A comparison of the maternal levels of serum proprotein convertase subtilisin/kexin type 9 in pregnant women with the complication of fetal open neural tube defects
It was aimed to evaluate the levels of maternal serum proprotein convertase subtilisin/kexin type 9 (PCSK9) in pregnant women with a fetus diagnosed with open neural tube defects (NTDs). This case‐control study included 38 pregnant women carrying fetuses with open NTDs and 44 age‐matched, pregnant w...
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Veröffentlicht in: | Congenital anomalies 2021-09, Vol.61 (5), p.169-176 |
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description | It was aimed to evaluate the levels of maternal serum proprotein convertase subtilisin/kexin type 9 (PCSK9) in pregnant women with a fetus diagnosed with open neural tube defects (NTDs). This case‐control study included 38 pregnant women carrying fetuses with open NTDs and 44 age‐matched, pregnant women with no specified risk factors. Comparisons were made of the groups in respect of demographic and clinical data and PCSK9 levels. To examine the performance of PCSK9 levels in the prediction of fetal open NTDs, receiver operating characteristic (ROC) curve analysis was used. In the first and second trimesters, PCSK9 levels were determined to be lower in the NTD group than in the control group (p = 0.010 and p = 0.015, respectively). In the first trimester, the lower PCSK9 levels in the NTD group were not statistically significant (p = 0.575). In the second trimester, the ROC curve value with the best balance of sensitivity/specificity for PCSK9 was 71.9 ng/ml (84.6% sensitivity, 51.7% specificity) and in the first and second trimester combined, 74.4 ng/ml (81.6% sensitivity, 45.5% specificity) (p = 0.015, p = 0.036, respectively). PCSK9 may be involved in the etiopathogenesis of open NTDs at the critical steps of fetal neuronal differentiation. Although it has limitations, PCSK9 may be used as an additional biomarker for the screening of NTDs. |
doi_str_mv | 10.1111/cga.12432 |
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This case‐control study included 38 pregnant women carrying fetuses with open NTDs and 44 age‐matched, pregnant women with no specified risk factors. Comparisons were made of the groups in respect of demographic and clinical data and PCSK9 levels. To examine the performance of PCSK9 levels in the prediction of fetal open NTDs, receiver operating characteristic (ROC) curve analysis was used. In the first and second trimesters, PCSK9 levels were determined to be lower in the NTD group than in the control group (p = 0.010 and p = 0.015, respectively). In the first trimester, the lower PCSK9 levels in the NTD group were not statistically significant (p = 0.575). In the second trimester, the ROC curve value with the best balance of sensitivity/specificity for PCSK9 was 71.9 ng/ml (84.6% sensitivity, 51.7% specificity) and in the first and second trimester combined, 74.4 ng/ml (81.6% sensitivity, 45.5% specificity) (p = 0.015, p = 0.036, respectively). PCSK9 may be involved in the etiopathogenesis of open NTDs at the critical steps of fetal neuronal differentiation. Although it has limitations, PCSK9 may be used as an additional biomarker for the screening of NTDs.</description><identifier>ISSN: 0914-3505</identifier><identifier>EISSN: 1741-4520</identifier><identifier>DOI: 10.1111/cga.12432</identifier><identifier>PMID: 34128273</identifier><language>eng</language><publisher>Kyoto, Japan: John Wiley & Sons Australia, Ltd</publisher><subject>Biomarkers ; Birth defects ; Case-Control Studies ; Defects ; Female ; Fetus ; Fetuses ; Humans ; Kexin ; Neural tube defects ; Neural Tube Defects - diagnosis ; Neural Tube Defects - etiology ; open neural tube defects ; Pregnancy ; Pregnant Women ; Proprotein Convertase 9 - blood ; proprotein convertase subtilisin/kexin type 9 ; Proprotein convertases ; Risk analysis ; Risk factors ; Sensitivity ; Statistical analysis ; Subtilisin</subject><ispartof>Congenital anomalies, 2021-09, Vol.61 (5), p.169-176</ispartof><rights>2021 Japanese Teratology Society</rights><rights>2021 Japanese Teratology Society.