIATION AFFILIATIONINFO
Proitsi P Proitsi Petroula P King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK; Department of Psychiatry, State Key Laboratory of Brain and Cognitive Sciences, and Centre for Genomic Sciences, Li Ka Shing Faculty of Medicine, the University of Hong Kong, Hong Kong. Electronic address: petroula.proitsi@kcl.ac.uk.
Lupton MK Lupton Michelle K MK King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK.
Velayudhan L Velayudhan Latha L King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK.
Hunter G Hunter Gillian G Centre for Integrative Physiology, University of Edinburgh, Edinburgh, UK.
Newhouse S Newhouse Stephen S King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK.
Lin K Lin Kuang K King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK.
Fogh I Fogh Isabella I King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK.
Tsolaki M Tsolaki Magda M Memory and Dementia Centre, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Daniilidou M Daniilidou Makrina M Laboratory of Biochemistry, Department of Chemistry, Aristotle University of Thessaloniki, Thessaloniki, Greece.
Pritchard M Pritchard Megan M King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK.
Craig D Craig David D Ageing group, Centre for Public Health, School of Medicine and Dentistry, Queen's University Belfast, Belfast, Northern Ireland, UK.
Todd S Todd Stephen S Ageing group, Centre for Public Health, School of Medicine and Dentistry, Queen's University Belfast, Belfast, Northern Ireland, UK.
Johnston JA Johnston Janet A JA Ageing group, Centre for Public Health, School of Medicine and Dentistry, Queen's University Belfast, Belfast, Northern Ireland, UK.
McGuinness B McGuinness Bernadette B Ageing group, Centre for Public Health, School of Medicine and Dentistry, Queen's University Belfast, Belfast, Northern Ireland, UK.
Kloszewska I Kloszewska Iwona I Department of Old Age Psychiatry & Psychotic Disorders, Medical University of Lodz, Lodz, Poland.
Soininen H Soininen Hilkka H Department of Neurology, Kuopio University Hospital and University of Eastern Finland, Kuopio, Finland.
Mecocci P Mecocci Patrizia P Section of Gerontology and Geriatrics, Department of Medicine, University of Perugia, Perugia, Italy.
Vellas B Vellas Bruno B Department of Internal and Geriatrics Medicine, INSERM U 1027, Gerontopole, Hôpitaux de Toulouse, Toulouse, France.
Passmore PA Passmore Peter A PA Ageing group, Centre for Public Health, School of Medicine and Dentistry, Queen's University Belfast, Belfast, Northern Ireland, UK.
Sims R Sims Rebecca R MRC Centre for Neuropsychiatric Genetics and Genomics, Department of Psychological Medicine and Neurology, School of Medicine, Cardiff University, Cardiff, UK.
Williams J Williams Julie J MRC Centre for Neuropsychiatric Genetics and Genomics, Department of Psychological Medicine and Neurology, School of Medicine, Cardiff University, Cardiff, UK.
Brayne C Brayne Carol C Department of Public Health and Primary Care, Cambridge Institute of Public Health, University of Cambridge, Cambridge, UK.
Alzheimer's Disease Neuroimaging Initiative
GERAD1 Consortium
Stewart R Stewart Robert R King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK.
Sham P Sham Pak P Department of Psychiatry, State Key Laboratory of Brain and Cognitive Sciences, and Centre for Genomic Sciences, Li Ka Shing Faculty of Medicine, the University of Hong Kong, Hong Kong.
Lovestone S Lovestone Simon S King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK; Department of Psychiatry, University of Oxford, Warneford Hospital, Oxford OX3 7JX, UK.
Powell JF Powell John F JF King's College London, Institute of Psychiatry, Psychology and Neuroscience, London, UK.
INVESTIGATORS
JOURNAL
VOLUME: 35
ISSUE: 12
TITLE: Neurobiology of aging
ISOABBREVIATION: Neurobiol. Aging
YEAR: 2014
MONTH: Dec
DAY:
MEDLINEDATE:
SEASON:
CITEDMEDIUM: Internet
ISSN: 1558-1497
ISSNTYPE: Electronic
MEDLINE JOURNAL
MEDLINETA: Neurobiol Aging
COUNTRY: United States
ISSNLINKING: 0197-4580
NLMUNIQUEID: 8100437
PUBLICATION TYPE
PUBLICATIONTYPE TEXT
Journal Article
Research Support, Non-U.S. Gov't
COMMENTS AND CORRECTIONS
GRANTS
GENERAL NOTE
KEYWORDS
KEYWORD
Environmental
Genetics
Genotype risk score
Late-onset Alzheimer's disease
Mediated pleiotropy
Type 2 diabetes mellitus
MESH HEADINGS
DESCRIPTORNAME QUALIFIERNAME
Alleles
Alzheimer Disease genetics
Comorbidity genetics
Diabetes Mellitus, Type 2 genetics
Genetic Predisposition to Disease genetics
Genome-Wide Association Study methods
Genotype methods
Humans methods
Meta-Analysis as Topic methods
Risk methods
SUPPLEMENTARY MESH
GENE SYMBOLS
CHEMICALS
OTHER ID's