Loading…
ProC® Global Assay in the Evaluation of Women with History of Severe Preeclampsia or HELLP Syndrome
Preeclampsia/HELLP syndrome has been associated with a high incidence of defects in the protein C pathway and increased anticardiolipin-antibodies/lupus anticoagulants. It is also apparent that thrombophilia is responsible for other pregnancy complications, such as recurrent spontaneous abortion, fe...
Saved in:
Published in: | Clinical and applied thrombosis/hemostasis 2002-10, Vol.8 (4), p.319-324 |
---|---|
Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Request full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
cited_by | cdi_FETCH-LOGICAL-c367t-9a24556a874124162933ad2c2ad7bf15a27953fae722585300418f716a9723923 |
---|---|
cites | cdi_FETCH-LOGICAL-c367t-9a24556a874124162933ad2c2ad7bf15a27953fae722585300418f716a9723923 |
container_end_page | 324 |
container_issue | 4 |
container_start_page | 319 |
container_title | Clinical and applied thrombosis/hemostasis |
container_volume | 8 |
creator | Heilmann, Lothar Tempelhoff, Georg-Friedrich v. Pollow, Kuhnhart |
description | Preeclampsia/HELLP syndrome has been associated with a high incidence of defects in the protein C pathway and increased anticardiolipin-antibodies/lupus anticoagulants. It is also apparent that thrombophilia is responsible for other pregnancy complications, such as recurrent spontaneous abortion, fetal growth restriction, intrauterine fetal death, and abruptio placentae. ProC® Global is a new global clotting assay designed to evaluate the abnormalities in the protein C anticoagulant pathway. It is based on the ability of endogenous activated protein C, generated by activation of protein C by Protac®, to prolong an activated partial thromboplastin time. A total of 61 patients with a history of severe preeclampsia or HELLP syndrome and 61 normal pregnant women (controls) were evaluated, 15 of whom had factor V Leiden mutation, 12 had protein C/S deficiency, 30 had a repeated lupus anticoagulants, and 27 increased anticardiolipin antibodies (ACA). All carriers of factor V Leiden mutation (N= 15) as well as all the patients with low activated protein C (APC) resistance ratio (N= 15) had a ProC® Global normalized ratio (NR) less than 0.80 (sensitivity 100%). Twenty-four patients positive for the lupus anticoagulants (LA) and 19 patients positive for ACA (> 5.0 IgG U/mL) had a ProC® Global NR less than 0.8, while six and eight, respectively, had a ProC® Global NR greater than 0.8 (sensitivity, 70%-80%). The detection of a reduced protein C/protein S activity ( |
doi_str_mv | 10.1177/107602960200800403 |
format | article |
fullrecord | <record><control><sourceid>proquest_AFRWT</sourceid><recordid>TN_cdi_proquest_miscellaneous_72808978</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sage_id>10.1177_107602960200800403</sage_id><sourcerecordid>2344186928</sourcerecordid><originalsourceid>FETCH-LOGICAL-c367t-9a24556a874124162933ad2c2ad7bf15a27953fae722585300418f716a9723923</originalsourceid><addsrcrecordid>eNp9kd9KwzAUxoMozn8v4IUEBO-qyUnbJJdjzE0YOFDxspy1qVbaZibtZC_lQ_hkZmwgKHgREg6_7zvfySHknLNrzqW84UymDHQ4jCnGYib2yBHXQkUgQeyHdwCiDTEgx96_McZ1qtNDMuCQcCUBjkgxd3b09UkntV1gTYfe45pWLe1eDR2vsO6xq2xLbUmfbWNa-lF1r3Ra-c669ab6YFbGGTp3xuQ1NktfIbWOTsez2Zw-rNvCBdkpOSix9uZsd5-Qp9vx42gaze4nd6PhLMpFKrtII8RJkqKSMYeYp6CFwAJywEIuSp4gSJ2IEk1InqhEhJG5KiVPUYd5NYgTcrX1XTr73hvfZU3lc1PX2Brb-0yCYkpLFcDLX-Cb7V0bsmUg4uCaathQsKVyZ713psyWrmrQrTPOss0Gsr8bCKKLnXW_aEzxI9l9eQButoDHF_PT9x_Lb5d1i0U</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2344186928</pqid></control><display><type>article</type><title>ProC® Global Assay in the Evaluation of Women with History of Severe Preeclampsia or HELLP Syndrome</title><source>SAGE Open Access</source><creator>Heilmann, Lothar ; Tempelhoff, Georg-Friedrich v. ; Pollow, Kuhnhart</creator><creatorcontrib>Heilmann, Lothar ; Tempelhoff, Georg-Friedrich v. ; Pollow, Kuhnhart</creatorcontrib><description>Preeclampsia/HELLP syndrome has been associated with a high incidence of defects in the protein C pathway and increased anticardiolipin-antibodies/lupus anticoagulants. It is also apparent that thrombophilia is responsible for other pregnancy complications, such as recurrent spontaneous abortion, fetal growth restriction, intrauterine fetal death, and abruptio placentae. ProC® Global is a new global clotting assay designed to evaluate the abnormalities in the protein C anticoagulant pathway. It is based on the ability of endogenous activated protein C, generated by activation of protein C by Protac®, to prolong an activated partial thromboplastin time. A total of 61 patients with a history of severe preeclampsia or HELLP syndrome and 61 normal pregnant women (controls) were evaluated, 15 of whom had factor V Leiden mutation, 12 had protein C/S deficiency, 30 had a repeated lupus anticoagulants, and 27 increased anticardiolipin antibodies (ACA). All carriers of factor V Leiden mutation (N= 15) as well as all the patients with low activated protein C (APC) resistance ratio (N= 15) had a ProC® Global normalized ratio (NR) less than 0.80 (sensitivity 100%). Twenty-four patients positive for the lupus anticoagulants (LA) and 19 patients positive for ACA (> 5.0 IgG U/mL) had a ProC® Global NR less than 0.8, while six and eight, respectively, had a ProC® Global NR greater than 0.8 (sensitivity, 70%-80%). The detection of a reduced protein C/protein S activity (<70%) was low (sensitivity, 33%-44%). In 25 cases with pathologic ProC® Global results, a thrombophilic defect (protein S/LA/ACA without APC resistance) was diagnosed in 18 women; but in 7 cases, no known thrombophilic defect was present. ProC® Global is a new screening test to identify patients with defects of the protein C system and an activated clotting system in preeclampsia but cannot correctly cover each thrombophilic component.</description><identifier>ISSN: 1076-0296</identifier><identifier>EISSN: 1938-2723</identifier><identifier>DOI: 10.1177/107602960200800403</identifier><identifier>PMID: 12518722</identifier><language>eng</language><publisher>Thousand Oaks, CA: SAGE Publications</publisher><subject>Adult ; Anticoagulants ; Biomarkers - blood ; Blood Coagulation Tests - standards ; Case-Control Studies ; Female ; Health risk assessment ; HELLP Syndrome - blood ; HELLP Syndrome - diagnosis ; HELLP Syndrome - etiology ; Humans ; Lupus ; Pre-Eclampsia - blood ; Pre-Eclampsia - diagnosis ; Pre-Eclampsia - etiology ; Preeclampsia ; Pregnancy ; Protein C - analysis ; Protein C - metabolism ; Proteins ; Reagent Kits, Diagnostic - standards ; Sensitivity and Specificity ; Thrombophilia - blood ; Thrombophilia - diagnosis</subject><ispartof>Clinical and applied thrombosis/hemostasis, 2002-10, Vol.8 (4), p.319-324</ispartof><rights>Copyright SAGE PUBLICATIONS, INC. Oct 2002</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c367t-9a24556a874124162933ad2c2ad7bf15a27953fae722585300418f716a9723923</citedby><cites>FETCH-LOGICAL-c367t-9a24556a874124162933ad2c2ad7bf15a27953fae722585300418f716a9723923</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/107602960200800403$$EPDF$$P50$$Gsage$$H</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2344186928?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,780,784,21966,25753,27853,27924,27925,37012,37013,44590,44945,45333</link.rule.ids><linktorsrc>$$Uhttps://journals.sagepub.com/doi/full/10.1177/107602960200800403?utm_source=summon&utm_medium=discovery-provider$$EView_record_in_SAGE_Publications$$FView_record_in_$$GSAGE_Publications</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12518722$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Heilmann, Lothar</creatorcontrib><creatorcontrib>Tempelhoff, Georg-Friedrich v.