How lifespan associated genes modulate aging changes: lessons from analysis of longitudinal data.

dc.contributor.authorYashin, Anatoliy I
dc.contributor.authorArbeev, Konstantin G
dc.contributor.authorWu, Deqing
dc.contributor.authorArbeeva, Liubov S
dc.contributor.authorKulminski, Alexander
dc.contributor.authorAkushevich, Igor
dc.contributor.authorCulminskaya, Irina
dc.contributor.authorStallard, Eric
dc.contributor.authorUkraintseva, Svetlana V
dc.coverage.spatialSwitzerland
dc.date.accessioned2017-06-06T14:57:58Z
dc.date.available2017-06-06T14:57:58Z
dc.date.issued2013
dc.description.abstractBACKGROUND AND OBJECTIVE: The influence of genes on human lifespan is mediated by biological processes that characterize body's functioning. The age trajectories of these processes contain important information about mechanisms linking aging, health, and lifespan. The objective of this paper is to investigate regularities of aging changes in different groups of individuals, including individuals with different genetic background, as well as their connections with health and lifespan. DATA AND METHOD: To reach this objective we used longitudinal data on four physiological variables, information about health and lifespan collected in the Framingham Heart Study (FHS), data on longevity alleles detected in earlier study, as well as methods of statistical modeling. RESULTS: We found that phenotypes of exceptional longevity and health are linked to distinct types of changes in physiological indices during aging. We also found that components of aging changes differ in groups of individuals with different genetic background. CONCLUSIONS: These results suggest that factors responsible for exceptional longevity and health are not necessary the same, and that postponing aging changes is associated with extreme longevity. The genetic factors which increase lifespan are associated with physiological changes typical of healthy and long-living individuals, smaller mortality risks from cancer and CVD and better estimates of adaptive capacity in statistical modeling. This indicates that extreme longevity and health related traits are likely to be less heterogeneous phenotypes than lifespan, and studying these phenotypes separately from lifespan may provide additional information about mechanisms of human aging and its relation to chronic diseases and lifespan.
dc.identifierhttps://www.ncbi.nlm.nih.gov/pubmed/23346098
dc.identifier.urihttps://hdl.handle.net/10161/14839
dc.languageeng
dc.publisherFrontiers Media SA
dc.relation.ispartofFront Genet
dc.relation.isversionof10.3389/fgene.2013.00003
dc.subjectage trajectories
dc.subjectgenetic dose
dc.subjectintegrative genetic mortality model
dc.subjectlongevity genes
dc.subjectphysiological variables
dc.titleHow lifespan associated genes modulate aging changes: lessons from analysis of longitudinal data.
dc.typeJournal article
duke.contributor.idYashin, Anatoliy I|0115822
duke.contributor.idArbeev, Konstantin G|0314903
duke.contributor.idWu, Deqing|0512187
duke.contributor.idArbeeva, Liubov S|0467626
duke.contributor.idKulminski, Alexander|0280429
duke.contributor.idAkushevich, Igor|0285458
duke.contributor.idCulminskaya, Irina|0334801
duke.contributor.idUkraintseva, Svetlana V|0314469
duke.contributor.orcidArbeev, Konstantin G|0000-0002-4195-7832
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/23346098
pubs.begin-page3
pubs.organisational-groupCenter for Population Health & Aging
pubs.organisational-groupDuke
pubs.organisational-groupDuke Cancer Institute
pubs.organisational-groupDuke Population Research Center
pubs.organisational-groupDuke Population Research Institute
pubs.organisational-groupInstitutes and Centers
pubs.organisational-groupInstitutes and Provost's Academic Units
pubs.organisational-groupPhysics
pubs.organisational-groupSanford School of Public Policy
pubs.organisational-groupSchool of Medicine
pubs.organisational-groupSocial Science Research Institute
pubs.organisational-groupStaff
pubs.organisational-groupTrinity College of Arts & Sciences
pubs.organisational-groupUniversity Institutes and Centers
pubs.publication-statusPublished online
pubs.volume4

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