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3072-44225ebc394ac45c961051dac0bce4909cc8ff424cc2a28fac8294e70e4f3d8c3</citedby><cites>FETCH-LOGICAL-c3072-44225ebc394ac45c961051dac0bce4909cc8ff424cc2a28fac8294e70e4f3d8c3</cites><orcidid>0000-0001-8567-9048 ; 0000-0002-0974-5717 ; 0000-0001-5437-1008 ; 0000-0002-5770-7555 ; 0000-0002-2494-4896 ; 0000-0002-8147-5379 ; 0000-0001-8209-8248</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fcga.12432$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fcga.12432$$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/34128273$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Erol, Seyit Ahmet</creatorcontrib><creatorcontrib>Tanacan, Atakan</creatorcontrib><creatorcontrib>Firat Oguz, Esra</creatorcontrib><creatorcontrib>Anuk, Ali Taner</creatorcontrib><creatorcontrib>Goncu Ayhan, Sule</creatorcontrib><creatorcontrib>Neselioglu, Salim</creatorcontrib><creatorcontrib>Sahin, Dilek</creatorcontrib><title>A comparison of the maternal levels of serum proprotein convertase subtilisin/kexin type 9 in pregnant women with the complication of fetal open neural tube defects</title><title>Congenital anomalies</title><addtitle>Congenit Anom (Kyoto)</addtitle><description>It was aimed to evaluate the levels of maternal serum proprotein convertase subtilisin/kexin type 9 (PCSK9) in pregnant women with a fetus diagnosed with open neural tube defects (NTDs). This case‐control study included 38 pregnant women carrying fetuses with open NTDs and 44 age‐matched, pregnant women with no specified risk factors. Comparisons were made of the groups in respect of demographic and clinical data and PCSK9 levels. To examine the performance of PCSK9 levels in the prediction of fetal open NTDs, receiver operating characteristic (ROC) curve analysis was used. In the first and second trimesters, PCSK9 levels were determined to be lower in the NTD group than in the control group (p = 0.010 and p = 0.015, respectively). In the first trimester, the lower PCSK9 levels in the NTD group were not statistically significant (p = 0.575). In the second trimester, the ROC curve value with the best balance of sensitivity/specificity for PCSK9 was 71.9 ng/ml (84.6% sensitivity, 51.7% specificity) and in the first and second trimester combined, 74.4 ng/ml (81.6% sensitivity, 45.5% specificity) (p = 0.015, p = 0.036, respectively). PCSK9 may be involved in the etiopathogenesis of open NTDs at the critical steps of fetal neuronal differentiation. Although it has limitations, PCSK9 may be used as an additional biomarker for the screening of NTDs.</description><subject>Biomarkers</subject><subject>Birth defects</subject><subject>Case-Control Studies</subject><subject>Defects</subject><subject>Female</subject><subject>Fetus</subject><subject>Fetuses</subject><subject>Humans</subject><subject>Kexin</subject><subject>Neural tube defects</subject><subject>Neural Tube Defects - diagnosis</subject><subject>Neural Tube Defects - etiology</subject><subject>open neural tube defects</subject><subject>Pregnancy</subject><subject>Pregnant Women</subject><subject>Proprotein Convertase 9 - blood</subject><subject>proprotein convertase subtilisin/kexin type 9</subject><subject>Proprotein convertases</subject><subject>Risk analysis</subject><subject>Risk factors</subject><subject>Sensitivity</subject><subject>Statistical analysis</subject><subject>Subtilisin</subject><issn>0914-3505</issn><issn>1741-4520</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kc1u1DAUhS0EokPLghdAltjAIh3_ZZIsRyNakCp1Q9eRc-emdXHsYDsd5n140DpNYYFU60q-uv58juxDyAfOznlea7jV51woKV6RFa8UL1Qp2GuyYg1XhSxZeULexXjPmNhsKvaWnEjFRS0quSJ_thT8MOpgonfU9zTdIR10wuC0pRYf0MZ5HDFMAx2Dz5XQuHzLPWBIOiKNU5eMNdG49U_8nc_ScUTa0NyNAW-ddoke_ICOHky6e3KYPa0Bnczi2mPKdn7MjMMp5D5NHdI99ggpnpE3vbYR3z_vp-Tm4uuP3bfi6vry-257VYBklSiUEqLEDmSjNKgSmg1nJd9rYB2galgDUPe9EgpAaFH3GmrRKKwYql7ua5Cn5POimx_5a8KY2sFEQGu1Qz_FVpSKS8F5zTL66T_03k_zn83UplaVqvlMfVkoCD7GgH07BjPocGw5a-fo2hxd-xRdZj8-K07dgPt_5N-sMrBegIOxeHxZqd1dbhfJR9mKpXQ</recordid><startdate>202109</startdate><enddate>202109</enddate><creator>Erol, Seyit Ahmet</creator><creator>Tanacan, Atakan</creator><creator>Firat Oguz, Esra</creator><creator>Anuk, Ali Taner</creator><creator>Goncu Ayhan, Sule</creator><creator>Neselioglu, Salim</creator><creator>Sahin, Dilek</creator><general>John Wiley & Sons Australia, Ltd</general><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>7QP</scope><scope>7TK</scope><scope>7U7</scope><scope>C1K</scope><scope>K9.</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0001-8567-9048</orcidid><orcidid>https://orcid.org/0000-0002-0974-5717</orcidid><orcidid>https://orcid.org/0000-0001-5437-1008</orcidid><orcidid>https://orcid.org/0000-0002-5770-7555</orcidid><orcidid>https://orcid.org/0000-0002-2494-4896</orcidid><orcidid>https://orcid.org/0000-0002-8147-5379</orcidid><orcidid>https://orcid.org/0000-0001-8209-8248</orcidid></search><sort><creationdate>202109</creationdate><title>A comparison of the maternal levels of serum proprotein convertase subtilisin/kexin type 9 in pregnant women with the complication of fetal open neural tube defects</title><author>Erol, Seyit Ahmet ; Tanacan, Atakan ; Firat Oguz, Esra ; Anuk, Ali