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LifeGene—a large prospective population-based study of global relevance

Identifieur interne : 000731 ( Istex/Corpus ); précédent : 000730; suivant : 000732

LifeGene—a large prospective population-based study of global relevance

Auteurs : Catarina Almqvist ; Hans-Olov Adami ; Paul W. Franks ; Leif Groop ; Erik Ingelsson ; Juha Kere ; Lauren Lissner ; Jan-Eric Litton ; Markus Maeurer ; Karl Michaëlsson ; Juni Palmgren ; Göran Pershagen ; Alexander Ploner ; Patrick F. Sullivan ; Gunnel Tybring ; Nancy L. Pedersen

Source :

RBID : ISTEX:D69D4F414337CEB1C730522FA7AD3D28855BC7FB

English descriptors

Abstract

Abstract: Studying gene-environment interactions requires that the amount and quality of the lifestyle data is comparable to what is available for the corresponding genomic data. Sweden has several crucial prerequisites for comprehensive longitudinal biomedical research, such as the personal identity number, the universally available national health care system, continuously updated population and health registries and a scientifically motivated population. LifeGene builds on these strengths to bridge the gap between basic research and clinical applications with particular attention to populations, through a unique design in a research-friendly setting. LifeGene is designed both as a prospective cohort study and an infrastructure with repeated contacts of study participants approximately every 5 years. Index persons aged 18–45 years old will be recruited and invited to include their household members (partner and any children). A comprehensive questionnaire addressing cutting-edge research questions will be administered through the web with short follow-ups annually. Biosamples and physical measurements will also be collected at baseline, and re-administered every 5 years thereafter. Event-based sampling will be a key feature of LifeGene. The household-based design will give the opportunity to involve young couples prior to and during pregnancy, allowing for the first study of children born into cohort with complete pre-and perinatal data from both the mother and father. Questions and sampling schemes will be tailored to the participants’ age and life events. The target of LifeGene is to enrol 500,000 Swedes and follow them longitudinally for at least 20 years.

