The Evaluation of Adropin and Autotaxin as Potential Markers of Endothelial Dysfunction in Preeclampsia
Endothelial dysfunction (ED) plays a prominent role in the pathogenesis of preeclampsia (PE). There is a need for non-invasive methods to assess endothelial function in preeclamptic patients. In the present study, adropin, autotaxin (ATX), and lysophosphatidic acid (LPA) were evaluated as indicators...
Gespeichert in:
Veröffentlicht in: | Angiology 2024-09, Vol.75 (8), p.779-785 |
---|---|
Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 785 |
---|---|
container_issue | 8 |
container_start_page | 779 |
container_title | Angiology |
container_volume | 75 |
creator | Karaca, Ece Ercan, Celal Caner Akdemir, Celal Sivrikoz, Tugba Sarac Salmaslioglu, Artur Verit, Fatma Ferda Gurdol, Figen Omer, Beyhan |
description | Endothelial dysfunction (ED) plays a prominent role in the pathogenesis of preeclampsia (PE). There is a need for non-invasive methods to assess endothelial function in preeclamptic patients. In the present study, adropin, autotaxin (ATX), and lysophosphatidic acid (LPA) were evaluated as indicators of ED. Patients diagnosed with PE and healthy pregnant women (n = 42 for each group) were compared. After measuring flow-mediated dilation (FMD), the participants were stratified as ED (+) or ED (−) based on a cut-off value of 6.5%. The PE patients were divided as early/late onset PE and severe/mild PE. Adropin, ATX, and LPA levels were measured, and their relevance to ED was evaluated. Student t, Mann–Whitney U, or ANOVA tests were used for statistics, as appropriate. Adropin levels were diminished in the ED (+) group, whereas ATX and LPA levels were increased. The decrease in adropin levels was more pronounced in severe PE, showing a positive correlation with the FMD. In the logistic regression model, adropin was the only parameter that was an independent variable for the FMD test (P < .001). Adropin measurements in serum may be of value for disease follow-up in patients with PE. |
doi_str_mv | 10.1177/00033197231183228 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_2852629916</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_00033197231183228</sage_id><sourcerecordid>2852629916</sourcerecordid><originalsourceid>FETCH-LOGICAL-c340t-ca7a31cf68156395d03b7601f6560f33c9f83acc16225fc673cc7af5bc2641203</originalsourceid><addsrcrecordid>eNp9kEtPwzAQhC0EouXxA7igHLmkeO3Yjo9VKQ-piB7KOXIdu01J4mIniP57Elq4IHFaze43I-0gdAV4BCDELcaYUpCCUICUEpIeoSHIBMfARHKMhv097oEBOgth00kGmJ-iARUsFamUQ7RarE00_VBlq5rC1ZGz0Tj3blvUkarzaNw2rlGfvQrR3DWmbgpVRs_Kvxkfenpa565Zm7Jf3-2CbWv9HdRZ5t4YXapqGwp1gU6sKoO5PMxz9Ho_XUwe49nLw9NkPIs1TXATayUUBW15CoxTyXJMl4JjsJxxbCnV0qZUaQ2cEGY1F1RroSxbasITIJieo5t97ta799aEJquKoE1Zqtq4NmQkZYQTKYF3KOxR7V0I3ths64tK-V0GOOv7zf7023muD_HtsjL5r-On0A4Y7YGgVibbuNbX3bv_JH4BNRKCgQ</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2852629916</pqid></control><display><type>article</type><title>The Evaluation of Adropin and Autotaxin as Potential Markers of Endothelial Dysfunction in Preeclampsia</title><source>Access via SAGE</source><source>MEDLINE</source><creator>Karaca, Ece ; Ercan, Celal Caner ; Akdemir, Celal ; Sivrikoz, Tugba Sarac ; Salmaslioglu, Artur ; Verit, Fatma Ferda ; Gurdol, Figen ; Omer, Beyhan</creator><creatorcontrib>Karaca, Ece ; Ercan, Celal Caner ; Akdemir, Celal ; Sivrikoz, Tugba Sarac ; Salmaslioglu, Artur ; Verit, Fatma Ferda ; Gurdol, Figen ; Omer, Beyhan</creatorcontrib><description>Endothelial dysfunction (ED) plays a prominent role in the pathogenesis of preeclampsia (PE). There is a need for non-invasive methods to assess endothelial function in preeclamptic patients. In the present study, adropin, autotaxin (ATX), and lysophosphatidic acid (LPA) were evaluated as indicators of ED. Patients diagnosed with PE and healthy pregnant women (n = 42 for each group) were compared. After measuring flow-mediated dilation (FMD), the participants were stratified as ED (+) or ED (−) based on a cut-off value of 6.5%. The PE patients were divided as early/late onset PE and severe/mild PE. Adropin, ATX, and LPA levels were measured, and their relevance to ED was evaluated. Student t, Mann–Whitney U, or ANOVA tests were used for statistics, as appropriate. Adropin levels were diminished in the ED (+) group, whereas ATX and LPA levels were increased. The decrease in adropin levels was more pronounced in severe PE, showing a positive correlation with the FMD. In the logistic regression model, adropin was the only parameter that was an independent variable for the FMD test (P < .001). Adropin measurements in serum may be of value for disease follow-up in patients with PE.</description><identifier>ISSN: 0003-3197</identifier><identifier>ISSN: 1940-1574</identifier><identifier>EISSN: 1940-1574</identifier><identifier>DOI: 10.1177/00033197231183228</identifier><identifier>PMID: 37587899</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Adult ; Biomarkers - blood ; Blood Proteins - analysis ; Case-Control Studies ; Endothelium, Vascular - physiopathology ; Female ; Humans ; Intercellular Signaling Peptides and Proteins - blood ; Lysophospholipids - blood ; Peptides - blood ; Phosphoric Diester Hydrolases - blood ; Pre-Eclampsia - blood ; Pre-Eclampsia - diagnosis ; Pre-Eclampsia - physiopathology ; Pregnancy ; Severity of Illness Index ; Vasodilation ; Young Adult</subject><ispartof>Angiology, 2024-09, Vol.75 (8), p.779-785</ispartof><rights>The Author(s) 2023</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c340t-ca7a31cf68156395d03b7601f6560f33c9f83acc16225fc673cc7af5bc2641203</citedby><cites>FETCH-LOGICAL-c340t-ca7a31cf68156395d03b7601f6560f33c9f83acc16225fc673cc7af5bc2641203</cites><orcidid>0000-0001-8320-0590 ; 0000-0002-5915-2055 ; 0000-0003-2922-5847</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/00033197231183228$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/00033197231183228$$EHTML$$P50$$Gsage$$H</linktohtml><link.rule.ids>314,780,784,21819,27924,27925,43621,43622</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37587899$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Karaca, Ece</creatorcontrib><creatorcontrib>Ercan, Celal Caner</creatorcontrib><creatorcontrib>Akdemir, Celal</creatorcontrib><creatorcontrib>Sivrikoz, Tugba Sarac</creatorcontrib><creatorcontrib>Salmaslioglu, Artur</creatorcontrib><creatorcontrib>Verit, Fatma Ferda</creatorcontrib><creatorcontrib>Gurdol, Figen</creatorcontrib><creatorcontrib>Omer, Beyhan</creatorcontrib><title>The Evaluation of Adropin and Autotaxin as Potential Markers of Endothelial Dysfunction in Preeclampsia</title><title>Angiology</title><addtitle>Angiology</addtitle><description>Endothelial dysfunction (ED) plays a prominent role in the pathogenesis of preeclampsia (PE). There is a need for non-invasive methods to assess endothelial function in preeclamptic patients. In the present study, adropin, autotaxin (ATX), and lysophosphatidic acid (LPA) were evaluated as indicators of ED. Patients diagnosed with PE and healthy pregnant women (n = 42 for each group) were compared. After measuring flow-mediated dilation (FMD), the participants were stratified as ED (+) or ED (−) based on a cut-off value of 6.5%. The PE patients were divided as early/late onset PE and severe/mild PE. Adropin, ATX, and LPA levels were measured, and their relevance to ED was evaluated. Student t, Mann–Whitney U, or ANOVA tests were used for statistics, as appropriate. Adropin levels were diminished in the ED (+) group, whereas ATX and LPA levels were increased. The decrease in adropin levels was more pronounced in severe PE, showing a positive correlation with the FMD. In the logistic regression model, adropin was the only parameter that was an independent variable for the FMD test (P < .001). Adropin measurements in serum may be of value for disease follow-up in patients with PE.