Serum microRNA profiling for the identification of predictive molecular markers of the response to controlled ovarian stimulation
To identify potential microRNA (miRNA) biomarkers of poor, normal and hyperresponse to controlled ovarian stimulation (COS). In the present study, we assessed 40 serum samples from patients undergoing COS. We used ten samples to standardize miRNAs detection in the serum. The remaining 30 samples wer...
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Veröffentlicht in: | JBRA assisted reproduction 2020, Vol.24 (2), p.97-103 |
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creator | Borges, Jr, Edson Mulato, Maria Gabriela Ferreira Souza, Setti, Amanda Iaconelli, Jr, Assumpto Vieira, Geraldo, Murilo Paes, de Almeida Ferreira Braga, Daniela |
description | To identify potential microRNA (miRNA) biomarkers of poor, normal and hyperresponse to controlled ovarian stimulation (COS).
In the present study, we assessed 40 serum samples from patients undergoing COS. We used ten samples to standardize miRNAs detection in the serum. The remaining 30 samples were split into three groups depending on the patient's response to COS: poor response (PR group, n=10), normal response (NR group, n=10), and hyperresponse (HR group, n=10). Aberrantly expressed miRNAs were identified using a large-scale expression analysis platform. Gene set enrichment analysis was performed to assess the biological processes potentially modulated by the identified miRNAs.
Twenty-two miRNAs were detected only in the PR or HR groups when compared with the NR group. From those, 11 presented poor dissociation curves and were excluded from further analysis. A bioinformatics analysis revealed that the selected 11 miRNAs target several genes involved in GnRH, estrogen and prolactin signaling, oocyte maturation, female pregnancy, and meiosis.
The large-scale analysis of miRNA expression identified distinct miRNA profiles for poor and hyperresponse to COS, which potentially modulate key processes for human assisted reproduction. All evidence suggests that the serum microRNA profiling may discriminate patients who will respond in an exacerbated manner from those who will respond insufficiently to COS. Further studies may validate these miRNAs, enabling the individualization of treatment and more successful outcomes. |
doi_str_mv | 10.5935/1518-0557.20190070 |
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In the present study, we assessed 40 serum samples from patients undergoing COS. We used ten samples to standardize miRNAs detection in the serum. The remaining 30 samples were split into three groups depending on the patient's response to COS: poor response (PR group, n=10), normal response (NR group, n=10), and hyperresponse (HR group, n=10). Aberrantly expressed miRNAs were identified using a large-scale expression analysis platform. Gene set enrichment analysis was performed to assess the biological processes potentially modulated by the identified miRNAs.
Twenty-two miRNAs were detected only in the PR or HR groups when compared with the NR group. From those, 11 presented poor dissociation curves and were excluded from further analysis. A bioinformatics analysis revealed that the selected 11 miRNAs target several genes involved in GnRH, estrogen and prolactin signaling, oocyte maturation, female pregnancy, and meiosis.
The large-scale analysis of miRNA expression identified distinct miRNA profiles for poor and hyperresponse to COS, which potentially modulate key processes for human assisted reproduction. All evidence suggests that the serum microRNA profiling may discriminate patients who will respond in an exacerbated manner from those who will respond insufficiently to COS. Further studies may validate these miRNAs, enabling the individualization of treatment and more successful outcomes.</description><identifier>ISSN: 1518-0557</identifier><identifier>ISSN: 1517-5693</identifier><identifier>EISSN: 1518-0557</identifier><identifier>DOI: 10.5935/1518-0557.20190070</identifier><identifier>PMID: 31693318</identifier><language>eng</language><publisher>Brazil: Sociedade Brasileira de Reprodução Humana (Brazilian Society of Assisted Reproduction)</publisher><subject>Birth rate ; Embryos ; Fluids ; Gene expression ; In vitro fertilization ; MicroRNAs ; Original Paper ; Patients ; Reproductive technologies ; Ultrasonic imaging ; Variables</subject><ispartof>JBRA assisted reproduction, 2020, Vol.24 (2), p.97-103</ispartof><rights>2020. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c430t-833615dc6a6a0910197a6db016f745eda15e2ef30415d539735fbe9008dd75e73</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7169915/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7169915/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,4010,27904,27905,27906,53772,53774</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31693318$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Borges, Jr, Edson</creatorcontrib><creatorcontrib>Mulato, Maria Gabriela Ferreira</creatorcontrib><creatorcontrib>Souza, Setti, Amanda</creatorcontrib><creatorcontrib>Iaconelli, Jr, Assumpto</creatorcontrib><creatorcontrib>Vieira, Geraldo, Murilo</creatorcontrib><creatorcontrib>Paes, de Almeida Ferreira Braga, Daniela</creatorcontrib><title>Serum microRNA profiling for the identification of predictive molecular markers of the response to controlled ovarian stimulation</title><title>JBRA assisted reproduction</title><addtitle>JBRA Assist Reprod</addtitle><description>To identify potential microRNA (miRNA) biomarkers of poor, normal and hyperresponse to controlled ovarian stimulation (COS).
