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Fetal concentrations of the growth factors TGF-[alpha] and TGF-[beta]1 in relation to normal and restricted fetal growth at term
Transforming growth factor-[alpha] (TGF-[alpha]) and TGF-[beta]1 are major anti-inflammatory cytokines and substantially contribute to normal pregnancy outcome. TGF-[alpha] stimulates placental mitosis, whereas TGF-[beta]1 is a critical regulator of trophoblast invasion and fetal growth. We aimed to...
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Published in: | Cytokine (Philadelphia, Pa.) Pa.), 2012-10, Vol.60 (1), p.157-161 |
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creator | Briana, Despina D Liosi, Sofia Gourgiotis, Dimitrios Boutsikou, Maria Marmarinos, Antonios Baka, Stavroula Hassiakos, Dimitrios Malamitsi-Puchner, Ariadne |
description | Transforming growth factor-[alpha] (TGF-[alpha]) and TGF-[beta]1 are major anti-inflammatory cytokines and substantially contribute to normal pregnancy outcome. TGF-[alpha] stimulates placental mitosis, whereas TGF-[beta]1 is a critical regulator of trophoblast invasion and fetal growth. We aimed to study cord blood TGF-[alpha] and TGF-[beta]1 concentrations in intrauterine-growth-restricted (IUGR, usually associated with abnormal trophoblast invasion, uteroplacental vascular insufficiency and enhanced inflammation) and appropriate-for-gestational-age-(AGA) pregnancies, and investigate possible correlations of the above concentrations with several demographic parameters of infants at birth. Plasma TGF-[alpha] and TGF-[beta]1 concentrations were determined by ELISA in 154 mixed arterio-venous cord blood samples from IUGR (n = 50) and AGA (n = 104) singleton full-term infants. After controlling for possible confounding factors (gender, birth-weight, gestational age, maternal age and parity), cord blood TGF-[alpha] and TGF-[beta]1 concentrations were significantly higher in IUGR than AGA group (b = 0.402, SE = 0.179, p = 0.027 and b = 0.152, SE = 0.061, p = 0.014, respectively). Delivery mode had an effect on cord blood TGF-[alpha] and TGF-[beta]1 concentrations, both being elevated in cases of vaginal delivery (b = -0.282, SE = 0.117, p = 0.018 and b = -0.123, SE = 0.059, p = 0.038, respectively). In conclusion, higher cord blood TGF-[alpha] and TGF-[beta]1 concentrations may represent a compensatory response to the inflammatory process characterizing the IUGR state. Additionally, higher cord blood TGF-[beta]1 concentrations in IUGRs could be attributed to increased shear stress, resulting from abnormal blood flow in IUGR fetal blood vessels. Finally, vaginal delivery-associated cytokine release may account for elevated TGF-[alpha] and TGF-[beta]1 concentrations. |
doi_str_mv | 10.1016/j.cyto.2012.06.005 |
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TGF-[alpha] stimulates placental mitosis, whereas TGF-[beta]1 is a critical regulator of trophoblast invasion and fetal growth. We aimed to study cord blood TGF-[alpha] and TGF-[beta]1 concentrations in intrauterine-growth-restricted (IUGR, usually associated with abnormal trophoblast invasion, uteroplacental vascular insufficiency and enhanced inflammation) and appropriate-for-gestational-age-(AGA) pregnancies, and investigate possible correlations of the above concentrations with several demographic parameters of infants at birth. Plasma TGF-[alpha] and TGF-[beta]1 concentrations were determined by ELISA in 154 mixed arterio-venous cord blood samples from IUGR (n = 50) and AGA (n = 104) singleton full-term infants. After controlling for possible confounding factors (gender, birth-weight, gestational age, maternal age and parity), cord blood TGF-[alpha] and TGF-[beta]1 concentrations were significantly higher in IUGR than AGA group (b = 0.402, SE = 0.179, p = 0.027 and b = 0.152, SE = 0.061, p = 0.014, respectively). Delivery mode had an effect on cord blood TGF-[alpha] and TGF-[beta]1 concentrations, both being elevated in cases of vaginal delivery (b = -0.282, SE = 0.117, p = 0.018 and b = -0.123, SE = 0.059, p = 0.038, respectively). In conclusion, higher cord blood TGF-[alpha] and TGF-[beta]1 concentrations may represent a compensatory response to the inflammatory process characterizing the IUGR state. Additionally, higher cord blood TGF-[beta]1 concentrations in IUGRs could be attributed to increased shear stress, resulting from abnormal blood flow in IUGR fetal blood vessels. Finally, vaginal delivery-associated cytokine release may account for elevated TGF-[alpha] and TGF-[beta]1 concentrations.