Association of cerebrospinal fluid Aβ42 with A2M gene in cognitively normal subjects

dc.contributor.authorMillard, Steven P.
dc.contributor.authorLutz, Franziska
dc.contributor.authorLi, Ge
dc.contributor.authorGalasko, Douglas R.
dc.contributor.authorFarlow, Martin R.
dc.contributor.authorQuinn, Joseph F.
dc.contributor.authorKaye, Jeffrey A.
dc.contributor.authorLeverenz, James B.
dc.contributor.authorTsuang, Debby
dc.contributor.authorYu, Chang-En
dc.contributor.authorPeskind, Elaine R.
dc.contributor.authorBekris, Lynn M.
dc.contributor.departmentDepartment of Neurology, IU School of Medicineen_US
dc.date.accessioned2016-03-03T15:54:52Z
dc.date.available2016-03-03T15:54:52Z
dc.date.issued2014-02
dc.description.abstractLow cerebrospinal fluid (CSF) Aβ42 levels correlate with increased brain Aβ deposition in Alzheimer’s disease (AD), which suggests a disruption in the degradation and clearance of Aβ from the brain. In addition, APOE ε4 carriers have lower CSF Aβ42 levels than non-carriers. The hypothesis of this investigation was that CSF Aβ42 levels correlate with regulatory region variation in genes that are biologically associated with degradation or clearance of Aβ from the brain. CSF Aβ42 levels were tested for associations with Aβ degradation and clearance genes and APOE ε4. Twenty-four SNPs located within the 5′ and 3′ regions of 12 genes were analyzed. The study sample consisted of 99 AD patients and 168 cognitively normal control subjects. CSF Aβ42 levels were associated with APOE ε4 status in controls but not in AD patientsen_US
dc.description.abstractA2M regulatory region SNPs were also associated with CSF Aβ42 levels in controls, but not in AD patients, even after adjusting for APOE ε4. These results suggest that genetic variation within the A2M gene influences CSF Aβ42 levels.en_US
dc.eprint.versionAuthor's manuscripten_US
dc.identifier.citationMillard, S. P., Lutz, F., Li, G., Galasko, D. R., Farlow, M. R., Quinn, J. F., … Bekris, L. M. (2014). Association of cerebrospinal fluid Aβ42 with A2M gene in cognitively normal subjects. Neurobiology of Aging, 35(2), 10.1016/j.neurobiolaging.2013.07.027. http://doi.org/10.1016/j.neurobiolaging.2013.07.027en_US
dc.identifier.issn0197-4580en_US
dc.identifier.urihttps://hdl.handle.net/1805/8672
dc.language.isoen_USen_US
dc.publisherElsevieren_US
dc.relation.isversionof10.1016/j.neurobiolaging.2013.07.027en_US
dc.relation.journalNeurobiology of agingen_US
dc.rightsPublisher Policyen_US
dc.sourcePMCen_US
dc.subjectAmyloid beta-Peptidesen_US
dc.subjectcerebrospinal fluiden_US
dc.subjectPeptide Fragmentsen_US
dc.subjectcerebrospinal fluiden_US
dc.subjectProteolysisen_US
dc.subjectalpha-Macroglobulinsen_US
dc.subjectgeneticsen_US
dc.titleAssociation of cerebrospinal fluid Aβ42 with A2M gene in cognitively normal subjectsen_US
dc.typeArticleen_US
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