In the present study, we assessed 40 serum samples from patients undergoing COS. We used ten samples to standardize miRNAs detection in the serum. The remaining 30 samples were split into three groups depending on the patient's response to COS: poor response (PR group, n=10), normal response (NR group, n=10), and hyperresponse (HR group, n=10). Aberrantly expressed miRNAs were identified using a large-scale expression analysis platform. Gene set enrichment analysis was performed to assess the biological processes potentially modulated by the identified miRNAs.
Twenty-two miRNAs were detected only in the PR or HR groups when compared with the NR group. From those, 11 presented poor dissociation curves and were excluded from further analysis. A bioinformatics analysis revealed that the selected 11 miRNAs target several genes involved in GnRH, estrogen and prolactin signaling, oocyte maturation, female pregnancy, and meiosis.
The large-scale analysis of miRNA expression identified distinct miRNA profiles for poor and hyperresponse to COS, which potentially modulate key processes for human assisted reproduction. All evidence suggests that the serum microRNA profiling may discriminate patients who will respond in an exacerbated manner from those who will respond insufficiently to COS. Further studies may validate these miRNAs, enabling the individualization of treatment and more successful outcomes.</description><subject>Birth rate</subject><subject>Embryos</subject><subject>Fluids</subject><subject>Gene expression</subject><subject>In vitro fertilization</subject><subject>MicroRNAs</subject><subject>Original Paper</subject><subject>Patients</subject><subject>Reproductive technologies</subject><subject>Ultrasonic imaging</subject><subject>Variables</subject><issn>1518-0557</issn><issn>1517-5693</issn><issn>1518-0557</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><recordid>eNpdkcFPHCEYxUnTphrdf6CHhqSXXlZhGGaGSxNjrJoYTao9ExY-FMvAFphNevQ_l4nuxnqCwO-9fO97CH2h5IgLxo8pp8OScN4fNYQKQnryAe3vHj--ue-hRc6PhFSMNqwln9Eeo51gjA776OkW0jTi0ekUf12f4HWK1nkX7rGNCZcHwM5AKM46rYqLAUdbGTBOF7cBPEYPevIq4VGlP5Dy_D-rEuR1DBlwiVjHUFL0HgyOG5WcCjgXN1bZ7HiIPlnlMyxezwP0--fZ3enF8urm_PL05GqpW0bKcmCso9zoTnWKCFrD9KozK0I727ccjKIcGrCMtJXiTPSM2xXUxQzG9Bx6doB-vPiup9UIRtdUSXm5Tq6O_k9G5eT_P8E9yPu4kX1dlqC8Gnx_NUjx7wS5yNFlDd6rAHHKsmG04Zy3w4x-e4c-ximFGq9Sohta0TWiUs0LVXefcwK7G4YSOZcs5w7l3KHcllxFX9_G2Em2lbJnxFGkgQ</recordid><startdate>2020</startdate><enddate>2020</enddate><creator>Borges, Jr, Edson</creator><creator>Mulato, Maria Gabriela Ferreira</creator><creator>Souza, Setti, Amanda</creator><creator>Iaconelli, Jr, Assumpto</creator><creator>Vieira, Geraldo, Murilo</creator><creator>Paes, de Almeida Ferreira Braga, Daniela</creator><general>Sociedade Brasileira de Reprodução Humana (Brazilian Society of Assisted Reproduction)</general><general>Brazilian Society of Assisted Reproduction</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>2020</creationdate><title>Serum microRNA profiling for the identification of predictive molecular markers of the response to controlled ovarian stimulation</title><author>Borges, Jr, Edson ; Mulato, Maria Gabriela Ferreira ; Souza, Setti, Amanda ; Iaconelli, Jr, Assumpto ; Vieira, Geraldo, Murilo ; Paes, de Almeida Ferreira Braga, Daniela</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c430t-833615dc6a6a0910197a6db016f745eda15e2ef30415d539735fbe9008dd75e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Birth rate</topic><topic>Embryos</topic><topic>Fluids</topic><topic>Gene expression</topic><topic>In vitro