</description><subject>Adult</subject><subject>Biomarkers - blood</subject><subject>Blood Proteins - analysis</subject><subject>Case-Control Studies</subject><subject>Endothelium, Vascular - physiopathology</subject><subject>Female</subject><subject>Humans</subject><subject>Intercellular Signaling Peptides and Proteins - blood</subject><subject>Lysophospholipids - blood</subject><subject>Peptides - blood</subject><subject>Phosphoric Diester Hydrolases - blood</subject><subject>Pre-Eclampsia - blood</subject><subject>Pre-Eclampsia - diagnosis</subject><subject>Pre-Eclampsia - physiopathology</subject><subject>Pregnancy</subject><subject>Severity of Illness Index</subject><subject>Vasodilation</subject><subject>Young Adult</subject><issn>0003-3197</issn><issn>1940-1574</issn><issn>1940-1574</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEtPwzAQhC0EouXxA7igHLmkeO3Yjo9VKQ-piB7KOXIdu01J4mIniP57Elq4IHFaze43I-0gdAV4BCDELcaYUpCCUICUEpIeoSHIBMfARHKMhv097oEBOgth00kGmJ-iARUsFamUQ7RarE00_VBlq5rC1ZGz0Tj3blvUkarzaNw2rlGfvQrR3DWmbgpVRs_Kvxkfenpa565Zm7Jf3-2CbWv9HdRZ5t4YXapqGwp1gU6sKoO5PMxz9Ho_XUwe49nLw9NkPIs1TXATayUUBW15CoxTyXJMl4JjsJxxbCnV0qZUaQ2cEGY1F1RroSxbasITIJieo5t97ta799aEJquKoE1Zqtq4NmQkZYQTKYF3KOxR7V0I3ths64tK-V0GOOv7zf7023muD_HtsjL5r-On0A4Y7YGgVibbuNbX3bv_JH4BNRKCgQ</recordid><startdate>20240901</startdate><enddate>20240901</enddate><creator>Karaca, Ece</creator><creator>Ercan, Celal Caner</creator><creator>Akdemir, Celal</creator><creator>Sivrikoz, Tugba Sarac</creator><creator>Salmaslioglu, Artur</creator><creator>Verit, Fatma Ferda</creator><creator>Gurdol, Figen</creator><creator>Omer, Beyhan</creator><general>SAGE Publications</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><orcidid>https://orcid.org/0000-0001-8320-0590</orcidid><orcidid>https://orcid.org/0000-0002-5915-2055</orcidid><orcidid>https://orcid.org/0000-0003-2922-5847</orcidid></search><sort><creationdate>20240901</creationdate><title>The Evaluation of Adropin and Autotaxin as Potential Markers of Endothelial Dysfunction in Preeclampsia</title><author>Karaca, Ece ; Ercan, Celal Caner ; Akdemir, Celal ; Sivrikoz, Tugba Sarac ; Salmaslioglu, Artur ; Verit, Fatma Ferda ; Gurdol, Figen ; Omer, Beyhan</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c340t-ca7a31cf68156395d03b7601f6560f33c9f83acc16225fc673cc7af5bc2641203</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Adult</topic><topic>Biomarkers - blood</topic><topic>Blood Proteins - analysis</topic><topic>Case-Control Studies</topic><topic>Endothelium, Vascular - physiopathology</topic><topic>Female</topic><topic>Humans</topic><topic>Intercellular Signaling Peptides and Proteins - blood</topic><topic>Lysophospholipids - blood</topic><topic>Peptides - blood</topic><topic>Phosphoric Diester Hydrolases - blood</topic><topic>Pre-Eclampsia - blood</topic><topic>Pre-Eclampsia - diagnosis</topic><topic>Pre-Eclampsia - physiopathology</topic><topic>Pregnancy</topic><topic>Severity of Illness Index</topic><topic>Vasodilation</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Karaca, Ece</creatorcontrib><creatorcontrib>Ercan, Celal Caner</creatorcontrib><creatorcontrib>Akdemir, Celal</creatorcontrib><creatorcontrib>Sivrikoz, Tugba Sarac</creatorcontrib><creatorcontrib>Salmaslioglu, Artur</creatorcontrib><creatorcontrib>Verit, Fatma