Cargando…
The relationship between cerebrospinal fluid tau markers, hippocampal volume, and delayed primacy performance in cognitively intact elderly individuals
BACKGROUND: Primacy performance in recall has been shown to predict cognitive decline in cognitively intact elderly and conversion from mild cognitive impairment to Alzheimer's disease (AD). Delayed primacy performance, but not delayed nonprimacy performance, has been shown to be associated wit...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527326/ https://www.ncbi.nlm.nih.gov/pubmed/26258161 http://dx.doi.org/10.1016/j.dadm.2014.11.002 |
_version_ | 1782384555684003840 |
---|---|
author | Bruno, Davide Grothe, Michel J. Nierenberg, Jay Teipel, Stefan J. Zetterberg, Henrik Blennow, Kaj Pomara, Nunzio |
author_facet | Bruno, Davide Grothe, Michel J. Nierenberg, Jay Teipel, Stefan J. Zetterberg, Henrik Blennow, Kaj Pomara, Nunzio |
author_sort | Bruno, Davide |
collection | PubMed |
description | BACKGROUND: Primacy performance in recall has been shown to predict cognitive decline in cognitively intact elderly and conversion from mild cognitive impairment to Alzheimer's disease (AD). Delayed primacy performance, but not delayed nonprimacy performance, has been shown to be associated with hippocampal volume in cognitively intact older individuals. Because presence of neurofibrillary tangles is an early sign of AD-related pathology, we set out to test whether cerebrospinal fluid (CSF) levels of tau had an effect on delayed primacy performance, while controlling for hippocampal volume and CSF amyloid-β 1-42 levels. METHODS: Forty-seven individuals, aged 60 years or older and cognitively intact, underwent a multisession study including lumbar puncture, a magnetic resonance imaging (MRI) scan of the head, and memory testing. RESULTS: Our regression analyses show that CSF levels of hyperphosphorylated (P) tau are only associated with reduced delayed primacy performance when hippocampal volumes are smaller. CONCLUSION: Our findings suggest that hippocampal size may play a protective role against the negative effects of P tau on memory. |
format | Online Article Text |
id | pubmed-4527326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-45273262016-03-01 The relationship between cerebrospinal fluid tau markers, hippocampal volume, and delayed primacy performance in cognitively intact elderly individuals Bruno, Davide Grothe, Michel J. Nierenberg, Jay Teipel, Stefan J. Zetterberg, Henrik Blennow, Kaj Pomara, Nunzio Alzheimers Dement (Amst) Cerebrospinal Fluid Biomarker BACKGROUND: Primacy performance in recall has been shown to predict cognitive decline in cognitively intact elderly and conversion from mild cognitive impairment to Alzheimer's disease (AD). Delayed primacy performance, but not delayed nonprimacy performance, has been shown to be associated with hippocampal volume in cognitively intact older individuals. Because presence of neurofibrillary tangles is an early sign of AD-related pathology, we set out to test whether cerebrospinal fluid (CSF) levels of tau had an effect on delayed primacy performance, while controlling for hippocampal volume and CSF amyloid-β 1-42 levels. METHODS: Forty-seven individuals, aged 60 years or older and cognitively intact, underwent a multisession study including lumbar puncture, a magnetic resonance imaging (MRI) scan of the head, and memory testing. RESULTS: Our regression analyses show that CSF levels of hyperphosphorylated (P) tau are only associated with reduced delayed primacy performance when hippocampal volumes are smaller. CONCLUSION: Our findings suggest that hippocampal size may play a protective role against the negative effects of P tau on memory. Elsevier 2015-03-29 /pmc/articles/PMC4527326/ /pubmed/26258161 http://dx.doi.org/10.1016/j.dadm.2014.11.002 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Cerebrospinal Fluid Biomarker Bruno, Davide Grothe, Michel J. Nierenberg, Jay Teipel, Stefan J. Zetterberg, Henrik Blennow, Kaj Pomara, Nunzio The relationship between cerebrospinal fluid tau markers, hippocampal volume, and delayed primacy performance in cognitively intact elderly individuals |
title | The relationship between cerebrospinal fluid tau markers, hippocampal volume, and delayed primacy performance in cognitively intact elderly individuals |
title_full | The relationship between cerebrospinal fluid tau markers, hippocampal volume, and delayed primacy performance in cognitively intact elderly individuals |
title_fullStr | The relationship between cerebrospinal fluid tau markers, hippocampal volume, and delayed primacy performance in cognitively intact elderly individuals |
title_full_unstemmed | The relationship between cerebrospinal fluid tau markers, hippocampal volume, and delayed primacy performance in cognitively intact elderly individuals |
title_short | The relationship between cerebrospinal fluid tau markers, hippocampal volume, and delayed primacy performance in cognitively intact elderly individuals |
title_sort | relationship between cerebrospinal fluid tau markers, hippocampal volume, and delayed primacy performance in cognitively intact elderly individuals |
topic | Cerebrospinal Fluid Biomarker |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527326/ https://www.ncbi.nlm.nih.gov/pubmed/26258161 http://dx.doi.org/10.1016/j.dadm.2014.11.002 |
work_keys_str_mv | AT brunodavide therelationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT grothemichelj therelationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT nierenbergjay therelationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT teipelstefanj therelationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT zetterberghenrik therelationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT blennowkaj therelationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT pomaranunzio therelationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT brunodavide relationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT grothemichelj relationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT nierenbergjay relationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT teipelstefanj relationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT zetterberghenrik relationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT blennowkaj relationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals AT pomaranunzio relationshipbetweencerebrospinalfluidtaumarkershippocampalvolumeanddelayedprimacyperformanceincognitivelyintactelderlyindividuals |