fertilization</topic><topic>MicroRNAs</topic><topic>Original Paper</topic><topic>Patients</topic><topic>Reproductive technologies</topic><topic>Ultrasonic imaging</topic><topic>Variables</topic><toplevel>online_resources</toplevel><creatorcontrib>Borges, Jr, Edson</creatorcontrib><creatorcontrib>Mulato, Maria Gabriela Ferreira</creatorcontrib><creatorcontrib>Souza, Setti, Amanda</creatorcontrib><creatorcontrib>Iaconelli, Jr, Assumpto</creatorcontrib><creatorcontrib>Vieira, Geraldo, Murilo</creatorcontrib><creatorcontrib>Paes, de Almeida Ferreira Braga, Daniela</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Publicly Available Content Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>JBRA assisted reproduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Borges, Jr, Edson</au><au>Mulato, Maria Gabriela Ferreira</au><au>Souza, Setti, Amanda</au><au>Iaconelli, Jr, Assumpto</au><au>Vieira, Geraldo, Murilo</au><au>Paes, de Almeida Ferreira Braga, Daniela</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum microRNA profiling for the identification of predictive molecular markers of the response to controlled ovarian stimulation</atitle><jtitle>JBRA assisted reproduction</jtitle><addtitle>JBRA Assist Reprod</addtitle><date>2020</date><risdate>2020</risdate><volume>24</volume><issue>2</issue><spage>97</spage><epage>103</epage><pages>97-103</pages><issn>1518-0557</issn><issn>1517-5693</issn><eissn>1518-0557</eissn><abstract>To identify potential microRNA (miRNA) biomarkers of poor, normal and hyperresponse to controlled ovarian stimulation (COS).
In the present study, we assessed 40 serum samples from patients undergoing COS. We used ten samples to standardize miRNAs detection in the serum. The remaining 30 samples were split into three groups depending on the patient's response to COS: poor response (PR group, n=10), normal response (NR group, n=10), and hyperresponse (HR group, n=10). Aberrantly expressed miRNAs were identified using a large-scale expression analysis platform. Gene set enrichment analysis was performed to assess the biological processes potentially modulated by the identified miRNAs.
Twenty-two miRNAs were detected only in the PR or HR groups when compared with the NR group. From those, 11 presented poor dissociation curves and were excluded from further analysis. A bioinformatics analysis revealed that the selected 11 miRNAs target several genes involved in GnRH, estrogen and prolactin signaling, oocyte maturation, female pregnancy, and meiosis.
The large-scale analysis of miRNA expression identified distinct miRNA profiles for poor and hyperresponse to COS, which potentially modulate key processes for human assisted reproduction. All evidence suggests that the serum microRNA profiling may discriminate patients who will respond in an exacerbated manner from those who will respond insufficiently to COS. Further studies may validate these miRNAs, enabling the individualization of treatment and more successful outcomes.</abstract><cop>Brazil</cop><pub>Sociedade Brasileira de Reprodução Humana (Brazilian Society of Assisted Reproduction)</pub><pmid>31693318</pmid><doi>10.5935/1518-0557.20190070</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Birth rate Embryos Fluids Gene expression In vitro fertilization MicroRNAs Original Paper Patients Reproductive technologies Ultrasonic imaging Variables |
title | Serum microRNA profiling for the identification of predictive molecular markers of the response to controlled ovarian stimulation |
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