PM.06 Low Molecular Heparin Within the Uteroplacental Unit
Background Perturbation of the uteroplacental haemostasis has been implicated in placenta mediated pregnancy complications in thrombophilic women. LMWH may be effective in altering local thrombin production in the uteroplacental compartment. Aim We determined the effects of LMWH (tinzaparin) on the...
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Veröffentlicht in: | Archives of disease in childhood. Fetal and neonatal edition 2013-04, Vol.98 (Suppl 1), p.A27-A27 |
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description | Background Perturbation of the uteroplacental haemostasis has been implicated in placenta mediated pregnancy complications in thrombophilic women. LMWH may be effective in altering local thrombin production in the uteroplacental compartment. Aim We determined the effects of LMWH (tinzaparin) on the peripheral, uteroplacental and fetal circulation and on haemostatic gene and antigen expression in placental tissue. Method Eight women on antenatal LMWH prophylaxis (tinzaparin 75 IU/kg) due to moderate risk of VTE undergoing caesarean section (CS) and a control group of 15 healthy pregnant women undergoing CS had venous blood taken from the peripheral and uterine vein before delivery of placenta. Simultaneously, cord venous blood and placental biopsy was collected. Tissue factor pathway inhibitor (TFPI), thrombin antithrombin (TAT) and endogenous thrombin potential (ETP) were measured. Real-time PCR and ELISA were used to quantify mRNA and protein expression of TFPI and TF in placental tissue. Results TAT levels within uterine vein are significantly higher compared to maternal peripheral circulation in both the control group (P < 0.0001) and LMWH group (P < 0.02). In the LMWH group, TAT is reduced compared with controls in the uterine vein (P < 0.001). ETP and TFPI within uterine circulation is reduced significantly in the LMWH group (P < 0.05) and (P < 0.02) respectively. Down-regulation of placental TFPI and TFPI2 mRNA expression was also found (p < 0.05). Placental TF mRNA expression in LMWH group showed a non significant increase compared to control and this is replicated in placental TF antigen expression. Conclusion TAT is reduced in uteroplacental circulation in thrombophilic women on LMWH prophylaxis and this is mirrored by decreased ETP in uteroplacental circulation. LMWH may be effective in reducing in- vivo thrombin production in the uteroplacental circulation of thrombophilic women. |
doi_str_mv | 10.1136/archdischild-2013-303966.091 |
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LMWH may be effective in altering local thrombin production in the uteroplacental compartment. Aim We determined the effects of LMWH (tinzaparin) on the peripheral, uteroplacental and fetal circulation and on haemostatic gene and antigen expression in placental tissue. Method Eight women on antenatal LMWH prophylaxis (tinzaparin 75 IU/kg) due to moderate risk of VTE undergoing caesarean section (CS) and a control group of 15 healthy pregnant women undergoing CS had venous blood taken from the peripheral and uterine vein before delivery of placenta. Simultaneously, cord venous blood and placental biopsy was collected. Tissue factor pathway inhibitor (TFPI), thrombin antithrombin (TAT) and endogenous thrombin potential (ETP) were measured. Real-time PCR and ELISA were used to quantify mRNA and protein expression of TFPI and TF in placental tissue. Results TAT levels within uterine vein are significantly higher compared to maternal peripheral circulation in both the control group (P < 0.0001) and LMWH group (P < 0.02). In the LMWH group, TAT is reduced compared with controls in the uterine vein (P < 0.001). ETP and TFPI within uterine circulation is reduced significantly in the LMWH group (P < 0.05) and (P < 0.02) respectively. Down-regulation of placental TFPI and TFPI2 mRNA expression was also found (p < 0.05). Placental TF mRNA expression in LMWH group showed a non significant increase compared to control and this is replicated in placental TF antigen expression. Conclusion TAT is reduced in uteroplacental circulation in thrombophilic women on LMWH prophylaxis and this is mirrored by decreased ETP in uteroplacental circulation. LMWH may be effective in reducing in- vivo thrombin production in the uteroplacental circulation of thrombophilic women.]]