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Olfactory testing in consecutive patients referred with suspected dementia
BACKGROUND: Alzheimer’s disease (AD) is the most common cause of dementia and early and accurate diagnosis is important. Olfactory dysfunction is an early sign of AD. The contribution by test of olfactory function has been surveyed in AD vs a line of conditions but remains to be settled in the worku...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477688/ https://www.ncbi.nlm.nih.gov/pubmed/28633628 http://dx.doi.org/10.1186/s12877-017-0516-2 |
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author | Christensen, Ib Thrane Larsson, Elna-Marie Holm, Ida E. Nielsen, Ole B.F. Andersen, Stig |
author_facet | Christensen, Ib Thrane Larsson, Elna-Marie Holm, Ida E. Nielsen, Ole B.F. Andersen, Stig |
author_sort | Christensen, Ib Thrane |
collection | PubMed |
description | BACKGROUND: Alzheimer’s disease (AD) is the most common cause of dementia and early and accurate diagnosis is important. Olfactory dysfunction is an early sign of AD. The contribution by test of olfactory function has been surveyed in AD vs a line of conditions but remains to be settled in the workup of unselected patients referred with suspected dementia. METHODS: We performed a two-step investigation: first, a comparative study of healthy controls and probable AD patients to test the applicability of the chosen scents (cuisine study); second, a study of consecutive patients referred to our geriatric outpatient clinic for suspected dementia with the investigating personnel blinded to the results of the Olfactory Test (blinded study). RESULTS: The sum of scents detected discriminated patients with probable AD from controls in the cuisine study (n = 40; p < 0.001; area under ROC curve 0.94). In the blinded study (n = 50) the diagnosis was probable AD in 48%, minimal cognitive impairment in 24%, vascular dementia in 8%, alcohol induced impairment in 12%, depression in 4%, and Parkinson’s disease and Lewy body dementia in 2%. Area under the ROC-curve was 0.67. The odds ratio for probable AD with 2+ smell errors was 12 (95%-CI: 1.3–101; p = 0.026 (reference 0–1 smell errors)) age adjusted. None in the AD group had zero smell errors (Negative Predictive Value 100%). CONCLUSION: Olfactory testing may support to dismiss the diagnosis of probable AD in the workup of a mixed group of patients referred with cognitive impairment. Still, it had a low sensitivity for probable AD. |
format | Online Article Text |
id | pubmed-5477688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-54776882017-06-23 Olfactory testing in consecutive patients referred with suspected dementia Christensen, Ib Thrane Larsson, Elna-Marie Holm, Ida E. Nielsen, Ole B.F. Andersen, Stig BMC Geriatr Research Article BACKGROUND: Alzheimer’s disease (AD) is the most common cause of dementia and early and accurate diagnosis is important. Olfactory dysfunction is an early sign of AD. The contribution by test of olfactory function has been surveyed in AD vs a line of conditions but remains to be settled in the workup of unselected patients referred with suspected dementia. METHODS: We performed a two-step investigation: first, a comparative study of healthy controls and probable AD patients to test the applicability of the chosen scents (cuisine study); second, a study of consecutive patients referred to our geriatric outpatient clinic for suspected dementia with the investigating personnel blinded to the results of the Olfactory Test (blinded study). RESULTS: The sum of scents detected discriminated patients with probable AD from controls in the cuisine study (n = 40; p < 0.001; area under ROC curve 0.94). In the blinded study (n = 50) the diagnosis was probable AD in 48%, minimal cognitive impairment in 24%, vascular dementia in 8%, alcohol induced impairment in 12%, depression in 4%, and Parkinson’s disease and Lewy body dementia in 2%. Area under the ROC-curve was 0.67. The odds ratio for probable AD with 2+ smell errors was 12 (95%-CI: 1.3–101; p = 0.026 (reference 0–1 smell errors)) age adjusted. None in the AD group had zero smell errors (Negative Predictive Value 100%). CONCLUSION: Olfactory testing may support to dismiss the diagnosis of probable AD in the workup of a mixed group of patients referred with cognitive impairment. Still, it had a low sensitivity for probable AD. BioMed Central 2017-06-20 /pmc/articles/PMC5477688/ /pubmed/28633628 http://dx.doi.org/10.1186/s12877-017-0516-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Christensen, Ib Thrane Larsson, Elna-Marie Holm, Ida E. Nielsen, Ole B.F. Andersen, Stig Olfactory testing in consecutive patients referred with suspected dementia |
title | Olfactory testing in consecutive patients referred with suspected dementia |
title_full | Olfactory testing in consecutive patients referred with suspected dementia |
title_fullStr | Olfactory testing in consecutive patients referred with suspected dementia |
title_full_unstemmed | Olfactory testing in consecutive patients referred with suspected dementia |
title_short | Olfactory testing in consecutive patients referred with suspected dementia |
title_sort | olfactory testing in consecutive patients referred with suspected dementia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5477688/ https://www.ncbi.nlm.nih.gov/pubmed/28633628 http://dx.doi.org/10.1186/s12877-017-0516-2 |
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