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Acute Regression in Down Syndrome
Background: Acute regression has been reported in some individuals with Down syndrome (DS), typically occurring between the teenage years and mid to late 20s. Characterized by sudden, and often unexplained, reductions in language skills, functional living skills and reduced psychomotor activity, som...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391552/ https://www.ncbi.nlm.nih.gov/pubmed/34439728 http://dx.doi.org/10.3390/brainsci11081109 |
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author | Handen, Benjamin Clare, Isabel Laymon, Charles Petersen, Melissa Zaman, Shahid O’Bryant, Sid Minhas, Davneet Tudorascu, Dana Brown, Stephanie Christian, Bradley |
author_facet | Handen, Benjamin Clare, Isabel Laymon, Charles Petersen, Melissa Zaman, Shahid O’Bryant, Sid Minhas, Davneet Tudorascu, Dana Brown, Stephanie Christian, Bradley |
author_sort | Handen, Benjamin |
collection | PubMed |
description | Background: Acute regression has been reported in some individuals with Down syndrome (DS), typically occurring between the teenage years and mid to late 20s. Characterized by sudden, and often unexplained, reductions in language skills, functional living skills and reduced psychomotor activity, some individuals have been incorrectly diagnosed with Alzheimer’s disease (AD). Methods: This paper compares five individuals with DS who previously experienced acute regression with a matched group of 15 unaffected individuals with DS using a set of AD biomarkers. Results: While the sample was too small to conduct statistical analyses, findings suggest there are possible meaningful differences between the groups on proteomics biomarkers (e.g., NfL, total tau). Hippocampal, caudate and putamen volumes were slightly larger in the regression group, the opposite of what was hypothesized. A slightly lower amyloid load was found on the PET scans for the regression group, but no differences were noted on tau PET. Conclusions: Some proteomics biomarker findings suggest that individuals with DS who experience acute regression may be at increased risk for AD at an earlier age in comparison to unaffected adults with DS. However, due to the age of the group (mean 38 years), it may be too early to observe meaningful group differences on image-based biomarkers. |
format | Online Article Text |
id | pubmed-8391552 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83915522021-08-28 Acute Regression in Down Syndrome Handen, Benjamin Clare, Isabel Laymon, Charles Petersen, Melissa Zaman, Shahid O’Bryant, Sid Minhas, Davneet Tudorascu, Dana Brown, Stephanie Christian, Bradley Brain Sci Article Background: Acute regression has been reported in some individuals with Down syndrome (DS), typically occurring between the teenage years and mid to late 20s. Characterized by sudden, and often unexplained, reductions in language skills, functional living skills and reduced psychomotor activity, some individuals have been incorrectly diagnosed with Alzheimer’s disease (AD). Methods: This paper compares five individuals with DS who previously experienced acute regression with a matched group of 15 unaffected individuals with DS using a set of AD biomarkers. Results: While the sample was too small to conduct statistical analyses, findings suggest there are possible meaningful differences between the groups on proteomics biomarkers (e.g., NfL, total tau). Hippocampal, caudate and putamen volumes were slightly larger in the regression group, the opposite of what was hypothesized. A slightly lower amyloid load was found on the PET scans for the regression group, but no differences were noted on tau PET. Conclusions: Some proteomics biomarker findings suggest that individuals with DS who experience acute regression may be at increased risk for AD at an earlier age in comparison to unaffected adults with DS. However, due to the age of the group (mean 38 years), it may be too early to observe meaningful group differences on image-based biomarkers. MDPI 2021-08-23 /pmc/articles/PMC8391552/ /pubmed/34439728 http://dx.doi.org/10.3390/brainsci11081109 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Handen, Benjamin Clare, Isabel Laymon, Charles Petersen, Melissa Zaman, Shahid O’Bryant, Sid Minhas, Davneet Tudorascu, Dana Brown, Stephanie Christian, Bradley Acute Regression in Down Syndrome |
title | Acute Regression in Down Syndrome |
title_full | Acute Regression in Down Syndrome |
title_fullStr | Acute Regression in Down Syndrome |
title_full_unstemmed | Acute Regression in Down Syndrome |
title_short | Acute Regression in Down Syndrome |
title_sort | acute regression in down syndrome |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8391552/ https://www.ncbi.nlm.nih.gov/pubmed/34439728 http://dx.doi.org/10.3390/brainsci11081109 |
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