</description><identifier>ISSN: 1043-4666</identifier><identifier>DOI: 10.1016/j.cyto.2012.06.005</identifier><language>eng</language><subject>Age ; Birth ; Blood vessels ; Cord blood ; Cytokines ; Demography ; Enzyme-linked immunosorbent assay ; Fetuses ; Gestational age ; Growth factors ; Infants ; Inflammation ; Mechanical stimuli ; Mitosis ; Parity ; Placenta ; Pregnancy ; Trophoblasts ; Vagina</subject><ispartof>Cytokine (Philadelphia, Pa.), 2012-10, Vol.60 (1), p.157-161</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Briana, Despina D</creatorcontrib><creatorcontrib>Liosi, Sofia</creatorcontrib><creatorcontrib>Gourgiotis, Dimitrios</creatorcontrib><creatorcontrib>Boutsikou, Maria</creatorcontrib><creatorcontrib>Marmarinos, Antonios</creatorcontrib><creatorcontrib>Baka, Stavroula</creatorcontrib><creatorcontrib>Hassiakos, Dimitrios</creatorcontrib><creatorcontrib>Malamitsi-Puchner, Ariadne</creatorcontrib><title>Fetal concentrations of the growth factors TGF-[alpha] and TGF-[beta]1 in relation to normal and restricted fetal growth at term</title><title>Cytokine (Philadelphia, Pa.)</title><description>Transforming growth factor-[alpha] (TGF-[alpha]) and TGF-[beta]1 are major anti-inflammatory cytokines and substantially contribute to normal pregnancy outcome. TGF-[alpha] stimulates placental mitosis, whereas TGF-[beta]1 is a critical regulator of trophoblast invasion and fetal growth. We aimed to study cord blood TGF-[alpha] and TGF-[beta]1 concentrations in intrauterine-growth-restricted (IUGR, usually associated with abnormal trophoblast invasion, uteroplacental vascular insufficiency and enhanced inflammation) and appropriate-for-gestational-age-(AGA) pregnancies, and investigate possible correlations of the above concentrations with several demographic parameters of infants at birth. Plasma TGF-[alpha] and TGF-[beta]1 concentrations were determined by ELISA in 154 mixed arterio-venous cord blood samples from IUGR (n = 50) and AGA (n = 104) singleton full-term infants. After controlling for possible confounding factors (gender, birth-weight, gestational age, maternal age and parity), cord blood TGF-[alpha] and TGF-[beta]1 concentrations were significantly higher in IUGR than AGA group (b = 0.402, SE = 0.179, p = 0.027 and b = 0.152, SE = 0.061, p = 0.014, respectively). Delivery mode had an effect on cord blood TGF-[alpha] and TGF-[beta]1 concentrations, both being elevated in cases of vaginal delivery (b = -0.282, SE = 0.117, p = 0.018 and b = -0.123, SE = 0.059, p = 0.038, respectively). In conclusion, higher cord blood TGF-[alpha] and TGF-[beta]1 concentrations may represent a compensatory response to the inflammatory process characterizing the IUGR state. Additionally, higher cord blood TGF-[beta]1 concentrations in IUGRs could be attributed to increased shear stress, resulting from abnormal blood flow in IUGR fetal blood vessels. Finally, vaginal delivery-associated cytokine release may account for elevated TGF-[alpha] and TGF-[beta]1 concentrations.</description><subject>Age</subject><subject>Birth</subject><subject>Blood vessels</subject><subject>Cord blood</subject><subject>Cytokines</subject><subject>Demography</subject><subject>Enzyme-linked immunosorbent assay</subject><subject>Fetuses</subject><subject>Gestational age</subject><subject>Growth factors</subject><subject>Infants</subject><subject>Inflammation</subject><subject>Mechanical stimuli</subject><subject>Mitosis</subject><subject>Parity</subject><subject>Placenta</subject><subject>Pregnancy</subject><subject>Trophoblasts</subject><subject>Vagina</subject><issn>1043-4666</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqVjT1OAzEQhV2AlPBzAaopadZ41okDNWLhAOlQFBlnNruR1xPsiRAdR2cJuUCqpye973tK3aHRaNA97HT4Fta1wVobp42ZX6gpmpmtZs65iboqZWeMebKLxVT9NCQ-QuAUKEn20nMqwC1IR7DN_CUdtD4I5wLL16Z693Hf-RX4tPnvHyO_QugTZIpHHIQhcR5G7d8qU5HcB6ENtMevk9ULCOXhRl22Pha6PeW1um9els9v1T7z52Fk10NfAsXoE_GhrBHR1mjd_NGeMf0FDWFZlg</recordid><startdate>20121001</startdate><enddate>20121001</enddate><creator>Briana, Despina D</creator><creator>Liosi, Sofia</creator><creator>Gourgiotis, Dimitrios</creator><creator>Boutsikou, Maria</creator><creator>Marmarinos, Antonios</creator><creator>Baka, Stavroula</creator><creator>Hassiakos, Dimitrios</creator><creator>Malamitsi-Puchner, Ariadne</creator><scope>7T5</scope><scope>H94</scope></search><sort><creationdate>20121001</creationdate><title>Fetal concentrations of the growth factors