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dc.contributor.authorEvans, Barbara A.
dc.contributor.authorEvans, James E.
dc.contributor.authorBaker, Stephen P.
dc.contributor.authorKane, Kevin J.
dc.contributor.authorSwearer, Joan M.
dc.contributor.authorHinerfeld, Douglas A.
dc.contributor.authorCaselli, Richard J.
dc.contributor.authorRogaeva, Ekaterina
dc.contributor.authorSt. George-Hyslop, Peter
dc.contributor.authorMoonis, Majaz
dc.contributor.authorPollen, Daniel A.
dc.date2022-08-11T08:09:11.000
dc.date.accessioned2022-08-23T16:20:41Z
dc.date.available2022-08-23T16:20:41Z
dc.date.issued2009-05-30
dc.date.submitted2010-03-11
dc.identifier.citationDement Geriatr Cogn Disord. 2009;27(6):519-24. Epub 2009 May 29. <a href="http://dx.doi.org/10.1159/000221835">Link to article on publisher's site</a>
dc.identifier.issn1420-8008 (Linking)
dc.identifier.doi10.1159/000221835
dc.identifier.pmid19478483
dc.identifier.urihttp://hdl.handle.net/20.500.14038/35338
dc.description.abstractBACKGROUND/AIMS: It is not yet established whether statins (lipophilic or hydrophilic) reduce the risk of Alzheimer's disease and, if so, by differentially modifying brain lipid levels. Our aim was to assess changes in brain cholesterol metabolism as reflected in the cerebrospinal fluid (CSF) before and after treatment with either atorvastatin or simvastatin. METHODS: We carried out a longitudinal analysis of CSF cholesterol, lathosterol and 24(S)-hydroxycholesterol before and after treatment with maximum doses of statins in 10 asymptomatic subjects, 8 of whom were heterozygous for apolipoprotein E epsilon4, and in 6 presymptomatic PS1 subjects. RESULTS: Statins initially reduced CSF lathosterol cholesterol and 24(S)-hydroxycholesterol in both PS1 and non-PS1 subjects reaching a nadir at 6-7 months, followed by a return to baseline at 15 months with an overshoot at 2 years, tending to return to baseline thereafter. CONCLUSIONS: Possible long-term protective effects of statins are not likely largely related to the temporally-dependent biphasic effects of statin therapy upon the magnitude and direction of changes in CSF lipid levels and their subsequent return to baseline levels.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=19478483&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1159/000221835
dc.subjectAdult
dc.subjectAged
dc.subjectAlzheimer Disease
dc.subjectApolipoproteins E
dc.subjectCholesterol
dc.subjectFemale
dc.subjectHeptanoic Acids
dc.subjectHeterozygote
dc.subjectHumans
dc.subjectHydroxycholesterols
dc.subjectHydroxymethylglutaryl-CoA Reductase Inhibitors
dc.subjectMale
dc.subjectMiddle Aged
dc.subjectMutation
dc.subjectPilot Projects
dc.subjectPresenilin-1
dc.subjectPyrroles
dc.subjectSimvastatin
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.subjectTechnology and Innovation
dc.titleLong-term statin therapy and CSF cholesterol levels: implications for Alzheimer's disease
dc.typeJournal Article
dc.source.journaltitleDementia and geriatric cognitive disorders
dc.source.volume27
dc.source.issue6
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/infoservices/86
dc.identifier.contextkey1216191
html.description.abstract<p>BACKGROUND/AIMS: It is not yet established whether statins (lipophilic or hydrophilic) reduce the risk of Alzheimer's disease and, if so, by differentially modifying brain lipid levels. Our aim was to assess changes in brain cholesterol metabolism as reflected in the cerebrospinal fluid (CSF) before and after treatment with either atorvastatin or simvastatin.</p> <p>METHODS: We carried out a longitudinal analysis of CSF cholesterol, lathosterol and 24(S)-hydroxycholesterol before and after treatment with maximum doses of statins in 10 asymptomatic subjects, 8 of whom were heterozygous for apolipoprotein E epsilon4, and in 6 presymptomatic PS1 subjects.</p> <p>RESULTS: Statins initially reduced CSF lathosterol cholesterol and 24(S)-hydroxycholesterol in both PS1 and non-PS1 subjects reaching a nadir at 6-7 months, followed by a return to baseline at 15 months with an overshoot at 2 years, tending to return to baseline thereafter.</p> <p>CONCLUSIONS: Possible long-term protective effects of statins are not likely largely related to the temporally-dependent biphasic effects of statin therapy upon the magnitude and direction of changes in CSF lipid levels and their subsequent return to baseline levels.</p>
dc.identifier.submissionpathinfoservices/86
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.contributor.departmentDepartment of Cell Biology
dc.contributor.departmentInformation Services, Academic Computing Services
dc.contributor.departmentDepartment of Psychiatry
dc.contributor.departmentDepartment of Neurology
dc.source.pages519-24


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