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Substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in Parkinson’s disease
Substantia nigra (SN) hyperechogenicity is present in most Parkinson’s disease (PD) cases but is occasionally absent in some. To date, age, gender, disease severity, and other factors have been reported to be associated with SN hyperechogenicity in PD. Previous studies have discovered that excess ir...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250839/ https://www.ncbi.nlm.nih.gov/pubmed/32457446 http://dx.doi.org/10.1038/s41598-020-65537-5 |
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author | Li, Kai Ge, Yi-Lun Gu, Chen-Chen Zhang, Jin-Ru Jin, Hong Li, Jiao Cheng, Xiao-Yu Yang, Ya-Ping Wang, Fen Zhang, Ying-Chun Chen, Jing Mao, Cheng-Jie Liu, Chun-Feng |
author_facet | Li, Kai Ge, Yi-Lun Gu, Chen-Chen Zhang, Jin-Ru Jin, Hong Li, Jiao Cheng, Xiao-Yu Yang, Ya-Ping Wang, Fen Zhang, Ying-Chun Chen, Jing Mao, Cheng-Jie Liu, Chun-Feng |
author_sort | Li, Kai |
collection | PubMed |
description | Substantia nigra (SN) hyperechogenicity is present in most Parkinson’s disease (PD) cases but is occasionally absent in some. To date, age, gender, disease severity, and other factors have been reported to be associated with SN hyperechogenicity in PD. Previous studies have discovered that excess iron deposition in the SN underlies its hyperechogenicity in PD, which may also indicate the involvement of genes associated with iron metabolism in hyperechogenicity. The objective of our study is to explore the potential associations between variants in iron metabolism-associated genes and SN echogenicity in Han Chinese PD. Demographic profiles, clinical data, SN echogenicity and genotypes were obtained from 221 Han Chinese PD individuals with a sufficient bone window. Serum ferritin levels were quantified in 92 of these individuals by immunochemical assay. We then compared factors between PD individuals with SN hyperechogenicity and those with SN hypoechogenicity to identify factors that predispose to SN hyperechogenicity. Of our 221 participants, 122 (55.2%) displayed SN hyperechogenicity, and 99 (44.8%) displayed SN hypoechogenicity. Gender and serum ferritin levels were found to be associated with SN hyperechogenicity. In total, 14 genes were included in the sequencing part. After data processing, 34 common single nucleotide polymorphisms were included in our further analyses. In our data, we also found a significantly higher frequency of PANK2 rs3737084 (genotype: OR = 2.07, P = 0.013; allele: OR = 2.51, P = 0.002) in the SN hyperechogenic group and a higher frequency of PLA2G6 rs731821 (genotype: OR = 0.45, P = 0.016; allele: OR = 0.44, P = 0.011) in the SN hypoechogenic group. However, neither of the two variants was found to be correlated with serum ferritin. This study demonstrated that genetic factors, serum ferritin level, and gender may explain the interindividual variability in SN echogenicity in PD. This is an explorative study, and further replication is warranted in larger samples and different populations. |
format | Online Article Text |
id | pubmed-7250839 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72508392020-06-04 Substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in Parkinson’s disease Li, Kai Ge, Yi-Lun Gu, Chen-Chen Zhang, Jin-Ru Jin, Hong Li, Jiao Cheng, Xiao-Yu Yang, Ya-Ping Wang, Fen Zhang, Ying-Chun Chen, Jing Mao, Cheng-Jie Liu, Chun-Feng Sci Rep Article Substantia nigra (SN) hyperechogenicity is present in most Parkinson’s disease (PD) cases but is occasionally absent in some. To date, age, gender, disease severity, and other factors have been reported to be associated with SN hyperechogenicity in PD. Previous studies have discovered that excess iron deposition in the SN underlies its hyperechogenicity in PD, which may also indicate the involvement of genes associated with iron metabolism in hyperechogenicity. The objective of our study is to explore the potential associations between variants in iron metabolism-associated genes and SN echogenicity in Han Chinese PD. Demographic profiles, clinical data, SN echogenicity and genotypes were obtained from 221 Han Chinese PD individuals with a sufficient bone window. Serum ferritin levels were quantified in 92 of these individuals by immunochemical assay. We then compared factors between PD individuals with SN hyperechogenicity and those with SN hypoechogenicity to identify factors that predispose to SN hyperechogenicity. Of our 221 participants, 122 (55.2%) displayed SN hyperechogenicity, and 99 (44.8%) displayed SN hypoechogenicity. Gender and serum ferritin levels were found to be associated with SN hyperechogenicity. In total, 14 genes were included in the sequencing part. After data processing, 34 common single nucleotide polymorphisms were included in our further analyses. In our data, we also found a significantly higher frequency of PANK2 rs3737084 (genotype: OR = 2.07, P = 0.013; allele: OR = 2.51, P = 0.002) in the SN hyperechogenic group and a higher frequency of PLA2G6 rs731821 (genotype: OR = 0.45, P = 0.016; allele: OR = 0.44, P = 0.011) in the SN hypoechogenic group. However, neither of the two variants was found to be correlated with serum ferritin. This study demonstrated that genetic factors, serum ferritin level, and gender may explain the interindividual variability in SN echogenicity in PD. This is an explorative study, and further replication is warranted in larger samples and different populations. Nature Publishing Group UK 2020-05-26 /pmc/articles/PMC7250839/ /pubmed/32457446 http://dx.doi.org/10.1038/s41598-020-65537-5 Text en © The Author(s) 2020 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 Li, Kai Ge, Yi-Lun Gu, Chen-Chen Zhang, Jin-Ru Jin, Hong Li, Jiao Cheng, Xiao-Yu Yang, Ya-Ping Wang, Fen Zhang, Ying-Chun Chen, Jing Mao, Cheng-Jie Liu, Chun-Feng Substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in Parkinson’s disease |
title | Substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in Parkinson’s disease |
title_full | Substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in Parkinson’s disease |
title_fullStr | Substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in Parkinson’s disease |
title_full_unstemmed | Substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in Parkinson’s disease |
title_short | Substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in Parkinson’s disease |
title_sort | substantia nigra echogenicity is associated with serum ferritin, gender and iron-related genes in parkinson’s disease |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7250839/ https://www.ncbi.nlm.nih.gov/pubmed/32457446 http://dx.doi.org/10.1038/s41598-020-65537-5 |
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