Url:
DOI: 10.1007/s10654-010-9521-x

Links to Exploration step

ISTEX:D69D4F414337CEB1C730522FA7AD3D28855BC7FB

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<div type="abstract" xml:lang="en">Abstract: Studying gene-environment interactions requires that the amount and quality of the lifestyle data is comparable to what is available for the corresponding genomic data. Sweden has several crucial prerequisites for comprehensive longitudinal biomedical research, such as the personal identity number, the universally available national health care system, continuously updated population and health registries and a scientifically motivated population. LifeGene builds on these strengths to bridge the gap between basic research and clinical applications with particular attention to populations, through a unique design in a research-friendly setting. LifeGene is designed both as a prospective cohort study and an infrastructure with repeated contacts of study participants approximately every 5 years. Index persons aged 18–45 years old will be recruited and invited to include their household members (partner and any children). A comprehensive questionnaire addressing cutting-edge research questions will be administered through the web with short follow-ups annually. Biosamples and physical measurements will also be collected at baseline, and re-administered every 5 years thereafter. Event-based sampling will be a key feature of LifeGene. The household-based design will give the opportunity to involve young couples prior to and during pregnancy, allowing for the first study of children born into cohort with complete pre-and perinatal data from both the mother and father. Questions and sampling schemes will be tailored to the participants’ age and life events. The target of LifeGene is to enrol 500,000 Swedes and follow them longitudinally for at least 20 years.</div>
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<OrgAddress>
<City>Uppsala</City>
<Country Code="SE">Sweden</Country>
</OrgAddress>
</Affiliation>
<Affiliation ID="Aff12">
<OrgDivision>Department of Mathematical Statistics</OrgDivision>
<OrgName>Stockholm University</OrgName>
<OrgAddress>
<City>Stockholm</City>
<Country Code="SE">Sweden</Country>
</OrgAddress>
</Affiliation>
<Affiliation ID="Aff13">
<OrgDivision>Institute of Environmental Medicine</OrgDivision>
<OrgName>Karolinska Institutet</OrgName>
<OrgAddress>
<City>Stockholm</City>
<Country Code="SE">Sweden</Country>
</OrgAddress>
</Affiliation>
<Affiliation ID="Aff14">
<OrgDivision>Department of Genetics</OrgDivision>
<OrgName>University of North Carolina at Chapel Hill</OrgName>
<OrgAddress>
<City>Chapel Hill</City>
<State>NC</State>
<Country Code="US">USA</Country>
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<Heading>Abstract</Heading>
<Para>Studying gene-environment interactions requires that the amount and quality of the lifestyle data is comparable to what is available for the corresponding genomic data. Sweden has several crucial prerequisites for comprehensive longitudinal biomedical research, such as the personal identity number, the universally available national health care system, continuously updated population and health registries and a scientifically motivated population. LifeGene builds on these strengths to bridge the gap between basic research and clinical applications with particular attention to populations, through a unique design in a research-friendly setting. LifeGene is designed both as a prospective cohort study and an infrastructure with repeated contacts of study participants approximately every 5 years. Index persons aged 18–45 years old will be recruited and invited to include their household members (partner and any children). A comprehensive questionnaire addressing cutting-edge research questions will be administered through the web with short follow-ups annually. Biosamples and physical measurements will also be collected at baseline, and re-administered every 5 years thereafter. Event-based sampling will be a key feature of LifeGene. The household-based design will give the opportunity to involve young couples prior to and during pregnancy, allowing for the first study of children born into cohort with complete pre-and perinatal data from both the mother and father. Questions and sampling schemes will be tailored to the participants’ age and life events. The target of LifeGene is to enrol 500,000 Swedes and follow them longitudinally for at least 20 years.</Para>
</Abstract>
<KeywordGroup Language="En" OutputMedium="All">
<Heading>Keywords</Heading>
<Keyword>Biobank</Keyword>
<Keyword>Cohort study</Keyword>
<Keyword>Epidemiology</Keyword>
<Keyword>Prospective study</Keyword>
<Keyword>Questionnaires</Keyword>
<Keyword>Population genetics</Keyword>
</KeywordGroup>
<AbbreviationGroup>
<Heading>Abbreviations</Heading>
<DefinitionList>
<DefinitionListEntry>
<Term>DLW</Term>
<Description>
<Para>Doubly labelled water</Para>
</Description>
</DefinitionListEntry>
<DefinitionListEntry>
<Term>DNA</Term>
<Description>
<Para>Deoxyribonucleic acid</Para>
</Description>
</DefinitionListEntry>
<DefinitionListEntry>
<Term>EDTA</Term>
<Description>
<Para>Ethylenediaminetetraacetic acid</Para>
</Description>
</DefinitionListEntry>
<DefinitionListEntry>
<Term>GWAS</Term>
<Description>
<Para>Genome wide association studies</Para>
</Description>
</DefinitionListEntry>
<DefinitionListEntry>
<Term>ILI</Term>
<Description>
<Para>Influenza-like illness</Para>
</Description>
</DefinitionListEntry>
<DefinitionListEntry>
<Term>PCR</Term>
<Description>
<Para>Polymerase chain reaction</Para>
</Description>
</DefinitionListEntry>
<DefinitionListEntry>
<Term>WHO</Term>
<Description>
<Para>World Health Organisation</Para>
</Description>
</DefinitionListEntry>
</DefinitionList>
</AbbreviationGroup>
</ArticleHeader>
<NoBody></NoBody>
</Article>
</Issue>
</Volume>
</Journal>
</Publisher>
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<titleInfo lang="en">
<title>LifeGene—a large prospective population-based study of global relevance</title>
</titleInfo>
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<title>LifeGene—a large prospective population-based study of global relevance</title>
</titleInfo>
<name type="personal" displayLabel="corresp">
<namePart type="given">Catarina</namePart>
<namePart type="family">Almqvist</namePart>
<affiliation>Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Box 281, SE-171 77, Stockholm, Sweden</affiliation>
<affiliation>Astrid Lindgren Children’s Hospital, Karolinska University Hospital, Stockholm, Sweden</affiliation>
<affiliation>E-mail: catarina.almqvist@ki.se</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Hans-Olov</namePart>
