Genome-Wide Expression Profiles for Ischemic Stroke: A Meta-Analysis
Genome-wide expression studies (GWES), using microarray platforms, have allowed a deeper understanding of the molecular factors involved in the pathophysiology of ischemic stroke (IS), one of the main global causes of mortality and disability. In the current work, we carried out a meta-analysis of a...
Gespeichert in:
Veröffentlicht in: | Journal of stroke and cerebrovascular diseases 2018-11, Vol.27 (11), p.3336-3341 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 3341 |
---|---|
container_issue | 11 |
container_start_page | 3336 |
container_title | Journal of stroke and cerebrovascular diseases |
container_volume | 27 |
creator | Moreno-Ramírez, Carlos E. Gutiérrez-Garzón, Eulogia Barreto, George E. Forero, Diego A. |
description | Genome-wide expression studies (GWES), using microarray platforms, have allowed a deeper understanding of the molecular factors involved in the pathophysiology of ischemic stroke (IS), one of the main global causes of mortality and disability.
In the current work, we carried out a meta-analysis of available GWES for IS. Bioinformatics and computational biology analyses were applied to identify enriched functional categories and convergence with other genomic datasets for IS.
Three primary datasets were included and in the meta-analyses for GWES and IS, 41 differentially expressed (DE) genes were identified using a random effects model. Thirteen of these genes were downregulated and 28 were upregulated. An analysis of functional categories found a significant enrichment for the Gene Ontology Term “Inflammatory Response” and for binding sites for the PAX2 transcription factor.
The list of DE genes identified in this meta-analysis of GWES for IS is useful for future genetic and molecular studies, which would allow the identification of novel mechanisms involved in the pathophysiology of IS. Several of the DE genes found in this meta-analysis have known functional roles related to mechanisms involved in the pathophysiology of IS. It is recognized the role of the inflammatory response in the pathophysiology of IS. |
doi_str_mv | 10.1016/j.jstrokecerebrovasdis.2018.07.035 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2098770094</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S1052305718304282</els_id><sourcerecordid>2098770094</sourcerecordid><originalsourceid>FETCH-LOGICAL-c404t-8a194900cfbfd9df68c82c1b5217e20bb771d9fde280e58ed17cadac00d9f2c33</originalsourceid><addsrcrecordid>eNqVkE1v1DAQhq0K1JbCX6hyRJUSZpz12ult-0GptAgkQBwtx56o3ibx4slW9N-TsoUTF04zGj16X80jxBlChYDLd5tqw1NO9-QpU5vTg-MQuZKApgJdQa0OxDGqWpZGIb6Yd1CyrEHpI_GKeQOAqIw6FEf1HLeUiMfi6obGNFD5PQYqrn9uMzHHNBafc-piT1x0KRe37O9oiL748rv-vFgVH2ly5Wp0_SNHfi1edq5nevM8T8S399dfLz-U6083t5erdekXsJhK47BZNAC-a7vQhG5pvJEeWyVRk4S21RpD0wWSBkgZCqi9C84DzFfp6_pEvN3nbnP6sSOe7BDZU9-7kdKOrYTGaA3QLGb0Yo_6nJgzdXab4-Dyo0WwTzbtxv7Lpn2yaUHb2eYccvrct2sHCn8j_uibgfUeoPnrh0jZso80egoxk59sSPF_-n4BoRmUtw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2098770094</pqid></control><display><type>article</type><title>Genome-Wide Expression Profiles for Ischemic Stroke: A Meta-Analysis</title><source>Access via ScienceDirect (Elsevier)</source><creator>Moreno-Ramírez, Carlos E. ; Gutiérrez-Garzón, Eulogia ; Barreto, George E. ; Forero, Diego A.</creator><creatorcontrib>Moreno-Ramírez, Carlos E. ; Gutiérrez-Garzón, Eulogia ; Barreto, George E. ; Forero, Diego A.</creatorcontrib><description>Genome-wide expression studies (GWES), using microarray platforms, have allowed a deeper understanding of the molecular factors involved in the pathophysiology of ischemic stroke (IS), one of the main global causes of mortality and disability.
In the current work, we carried out a meta-analysis of available GWES for IS. Bioinformatics and computational biology analyses were applied to identify enriched functional categories and convergence with other genomic datasets for IS.
Three primary datasets were included and in the meta-analyses for GWES and IS, 41 differentially expressed (DE) genes were identified using a random effects model. Thirteen of these genes were downregulated and 28 were upregulated. An analysis of functional categories found a significant enrichment for the Gene Ontology Term “Inflammatory Response” and for binding sites for the PAX2 transcription factor.
