Pre-pregnancy endothelial dysfunction and birth outcomes: The Coronary Artery Risk Development in Young Adults (CARDIA) Study
Endothelial dysfunction is a form of subclinical cardiovascular disease that may be involved in preterm birth and small-for-gestational-age deliveries. However, concentrations of biomarkers of endothelial dysfunction before pregnancy have rarely been measured. We hypothesized that higher levels of b...
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Veröffentlicht in: | Hypertension research 2018-04, Vol.41 (4), p.282-289 |
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description | Endothelial dysfunction is a form of subclinical cardiovascular disease that may be involved in preterm birth and small-for-gestational-age deliveries. However, concentrations of biomarkers of endothelial dysfunction before pregnancy have rarely been measured. We hypothesized that higher levels of biomarkers of endothelial dysfunction (cellular adhesion molecules and selectins) would be associated with odds of preterm birth and/or small-for-gestational-age deliveries. We included 235 women from the Coronary Artery Risk Development in Young Adults (CARDIA) study who were nulliparous at Y7, reported ≥1 live birth through Y25, and had ≥1 biomarker measured at Y7. We tested for associations between individual biomarkers and an averaged z-score representing total endothelial dysfunction with preterm birth and/or small-for-gestational-age deliveries using Poisson regression, adjusted for demographic and clinical characteristics at the exam immediately preceding index birth. At Y7, total evidence of endothelial dysfunction was similar in women who did (n = 59) and did not have (n = 176) preterm birth and/or small-for-gestational-age deliveries. There was no association between biomarkers of endothelial dysfunction (either individual biomarker or total score) with odds of preterm birth and/or small-for-gestational-age deliveries after adjustment: IRR = 1.01, 95% CI: 0.74, 1.39, p = 0.93 for total endothelial biomarker score. Associations were not modified by race. We conclude that biomarkers of endothelial dysfunction in nulliparous women, measured ~3 years before pregnancy, did not identify women at risk for preterm birth and/or small-for-gestational-age deliveries. This suggests that the maternal endothelial dysfunction that is believed to contribute to these birth outcomes may not be detectable before pregnancy. |
doi_str_mv | 10.1038/s41440-018-0017-5 |
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However, concentrations of biomarkers of endothelial dysfunction before pregnancy have rarely been measured. We hypothesized that higher levels of biomarkers of endothelial dysfunction (cellular adhesion molecules and selectins) would be associated with odds of preterm birth and/or small-for-gestational-age deliveries. We included 235 women from the Coronary Artery Risk Development in Young Adults (CARDIA) study who were nulliparous at Y7, reported ≥1 live birth through Y25, and had ≥1 biomarker measured at Y7. We tested for associations between individual biomarkers and an averaged z-score representing total endothelial dysfunction with preterm birth and/or small-for-gestational-age deliveries using Poisson regression, adjusted for demographic and clinical characteristics at the exam immediately preceding index birth. At Y7, total evidence of endothelial dysfunction was similar in women who did (n = 59) and did not have (n = 176) preterm birth and/or small-for-gestational-age deliveries. There was no association between biomarkers of endothelial dysfunction (either individual biomarker or total score) with odds of preterm birth and/or small-for-gestational-age deliveries after adjustment: IRR = 1.01, 95% CI: 0.74, 1.39, p = 0.93 for total endothelial biomarker score. Associations were not modified by race. We conclude that biomarkers of endothelial dysfunction in nulliparous women, measured ~3 years before pregnancy, did not identify women at risk for preterm birth and/or small-for-gestational-age deliveries. This suggests that the maternal endothelial dysfunction that is believed to contribute to these birth outcomes may not be detectable before pregnancy.