Plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p: Novel diagnostic biomarkers for gestational diabetes mellitus

Aim To explore whether plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p can be used as diagnostic biomarkers in gestational diabetes mellitus (GDM) and to investigate the relationship between those microRNAs and the risk factors of GDM (body mass index [BMI], insulin resistance [IR] and tumor necrosis fact...

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Veröffentlicht in:The journal of obstetrics and gynaecology research 2017-06, Vol.43 (6), p.974-981
Hauptverfasser: Cao, Ya‐Lei, Jia, Yan‐Ju, Xing, Bao‐Heng, Shi, Dan‐Dan, Dong, Xiu‐Juan
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container_issue 6
container_start_page 974
container_title The journal of obstetrics and gynaecology research
container_volume 43
creator Cao, Ya‐Lei
Jia, Yan‐Ju
Xing, Bao‐Heng
Shi, Dan‐Dan
Dong, Xiu‐Juan
description Aim To explore whether plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p can be used as diagnostic biomarkers in gestational diabetes mellitus (GDM) and to investigate the relationship between those microRNAs and the risk factors of GDM (body mass index [BMI], insulin resistance [IR] and tumor necrosis factor‐α (TNF‐α)). Methods A total of 85 pregnant women with GDM and 72 pregnant women without GDM were enrolled in this study. The plasma concentration of microRNAs (microRNA‐16‐5p, ‐17‐5p, ‐19a‐3p, ‐19b‐3p, ‐20a‐5p) was measured using quantitative reverse transcription–polymerase chain reaction (qRT‐PCR). Spearman's correlation analysis was used to evaluate the correlation between those microRNAs and the risk factors of GDM, and receiver operating characteristic curve analysis was used to evaluate diagnostic sensitivity and specificity. Results Compared with non‐GDM women, the relative and absolute expression of plasma microRNA‐16‐5p, ‐17‐5p, ‐20a‐5p from GDM women were significantly upregulated, when those women were diagnosed as GDM. During pregnancy, the expression of those microRNAs from GDM women also were significantly upregulated. The expression of those microRNAs was also positively correlated with IR, a risk factor of GDM. Plasma microRNA‐16‐5p, ‐17‐5p, ‐20a‐5p reflected an obvious separation between GDM women and non‐GDM women, with areas under the curve of 0.92 (95%CI: 0.871–0.984), 0.88 (95%CI: 0.798–0.962), and 0.74 (95%CI: 0.618–0.870), respectively, cut‐offs >2554, 1820, 3886 copies/μL, respectively; sensitivity 41.6%, 21.4% and 17.8%, respectively; and specificity 95.8%, 95.4% and 95.4%, respectively. Conclusion Plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p are potential diagnostic biomarkers in GDM.
doi_str_mv 10.1111/jog.13317
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Methods A total of 85 pregnant women with GDM and 72 pregnant women without GDM were enrolled in this study. The plasma concentration of microRNAs (microRNA‐16‐5p, ‐17‐5p, ‐19a‐3p, ‐19b‐3p, ‐20a‐5p) was measured using quantitative reverse transcription–polymerase chain reaction (qRT‐PCR). Spearman's correlation analysis was used to evaluate the correlation between those microRNAs and the risk factors of GDM, and receiver operating characteristic curve analysis was used to evaluate diagnostic sensitivity and specificity. Results Compared with non‐GDM women, the relative and absolute expression of plasma microRNA‐16‐5p, ‐17‐5p, ‐20a‐5p from GDM women were significantly upregulated, when those women were diagnosed as GDM. During pregnancy, the expression of those microRNAs from GDM women also were significantly upregulated. The expression of those microRNAs was