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Identification of a panel of five serum miRNAs as a biomarker for Parkinson's disease
Abstract Background and objective Parkinson's disease (PD) is the second most common age-related neurodegenerative disorder after Alzheimer's disease. The aim of this work was to determine whether the differences of serum miRNAs profiling could distinguish PD patients from healthy individu...
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Published in: | Parkinsonism & related disorders 2016-01, Vol.22, p.68-73 |
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creator | Ding, Haixia Huang, Zhen Chen, Mengjie Wang, Cheng Chen, Xi Chen, Jiangning Zhang, Junfeng |
description | Abstract Background and objective Parkinson's disease (PD) is the second most common age-related neurodegenerative disorder after Alzheimer's disease. The aim of this work was to determine whether the differences of serum miRNAs profiling could distinguish PD patients from healthy individuals. Methods We collected serum samples from 106 sporadic PD patients and 91 age/gender-matched healthy controls. Serum miRNAs were analysed by Solexa sequencing followed by a qRT-PCR examination. The qRT-PCR assay, which was divided into two phases, was used to validate the expression of miRNAs screened by Solexa sequencing. Receiver operating characteristic (ROC) curve analysis and clustering analysis were performed to determine the diagnostic usefulness of the selected miRNAs for PD. Results In this study, we generated a profile of 5 serum miRNAs: miR-195 was up-regulated, and miR-185, miR-15b, miR-221 and miR-181a were down-regulated. Conclusion This group of five miRNAs can precisely distinguish PD patients from health individuals and may be used as a potential serum-based biomarker for the diagnosis of PD. |
doi_str_mv | 10.1016/j.parkreldis.2015.11.014 |
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The aim of this work was to determine whether the differences of serum miRNAs profiling could distinguish PD patients from healthy individuals. Methods We collected serum samples from 106 sporadic PD patients and 91 age/gender-matched healthy controls. Serum miRNAs were analysed by Solexa sequencing followed by a qRT-PCR examination. The qRT-PCR assay, which was divided into two phases, was used to validate the expression of miRNAs screened by Solexa sequencing. Receiver operating characteristic (ROC) curve analysis and clustering analysis were performed to determine the diagnostic usefulness of the selected miRNAs for PD. Results In this study, we generated a profile of 5 serum miRNAs: miR-195 was up-regulated, and miR-185, miR-15b, miR-221 and miR-181a were down-regulated. Conclusion This group of five miRNAs can precisely distinguish PD patients from health individuals and may be used as a potential serum-based biomarker for the diagnosis of PD.</description><identifier>ISSN: 1353-8020</identifier><identifier>EISSN: 1873-5126</identifier><identifier>DOI: 10.1016/j.parkreldis.2015.11.014</identifier><identifier>PMID: 26631952</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>Adult ; Aged ; Area Under Curve ; Biomarkers - blood ; Case-Control Studies ; Down-Regulation ; Female ; Humans ; Male ; MicroRNAs - blood ; Middle Aged ; Neurology ; Parkinson Disease - blood ; Parkinson Disease - diagnosis ; Parkinson's disease ; Real-Time Polymerase Chain Reaction ; ROC Curve ; Sensitivity and Specificity ; Serum miRNA ; Transcriptome ; Up-Regulation</subject><ispartof>Parkinsonism & related disorders, 2016-01, Vol.22, p.68-73</ispartof><rights>Elsevier Ltd</rights><rights>2015 Elsevier Ltd</rights><rights>Copyright © 2015 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c554t-ce471fa4b8d347ffe01210452fbc732ee312dba97256ea47a92c889f6ea366f63</citedby><cites>FETCH-LOGICAL-c554t-ce471fa4b8d347ffe01210452fbc732ee312dba97256ea47a92c889f6ea366f63</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26631952$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ding, Haixia</creatorcontrib><creatorcontrib>Huang, Zhen</creatorcontrib><creatorcontrib>Chen, Mengjie</creatorcontrib><creatorcontrib>Wang, Cheng</creatorcontrib><creatorcontrib>Chen, Xi</creatorcontrib><creatorcontrib>Chen, Jiangning</creatorcontrib><creatorcontrib>Zhang, Junfeng</creatorcontrib><title>Identification of a panel of five serum miRNAs as a biomarker for Parkinson's disease</title><title>Parkinsonism & related disorders</title><addtitle>Parkinsonism Relat Disord</addtitle><description>Abstract Background and objective Parkinson's disease (PD) is the second most common age-related neurodegenerative disorder after Alzheimer's disease. The aim of this work was to determine whether the differences of serum miRNAs profiling could distinguish PD patients from healthy individuals. Methods We collected serum samples from 106 sporadic PD patients and 91 age/gender-matched healthy controls. Serum miRNAs were analysed by Solexa sequencing followed by a qRT-PCR examination. The qRT-PCR assay, which was divided into two phases, was used to validate the expression of miRNAs screened by Solexa sequencing. Receiver operating characteristic (ROC) curve analysis and clustering analysis were performed to determine the diagnostic usefulness of the selected miRNAs for PD. Results In this study, we generated a profile of 5 serum miRNAs: miR-195 was up-regulated, and miR-185, miR-15b, miR-221 and miR-181a were down-regulated. Conclusion This group of five miRNAs can precisely distinguish PD patients from health individuals and may be used as a potential serum-based biomarker for the diagnosis of PD.