The list of DE genes identified in this meta-analysis of GWES for IS is useful for future genetic and molecular studies, which would allow the identification of novel mechanisms involved in the pathophysiology of IS. Several of the DE genes found in this meta-analysis have known functional roles related to mechanisms involved in the pathophysiology of IS. It is recognized the role of the inflammatory response in the pathophysiology of IS.</description><identifier>ISSN: 1052-3057</identifier><identifier>EISSN: 1532-8511</identifier><identifier>DOI: 10.1016/j.jstrokecerebrovasdis.2018.07.035</identifier><identifier>PMID: 30166211</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>bioinformatics ; computational biology ; genome-wide expression ; Ischemic stroke ; meta-analysis ; neurogenetics</subject><ispartof>Journal of stroke and cerebrovascular diseases, 2018-11, Vol.27 (11), p.3336-3341</ispartof><rights>2018</rights><rights>Copyright © 2018. Published by Elsevier Inc.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c404t-8a194900cfbfd9df68c82c1b5217e20bb771d9fde280e58ed17cadac00d9f2c33</citedby><cites>FETCH-LOGICAL-c404t-8a194900cfbfd9df68c82c1b5217e20bb771d9fde280e58ed17cadac00d9f2c33</cites><orcidid>0000-0002-2025-2454 ; 0000-0001-9175-3363</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.jstrokecerebrovasdis.2018.07.035$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30166211$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Moreno-Ramírez, Carlos E.</creatorcontrib><creatorcontrib>Gutiérrez-Garzón, Eulogia</creatorcontrib><creatorcontrib>Barreto, George E.</creatorcontrib><creatorcontrib>Forero, Diego A.</creatorcontrib><title>Genome-Wide Expression Profiles for Ischemic Stroke: A Meta-Analysis</title><title>Journal of stroke and cerebrovascular diseases</title><addtitle>J Stroke Cerebrovasc Dis</addtitle><description>Genome-wide expression studies (GWES), using microarray platforms, have allowed a deeper understanding of the molecular factors involved in the pathophysiology of ischemic stroke (IS), one of the main global causes of mortality and disability.
In the current work, we carried out a meta-analysis of available GWES for IS. Bioinformatics and computational biology analyses were applied to identify enriched functional categories and convergence with other genomic datasets for IS.
Three primary datasets were included and in the meta-analyses for GWES and IS, 41 differentially expressed (DE) genes were identified using a random effects model. Thirteen of these genes were downregulated and 28 were upregulated. An analysis of functional categories found a significant enrichment for the Gene Ontology Term “Inflammatory Response” and for binding sites for the PAX2 transcription factor.
The list of DE genes identified in this meta-analysis of GWES for IS is useful for future genetic and molecular studies, which would allow the identification of novel mechanisms involved in the pathophysiology of IS. Several of the DE genes found in this meta-analysis have known functional roles related to mechanisms involved in the pathophysiology of IS. It is recognized the role of the inflammatory response in the pathophysiology of IS.</description><subject>bioinformatics</subject><subject>computational biology</subject><subject>genome-wide expression</subject><subject>Ischemic stroke</subject><subject>meta-analysis</subject><subject>neurogenetics</subject><issn>1052-3057</issn><issn>1532-8511</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNqVkE1v1DAQhq0K1JbCX6hyRJUSZpz12ult-0GptAgkQBwtx56o3ibx4slW9N-TsoUTF04zGj16X80jxBlChYDLd5tqw1NO9-QpU5vTg-MQuZKApgJdQa0OxDGqWpZGIb6Yd1CyrEHpI_GKeQOAqIw6FEf1HLeUiMfi6obGNFD5PQYqrn9uMzHHNBafc-piT1x0KRe37O9oiL748rv-vFgVH2ly5Wp0_SNHfi1edq5nevM8T8S399dfLz-U6083t5erdekXsJhK47BZNAC-a7vQhG5pvJEeWyVRk4S21RpD0wWSBkgZCqi9C84DzFfp6_pEvN3nbnP6sSOe7BDZU9-7kdKOrYTGaA3QLGb0Yo_6nJgzdXab4-Dyo0WwTzbtxv7Lpn2yaUHb2eYccvrct2sHCn8j_uibgfUeoPnrh0jZso80egoxk59sSPF_-n4BoRmUtw</recordid><startdate>20181101</startdate><enddate>20181101</enddate><creator>Moreno-Ramírez, Carlos E.</creator><creator>Gutiérrez-Garzón, Eulogia</creator><creator>Barreto, George E.</creator><creator>Forero, Diego A.