also positively correlated with IR, a risk factor of GDM. Plasma microRNA‐16‐5p, ‐17‐5p, ‐20a‐5p reflected an obvious separation between GDM women and non‐GDM women, with areas under the curve of 0.92 (95%CI: 0.871–0.984), 0.88 (95%CI: 0.798–0.962), and 0.74 (95%CI: 0.618–0.870), respectively, cut‐offs &gt;2554, 1820, 3886 copies/μL, respectively; sensitivity 41.6%, 21.4% and 17.8%, respectively; and specificity 95.8%, 95.4% and 95.4%, respectively. Conclusion Plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p are potential diagnostic biomarkers in GDM.</description><identifier>ISSN: 1341-8076</identifier><identifier>EISSN: 1447-0756</identifier><identifier>DOI: 10.1111/jog.13317</identifier><identifier>PMID: 28621051</identifier><language>eng</language><publisher>Australia: Wiley Subscription Services, Inc</publisher><subject>Adult ; biomarker ; Biomarkers ; Biomarkers - blood ; Body mass ; Body mass index ; Correlation analysis ; Diabetes ; Diabetes mellitus ; Diabetes, Gestational - blood ; Female ; gestational diabetes mellitus ; Humans ; Insulin ; microRNA ; MicroRNAs ; MicroRNAs - blood ; miRNA ; Polymerase chain reaction ; Pregnancy ; Reverse transcription ; risk factor ; Risk factors ; ROC Curve ; Tumor necrosis factor ; Tumor necrosis factor-TNF ; Young Adult</subject><ispartof>The journal of obstetrics and gynaecology research, 2017-06, Vol.43 (6), p.974-981</ispartof><rights>2017 Japan Society of Obstetrics and Gynecology</rights><rights>2017 Japan Society of Obstetrics and Gynecology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3587-fdb07e4ce68ac0dd3442419b48defa851c07da2318a9784b49bcbce49d678a5a3</citedby><cites>FETCH-LOGICAL-c3587-fdb07e4ce68ac0dd3442419b48defa851c07da2318a9784b49bcbce49d678a5a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fjog.13317$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fjog.13317$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27901,27902,45550,45551</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28621051$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cao, Ya‐Lei</creatorcontrib><creatorcontrib>Jia, Yan‐Ju</creatorcontrib><creatorcontrib>Xing, Bao‐Heng</creatorcontrib><creatorcontrib>Shi, Dan‐Dan</creatorcontrib><creatorcontrib>Dong, Xiu‐Juan</creatorcontrib><title>Plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p: Novel diagnostic biomarkers for gestational diabetes mellitus</title><title>The journal of obstetrics and gynaecology research</title><addtitle>J Obstet Gynaecol Res</addtitle><description>Aim To explore whether plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p can be used as diagnostic biomarkers in gestational diabetes mellitus (GDM) and to investigate the relationship between those microRNAs and the risk factors of GDM (body mass index [BMI], insulin resistance [IR] and tumor necrosis factor‐α (TNF‐α)). Methods A total of 85 pregnant women with GDM and 72 pregnant women without GDM were enrolled in this study. The plasma concentration of microRNAs (microRNA‐16‐5p, ‐17‐5p, ‐19a‐3p, ‐19b‐3p, ‐20a‐5p) was measured using quantitative reverse transcription–polymerase chain reaction (qRT‐PCR). Spearman's correlation analysis was used to evaluate the correlation between those microRNAs and the risk factors of GDM, and receiver operating characteristic curve analysis was used to evaluate diagnostic sensitivity and specificity. Results Compared with non‐GDM women, the relative and absolute expression of plasma microRNA‐16‐5p, ‐17‐5p, ‐20a‐5p from GDM women were significantly upregulated, when those women were diagnosed as GDM. During pregnancy, the expression of those microRNAs from GDM women also