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Placental Vitamin D-Binding Protein Expression in Human Idiopathic Fetal Growth Restriction
Vitamin D-binding protein is a multifunctional serum protein with multiple actions related to normal health. Vitamin D-binding protein transports vitamin D and influences the metabolism of this key hormone but it also has additional immunomodulatory and actin-clearing properties. We investigated whe...
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Published in: | Journal of pregnancy 2017-01, Vol.2017 (2017), p.1-5 |
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creator | Georgiou, Harry M. Brennecke, Shaun Patrick Kalionis, Bill Yong, Hannah E. J. Chollangi, Tejasvy Wookey, Alice F. Murthi, Padma |
description | Vitamin D-binding protein is a multifunctional serum protein with multiple actions related to normal health. Vitamin D-binding protein transports vitamin D and influences the metabolism of this key hormone but it also has additional immunomodulatory and actin-clearing properties. We investigated whether vitamin D-binding protein expression is altered in fetal growth restriction-associated placental dysfunction. Protein was extracted from 35 placentae derived from 17 healthy control subjects and 18 gestation-matched subjects with fetal growth restriction (FGR). FGR subjects were further subdivided as idiopathic (n=9) and nonidiopathic (n=9). Vitamin D-binding protein and 25(OH) vitamin D were measured by ELISA and normalized to protein concentration. The results showed significantly reduced levels of placental vitamin D-binding protein (control versus FGR, p |
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J. ; Chollangi, Tejasvy ; Wookey, Alice F. ; Murthi, Padma</creator><contributor>Wing, Deborah A.</contributor><creatorcontrib>Georgiou, Harry M. ; Brennecke, Shaun Patrick ; Kalionis, Bill ; Yong, Hannah E. J. ; Chollangi, Tejasvy ; Wookey, Alice F. ; Murthi, Padma ; Wing, Deborah A.</creatorcontrib><description>Vitamin D-binding protein is a multifunctional serum protein with multiple actions related to normal health. Vitamin D-binding protein transports vitamin D and influences the metabolism of this key hormone but it also has additional immunomodulatory and actin-clearing properties. We investigated whether vitamin D-binding protein expression is altered in fetal growth restriction-associated placental dysfunction. Protein was extracted from 35 placentae derived from 17 healthy control subjects and 18 gestation-matched subjects with fetal growth restriction (FGR). FGR subjects were further subdivided as idiopathic (n=9) and nonidiopathic (n=9). Vitamin D-binding protein and 25(OH) vitamin D were measured by ELISA and normalized to protein concentration. The results showed significantly reduced levels of placental vitamin D-binding protein (control versus FGR, p<0.05, Student’s t-test) that were strongly associated with idiopathic fetal growth restriction (p<0.01, Kruskal-Wallis), whereas levels of vitamin D-binding protein were not associated with placental 25(OH) vitamin D stores (p=0.295, Pearson’s correlation). As such, vitamin D-binding protein may be a factor in unexplained placental dysfunction associated with idiopathic fetal growth restriction and may potentially serve as a biomarker of this disease.</description><identifier>ISSN: 2090-2727</identifier><identifier>EISSN: 2090-2735</identifier><identifier>DOI: 10.1155/2017/5120267</identifier><identifier>PMID: 28293436</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Adult ; Biomarkers - blood ; Case-Control Studies ; Chi-Square Distribution ; Diabetes ; Enzyme-Linked Immunosorbent Assay ; Female ; Fetal Development ; Fetal Growth Retardation - metabolism ; Health risk assessment ; Humans ; Hypertension ; Inflammation ; Metabolism ; Metabolites ; Obstetrics ; Placenta ; Placenta - metabolism ; Preeclampsia ; Pregnancy ; Proteins ; Studies ; Vitamin D ; Vitamin D-Binding Protein - metabolism ; Womens health</subject><ispartof>Journal of pregnancy, 2017-01, Vol.2017 (2017), p.1-5</ispartof><rights>Copyright © 2017 Alice F. Wookey et al.