</description><identifier>ISSN: 0916-9636</identifier><identifier>EISSN: 1348-4214</identifier><identifier>DOI: 10.1038/s41440-018-0017-5</identifier><identifier>PMID: 29449706</identifier><language>eng</language><publisher>England: Nature Publishing Group</publisher><subject>Adolescent ; Adult ; Age ; Biomarkers ; Blood Pressure ; Cell Adhesion Molecules - blood ; Coronary Artery Disease - physiopathology ; Coronary vessels ; Endothelium, Vascular - physiopathology ; Female ; Health risk assessment ; Humans ; Infant, Small for Gestational Age ; Negative Results ; Nitric oxide ; Obstetric Labor, Premature ; Pregnancy ; Pregnancy - physiology ; Pregnancy Outcome ; Premature birth ; Risk Assessment ; Socioeconomic Factors ; Vein & artery diseases ; Young Adult ; Young adults</subject><ispartof>Hypertension research, 2018-04, Vol.41 (4), p.282-289</ispartof><rights>Copyright Nature Publishing Group Apr 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c381t-6de4eedaee76d936c6980e6496f992ffeb7845a3f837ce1da9b2e617be2ad6d03</citedby><cites>FETCH-LOGICAL-c381t-6de4eedaee76d936c6980e6496f992ffeb7845a3f837ce1da9b2e617be2ad6d03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29449706$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Lane-Cordova, Abbi D</creatorcontrib><creatorcontrib>Gunderson, Erica P</creatorcontrib><creatorcontrib>Carnethon, Mercedes R</creatorcontrib><creatorcontrib>Catov, Janet M</creatorcontrib><creatorcontrib>Reiner, Alex P</creatorcontrib><creatorcontrib>Lewis, Cora E</creatorcontrib><creatorcontrib>Dude, Annie M</creatorcontrib><creatorcontrib>Greenland, Philip</creatorcontrib><creatorcontrib>Jacobs, Jr, David R</creatorcontrib><title>Pre-pregnancy endothelial dysfunction and birth outcomes: The Coronary Artery Risk Development in Young Adults (CARDIA) Study</title><title>Hypertension research</title><addtitle>Hypertens Res</addtitle><description>Endothelial dysfunction is a form of subclinical cardiovascular disease that may be involved in preterm birth and small-for-gestational-age deliveries. However, concentrations of biomarkers of endothelial dysfunction before pregnancy have rarely been measured. We hypothesized that higher levels of biomarkers of endothelial dysfunction (cellular adhesion molecules and selectins) would be associated with odds of preterm birth and/or small-for-gestational-age deliveries. We included 235 women from the Coronary Artery Risk Development in Young Adults (CARDIA) study who were nulliparous at Y7, reported ≥1 live birth through Y25, and had ≥1 biomarker measured at Y7. We tested for associations between individual biomarkers and an averaged z-score representing total endothelial dysfunction with preterm birth and/or small-for-gestational-age deliveries using Poisson regression, adjusted for demographic and clinical characteristics at the exam immediately preceding index birth. At Y7, total evidence of endothelial dysfunction was similar in women who did (n = 59) and did not have (n = 176) preterm birth and/or small-for-gestational-age deliveries. There was no association between biomarkers of endothelial dysfunction (either individual biomarker or total score) with odds of preterm birth and/or small-for-gestational-age deliveries after adjustment: IRR = 1.01, 95% CI: 0.74, 1.39, p = 0.93 for total endothelial biomarker score. Associations were not modified by race. We conclude that biomarkers of endothelial dysfunction in nulliparous women, measured ~3 years before pregnancy, did not identify women at risk for preterm birth and/or small-for-gestational-age deliveries. This suggests that the maternal endothelial dysfunction that is believed to contribute to these birth outcomes may not be detectable before pregnancy.