></description><identifier>ISSN: 1359-2998</identifier><identifier>EISSN: 1468-2052</identifier><identifier>DOI: 10.1136/archdischild-2013-303966.091</identifier><language>eng</language><publisher>London: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher><subject>Blood ; Prophylaxis</subject><ispartof>Archives of disease in childhood. Fetal and neonatal edition, 2013-04, Vol.98 (Suppl 1), p.A27-A27</ispartof><rights>2013, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><rights>Copyright: 2013 (c) 2013, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttp://fn.bmj.com/content/98/Suppl_1/A27.1.full.pdf$$EPDF$$P50$$Gbmj$$H</linktopdf><linktohtml>$$Uhttp://fn.bmj.com/content/98/Suppl_1/A27.1.full$$EHTML$$P50$$Gbmj$$H</linktohtml><link.rule.ids>114,115,314,780,784,3196,23571,27924,27925,77600,77631</link.rule.ids></links><search><creatorcontrib>Ismail, SK</creatorcontrib><creatorcontrib>Norris, L</creatorcontrib><creatorcontrib>Kelly, L</creatorcontrib><creatorcontrib>Higgins, JR</creatorcontrib><title>PM.06 Low Molecular Heparin Within the Uteroplacental Unit</title><title>Archives of disease in childhood. Fetal and neonatal edition</title><addtitle>Arch Dis Child Fetal Neonatal Ed</addtitle><description><![CDATA[Background Perturbation of the uteroplacental haemostasis has been implicated in placenta mediated pregnancy complications in thrombophilic women. LMWH may be effective in altering local thrombin production in the uteroplacental compartment. Aim We determined the effects of LMWH (tinzaparin) on the peripheral, uteroplacental and fetal circulation and on haemostatic gene and antigen expression in placental tissue. Method Eight women on antenatal LMWH prophylaxis (tinzaparin 75 IU/kg) due to moderate risk of VTE undergoing caesarean section (CS) and a control group of 15 healthy pregnant women undergoing CS had venous blood taken from the peripheral and uterine vein before delivery of placenta. Simultaneously, cord venous blood and placental biopsy was collected. Tissue factor pathway inhibitor (TFPI), thrombin antithrombin (TAT) and endogenous thrombin potential (ETP) were measured. Real-time PCR and ELISA were used to quantify mRNA and protein expression of TFPI and TF in placental tissue. Results TAT levels within uterine vein are significantly higher compared to maternal peripheral circulation in both the control group (P < 0.0001) and LMWH group (P < 0.02). In the LMWH group, TAT is reduced compared with controls in the uterine vein (P < 0.001). ETP and TFPI within uterine circulation is reduced significantly in the LMWH group (P < 0.05) and (P < 0.02) respectively. Down-regulation of placental TFPI and TFPI2 mRNA expression was also found (p < 0.05). Placental TF mRNA expression in LMWH group showed a non significant increase compared to control and this is replicated in placental TF antigen expression. Conclusion TAT is reduced in uteroplacental circulation in thrombophilic women on LMWH prophylaxis and this is mirrored by decreased ETP in uteroplacental circulation. LMWH may be effective in reducing in- vivo thrombin production in the uteroplacental circulation of thrombophilic women.]]