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Homocysteine as a Risk Factor for Cognitive Impairment in Stroke Patients

dc.contributor.authorSachdev, Perminder Singh
dc.contributor.authorValenzuela, Michael
dc.contributor.authorBrodaty, Henry
dc.contributor.authorWang, Xing
dc.contributor.authorLooi, Jeffrey
dc.contributor.authorLorentz, Lisa
dc.contributor.authorHoward, Lesley
dc.contributor.authorJones, Megan
dc.contributor.authorZagami, Alessandro
dc.contributor.authorGillies, David
dc.contributor.authorWilcken, David
dc.date.accessioned2015-12-13T22:36:58Z
dc.date.available2015-12-13T22:36:58Z
dc.date.issued2003
dc.date.updated2015-12-11T09:34:26Z
dc.description.abstractBackground: Elevated total homocysteine (tHcy) levels are associated with an increased risk of cerebrovascular disease. It is uncertain whether tHcy is also an independent risk factor for cognitive impairment. Methods: We examined 95 stroke subjects 3 months after their strokes, and 55 healthy comparison subjects, with a detailed neuropsychological assessment, and MRI brain scans in a proportion (n = 97). Baseline measurements of tHcy, serum folate and B12, creatinine and plasma fibrinogen levels were obtained. Results: tHcy levels were higher in the stroke subjects by a mean 34%. These levels were significantly correlated with the first factor of a principal component analysis of the neuropsychological data, after controlling for age, folate, B12 and creatinine levels. The correlation of Hcy levels was particularly significant with frontal-executive functioning and attention. tHcy levels were significantly correlated with number of infarcts and total stroke volume in the stroke group, but not with T2-weighted deep white matter hyperintensity scores, after correction for age. In the control group, tHcy levels were significantly correlated with ventricle-to-brain ratios as measures of brain atrophy. Conclusion: This study provides evidence that high tHcy levels are associated with cognitive impairment, in particular that of frontal-executive function. The major component of this association is accounted for by small and large strokes, but non-vascular neurotoxic effects of tHcy also appear to play a role. tHcy must receive greater attention as a risk factor for cognitive impairment.
dc.identifier.issn1420-8008
dc.identifier.urihttp://hdl.handle.net/1885/77025
dc.publisherS Karger AG
dc.sourceDementia and Geriatric Cognitive Disorders
dc.subjectKeywords: creatinine; cyanocobalamin; fibrinogen; folic acid; homocysteine; adult; age; aged; article; attention; brain atrophy; brain function; brain scintiscanning; cognitive defect; controlled study; correlation analysis; creatinine blood level; female; fibrinog Brain scans; Cognitive impairment; Homocysteine; MRI; Total homocysteine
dc.titleHomocysteine as a Risk Factor for Cognitive Impairment in Stroke Patients
dc.typeJournal article
local.bibliographicCitation.lastpage162
local.bibliographicCitation.startpage155
local.contributor.affiliationSachdev, Perminder Singh, University of New South Wales (Prince of Wales Hospital)
local.contributor.affiliationValenzuela, Michael, University of New South Wales
local.contributor.affiliationBrodaty, Henry, Prince of Wales Hospital
local.contributor.affiliationWang, Xing, University of New South Wales
local.contributor.affiliationLooi, Jeffrey, College of Medicine, Biology and Environment, ANU
local.contributor.affiliationLorentz, Lisa, University of New South Wales
local.contributor.affiliationHoward, Lesley, Prince of Wales Hospital
local.contributor.affiliationJones, Megan, Prince of Wales Hospital
local.contributor.affiliationZagami, Alessandro, Prince of Wales Hospital
local.contributor.affiliationGillies, David, University of New South Wales, ADFA
local.contributor.affiliationWilcken, David, University of New South Wales
local.contributor.authoruidLooi, Jeffrey, u4593152
local.description.notesImported from ARIES
local.description.refereedYes
local.identifier.absfor110319 - Psychiatry (incl. Psychotherapy)
local.identifier.absfor110999 - Neurosciences not elsewhere classified
local.identifier.ariespublicationMigratedxPub5871
local.identifier.citationvolume15
local.identifier.doi10.1159/000068481
local.identifier.scopusID2-s2.0-12244287634
local.type.statusPublished Version

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