Taner ; Goncu Ayhan, Sule ; Neselioglu, Salim ; Sahin, Dilek</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3072-44225ebc394ac45c961051dac0bce4909cc8ff424cc2a28fac8294e70e4f3d8c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>Biomarkers</topic><topic>Birth defects</topic><topic>Case-Control Studies</topic><topic>Defects</topic><topic>Female</topic><topic>Fetus</topic><topic>Fetuses</topic><topic>Humans</topic><topic>Kexin</topic><topic>Neural tube defects</topic><topic>Neural Tube Defects - diagnosis</topic><topic>Neural Tube Defects - etiology</topic><topic>open neural tube defects</topic><topic>Pregnancy</topic><topic>Pregnant Women</topic><topic>Proprotein Convertase 9 - blood</topic><topic>proprotein convertase subtilisin/kexin type 9</topic><topic>Proprotein convertases</topic><topic>Risk analysis</topic><topic>Risk factors</topic><topic>Sensitivity</topic><topic>Statistical analysis</topic><topic>Subtilisin</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Erol, Seyit Ahmet</creatorcontrib><creatorcontrib>Tanacan, Atakan</creatorcontrib><creatorcontrib>Firat Oguz, Esra</creatorcontrib><creatorcontrib>Anuk, Ali Taner</creatorcontrib><creatorcontrib>Goncu Ayhan, Sule</creatorcontrib><creatorcontrib>Neselioglu, Salim</creatorcontrib><creatorcontrib>Sahin, Dilek</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Congenital anomalies</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Erol, Seyit Ahmet</au><au>Tanacan, Atakan</au><au>Firat Oguz, Esra</au><au>Anuk, Ali Taner</au><au>Goncu Ayhan, Sule</au><au>Neselioglu, Salim</au><au>Sahin, Dilek</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A comparison of the maternal levels of serum proprotein convertase subtilisin/kexin type 9 in pregnant women with the complication of fetal open neural tube defects</atitle><jtitle>Congenital anomalies</jtitle><addtitle>Congenit Anom (Kyoto)</addtitle><date>2021-09</date><risdate>2021</risdate><volume>61</volume><issue>5</issue><spage>169</spage><epage>176</epage><pages>169-176</pages><issn>0914-3505</issn><eissn>1741-4520</eissn><abstract>It was aimed to evaluate the levels of maternal serum proprotein convertase subtilisin/kexin type 9 (PCSK9) in pregnant women with a fetus diagnosed with open neural tube defects (NTDs). This case‐control study included 38 pregnant women carrying fetuses with open NTDs and 44 age‐matched, pregnant women with no specified risk factors. Comparisons were made of the groups in respect of demographic and clinical data and PCSK9 levels. To examine the performance of PCSK9 levels in the prediction of fetal open NTDs, receiver operating characteristic (ROC) curve analysis was used. In the first and second trimesters, PCSK9 levels were determined to be lower in the NTD group than in the control group (p = 0.010 and p = 0.015, respectively). In the first trimester, the lower PCSK9 levels in the NTD group were not statistically significant (p = 0.575). In the second trimester, the ROC curve value with the best balance of sensitivity/specificity for PCSK9 was 71.9 ng/ml (84.6% sensitivity, 51.7% specificity) and in the first and second trimester combined, 74.4 ng/ml (81.6% sensitivity, 45.5% specificity) (p = 0.015, p = 0.036, respectively). PCSK9 may be involved in the etiopathogenesis of open NTDs at the critical steps of fetal neuronal differentiation. Although it has limitations, PCSK9 may be used as an additional biomarker for the screening of NTDs.</abstract><cop>Kyoto, Japan</cop><pub>John Wiley & Sons Australia, Ltd</pub><pmid>34128273</pmid><doi>10.1111/cga.12432</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0001-8567-9048</orcidid><orcidid>https://orcid.org/0000-0002-0974-5717</orcidid><orcidid>https://orcid.org/0000-0001-5437-1008</orcidid><orcidid>https://orcid.org/0000-0002-5770-7555</orcidid><orcidid>https://orcid.org/0000-0002-2494-4896</orcidid><orcidid>https://orcid.org/0000-0002-8147-5379</orcidid><orcidid>https://orcid.org/0000-0001-8209-8248</orcidid></addata></record> |
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subjects | Biomarkers Birth defects Case-Control Studies Defects Female Fetus Fetuses Humans Kexin Neural tube defects Neural Tube Defects - diagnosis Neural Tube Defects - etiology open neural tube defects Pregnancy Pregnant Women Proprotein Convertase 9 - blood proprotein convertase subtilisin/kexin type 9 Proprotein convertases Risk analysis Risk factors Sensitivity Statistical analysis Subtilisin |
title | A comparison of the maternal levels of serum proprotein convertase subtilisin/kexin type 9 in pregnant women with the complication of fetal open neural tube defects |
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