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MTRNR2L12: A Candidate Blood Marker of Early Alzheimer’s Disease-Like Dementia in Adults with Down Syndrome

Morphological abnormalities observed typically in the brains of adults with Down syndrome are identical with those present in patients with Alzheimer’s disease. However, only some adults with Down syndrome suffer from early dementia, whereas others remain unaffected. We aimed to identify the genomic...

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Detalles Bibliográficos
Autores principales: Bik-Multanowski, Miroslaw, Pietrzyk, Jacek J., Midro, Alina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: IOS Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878308/
https://www.ncbi.nlm.nih.gov/pubmed/25720405
http://dx.doi.org/10.3233/JAD-143030
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author Bik-Multanowski, Miroslaw
Pietrzyk, Jacek J.
Midro, Alina
author_facet Bik-Multanowski, Miroslaw
Pietrzyk, Jacek J.
Midro, Alina
author_sort Bik-Multanowski, Miroslaw
collection PubMed
description Morphological abnormalities observed typically in the brains of adults with Down syndrome are identical with those present in patients with Alzheimer’s disease. However, only some adults with Down syndrome suffer from early dementia, whereas others remain unaffected. We aimed to identify the genomic background responsible for this observation. We performed cognitive assessment and genome expression analysis of blood mononuclear cells in seniors with Down syndrome. Unaffected elderly patients and younger patients with severe cognitive disability or cognitive deterioration differed significantly with regard to the MTRNR2L12 gene. Our findings suggest the potential value of this gene as a blood marker of early dementia in individuals with Down syndrome.
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spelling pubmed-48783082016-06-09 MTRNR2L12: A Candidate Blood Marker of Early Alzheimer’s Disease-Like Dementia in Adults with Down Syndrome Bik-Multanowski, Miroslaw Pietrzyk, Jacek J. Midro, Alina J Alzheimers Dis Research Article Morphological abnormalities observed typically in the brains of adults with Down syndrome are identical with those present in patients with Alzheimer’s disease. However, only some adults with Down syndrome suffer from early dementia, whereas others remain unaffected. We aimed to identify the genomic background responsible for this observation. We performed cognitive assessment and genome expression analysis of blood mononuclear cells in seniors with Down syndrome. Unaffected elderly patients and younger patients with severe cognitive disability or cognitive deterioration differed significantly with regard to the MTRNR2L12 gene. Our findings suggest the potential value of this gene as a blood marker of early dementia in individuals with Down syndrome. IOS Press 2015-05-07 /pmc/articles/PMC4878308/ /pubmed/25720405 http://dx.doi.org/10.3233/JAD-143030 Text en IOS Press and the authors. All rights reserved This article is published online with Open Access and distributed under the terms of the Creative Commons Attribution Non-Commercial License.
spellingShingle Research Article
Bik-Multanowski, Miroslaw
Pietrzyk, Jacek J.
Midro, Alina
MTRNR2L12: A Candidate Blood Marker of Early Alzheimer’s Disease-Like Dementia in Adults with Down Syndrome
title MTRNR2L12: A Candidate Blood Marker of Early Alzheimer’s Disease-Like Dementia in Adults with Down Syndrome
title_full MTRNR2L12: A Candidate Blood Marker of Early Alzheimer’s Disease-Like Dementia in Adults with Down Syndrome
title_fullStr MTRNR2L12: A Candidate Blood Marker of Early Alzheimer’s Disease-Like Dementia in Adults with Down Syndrome
title_full_unstemmed MTRNR2L12: A Candidate Blood Marker of Early Alzheimer’s Disease-Like Dementia in Adults with Down Syndrome
title_short MTRNR2L12: A Candidate Blood Marker of Early Alzheimer’s Disease-Like Dementia in Adults with Down Syndrome
title_sort mtrnr2l12: a candidate blood marker of early alzheimer’s disease-like dementia in adults with down syndrome
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4878308/
https://www.ncbi.nlm.nih.gov/pubmed/25720405
http://dx.doi.org/10.3233/JAD-143030
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