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age</subject><subject>Biomarkers</subject><subject>Blood Pressure</subject><subject>Cell Adhesion Molecules - blood</subject><subject>Coronary Artery Disease - physiopathology</subject><subject>Coronary vessels</subject><subject>Endothelium, Vascular - physiopathology</subject><subject>Female</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Infant, Small for Gestational Age</subject><subject>Negative Results</subject><subject>Nitric oxide</subject><subject>Obstetric Labor, Premature</subject><subject>Pregnancy</subject><subject>Pregnancy - physiology</subject><subject>Pregnancy Outcome</subject><subject>Premature birth</subject><subject>Risk Assessment</subject><subject>Socioeconomic Factors</subject><subject>Vein & artery diseases</subject><subject>Young Adult</subject><subject>Young adults</subject><issn>0916-9636</issn><issn>1348-4214</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNpdkcFu1DAQhi0EokvhAbggS1zKIeCxHSfmUCnaUqhUCVTKgZPlxJPdlKy92E6lPfDuzbKlAk5zmG9-_aOPkJfA3gIT9bskQUpWMKgLxqAqykdkAULWheQgH5MF06AKrYQ6Is9SumGM16WGp-SIayl1xdSC_PoSsdhGXHnrux1F70Je4zjYkbpd6iff5SF4ar2j7RDzmoYpd2GD6T29XiNdhhi8jTvaxIzzuBrSD3qGtziG7QZ9poOn38PkV7Rx05gTPVk2V2cXzRv6NU9u95w86e2Y8MX9PCbfzj9cLz8Vl58_Xiyby6ITNeRCOZSIziJWymmhOqVrhkpq1WvN-x7bqpalFX0tqg7BWd1yVFC1yK1TjoljcnrI3U7tBl03N4t2NNs4bObyJtjB_Lvxw9qswq1RAgB4OQec3AfE8HPClM1mSB2Oo_UYpmQ4Y4JJBozP6Ov_0JswRT-_N1McqlLI3xQcqC6GlCL2D2WAmb1cc5BrZrlmL9fsS7z6-4uHiz82xR3y0KHn</recordid><startdate>20180401</startdate><enddate>20180401</enddate><creator>Lane-Cordova, Abbi D</creator><creator>Gunderson, Erica P</creator><creator>Carnethon, Mercedes R</creator><creator>Catov, Janet M</creator><creator>Reiner, Alex P</creator><creator>Lewis, Cora E</creator><creator>Dude, Annie M</creator><creator>Greenland, Philip</creator><creator>Jacobs, Jr, David R</creator><general>Nature Publishing Group</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>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>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180401</creationdate><title>Pre-pregnancy endothelial dysfunction and birth outcomes: The Coronary Artery Risk Development in Young Adults (CARDIA) Study</title><author>Lane-Cordova, Abbi D ; 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However, concentrations of biomarkers of endothelial dysfunction before pregnancy have rarely been measured. We hypothesized that higher levels of biomarkers of endothelial dysfunction (cellular adhesion molecules and selectins) would be associated with odds of preterm birth and/or small-for-gestational-age deliveries. We included 235 women from the Coronary Artery Risk Development in Young Adults (CARDIA) study who were nulliparous at Y7, reported ≥1 live birth through Y25, and had ≥1 biomarker measured at Y7. We tested for associations between individual biomarkers and an averaged z-score representing total endothelial dysfunction with preterm birth and/or small-for-gestational-age deliveries using Poisson regression, adjusted for demographic and clinical characteristics at the exam immediately preceding index birth. At Y7, total evidence of endothelial dysfunction was similar in women who did (n = 59) and did not have (n = 176) preterm birth and/or small-for-gestational-age deliveries. There was no association between biomarkers of endothelial dysfunction (either individual biomarker or total score) with odds of preterm birth and/or small-for-gestational-age deliveries after adjustment: IRR = 1.01, 95% CI: 0.74, 1.39, p = 0.93 for total endothelial biomarker score. Associations were not modified by race. We conclude that biomarkers of endothelial dysfunction in nulliparous women, measured ~3 years before pregnancy, did not identify women at risk for preterm birth and/or small-for-gestational-age deliveries. This suggests that the maternal endothelial dysfunction that is believed to contribute to these birth outcomes may not be detectable before pregnancy.</abstract><cop>England</cop><pub>Nature Publishing Group</pub><pmid>29449706</pmid><doi>10.1038/s41440-018-0017-5</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Age Biomarkers Blood Pressure Cell Adhesion Molecules - blood Coronary Artery Disease - physiopathology Coronary vessels Endothelium, Vascular - physiopathology Female Health risk assessment Humans Infant, Small for Gestational Age Negative Results Nitric oxide Obstetric Labor, Premature Pregnancy Pregnancy - physiology Pregnancy Outcome Premature birth Risk Assessment Socioeconomic Factors Vein & artery diseases Young Adult Young adults |
title | Pre-pregnancy endothelial dysfunction and birth outcomes: The Coronary Artery Risk Development in Young Adults (CARDIA) Study |
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