Cognitive dysfunction in relation to topography and burden of cerebral microbleeds

dc.authorid0000-0003-3448-9249en_US
dc.authorid0000-0002-6291-0312en_US
dc.authorid0000-0002-6404-4403en_US
dc.authorid0000-0002-0223-9336en_US
dc.authorid0000-0002-6527-4139en_US
dc.authorid0000-0002-7267-1431en_US
dc.contributor.authorBüyükşerbetçi, Gülseren
dc.contributor.authorSaka, Esen
dc.contributor.authorOğuz, Kader Karlı
dc.contributor.authorGöçmen, Rahşan
dc.contributor.authorArsava, Ethem Murat
dc.contributor.authorTopçuoğlu, Mehmet Akif
dc.date.accessioned2019-08-05T07:52:42Z
dc.date.available2019-08-05T07:52:42Z
dc.date.issued2018en_US
dc.departmentFakülteler, Tıp Fakültesi, Dahili Tıp Bilimleri Bölümüen_US
dc.descriptionBüyükşerbetçi, Gülseren (Balikesir Author)en_US
dc.description.abstractIntroduction: Contribution of cerebral microbleeds (CMBs) on cognitive dysfunctions in elderly patients with otherwise asymptomatic white matter lesions (WMLs) is not well-documented. Methods: MRI parameters of cerebral atrophy. CMBs and WMLs were herein analyzed in relation to global and main domains (attention, executive, memory, visuospatial, language) of cognitive function. Eightyfive patients older than 50, without neurodegenerative/cerebrovascular disease, but had CMBs were recruited from 2562 with T2*-gradient-echo MR imaging during one-year period. Results: Global cognition, evaluated by mini-mental status examination (MMSE), was impaired (score <= 24) in 42%. In contrast to CMBs load, WML burden and temporal atrophy were significantly higher in cases with MMSE <= 24. Cholinergic Pathways Hyperintensities Scale (CHIPS) was positively correlated with global cognitive dysfunction but its CMB counterpart, Cholinergic Pathways Bleeding Scale described herein, was not. However, burden of CMBs in thalamic/cortical regions predicted language dysfunction. Conclusion: Cognitive dysfunction associated with CMBs may be dependent on their distribution rather than their absolute number.en_US
dc.identifier.doi10.29399/npa.23018
dc.identifier.endpage90en_US
dc.identifier.issn1300-0667
dc.identifier.issn1309-4866
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-85044334169
dc.identifier.scopusqualityQ3
dc.identifier.startpage84en_US
dc.identifier.trdizinid308319
dc.identifier.urihttps://doi.org/10.29399/npa.23018
dc.identifier.urihttps://hdl.handle.net/20.500.12462/5796
dc.identifier.volume55en_US
dc.identifier.wosWOS:000450095400015
dc.identifier.wosqualityQ4
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.publisherAvesen_US
dc.relation.ispartofNoropsikiyatri Arsivi-Archives of Neuropsychiatryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.subjectCholinergicen_US
dc.subjectDementiaen_US
dc.subjectMicrobleeden_US
dc.subjectLacuneen_US
dc.subjectWhite Matteren_US
dc.subjectCortexen_US
dc.subjectCorticalen_US
dc.subjectMagnetic Resonance İmagingen_US
dc.subjectGradient Echoen_US
dc.titleCognitive dysfunction in relation to topography and burden of cerebral microbleedsen_US
dc.typeArticleen_US

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