<namePart type="family">Adami</namePart>
<affiliation>Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Box 281, SE-171 77, Stockholm, Sweden</affiliation>
<affiliation>Department of Epidemiology, Harvard School of Public Health, Boston, MA, USA</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Paul</namePart>
<namePart type="given">W.</namePart>
<namePart type="family">Franks</namePart>
<affiliation>Department of Public Health & Clinical Medicine, Section for Medicine, Umeå University Hospital Sweden, Umeå, Sweden</affiliation>
<affiliation>Department of Clinical Sciences, Genetic and Molecular Epidemiology Unit, Skåne University Hospital, Lund University, Malmo, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Leif</namePart>
<namePart type="family">Groop</namePart>
<affiliation>Department of Clinical Sciences, Diabetes and Endocrinology Unit, Lund University, Lund, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Erik</namePart>
<namePart type="family">Ingelsson</namePart>
<affiliation>Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Box 281, SE-171 77, Stockholm, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Juha</namePart>
<namePart type="family">Kere</namePart>
<affiliation>Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Lauren</namePart>
<namePart type="family">Lissner</namePart>
<affiliation>Department of Public Health and Community Medicine, University of Gothenburg, Gothenburg, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Jan-Eric</namePart>
<namePart type="family">Litton</namePart>
<affiliation>Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Box 281, SE-171 77, Stockholm, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">Markus</namePart>
<namePart type="family">Maeurer</namePart>
<affiliation>Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden</affiliation>
<affiliation>Swedish Institute for Infectious Disease Control, Stockholm, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">Karl</namePart>
<namePart type="family">Michaëlsson</namePart>
<affiliation>Department of Surgical Sciences, Uppsala University, Uppsala, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
</name>
<name type="personal">
<namePart type="given">Juni</namePart>
<namePart type="family">Palmgren</namePart>
<affiliation>Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Box 281, SE-171 77, Stockholm, Sweden</affiliation>
<affiliation>Department of Mathematical Statistics, Stockholm University, Stockholm, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">Göran</namePart>
<namePart type="family">Pershagen</namePart>
<affiliation>Institute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
</role>
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<name type="personal">
<namePart type="given">Alexander</namePart>
<namePart type="family">Ploner</namePart>
<affiliation>Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Box 281, SE-171 77, Stockholm, Sweden</affiliation>
<role>
<roleTerm type="text">author</roleTerm>
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<name type="personal">
<namePart type="given">Patrick</namePart>
<namePart type="given">F.</namePart>
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<affiliation>Department of Genetics, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA</affiliation>
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<namePart type="family">Tybring</namePart>
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<namePart type="family">Pedersen</namePart>
<affiliation>Department of Medical Epidemiology and Biostatistics, Karolinska Institutet, Box 281, SE-171 77, Stockholm, Sweden</affiliation>
<affiliation>E-mail: nancy.pedersen@ki.se</affiliation>
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<abstract lang="en">Abstract: Studying gene-environment interactions requires that the amount and quality of the lifestyle data is comparable to what is available for the corresponding genomic data. Sweden has several crucial prerequisites for comprehensive longitudinal biomedical research, such as the personal identity number, the universally available national health care system, continuously updated population and health registries and a scientifically motivated population. LifeGene builds on these strengths to bridge the gap between basic research and clinical applications with particular attention to populations, through a unique design in a research-friendly setting. LifeGene is designed both as a prospective cohort study and an infrastructure with repeated contacts of study participants approximately every 5 years. Index persons aged 18–45 years old will be recruited and invited to include their household members (partner and any children). A comprehensive questionnaire addressing cutting-edge research questions will be administered through the web with short follow-ups annually. Biosamples and physical measurements will also be collected at baseline, and re-administered every 5 years thereafter. Event-based sampling will be a key feature of LifeGene. The household-based design will give the opportunity to involve young couples prior to and during pregnancy, allowing for the first study of children born into cohort with complete pre-and perinatal data from both the mother and father. Questions and sampling schemes will be tailored to the participants’ age and life events. The target of LifeGene is to enrol 500,000 Swedes and follow them longitudinally for at least 20 years.</abstract>
<note>NEW STUDY</note>
<subject lang="en">
<genre>Keywords</genre>
<topic>Biobank</topic>
<topic>Cohort study</topic>
<topic>Epidemiology</topic>
<topic>Prospective study</topic>
<topic>Questionnaires</topic>
<topic>Population genetics</topic>
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<genre>Abbreviations</genre>
<topic>DLW : Doubly labelled water</topic>
<topic>DNA : Deoxyribonucleic acid</topic>
<topic>EDTA : Ethylenediaminetetraacetic acid</topic>
<topic>GWAS : Genome wide association studies</topic>
<topic>ILI : Influenza-like illness</topic>
<topic>PCR : Polymerase chain reaction</topic>
<topic>WHO : World Health Organisation</topic>
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<genre>Medicine & Public Health</genre>
<topic>Oncology</topic>
<topic>Cardiology</topic>
<topic>Infectious Diseases</topic>
<topic>Public Health/Gesundheitswesen</topic>
<topic>Epidemiology</topic>
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<identifier type="ISSN">0393-2990</identifier>
<identifier type="eISSN">1573-7284</identifier>
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<identifier type="VolumeIssueCount">12</identifier>
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<date>2011</date>
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