</rights><rights>Copyright © 2017 Alice F. Wookey et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.</rights><rights>Copyright © 2017 Alice F. Wookey et al. 2017</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c537t-a5983f30763eb8670d6c2a2dc3cf68f7237462927a24bbbf3041cc3c61a3b3ba3</citedby><cites>FETCH-LOGICAL-c537t-a5983f30763eb8670d6c2a2dc3cf68f7237462927a24bbbf3041cc3c61a3b3ba3</cites><orcidid>0000-0003-3070-6971 ; 0000-0003-2535-5134 ; 0000-0003-0553-9489 ; 0000-0002-0132-9858</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/1872584103/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/1872584103?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,724,777,781,882,25734,27905,27906,36993,36994,44571,53772,53774,74875</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28293436$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>Wing, Deborah A.</contributor><creatorcontrib>Georgiou, Harry M.</creatorcontrib><creatorcontrib>Brennecke, Shaun Patrick</creatorcontrib><creatorcontrib>Kalionis, Bill</creatorcontrib><creatorcontrib>Yong, Hannah E. J.</creatorcontrib><creatorcontrib>Chollangi, Tejasvy</creatorcontrib><creatorcontrib>Wookey, Alice F.</creatorcontrib><creatorcontrib>Murthi, Padma</creatorcontrib><title>Placental Vitamin D-Binding Protein Expression in Human Idiopathic Fetal Growth Restriction</title><title>Journal of pregnancy</title><addtitle>J Pregnancy</addtitle><description>Vitamin D-binding protein is a multifunctional serum protein with multiple actions related to normal health. Vitamin D-binding protein transports vitamin D and influences the metabolism of this key hormone but it also has additional immunomodulatory and actin-clearing properties. We investigated whether vitamin D-binding protein expression is altered in fetal growth restriction-associated placental dysfunction. Protein was extracted from 35 placentae derived from 17 healthy control subjects and 18 gestation-matched subjects with fetal growth restriction (FGR). FGR subjects were further subdivided as idiopathic (n=9) and nonidiopathic (n=9). Vitamin D-binding protein and 25(OH) vitamin D were measured by ELISA and normalized to protein concentration. The results showed significantly reduced levels of placental vitamin D-binding protein (control versus FGR, p<0.05, Student’s t-test) that were strongly associated with idiopathic fetal growth restriction (p<0.01, Kruskal-Wallis), whereas levels of vitamin D-binding protein were not associated with placental 25(OH) vitamin D stores (p=0.295, Pearson’s correlation). As such, vitamin D-binding protein may be a factor in unexplained placental dysfunction associated with idiopathic fetal growth restriction and may potentially serve as a biomarker of this disease.</description><subject>Adult</subject><subject>Biomarkers - blood</subject><subject>Case-Control Studies</subject><subject>Chi-Square Distribution</subject><subject>Diabetes</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Female</subject><subject>Fetal Development</subject><subject>Fetal Growth Retardation - metabolism</subject><subject>Health risk assessment</subject><subject>Humans</subject><subject>Hypertension</subject><subject>Inflammation</subject><subject>Metabolism</subject><subject>Metabolites</subject><subject>Obstetrics</subject><subject>Placenta</subject><subject>Placenta - metabolism</subject><subject>Preeclampsia</subject><subject>Pregnancy</subject><subject>Proteins</subject><subject>Studies</subject><subject>Vitamin