</creator><general>Elsevier Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2025-2454</orcidid><orcidid>https://orcid.org/0000-0001-9175-3363</orcidid></search><sort><creationdate>20181101</creationdate><title>Genome-Wide Expression Profiles for Ischemic Stroke: A Meta-Analysis</title><author>Moreno-Ramírez, Carlos E. ; Gutiérrez-Garzón, Eulogia ; Barreto, George E. ; Forero, Diego A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c404t-8a194900cfbfd9df68c82c1b5217e20bb771d9fde280e58ed17cadac00d9f2c33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>bioinformatics</topic><topic>computational biology</topic><topic>genome-wide expression</topic><topic>Ischemic stroke</topic><topic>meta-analysis</topic><topic>neurogenetics</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Moreno-Ramírez, Carlos E.</creatorcontrib><creatorcontrib>Gutiérrez-Garzón, Eulogia</creatorcontrib><creatorcontrib>Barreto, George E.</creatorcontrib><creatorcontrib>Forero, Diego A.</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of stroke and cerebrovascular diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Moreno-Ramírez, Carlos E.</au><au>Gutiérrez-Garzón, Eulogia</au><au>Barreto, George E.</au><au>Forero, Diego A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Genome-Wide Expression Profiles for Ischemic Stroke: A Meta-Analysis</atitle><jtitle>Journal of stroke and cerebrovascular diseases</jtitle><addtitle>J Stroke Cerebrovasc Dis</addtitle><date>2018-11-01</date><risdate>2018</risdate><volume>27</volume><issue>11</issue><spage>3336</spage><epage>3341</epage><pages>3336-3341</pages><issn>1052-3057</issn><eissn>1532-8511</eissn><abstract>Genome-wide expression studies (GWES), using microarray platforms, have allowed a deeper understanding of the molecular factors involved in the pathophysiology of ischemic stroke (IS), one of the main global causes of mortality and disability.
In the current work, we carried out a meta-analysis of available GWES for IS. Bioinformatics and computational biology analyses were applied to identify enriched functional categories and convergence with other genomic datasets for IS.
Three primary datasets were included and in the meta-analyses for GWES and IS, 41 differentially expressed (DE) genes were identified using a random effects model. Thirteen of these genes were downregulated and 28 were upregulated. An analysis of functional categories found a significant enrichment for the Gene Ontology Term “Inflammatory Response” and for binding sites for the PAX2 transcription factor.
The list of DE genes identified in this meta-analysis of GWES for IS is useful for future genetic and molecular studies, which would allow the identification of novel mechanisms involved in the pathophysiology of IS. Several of the DE genes found in this meta-analysis have known functional roles related to mechanisms involved in the pathophysiology of IS. It is recognized the role of the inflammatory response in the pathophysiology of IS.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>30166211</pmid><doi>10.1016/j.jstrokecerebrovasdis.2018.07.035</doi><tpages>6</tpages><orcidid>https://orcid.org/0000-0002-2025-2454</orcidid><orcidid>https://orcid.org/0000-0001-9175-3363</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1052-3057 |
ispartof | Journal of stroke and cerebrovascular diseases, 2018-11, Vol.27 (11), p.3336-3341 |
issn | 1052-3057 1532-8511 |
language | eng |
recordid | cdi_proquest_miscellaneous_2098770094 |
source | Access via ScienceDirect (Elsevier) |
subjects | bioinformatics computational biology genome-wide expression Ischemic stroke meta-analysis neurogenetics |
title | Genome-Wide Expression Profiles for Ischemic Stroke: A Meta-Analysis |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T11%3A11%3A41IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Genome-Wide%20Expression%20Profiles%20for%20Ischemic%20Stroke:%20A%20Meta-Analysis&rft.jtitle=Journal%20of%20stroke%20and%20cerebrovascular%20diseases&rft.au=Moreno-Ram%C3%ADrez,%20Carlos%20E.&rft.date=2018-11-01&rft.volume=27&rft.issue=11&rft.spage=3336&rft.epage=3341&rft.pages=3336-3341&rft.issn=1052-3057&rft.eissn=1532-8511&rft_id=info:doi/10.1016/j.jstrokecerebrovasdis.2018.07.035&rft_dat=%3Cproquest_cross%3E2098770094%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2098770094&rft_id=info:pmid/30166211&rft_els_id=S1052305718304282&rfr_iscdi=true |