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Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson’s disease
Multiple single nucleotide polymorphisms may contribute to cognitive decline in Parkinson’s disease. However, the mechanism by which these single nucleotide polymorphisms modify brain imaging phenotype remains unclear. The aim of this study was to investigate the potential effects of multiple single...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer - Medknow
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827791/ https://www.ncbi.nlm.nih.gov/pubmed/36255006 http://dx.doi.org/10.4103/1673-5374.355764 |
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author | Shen, Ting Pu, Jia-Li Jiang, Ya-Si Yue, Yu-Mei He, Ting-Ting Qu, Bo-Yi Zhao, Shuai Yan, Ya-Ping Lai, Hsin-Yi Zhang, Bao-Rong |
author_facet | Shen, Ting Pu, Jia-Li Jiang, Ya-Si Yue, Yu-Mei He, Ting-Ting Qu, Bo-Yi Zhao, Shuai Yan, Ya-Ping Lai, Hsin-Yi Zhang, Bao-Rong |
author_sort | Shen, Ting |
collection | PubMed |
description | Multiple single nucleotide polymorphisms may contribute to cognitive decline in Parkinson’s disease. However, the mechanism by which these single nucleotide polymorphisms modify brain imaging phenotype remains unclear. The aim of this study was to investigate the potential effects of multiple single nucleotide polymorphisms on brain imaging phenotype in Parkinson’s disease. Forty-eight Parkinson’s disease patients and 39 matched healthy controls underwent genotyping and 7T magnetic resonance imaging. A cognitive-weighted polygenic risk score model was designed, in which the effect sizes were determined individually for 36 single nucleotide polymorphisms. The correlations between polygenic risk score, neuroimaging features, and clinical data were analyzed. Furthermore, individual single nucleotide polymorphism analysis was performed to explore the main effects of genotypes and their interactive effects with Parkinson’s disease diagnosis. We found that, in Parkinson’s disease, the polygenic risk score was correlated with the neural activity of the hippocampus, parahippocampus, and fusiform gyrus, and with hippocampal-prefrontal and fusiform-temporal connectivity, as well as with gray matter alterations in the orbitofrontal cortex. In addition, we found that single nucleotide polymorphisms in α-synuclein (SNCA) were associated with white matter microstructural changes in the superior corona radiata, corpus callosum, and external capsule. A single nucleotide polymorphism in catechol-O-methyltransferase was associated with the neural activities of the lingual, fusiform, and occipital gyri, which are involved in visual cognitive dysfunction. Furthermore, DRD3 was associated with frontal and temporal lobe function and structure. In conclusion, imaging genetics is useful for providing a better understanding of the genetic pathways involved in the pathophysiologic processes underlying Parkinson’s disease. This study provides evidence of an association between genetic factors, cognitive functions, and multi-modality neuroimaging biomarkers in Parkinson’s disease. |
format | Online Article Text |
id | pubmed-9827791 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Wolters Kluwer - Medknow |
record_format | MEDLINE/PubMed |
spelling | pubmed-98277912023-01-10 Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson’s disease Shen, Ting Pu, Jia-Li Jiang, Ya-Si Yue, Yu-Mei He, Ting-Ting Qu, Bo-Yi Zhao, Shuai Yan, Ya-Ping Lai, Hsin-Yi Zhang, Bao-Rong Neural Regen Res Research Article Multiple single nucleotide polymorphisms may contribute to cognitive decline in Parkinson’s disease. However, the mechanism by which these single nucleotide polymorphisms modify brain imaging phenotype remains unclear. The aim of this study was to investigate the potential effects of multiple single nucleotide polymorphisms on brain imaging phenotype in Parkinson’s disease. Forty-eight Parkinson’s disease patients and 39 matched healthy controls underwent genotyping and 7T magnetic resonance imaging. A cognitive-weighted polygenic risk score model was designed, in which the effect sizes were determined individually for 36 single nucleotide polymorphisms. The correlations between polygenic risk score, neuroimaging features, and clinical data were analyzed. Furthermore, individual single nucleotide polymorphism analysis was performed to explore the main effects of genotypes and their interactive effects with Parkinson’s disease diagnosis. We found that, in Parkinson’s disease, the polygenic risk score was correlated with the neural activity of the hippocampus, parahippocampus, and fusiform gyrus, and with hippocampal-prefrontal and fusiform-temporal connectivity, as well as with gray matter alterations in the orbitofrontal cortex. In addition, we found that single nucleotide polymorphisms in α-synuclein (SNCA) were associated with white matter microstructural changes in the superior corona radiata, corpus callosum, and external capsule. A single nucleotide polymorphism in catechol-O-methyltransferase was associated with the neural activities of the lingual, fusiform, and occipital gyri, which are involved in visual cognitive dysfunction. Furthermore, DRD3 was associated with frontal and temporal lobe function and structure. In conclusion, imaging genetics is useful for providing a better understanding of the genetic pathways involved in the pathophysiologic processes underlying Parkinson’s disease. This study provides evidence of an association between genetic factors, cognitive functions, and multi-modality neuroimaging biomarkers in Parkinson’s disease. Wolters Kluwer - Medknow 2022-10-10 /pmc/articles/PMC9827791/ /pubmed/36255006 http://dx.doi.org/10.4103/1673-5374.355764 Text en Copyright: © Neural Regeneration Research https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms. |
spellingShingle | Research Article Shen, Ting Pu, Jia-Li Jiang, Ya-Si Yue, Yu-Mei He, Ting-Ting Qu, Bo-Yi Zhao, Shuai Yan, Ya-Ping Lai, Hsin-Yi Zhang, Bao-Rong Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson’s disease |
title | Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson’s disease |
title_full | Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson’s disease |
title_fullStr | Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson’s disease |
title_full_unstemmed | Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson’s disease |
title_short | Impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in Parkinson’s disease |
title_sort | impact of cognition-related single nucleotide polymorphisms on brain imaging phenotype in parkinson’s disease |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9827791/ https://www.ncbi.nlm.nih.gov/pubmed/36255006 http://dx.doi.org/10.4103/1673-5374.355764 |
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