Ferda</creatorcontrib><creatorcontrib>Gurdol, Figen</creatorcontrib><creatorcontrib>Omer, Beyhan</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>Angiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Karaca, Ece</au><au>Ercan, Celal Caner</au><au>Akdemir, Celal</au><au>Sivrikoz, Tugba Sarac</au><au>Salmaslioglu, Artur</au><au>Verit, Fatma Ferda</au><au>Gurdol, Figen</au><au>Omer, Beyhan</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The Evaluation of Adropin and Autotaxin as Potential Markers of Endothelial Dysfunction in Preeclampsia</atitle><jtitle>Angiology</jtitle><addtitle>Angiology</addtitle><date>2024-09-01</date><risdate>2024</risdate><volume>75</volume><issue>8</issue><spage>779</spage><epage>785</epage><pages>779-785</pages><issn>0003-3197</issn><issn>1940-1574</issn><eissn>1940-1574</eissn><abstract>Endothelial dysfunction (ED) plays a prominent role in the pathogenesis of preeclampsia (PE). There is a need for non-invasive methods to assess endothelial function in preeclamptic patients. In the present study, adropin, autotaxin (ATX), and lysophosphatidic acid (LPA) were evaluated as indicators of ED. Patients diagnosed with PE and healthy pregnant women (n = 42 for each group) were compared. After measuring flow-mediated dilation (FMD), the participants were stratified as ED (+) or ED (−) based on a cut-off value of 6.5%. The PE patients were divided as early/late onset PE and severe/mild PE. Adropin, ATX, and LPA levels were measured, and their relevance to ED was evaluated. Student t, Mann–Whitney U, or ANOVA tests were used for statistics, as appropriate. Adropin levels were diminished in the ED (+) group, whereas ATX and LPA levels were increased. The decrease in adropin levels was more pronounced in severe PE, showing a positive correlation with the FMD. In the logistic regression model, adropin was the only parameter that was an independent variable for the FMD test (P < .001). Adropin measurements in serum may be of value for disease follow-up in patients with PE.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>37587899</pmid><doi>10.1177/00033197231183228</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0001-8320-0590</orcidid><orcidid>https://orcid.org/0000-0002-5915-2055</orcidid><orcidid>https://orcid.org/0000-0003-2922-5847</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 0003-3197 |
ispartof | Angiology, 2024-09, Vol.75 (8), p.779-785 |
issn | 0003-3197 1940-1574 1940-1574 |
language | eng |
recordid | cdi_proquest_miscellaneous_2852629916 |
source | Access via SAGE; MEDLINE |
subjects | Adult Biomarkers - blood Blood Proteins - analysis Case-Control Studies Endothelium, Vascular - physiopathology Female Humans Intercellular Signaling Peptides and Proteins - blood Lysophospholipids - blood Peptides - blood Phosphoric Diester Hydrolases - blood Pre-Eclampsia - blood Pre-Eclampsia - diagnosis Pre-Eclampsia - physiopathology Pregnancy Severity of Illness Index Vasodilation Young Adult |
title | The Evaluation of Adropin and Autotaxin as Potential Markers of Endothelial Dysfunction in Preeclampsia |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T05%3A18%3A26IST&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=The%20Evaluation%20of%20Adropin%20and%20Autotaxin%20as%20Potential%20Markers%20of%20Endothelial%20Dysfunction%20in%20Preeclampsia&rft.jtitle=Angiology&rft.au=Karaca,%20Ece&rft.date=2024-09-01&rft.volume=75&rft.issue=8&rft.spage=779&rft.epage=785&rft.pages=779-785&rft.issn=0003-3197&rft.eissn=1940-1574&rft_id=info:doi/10.1177/00033197231183228&rft_dat=%3Cproquest_cross%3E2852629916%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=2852629916&rft_id=info:pmid/37587899&rft_sage_id=10.1177_00033197231183228&rfr_iscdi=true |