></description><subject>Blood</subject><subject>Prophylaxis</subject><issn>1359-2998</issn><issn>1468-2052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqVkMtKw0AYhQdRsFbfIaDb1Lkkc4FutKgVWi9grbthMpmQ1DSJM1PUnRtf1CdxSkTcujo_h3P-Ax8AJwiOECL0VFld5pXTZVXnMYaIxAQSQekICrQDBiihPNgp3g03SUWMheD74MC5FYQQMcYGYHw3H0H69fE5a1-jeVsbvamVjaamU7ZqomXlyyC-NNHCG9t2tdKm8aqOFk3lD8FeoWpnjn50CBaXFw-TaTy7vbqenM3iDGOEYpLAhBY5y1KBscKCYpQJzkmeQ5UVKYdJTrkpTKaFMMElCWUF1TrTjOacUDIEx_3fzrYvG-O8XLUb24RJiViopxAJElLjPqVt65w1hexstVb2XSIot7zkX15yy0v2vGTgFepxX6-cN2-_XWWfJWWEpfLmcSKXT5yS-4TL85BnfT5br_639A3N-4Kc</recordid><startdate>201304</startdate><enddate>201304</enddate><creator>Ismail, SK</creator><creator>Norris, L</creator><creator>Kelly, L</creator><creator>Higgins, JR</creator><general>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</general><general>BMJ Publishing Group LTD</general><scope>BSCLL</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>BTHHO</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></search><sort><creationdate>201304</creationdate><title>PM.06 Low Molecular Heparin Within the Uteroplacental Unit</title><author>Ismail, SK ; Norris, L ; Kelly, L ; Higgins, JR</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b2211-34046fd7b5922a29621b9883dd0abf5804d68efebc99e3dd3467f6ccbc76d8363</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Blood</topic><topic>Prophylaxis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ismail, SK</creatorcontrib><creatorcontrib>Norris, L</creatorcontrib><creatorcontrib>Kelly, L</creatorcontrib><creatorcontrib>Higgins, JR</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>BMJ Journals</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>Archives of disease in childhood. Fetal and neonatal edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ismail, SK</au><au>Norris, L</au><au>Kelly, L</au><au>Higgins, JR</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>PM.06 Low Molecular Heparin Within the Uteroplacental Unit</atitle><jtitle>Archives of disease in childhood. Fetal and neonatal edition</jtitle><addtitle>Arch Dis Child Fetal Neonatal Ed</addtitle><date>2013-04</date><risdate>2013</risdate><volume>98</volume><issue>Suppl 1</issue><spage>A27</spage><epage>A27</epage><pages>A27-A27</pages><issn>1359-2998</issn><eissn>1468-2052</eissn><abstract><![CDATA[Background Perturbation of the uteroplacental haemostasis has been implicated in placenta mediated pregnancy complications in thrombophilic women. LMWH may be effective in altering local thrombin production in the uteroplacental compartment. Aim We determined the effects of LMWH (tinzaparin) on the peripheral, uteroplacental and fetal circulation and on haemostatic gene and antigen expression in placental tissue. Method Eight women on antenatal LMWH prophylaxis (tinzaparin 75 IU/kg) due to moderate risk of VTE undergoing caesarean section (CS) and a control group of 15 healthy pregnant women undergoing CS had venous blood taken from the peripheral and uterine vein before delivery of placenta. Simultaneously, cord venous blood and placental biopsy was collected. Tissue factor pathway inhibitor (TFPI), thrombin antithrombin (TAT) and endogenous thrombin potential (ETP) were measured. Real-time PCR and ELISA were used to quantify mRNA and protein expression of TFPI and TF in placental tissue. Results TAT levels within uterine vein are significantly higher compared to maternal peripheral circulation in both the control group (P < 0.0001) and LMWH group (P < 0.02). In the LMWH group, TAT is reduced compared with controls in the uterine vein (P < 0.001). ETP and TFPI within uterine circulation is reduced significantly in the LMWH group (P < 0.05) and (P < 0.02) respectively. Down-regulation of placental TFPI and TFPI2 mRNA expression was also found (p < 0.05). Placental TF mRNA expression in LMWH group showed a non significant increase compared to control and this is replicated in placental TF antigen expression. Conclusion TAT is reduced in uteroplacental circulation in thrombophilic women on LMWH prophylaxis and this is mirrored by decreased ETP in uteroplacental circulation. LMWH may be effective in reducing in- vivo thrombin production in the uteroplacental circulation of thrombophilic women.]]></abstract><cop>London</cop><pub>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</pub><doi>10.1136/archdischild-2013-303966.091</doi><oa>free_for_read</oa></addata></record> |
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title | PM.06 Low Molecular Heparin Within the Uteroplacental Unit |
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