Comparison of Brief Cognitive Tests and CSF Biomarkers in Predicting Alzheimer's Disease in Mild Cognitive Impairment: Six-Year Follow-Up Study.
(2012) In PLoS ONE 7(6).- Abstract
- INTRODUCTION:
Early identification of Alzheimer's disease (AD) is needed both for clinical trials and in clinical practice. In this study, we compared brief cognitive tests and cerebrospinal fluid (CSF) biomarkers in predicting conversion from mild cognitive impairment (MCI) to AD.
METHODS:
At a memory clinic, 133 patients with MCI were followed until development of dementia or until they had been stable over a mean period of 5.9 years (range 3.2-8.8 years). The Mini-Mental State Examination (MMSE), the clock drawing test, total tau, tau phosphorylated at Thr(181) (P-tau) and amyloid-β(1-42) (Aβ(42)) were assessed at baseline.
RESULTS:
During clinical follow-up, 47% remained... (More) - INTRODUCTION:
Early identification of Alzheimer's disease (AD) is needed both for clinical trials and in clinical practice. In this study, we compared brief cognitive tests and cerebrospinal fluid (CSF) biomarkers in predicting conversion from mild cognitive impairment (MCI) to AD.
METHODS:
At a memory clinic, 133 patients with MCI were followed until development of dementia or until they had been stable over a mean period of 5.9 years (range 3.2-8.8 years). The Mini-Mental State Examination (MMSE), the clock drawing test, total tau, tau phosphorylated at Thr(181) (P-tau) and amyloid-β(1-42) (Aβ(42)) were assessed at baseline.
RESULTS:
During clinical follow-up, 47% remained cognitively stable and 53% developed dementia, with an incidence of 13.8%/year. In the group that developed dementia the prevalence of AD was 73.2%, vascular dementia 14.1%, dementia with Lewy bodies (DLB) 5.6%, progressive supranuclear palsy (PSP) 4.2%, semantic dementia 1.4% and dementia due to brain tumour 1.4%. When predicting subsequent development of AD among patients with MCI, the cognitive tests classified 81% of the cases correctly (AUC, 0.85; 95% CI, 0.77-0.90) and CSF biomarkers 83% (AUC, 0.89; 95% CI, 0.82-0.94). The combination of cognitive tests and CSF (AUC, 0.93; 95% CI 0.87 to 0.96) was significantly better than the cognitive tests (p = 0.01) and the CSF biomarkers (p = 0.04) alone when predicting AD.
CONCLUSIONS:
The MMSE and the clock drawing test were as accurate as CSF biomarkers in predicting future development of AD in patients with MCI. Combining both instruments provided significantly greater accuracy than cognitive tests or CSF biomarkers alone in predicting AD. (Less)
Please use this url to cite or link to this publication:
https://lup.lub.lu.se/record/2967492
- author
- Palmqvist, Sebastian LU ; Hertze, Joakim LU ; Minthon, Lennart LU ; Wattmo, Carina LU ; Zetterberg, Henrik ; Blennow, Kaj ; Londos, Elisabet LU and Hansson, Oskar LU
- organization
- publishing date
- 2012
- type
- Contribution to journal
- publication status
- published
- subject
- in
- PLoS ONE
- volume
- 7
- issue
- 6
- article number
- e38639
- publisher
- Public Library of Science (PLoS)
- external identifiers
-
- wos:000305730900015
- pmid:22761691
- scopus:84862676596
- ISSN
- 1932-6203
- DOI
- 10.1371/journal.pone.0038639
- language
- English
- LU publication?
- yes
- id
- 422b84d0-d1e9-48cb-82a4-efbbed5b0747 (old id 2967492)
- alternative location
- http://www.ncbi.nlm.nih.gov/pubmed/22761691?dopt=Abstract
- date added to LUP
- 2016-04-01 14:19:36
- date last changed
- 2022-05-19 23:57:06
@article{422b84d0-d1e9-48cb-82a4-efbbed5b0747, abstract = {{INTRODUCTION:<br/><br> Early identification of Alzheimer's disease (AD) is needed both for clinical trials and in clinical practice. In this study, we compared brief cognitive tests and cerebrospinal fluid (CSF) biomarkers in predicting conversion from mild cognitive impairment (MCI) to AD.<br/><br> <br/><br> METHODS:<br/><br> At a memory clinic, 133 patients with MCI were followed until development of dementia or until they had been stable over a mean period of 5.9 years (range 3.2-8.8 years). The Mini-Mental State Examination (MMSE), the clock drawing test, total tau, tau phosphorylated at Thr(181) (P-tau) and amyloid-β(1-42) (Aβ(42)) were assessed at baseline.<br/><br> <br/><br> RESULTS:<br/><br> During clinical follow-up, 47% remained cognitively stable and 53% developed dementia, with an incidence of 13.8%/year. In the group that developed dementia the prevalence of AD was 73.2%, vascular dementia 14.1%, dementia with Lewy bodies (DLB) 5.6%, progressive supranuclear palsy (PSP) 4.2%, semantic dementia 1.4% and dementia due to brain tumour 1.4%. When predicting subsequent development of AD among patients with MCI, the cognitive tests classified 81% of the cases correctly (AUC, 0.85; 95% CI, 0.77-0.90) and CSF biomarkers 83% (AUC, 0.89; 95% CI, 0.82-0.94). The combination of cognitive tests and CSF (AUC, 0.93; 95% CI 0.87 to 0.96) was significantly better than the cognitive tests (p = 0.01) and the CSF biomarkers (p = 0.04) alone when predicting AD.<br/><br> <br/><br> CONCLUSIONS:<br/><br> The MMSE and the clock drawing test were as accurate as CSF biomarkers in predicting future development of AD in patients with MCI. Combining both instruments provided significantly greater accuracy than cognitive tests or CSF biomarkers alone in predicting AD.}}, author = {{Palmqvist, Sebastian and Hertze, Joakim and Minthon, Lennart and Wattmo, Carina and Zetterberg, Henrik and Blennow, Kaj and Londos, Elisabet and Hansson, Oskar}}, issn = {{1932-6203}}, language = {{eng}}, number = {{6}}, publisher = {{Public Library of Science (PLoS)}}, series = {{PLoS ONE}}, title = {{Comparison of Brief Cognitive Tests and CSF Biomarkers in Predicting Alzheimer's Disease in Mild Cognitive Impairment: Six-Year Follow-Up Study.}}, url = {{https://lup.lub.lu.se/search/files/3912628/3350466.pdf}}, doi = {{10.1371/journal.pone.0038639}}, volume = {{7}}, year = {{2012}}, }