TGF-[alpha] and TGF-[beta]1 in relation to normal and restricted fetal growth at term</title><author>Briana, Despina D ; Liosi, Sofia ; Gourgiotis, Dimitrios ; Boutsikou, Maria ; Marmarinos, Antonios ; Baka, Stavroula ; Hassiakos, Dimitrios ; Malamitsi-Puchner, Ariadne</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_11132136583</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Age</topic><topic>Birth</topic><topic>Blood vessels</topic><topic>Cord blood</topic><topic>Cytokines</topic><topic>Demography</topic><topic>Enzyme-linked immunosorbent assay</topic><topic>Fetuses</topic><topic>Gestational age</topic><topic>Growth factors</topic><topic>Infants</topic><topic>Inflammation</topic><topic>Mechanical stimuli</topic><topic>Mitosis</topic><topic>Parity</topic><topic>Placenta</topic><topic>Pregnancy</topic><topic>Trophoblasts</topic><topic>Vagina</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Briana, Despina D</creatorcontrib><creatorcontrib>Liosi, Sofia</creatorcontrib><creatorcontrib>Gourgiotis, Dimitrios</creatorcontrib><creatorcontrib>Boutsikou, Maria</creatorcontrib><creatorcontrib>Marmarinos, Antonios</creatorcontrib><creatorcontrib>Baka, Stavroula</creatorcontrib><creatorcontrib>Hassiakos, Dimitrios</creatorcontrib><creatorcontrib>Malamitsi-Puchner, Ariadne</creatorcontrib><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><jtitle>Cytokine (Philadelphia, Pa.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Briana, Despina D</au><au>Liosi, Sofia</au><au>Gourgiotis, Dimitrios</au><au>Boutsikou, Maria</au><au>Marmarinos, Antonios</au><au>Baka, Stavroula</au><au>Hassiakos, Dimitrios</au><au>Malamitsi-Puchner, Ariadne</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fetal concentrations of the growth factors TGF-[alpha] and TGF-[beta]1 in relation to normal and restricted fetal growth at term</atitle><jtitle>Cytokine (Philadelphia, Pa.)</jtitle><date>2012-10-01</date><risdate>2012</risdate><volume>60</volume><issue>1</issue><spage>157</spage><epage>161</epage><pages>157-161</pages><issn>1043-4666</issn><abstract>Transforming growth factor-[alpha] (TGF-[alpha]) and TGF-[beta]1 are major anti-inflammatory cytokines and substantially contribute to normal pregnancy outcome. TGF-[alpha] stimulates placental mitosis, whereas TGF-[beta]1 is a critical regulator of trophoblast invasion and fetal growth. We aimed to study cord blood TGF-[alpha] and TGF-[beta]1 concentrations in intrauterine-growth-restricted (IUGR, usually associated with abnormal trophoblast invasion, uteroplacental vascular insufficiency and enhanced inflammation) and appropriate-for-gestational-age-(AGA) pregnancies, and investigate possible correlations of the above concentrations with several demographic parameters of infants at birth. Plasma TGF-[alpha] and TGF-[beta]1 concentrations were determined by ELISA in 154 mixed arterio-venous cord blood samples from IUGR (n = 50) and AGA (n = 104) singleton full-term infants. After controlling for possible confounding factors (gender, birth-weight, gestational age, maternal age and parity), cord blood TGF-[alpha] and TGF-[beta]1 concentrations were significantly higher in IUGR than AGA group (b = 0.402, SE = 0.179, p = 0.027 and b = 0.152, SE = 0.061, p = 0.014, respectively). Delivery mode had an effect on cord blood TGF-[alpha] and TGF-[beta]1 concentrations, both being elevated in cases of vaginal delivery (b = -0.282, SE = 0.117, p = 0.018 and b = -0.123, SE = 0.059, p = 0.038, respectively). In conclusion, higher cord blood TGF-[alpha] and TGF-[beta]1 concentrations may represent a compensatory response to the inflammatory process characterizing the IUGR state. Additionally, higher cord blood TGF-[beta]1 concentrations in IUGRs could be attributed to increased shear stress, resulting from abnormal blood flow in IUGR fetal blood vessels. Finally, vaginal delivery-associated cytokine release may account for elevated TGF-[alpha] and TGF-[beta]1 concentrations.</abstract><doi>10.1016/j.cyto.2012.06.005</doi></addata></record> |
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subjects | Age Birth Blood vessels Cord blood Cytokines Demography Enzyme-linked immunosorbent assay Fetuses Gestational age Growth factors Infants Inflammation Mechanical stimuli Mitosis Parity Placenta Pregnancy Trophoblasts Vagina |
title | Fetal concentrations of the growth factors TGF-[alpha] and TGF-[beta]1 in relation to normal and restricted fetal growth at term |
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