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Early diagnosis of Alzheimer’s disease from elevated olfactory mucosal miR-206 level

MicroRNA-206, which suppresses the expression of brain-derived neurotrophic factor, is known to be elevated in the brains of Alzheimer’s disease (AD) patients. We performed intranasal biopsy of the olfactory epithelia of early dementia patients (n = 24) and cognitively healthy controls (n = 9). Pati...

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Autores principales: Moon, Jangsup, Lee, Soon-Tae, Kong, Il Gyu, Byun, Jung-Ick, Sunwoo, Jun-Sang, Shin, Jung-Won, Shim, Ji-Young, Park, Ji-Hyun, Jeon, Daejong, Jung, Keun-Hwa, Jung, Ki-Young, Kim, Dong-Young, Lee, Sang Kun, Kim, Manho, Chu, Kon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740889/
https://www.ncbi.nlm.nih.gov/pubmed/26842588
http://dx.doi.org/10.1038/srep20364
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author Moon, Jangsup
Lee, Soon-Tae
Kong, Il Gyu
Byun, Jung-Ick
Sunwoo, Jun-Sang
Shin, Jung-Won
Shim, Ji-Young
Park, Ji-Hyun
Jeon, Daejong
Jung, Keun-Hwa
Jung, Ki-Young
Kim, Dong-Young
Lee, Sang Kun
Kim, Manho
Chu, Kon
author_facet Moon, Jangsup
Lee, Soon-Tae
Kong, Il Gyu
Byun, Jung-Ick
Sunwoo, Jun-Sang
Shin, Jung-Won
Shim, Ji-Young
Park, Ji-Hyun
Jeon, Daejong
Jung, Keun-Hwa
Jung, Ki-Young
Kim, Dong-Young
Lee, Sang Kun
Kim, Manho
Chu, Kon
author_sort Moon, Jangsup
collection PubMed
description MicroRNA-206, which suppresses the expression of brain-derived neurotrophic factor, is known to be elevated in the brains of Alzheimer’s disease (AD) patients. We performed intranasal biopsy of the olfactory epithelia of early dementia patients (n = 24) and cognitively healthy controls (n = 9). Patients with significant depression (n = 8) were analyzed separately, as their cognitive impairments were thought to be caused by their depression. Real-time PCR was performed on the biopsied tissues. The relative microRNA-206 level exhibited a 7.8-fold increase (P = 0.004) in the mild cognitive impairment group (CDR 0.5; n = 13) and a 41.5-fold increase (P < 0.001) in the CDR 1 group (n = 11). However, this level was not increased in the depression group, even in those with cognitive decline. Using the optimal cutoff value, the sensitivity/specificity for diagnosing CDR 0.5 and CDR 1 dementia were 87.5%/94.1% and 90.9%/93.3%, respectively. In ROC analysis, the AUCs were 0.942 and 0.976 in the CDR 0.5 and CDR 1 groups, respectively. The olfactory mucosal microRNA-206 level and cognitive assessment scores were significantly correlated in the non-depressed subjects with cognitive impairment. In conclusion, the olfactory mucosal microRNA-206 level can be easily measured, and it can be utilized as an excellent biomarker for the diagnosis of early AD, including mild cognitive impairment.
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spelling pubmed-47408892016-02-09 Early diagnosis of Alzheimer’s disease from elevated olfactory mucosal miR-206 level Moon, Jangsup Lee, Soon-Tae Kong, Il Gyu Byun, Jung-Ick Sunwoo, Jun-Sang Shin, Jung-Won Shim, Ji-Young Park, Ji-Hyun Jeon, Daejong Jung, Keun-Hwa Jung, Ki-Young Kim, Dong-Young Lee, Sang Kun Kim, Manho Chu, Kon Sci Rep Article MicroRNA-206, which suppresses the expression of brain-derived neurotrophic factor, is known to be elevated in the brains of Alzheimer’s disease (AD) patients. We performed intranasal biopsy of the olfactory epithelia of early dementia patients (n = 24) and cognitively healthy controls (n = 9). Patients with significant depression (n = 8) were analyzed separately, as their cognitive impairments were thought to be caused by their depression. Real-time PCR was performed on the biopsied tissues. The relative microRNA-206 level exhibited a 7.8-fold increase (P = 0.004) in the mild cognitive impairment group (CDR 0.5; n = 13) and a 41.5-fold increase (P < 0.001) in the CDR 1 group (n = 11). However, this level was not increased in the depression group, even in those with cognitive decline. Using the optimal cutoff value, the sensitivity/specificity for diagnosing CDR 0.5 and CDR 1 dementia were 87.5%/94.1% and 90.9%/93.3%, respectively. In ROC analysis, the AUCs were 0.942 and 0.976 in the CDR 0.5 and CDR 1 groups, respectively. The olfactory mucosal microRNA-206 level and cognitive assessment scores were significantly correlated in the non-depressed subjects with cognitive impairment. In conclusion, the olfactory mucosal microRNA-206 level can be easily measured, and it can be utilized as an excellent biomarker for the diagnosis of early AD, including mild cognitive impairment. Nature Publishing Group 2016-02-04 /pmc/articles/PMC4740889/ /pubmed/26842588 http://dx.doi.org/10.1038/srep20364 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Moon, Jangsup
Lee, Soon-Tae
Kong, Il Gyu
Byun, Jung-Ick
Sunwoo, Jun-Sang
Shin, Jung-Won
Shim, Ji-Young
Park, Ji-Hyun
Jeon, Daejong
Jung, Keun-Hwa
Jung, Ki-Young
Kim, Dong-Young
Lee, Sang Kun
Kim, Manho
Chu, Kon
Early diagnosis of Alzheimer’s disease from elevated olfactory mucosal miR-206 level
title Early diagnosis of Alzheimer’s disease from elevated olfactory mucosal miR-206 level
title_full Early diagnosis of Alzheimer’s disease from elevated olfactory mucosal miR-206 level
title_fullStr Early diagnosis of Alzheimer’s disease from elevated olfactory mucosal miR-206 level
title_full_unstemmed Early diagnosis of Alzheimer’s disease from elevated olfactory mucosal miR-206 level
title_short Early diagnosis of Alzheimer’s disease from elevated olfactory mucosal miR-206 level
title_sort early diagnosis of alzheimer’s disease from elevated olfactory mucosal mir-206 level
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4740889/
https://www.ncbi.nlm.nih.gov/pubmed/26842588
http://dx.doi.org/10.1038/srep20364
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