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The accelerated aging model reveals critical mechanisms of late-onset Parkinson’s disease

BACKGROUND: Late-onset Parkinson’s disease (LOPD) is a common neurodegenerative disorder and lacks disease-modifying treatments, attracting major attentions as the aggravating trend of aging population. There were numerous evidences supported that accelerated aging was the primary risk factor for LO...

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Autores principales: Li, Shiyan, Liu, Hongxin, Bian, Shiyu, Sha, Xianzheng, Li, Yixue, Wang, Yin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288517/
https://www.ncbi.nlm.nih.gov/pubmed/32536974
http://dx.doi.org/10.1186/s13040-020-00215-w
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author Li, Shiyan
Liu, Hongxin
Bian, Shiyu
Sha, Xianzheng
Li, Yixue
Wang, Yin
author_facet Li, Shiyan
Liu, Hongxin
Bian, Shiyu
Sha, Xianzheng
Li, Yixue
Wang, Yin
author_sort Li, Shiyan
collection PubMed
description BACKGROUND: Late-onset Parkinson’s disease (LOPD) is a common neurodegenerative disorder and lacks disease-modifying treatments, attracting major attentions as the aggravating trend of aging population. There were numerous evidences supported that accelerated aging was the primary risk factor for LOPD, thus pointed out that the mechanisms of PD should be revealed thoroughly based on aging acceleration. However, how PD was triggered by accelerated aging remained unclear and the systematic prediction model was needed to study the mechanisms of PD. RESULTS: In this paper, an improved PD predictor was presented by comparing with the normal aging process, and both aging and PD markers were identified herein using machine learning methods. Based on the aging scores, the aging acceleration network was constructed thereby, where the enrichment analysis shed light on key characteristics of LOPD. As a result, dysregulated energy metabolisms, the cell apoptosis, neuroinflammation and the ion imbalances were identified as crucial factors linking accelerated aging and PD coordinately, along with dysfunctions in the immune system. CONCLUSIONS: In short, mechanisms between aging and LOPD were integrated by our computational pipeline.
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spelling pubmed-72885172020-06-11 The accelerated aging model reveals critical mechanisms of late-onset Parkinson’s disease Li, Shiyan Liu, Hongxin Bian, Shiyu Sha, Xianzheng Li, Yixue Wang, Yin BioData Min Research BACKGROUND: Late-onset Parkinson’s disease (LOPD) is a common neurodegenerative disorder and lacks disease-modifying treatments, attracting major attentions as the aggravating trend of aging population. There were numerous evidences supported that accelerated aging was the primary risk factor for LOPD, thus pointed out that the mechanisms of PD should be revealed thoroughly based on aging acceleration. However, how PD was triggered by accelerated aging remained unclear and the systematic prediction model was needed to study the mechanisms of PD. RESULTS: In this paper, an improved PD predictor was presented by comparing with the normal aging process, and both aging and PD markers were identified herein using machine learning methods. Based on the aging scores, the aging acceleration network was constructed thereby, where the enrichment analysis shed light on key characteristics of LOPD. As a result, dysregulated energy metabolisms, the cell apoptosis, neuroinflammation and the ion imbalances were identified as crucial factors linking accelerated aging and PD coordinately, along with dysfunctions in the immune system. CONCLUSIONS: In short, mechanisms between aging and LOPD were integrated by our computational pipeline. BioMed Central 2020-06-10 /pmc/articles/PMC7288517/ /pubmed/32536974 http://dx.doi.org/10.1186/s13040-020-00215-w Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. 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 in a credit line to the data.
spellingShingle Research
Li, Shiyan
Liu, Hongxin
Bian, Shiyu
Sha, Xianzheng
Li, Yixue
Wang, Yin
The accelerated aging model reveals critical mechanisms of late-onset Parkinson’s disease
title The accelerated aging model reveals critical mechanisms of late-onset Parkinson’s disease
title_full The accelerated aging model reveals critical mechanisms of late-onset Parkinson’s disease
title_fullStr The accelerated aging model reveals critical mechanisms of late-onset Parkinson’s disease
title_full_unstemmed The accelerated aging model reveals critical mechanisms of late-onset Parkinson’s disease
title_short The accelerated aging model reveals critical mechanisms of late-onset Parkinson’s disease
title_sort accelerated aging model reveals critical mechanisms of late-onset parkinson’s disease
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7288517/
https://www.ncbi.nlm.nih.gov/pubmed/32536974
http://dx.doi.org/10.1186/s13040-020-00215-w
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