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Associations between apolipoprotein E phenotype, glucose metabolism and cognitive function in men. An explorative study in a population sample

dc.contributor.authorHelkala, E. L.en_US
dc.contributor.authorLakka, T. A. (Timo A.)en_US
dc.contributor.authorVanhanen, M.en_US
dc.contributor.authorTuomainen, T. P.en_US
dc.contributor.authorEhnholm, Christianen_US
dc.contributor.authorKaplan, George A.en_US
dc.contributor.authorSalonen, Jukka T.en_US
dc.date.accessioned2010-06-01T19:46:23Z
dc.date.available2010-06-01T19:46:23Z
dc.date.issued2001-12en_US
dc.identifier.citationHelkala, E-L.; Lakka, T.; Vanhanen, M.; Tuomainen, T-P.; Ehnholm, C.; Kaplan, G.A.; Salonen, J.T. (2001). "Associations between apolipoprotein E phenotype, glucose metabolism and cognitive function in men. An explorative study in a population sample." Diabetic Medicine 18(12): 991-997. <http://hdl.handle.net/2027.42/72906>en_US
dc.identifier.issn0742-3071en_US
dc.identifier.issn1464-5491en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/72906
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=11903399&dopt=citationen_US
dc.description.abstractAims  To investigate the associations of the apolipoprotein E phenotype (apoE) and disturbed glucose metabolism with cognitive function in a random population sample. Methods  A cross-sectional study was conducted, in which 528 men aged 54 or 60 years were recruited randomly from a larger population-based sample of 1516 men. A subject was defined as having abnormal glucose tolerance (AGT), if he had a clinical diagnosis of diabetes, with either dietary or oral antidiabetic treatment or showed impaired glucose tolerance in an oral glucose tolerance test. The subjects were divided into three groups according to apolipoprotein E phenotypes: (a) E2/4, E3/4 or E4/4 (apoE E4); (b) E 3/3 (apoE E3); and (c) E2/2 or E2/3 (apoE E2). Memory function was examined using a word-list learning with Buschke's selective reminding method and test. Executive functions were assessed with the Trail Making Test A and B. Results  Those subjects with apoE E2 and abnormal glucose metabolism demonstrated the worst cognitive executive control compared to other groups. Simple cognitive speed did not differ between the groups. Conclusions  The exploratory analyses revealed that subjects with apoE E2 allele and AGT had worse glycaemic control and cognitive executive control compared to other groups. Different apolipoprotein phenotypes together with impaired glucose tolerance may have different cumulative adverse effects on age-related cognitive performance. Some subgroups of subjects may be especially vulnerable to cognitive impairment. Diabet. Med. 18, 991–997 (2001)en_US
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dc.publisherBlackwell Science Ltden_US
dc.rightsBritish Diabetic Associationen_US
dc.subject.otherCognitive Functionsen_US
dc.subject.otherGlucose Metabolismen_US
dc.subject.otherApolipoprotein E Phenotypeen_US
dc.titleAssociations between apolipoprotein E phenotype, glucose metabolism and cognitive function in men. An explorative study in a population sampleen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMedicine (General)en_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationum†† Department of Epidemiology, University of Michigan, School of Public Health, Ann Arbor, Michigan, USAen_US
dc.contributor.affiliationother* Department of Public Health and General Practice of University of Kuopio, Kuopio, Finland,en_US
dc.contributor.affiliationother† Research Institute of Public Health, University of Kuopio anden_US
dc.contributor.affiliationother† Research Institute of Exercise Medicine, Kuopio,en_US
dc.contributor.affiliationother§ Department of Neurology, University Hospital and University of Kuopio, Kuopio, Finland,en_US
dc.contributor.affiliationother** National Public Health Institute, Helsinki, Finland,en_US
dc.identifier.pmid11903399en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/72906/1/j.0742-3071.2001.00588.x.pdf
dc.identifier.doi10.1046/j.0742-3071.2001.00588.xen_US
dc.identifier.sourceDiabetic Medicineen_US
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dc.owningcollnameInterdisciplinary and Peer-Reviewed


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