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Diagonal Earlobe Crease is a Visible Sign for Cerebral Small Vessel Disease and Amyloid-β

We investigated the frequency and clinical significance of diagonal earlobe crease (DELC) in cognitively impaired patients using imaging biomarkers, such as white matter hyperintensities (WMH) on MRI and amyloid-β (Aβ) PET. A total of 471 cognitively impaired patients and 243 cognitively normal (CN)...

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Autores principales: Lee, Jin San, Park, Seongbeom, Kim, Hee Jin, Kim, Yeshin, Jang, Hyemin, Kim, Ko Woon, Rhee, Hak Young, Yoon, Sung Sang, Hwang, Kyoung Jin, Park, Key-Chung, Moon, Seung Hwan, Kim, Sung Tae, Lockhart, Samuel N., Na, Duk L., Seo, Sang Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645376/
https://www.ncbi.nlm.nih.gov/pubmed/29042572
http://dx.doi.org/10.1038/s41598-017-13370-8
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author Lee, Jin San
Park, Seongbeom
Kim, Hee Jin
Kim, Yeshin
Jang, Hyemin
Kim, Ko Woon
Rhee, Hak Young
Yoon, Sung Sang
Hwang, Kyoung Jin
Park, Key-Chung
Moon, Seung Hwan
Kim, Sung Tae
Lockhart, Samuel N.
Na, Duk L.
Seo, Sang Won
author_facet Lee, Jin San
Park, Seongbeom
Kim, Hee Jin
Kim, Yeshin
Jang, Hyemin
Kim, Ko Woon
Rhee, Hak Young
Yoon, Sung Sang
Hwang, Kyoung Jin
Park, Key-Chung
Moon, Seung Hwan
Kim, Sung Tae
Lockhart, Samuel N.
Na, Duk L.
Seo, Sang Won
author_sort Lee, Jin San
collection PubMed
description We investigated the frequency and clinical significance of diagonal earlobe crease (DELC) in cognitively impaired patients using imaging biomarkers, such as white matter hyperintensities (WMH) on MRI and amyloid-β (Aβ) PET. A total of 471 cognitively impaired patients and 243 cognitively normal (CN) individuals were included in this study. Compared with CN individuals, cognitively impaired patients had a greater frequency of DELC (OR 1.6, 95% CI 1.1–2.2, P = 0.007). This relationship was more prominent in patients with dementia (OR 1.8, 95% CI 1.2–2.7, P = 0.002) and subcortical vascular cognitive impairment (OR 2.4, 95% CI 1.6–3.6, P < 0.001). Compared with Aβ-negative cognitively impaired patients with minimal WMH, Aβ-positive patients with moderate to severe WMH were significantly more likely to exhibit DELC (OR 7.3, 95% CI 3.4–16.0, P < 0.001). We suggest that DELC can serve as a useful supportive sign, not only for the presence of cognitive impairment, but also for cerebral small vessel disease (CSVD) and Aβ-positivity. The relationship between DELC and Aβ-positivity might be explained by the causative role of CSVD in Aβ accumulation.
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spelling pubmed-56453762017-10-26 Diagonal Earlobe Crease is a Visible Sign for Cerebral Small Vessel Disease and Amyloid-β Lee, Jin San Park, Seongbeom Kim, Hee Jin Kim, Yeshin Jang, Hyemin Kim, Ko Woon Rhee, Hak Young Yoon, Sung Sang Hwang, Kyoung Jin Park, Key-Chung Moon, Seung Hwan Kim, Sung Tae Lockhart, Samuel N. Na, Duk L. Seo, Sang Won Sci Rep Article We investigated the frequency and clinical significance of diagonal earlobe crease (DELC) in cognitively impaired patients using imaging biomarkers, such as white matter hyperintensities (WMH) on MRI and amyloid-β (Aβ) PET. A total of 471 cognitively impaired patients and 243 cognitively normal (CN) individuals were included in this study. Compared with CN individuals, cognitively impaired patients had a greater frequency of DELC (OR 1.6, 95% CI 1.1–2.2, P = 0.007). This relationship was more prominent in patients with dementia (OR 1.8, 95% CI 1.2–2.7, P = 0.002) and subcortical vascular cognitive impairment (OR 2.4, 95% CI 1.6–3.6, P < 0.001). Compared with Aβ-negative cognitively impaired patients with minimal WMH, Aβ-positive patients with moderate to severe WMH were significantly more likely to exhibit DELC (OR 7.3, 95% CI 3.4–16.0, P < 0.001). We suggest that DELC can serve as a useful supportive sign, not only for the presence of cognitive impairment, but also for cerebral small vessel disease (CSVD) and Aβ-positivity. The relationship between DELC and Aβ-positivity might be explained by the causative role of CSVD in Aβ accumulation. Nature Publishing Group UK 2017-10-17 /pmc/articles/PMC5645376/ /pubmed/29042572 http://dx.doi.org/10.1038/s41598-017-13370-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Lee, Jin San
Park, Seongbeom
Kim, Hee Jin
Kim, Yeshin
Jang, Hyemin
Kim, Ko Woon
Rhee, Hak Young
Yoon, Sung Sang
Hwang, Kyoung Jin
Park, Key-Chung
Moon, Seung Hwan
Kim, Sung Tae
Lockhart, Samuel N.
Na, Duk L.
Seo, Sang Won
Diagonal Earlobe Crease is a Visible Sign for Cerebral Small Vessel Disease and Amyloid-β
title Diagonal Earlobe Crease is a Visible Sign for Cerebral Small Vessel Disease and Amyloid-β
title_full Diagonal Earlobe Crease is a Visible Sign for Cerebral Small Vessel Disease and Amyloid-β
title_fullStr Diagonal Earlobe Crease is a Visible Sign for Cerebral Small Vessel Disease and Amyloid-β
title_full_unstemmed Diagonal Earlobe Crease is a Visible Sign for Cerebral Small Vessel Disease and Amyloid-β
title_short Diagonal Earlobe Crease is a Visible Sign for Cerebral Small Vessel Disease and Amyloid-β
title_sort diagonal earlobe crease is a visible sign for cerebral small vessel disease and amyloid-β
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5645376/
https://www.ncbi.nlm.nih.gov/pubmed/29042572
http://dx.doi.org/10.1038/s41598-017-13370-8
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