D</subject><subject>Vitamin D-Binding Protein - metabolism</subject><subject>Womens health</subject><issn>2090-2727</issn><issn>2090-2735</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNkk1v1DAQhi0EotXSG2cUiQsShNoeJ3YuSFD6sVIlKgRcOFgTx9n1Kom3dkLh3-Owy0I54Yvtmcevxu8MIU8Zfc1YUZxyyuRpwTjlpXxAjjmtaM4lFA8PZy6PyEmMG5qWUIwy_pgcccUrEFAek683HRo7jNhlX9yIvRuy9_k7NzRuWGU3wY82Rc6_b4ON0fkhS7erqcchWzbOb3FcO5Nd2Pn5ZfB34zr7aOMYnBkT_IQ8arGL9mS_L8jni_NPZ1f59YfL5dnb69wUIMcci0pBC1SWYGtVStqUhiNvDJi2VK3kIEXJKy6Ri7quEymYScmSIdRQIyzIcqfbeNzobXA9hh_ao9O_Aj6sNIbRmc5qAcwKQQGEbEUFBq2yIFpLFVasamzSerPT2k51b5vZmoDdPdH7mcGt9cp_0wUA45VMAi_2AsHfTskM3btobNfhYP0UNVNSqgIKphL6_B9046cwJKtmihdKsFTpgrzaUSb4GINtD8Uwquch0PMQ6P0QJPzZ3x84wL9bnoCXO2Cduox37j_lbGJsi39opkoqAX4Ca9XCUw</recordid><startdate>20170101</startdate><enddate>20170101</enddate><creator>Georgiou, Harry M.</creator><creator>Brennecke, Shaun Patrick</creator><creator>Kalionis, Bill</creator><creator>Yong, Hannah E. 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J.</au><au>Chollangi, Tejasvy</au><au>Wookey, Alice F.</au><au>Murthi, Padma</au><au>Wing, Deborah A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Placental Vitamin D-Binding Protein Expression in Human Idiopathic Fetal Growth Restriction</atitle><jtitle>Journal of pregnancy</jtitle><addtitle>J Pregnancy</addtitle><date>2017-01-01</date><risdate>2017</risdate><volume>2017</volume><issue>2017</issue><spage>1</spage><epage>5</epage><pages>1-5</pages><issn>2090-2727</issn><eissn>2090-2735</eissn><abstract>Vitamin D-binding protein is a multifunctional serum protein with multiple actions related to normal health. Vitamin D-binding protein transports vitamin D and influences the metabolism of this key hormone but it also has additional immunomodulatory and actin-clearing properties. We investigated whether vitamin D-binding protein expression is altered in fetal growth restriction-associated placental dysfunction. Protein was extracted from 35 placentae derived from 17 healthy control subjects and 18 gestation-matched subjects with fetal growth restriction (FGR). FGR subjects were further subdivided as idiopathic (n=9) and nonidiopathic (n=9). Vitamin D-binding protein and 25(OH) vitamin D were measured by ELISA and normalized to protein concentration. The results showed significantly reduced levels of placental vitamin D-binding protein (control versus FGR, p<0.05, Student’s t-test) that were strongly associated with idiopathic fetal growth restriction (p<0.01, Kruskal-Wallis), whereas levels of vitamin D-binding protein were not associated with placental 25(OH) vitamin D stores (p=0.295, Pearson’s correlation). As such, vitamin D-binding protein may be a factor in unexplained placental dysfunction associated with idiopathic fetal growth restriction and may potentially serve as a biomarker of this disease.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>28293436</pmid><doi>10.1155/2017/5120267</doi><tpages>5</tpages><orcidid>https://orcid.org/0000-0003-3070-6971</orcidid><orcidid>https://orcid.org/0000-0003-2535-5134</orcidid><orcidid>https://orcid.org/0000-0003-0553-9489</orcidid><orcidid>https://orcid.org/0000-0002-0132-9858</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biomarkers - blood Case-Control Studies Chi-Square Distribution Diabetes Enzyme-Linked Immunosorbent Assay Female Fetal Development Fetal Growth Retardation - metabolism Health risk assessment Humans Hypertension Inflammation Metabolism Metabolites Obstetrics Placenta Placenta - metabolism Preeclampsia Pregnancy Proteins Studies Vitamin D Vitamin D-Binding Protein - metabolism Womens health |
title | Placental Vitamin D-Binding Protein Expression in Human Idiopathic Fetal Growth Restriction |
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