were significantly upregulated. The expression of those microRNAs was also positively correlated with IR, a risk factor of GDM. Plasma microRNA‐16‐5p, ‐17‐5p, ‐20a‐5p reflected an obvious separation between GDM women and non‐GDM women, with areas under the curve of 0.92 (95%CI: 0.871–0.984), 0.88 (95%CI: 0.798–0.962), and 0.74 (95%CI: 0.618–0.870), respectively, cut‐offs &gt;2554, 1820, 3886 copies/μL, respectively; sensitivity 41.6%, 21.4% and 17.8%, respectively; and specificity 95.8%, 95.4% and 95.4%, respectively. Conclusion Plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p are potential diagnostic biomarkers in GDM.</description><subject>Adult</subject><subject>biomarker</subject><subject>Biomarkers</subject><subject>Biomarkers - blood</subject><subject>Body mass</subject><subject>Body mass index</subject><subject>Correlation analysis</subject><subject>Diabetes</subject><subject>Diabetes mellitus</subject><subject>Diabetes, Gestational - blood</subject><subject>Female</subject><subject>gestational diabetes mellitus</subject><subject>Humans</subject><subject>Insulin</subject><subject>microRNA</subject><subject>MicroRNAs</subject><subject>MicroRNAs - blood</subject><subject>miRNA</subject><subject>Polymerase chain reaction</subject><subject>Pregnancy</subject><subject>Reverse transcription</subject><subject>risk factor</subject><subject>Risk factors</subject><subject>ROC Curve</subject><subject>Tumor necrosis factor</subject><subject>Tumor necrosis factor-TNF</subject><subject>Young Adult</subject><issn>1341-8076</issn><issn>1447-0756</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1KxDAUhYMojn8LX0ACbhTsmNukTepOxF_EEdF1SZN0yNhOxqZV3PkIPqNPYqYzuhDMIjkXvhzOvRehXSBDCOd44sZDoBT4CtoAxnhEeJKuBk0ZRILwdIA2vZ8QAjwDsY4GsUhjIAlsoPa-kr6WuLaqcQ93p18fn5CGK5kd4bnmvcZyqudlTGRfn-A792oqrK0cT51vrcKFdbVsnk3jcekaPDa-la11U9lThWmNx7WpKtt2fhutlbLyZmf5bqGni_PHs6vodnR5fXZ6GymaCB6VuiDcMGVSIRXRmjIWM8gKJrQppUhAEa5lTEHIjAtWsKxQhTIs0ykXMpF0Cx0sfGeNe-lCory2XoUQcmpc53PIgPBMUMoCuv8HnbiuCennVExYRlhPHS6oMCzvG1Pms8aGtt9zIPl8FeHXOO9XEdi9pWNX1Eb_kj-zD8DxAnizlXn_3ym_GV0uLL8BQviW1Q</recordid><startdate>201706</startdate><enddate>201706</enddate><creator>Cao, Ya‐Lei</creator><creator>Jia, Yan‐Ju</creator><creator>Xing, Bao‐Heng</creator><creator>Shi, Dan‐Dan</creator><creator>Dong, Xiu‐Juan</creator><general>Wiley Subscription Services, Inc</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>7T5</scope><scope>7TO</scope><scope>H94</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201706</creationdate><title>Plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p: Novel diagnostic biomarkers for gestational diabetes mellitus</title><author>Cao, Ya‐Lei ; Jia, Yan‐Ju ; Xing, Bao‐Heng ; Shi, Dan‐Dan ; Dong, Xiu‐Juan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3587-fdb07e4ce68ac0dd3442419b48defa851c07da2318a9784b49bcbce49d678a5a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adult</topic><topic>biomarker</topic><topic>Biomarkers</topic><topic>Biomarkers - blood</topic><topic>Body mass</topic><topic>Body mass index</topic><topic>Correlation analysis</topic><topic>Diabetes</topic><topic>Diabetes mellitus</topic><topic>Diabetes, Gestational - blood</topic><topic>Female</topic><topic>gestational diabetes mellitus</topic><topic>Humans</topic><topic>Insulin</topic><topic>microRNA</topic><topic>MicroRNAs</topic><topic>MicroRNAs - blood</topic><topic>miRNA</topic><topic>Polymerase chain reaction</topic><topic>Pregnancy</topic><topic>Reverse transcription</topic><topic>risk factor</topic><topic>Risk factors</topic><topic>ROC Curve</topic><topic>Tumor necrosis factor</topic><topic>Tumor necrosis