</description><subject>Adult</subject><subject>Aged</subject><subject>Area Under Curve</subject><subject>Biomarkers - blood</subject><subject>Case-Control Studies</subject><subject>Down-Regulation</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>MicroRNAs - blood</subject><subject>Middle Aged</subject><subject>Neurology</subject><subject>Parkinson Disease - blood</subject><subject>Parkinson Disease - diagnosis</subject><subject>Parkinson's disease</subject><subject>Real-Time Polymerase Chain Reaction</subject><subject>ROC Curve</subject><subject>Sensitivity and Specificity</subject><subject>Serum miRNA</subject><subject>Transcriptome</subject><subject>Up-Regulation</subject><issn>1353-8020</issn><issn>1873-5126</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><recordid>eNqNUVFL3jAUDTKZzu0vjLxtL625SdOmLwMn2xRERedzSNMbyGfbfEtawX9vyqcTfBICOYFz78k5hxAKrAQG9fGm3Jp4H3HofSo5A1kClAyqPXIIqhGFBF5_yFhIUSjG2QH5lNKGMdZIJj6SA17XAlrJD8ndeY_T7J23ZvZhosFRQ7dmwmGFzj8gTRiXkY7-5vIkUZMP7XwYsz5G6kKk1xn6KYXpW6L5P2gSfib7zgwJvzzfR-Tu96-_p2fFxdWf89OTi8JKWc2FxaoBZ6pO9aJqnEMGHFgluetsIziiAN53pm24rNFUjWm5Vap1-SHq2tXiiHzf7d3G8G_BNOvRJ4vDkA2EJWloJBdSglKZqnZUG0NKEZ3eRp9dPGpgeg1Vb_RrqHoNVQPoHGoe_fqssnQj9v8HX1LMhJ87AmavDx6jTtbjZLH3Ee2s--Dfo_LjzRI7-Cn3MtzjI6ZNWOKUs9SgE9dM367lrt2CFIwJ1YoneUCh8w</recordid><startdate>20160101</startdate><enddate>20160101</enddate><creator>Ding, Haixia</creator><creator>Huang, Zhen</creator><creator>Chen, Mengjie</creator><creator>Wang, Cheng</creator><creator>Chen, Xi</creator><creator>Chen, Jiangning</creator><creator>Zhang, Junfeng</creator><general>Elsevier Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20160101</creationdate><title>Identification of a panel of five serum miRNAs as a biomarker for Parkinson's disease</title><author>Ding, Haixia ; Huang, Zhen ; Chen, Mengjie ; Wang, Cheng ; Chen, Xi ; Chen, Jiangning ; Zhang, Junfeng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c554t-ce471fa4b8d347ffe01210452fbc732ee312dba97256ea47a92c889f6ea366f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Area Under Curve</topic><topic>Biomarkers - blood</topic><topic>Case-Control Studies</topic><topic>Down-Regulation</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>MicroRNAs - blood</topic><topic>Middle Aged</topic><topic>Neurology</topic><topic>Parkinson Disease - blood</topic><topic>Parkinson Disease - diagnosis</topic><topic>Parkinson's disease</topic><topic>Real-Time Polymerase Chain Reaction</topic><topic>ROC Curve</topic><topic>Sensitivity and Specificity</topic><topic>Serum miRNA</topic><topic>Transcriptome</topic><topic>Up-Regulation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ding, Haixia</creatorcontrib><creatorcontrib>Huang, Zhen</creatorcontrib><creatorcontrib>Chen, Mengjie</creatorcontrib><creatorcontrib>Wang, Cheng</creatorcontrib><creatorcontrib>Chen, Xi</creatorcontrib><creatorcontrib>Chen, Jiangning</creatorcontrib><creatorcontrib>Zhang, Junfeng</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Parkinsonism & related disorders</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ding, Haixia</au><au>Huang, Zhen</au><au>Chen, Mengjie</au><au>Wang, Cheng</au><au>Chen, Xi</au><au>Chen, Jiangning</au><au>Zhang, Junfeng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Identification of a panel of five serum miRNAs as a biomarker for Parkinson's disease</atitle><jtitle>Parkinsonism & related disorders</jtitle><addtitle>Parkinsonism Relat Disord</addtitle><date>2016-01-01</date><risdate>2016</risdate><volume>22</volume><spage>68</spage><epage>73</epage><pages>68-73</pages><issn>1353-8020</issn><eissn>1873-5126</eissn><abstract>Abstract Background and objective Parkinson's disease (PD) is the second most common age-related neurodegenerative disorder after Alzheimer's disease. The aim of this work was to determine whether the differences of serum miRNAs profiling could distinguish PD patients from healthy individuals. Methods We collected serum samples from 106 sporadic PD patients and 91 age/gender-matched healthy controls. Serum miRNAs were analysed by Solexa sequencing followed by a qRT-PCR examination. The qRT-PCR assay, which was divided into two phases, was used to validate the expression of miRNAs screened by Solexa sequencing. Receiver operating characteristic (ROC) curve analysis and clustering analysis were performed to determine the diagnostic usefulness of the selected miRNAs for PD. Results In this study, we generated a profile of 5 serum miRNAs: miR-195 was up-regulated, and miR-185, miR-15b, miR-221 and miR-181a were down-regulated. Conclusion This group of five miRNAs can precisely distinguish PD patients from health individuals and may be used as a potential serum-based biomarker for the diagnosis of PD.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>26631952</pmid><doi>10.1016/j.parkreldis.2015.11.014</doi><tpages>6</tpages></addata></record> |
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subjects | Adult Aged Area Under Curve Biomarkers - blood Case-Control Studies Down-Regulation Female Humans Male MicroRNAs - blood Middle Aged Neurology Parkinson Disease - blood Parkinson Disease - diagnosis Parkinson's disease Real-Time Polymerase Chain Reaction ROC Curve Sensitivity and Specificity Serum miRNA Transcriptome Up-Regulation |
title | Identification of a panel of five serum miRNAs as a biomarker for Parkinson's disease |
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