factor-TNF</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cao, Ya‐Lei</creatorcontrib><creatorcontrib>Jia, Yan‐Ju</creatorcontrib><creatorcontrib>Xing, Bao‐Heng</creatorcontrib><creatorcontrib>Shi, Dan‐Dan</creatorcontrib><creatorcontrib>Dong, Xiu‐Juan</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Immunology Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>The journal of obstetrics and gynaecology research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cao, Ya‐Lei</au><au>Jia, Yan‐Ju</au><au>Xing, Bao‐Heng</au><au>Shi, Dan‐Dan</au><au>Dong, Xiu‐Juan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p: Novel diagnostic biomarkers for gestational diabetes mellitus</atitle><jtitle>The journal of obstetrics and gynaecology research</jtitle><addtitle>J Obstet Gynaecol Res</addtitle><date>2017-06</date><risdate>2017</risdate><volume>43</volume><issue>6</issue><spage>974</spage><epage>981</epage><pages>974-981</pages><issn>1341-8076</issn><eissn>1447-0756</eissn><abstract>Aim To explore whether plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p can be used as diagnostic biomarkers in gestational diabetes mellitus (GDM) and to investigate the relationship between those microRNAs and the risk factors of GDM (body mass index [BMI], insulin resistance [IR] and tumor necrosis factor‐α (TNF‐α)). Methods A total of 85 pregnant women with GDM and 72 pregnant women without GDM were enrolled in this study. The plasma concentration of microRNAs (microRNA‐16‐5p, ‐17‐5p, ‐19a‐3p, ‐19b‐3p, ‐20a‐5p) was measured using quantitative reverse transcription–polymerase chain reaction (qRT‐PCR). Spearman's correlation analysis was used to evaluate the correlation between those microRNAs and the risk factors of GDM, and receiver operating characteristic curve analysis was used to evaluate diagnostic sensitivity and specificity. Results Compared with non‐GDM women, the relative and absolute expression of plasma microRNA‐16‐5p, ‐17‐5p, ‐20a‐5p from GDM women were significantly upregulated, when those women were diagnosed as GDM. During pregnancy, the expression of those microRNAs from GDM women also were significantly upregulated. The expression of those microRNAs was also positively correlated with IR, a risk factor of GDM. Plasma microRNA‐16‐5p, ‐17‐5p, ‐20a‐5p reflected an obvious separation between GDM women and non‐GDM women, with areas under the curve of 0.92 (95%CI: 0.871–0.984), 0.88 (95%CI: 0.798–0.962), and 0.74 (95%CI: 0.618–0.870), respectively, cut‐offs &gt;2554, 1820, 3886 copies/μL, respectively; sensitivity 41.6%, 21.4% and 17.8%, respectively; and specificity 95.8%, 95.4% and 95.4%, respectively. Conclusion Plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p are potential diagnostic biomarkers in GDM.</abstract><cop>Australia</cop><pub>Wiley Subscription Services, Inc</pub><pmid>28621051</pmid><doi>10.1111/jog.13317</doi><tpages>8</tpages></addata></record>
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identifier ISSN: 1341-8076
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source Wiley Online Library - AutoHoldings Journals; MEDLINE
subjects Adult
biomarker
Biomarkers
Biomarkers - blood
Body mass
Body mass index
Correlation analysis
Diabetes
Diabetes mellitus
Diabetes, Gestational - blood
Female
gestational diabetes mellitus
Humans
Insulin
microRNA
MicroRNAs
MicroRNAs - blood
miRNA
Polymerase chain reaction
Pregnancy
Reverse transcription
risk factor
Risk factors
ROC Curve
Tumor necrosis factor
Tumor necrosis factor-TNF
Young Adult
title Plasma microRNA‐16‐5p, ‐17‐5p and ‐20a‐5p: Novel diagnostic biomarkers for gestational diabetes mellitus
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