</creatorcontrib><creatorcontrib>Pollow, Kuhnhart</creatorcontrib><title>ProC® Global Assay in the Evaluation of Women with History of Severe Preeclampsia or HELLP Syndrome</title><title>Clinical and applied thrombosis/hemostasis</title><addtitle>Clin Appl Thromb Hemost</addtitle><description>Preeclampsia/HELLP syndrome has been associated with a high incidence of defects in the protein C pathway and increased anticardiolipin-antibodies/lupus anticoagulants. It is also apparent that thrombophilia is responsible for other pregnancy complications, such as recurrent spontaneous abortion, fetal growth restriction, intrauterine fetal death, and abruptio placentae. ProC® Global is a new global clotting assay designed to evaluate the abnormalities in the protein C anticoagulant pathway. It is based on the ability of endogenous activated protein C, generated by activation of protein C by Protac®, to prolong an activated partial thromboplastin time. A total of 61 patients with a history of severe preeclampsia or HELLP syndrome and 61 normal pregnant women (controls) were evaluated, 15 of whom had factor V Leiden mutation, 12 had protein C/S deficiency, 30 had a repeated lupus anticoagulants, and 27 increased anticardiolipin antibodies (ACA). All carriers of factor V Leiden mutation (N= 15) as well as all the patients with low activated protein C (APC) resistance ratio (N= 15) had a ProC® Global normalized ratio (NR) less than 0.80 (sensitivity 100%). Twenty-four patients positive for the lupus anticoagulants (LA) and 19 patients positive for ACA (> 5.0 IgG U/mL) had a ProC® Global NR less than 0.8, while six and eight, respectively, had a ProC® Global NR greater than 0.8 (sensitivity, 70%-80%). The detection of a reduced protein C/protein S activity (<70%) was low (sensitivity, 33%-44%). In 25 cases with pathologic ProC® Global results, a thrombophilic defect (protein S/LA/ACA without APC resistance) was diagnosed in 18 women; but in 7 cases, no known thrombophilic defect was present. ProC® Global is a new screening test to identify patients with defects of the protein C system and an activated clotting system in preeclampsia but cannot correctly cover each thrombophilic component.</description><subject>Adult</subject><subject>Anticoagulants</subject><subject>Biomarkers - blood</subject><subject>Blood Coagulation Tests - standards</subject><subject>Case-Control Studies</subject><subject>Female</subject><subject>Health risk assessment</subject><subject>HELLP Syndrome - blood</subject><subject>HELLP Syndrome - diagnosis</subject><subject>HELLP Syndrome - etiology</subject><subject>Humans</subject><subject>Lupus</subject><subject>Pre-Eclampsia - blood</subject><subject>Pre-Eclampsia - diagnosis</subject><subject>Pre-Eclampsia - etiology</subject><subject>Preeclampsia</subject><subject>Pregnancy</subject><subject>Protein C - analysis</subject><subject>Protein C - metabolism</subject><subject>Proteins</subject><subject>Reagent Kits, Diagnostic - standards</subject><subject>Sensitivity and Specificity</subject><subject>Thrombophilia - blood</subject><subject>Thrombophilia - diagnosis</subject><issn>1076-0296</issn><issn>1938-2723</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2002</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><recordid>eNp9kd9KwzAUxoMozn8v4IUEBO-qyUnbJJdjzE0YOFDxspy1qVbaZibtZC_lQ_hkZmwgKHgREg6_7zvfySHknLNrzqW84UymDHQ4jCnGYib2yBHXQkUgQeyHdwCiDTEgx96_McZ1qtNDMuCQcCUBjkgxd3b09UkntV1gTYfe45pWLe1eDR2vsO6xq2xLbUmfbWNa-lF1r3Ra-c669ab6YFbGGTp3xuQ1NktfIbWOTsez2Zw-rNvCBdkpOSix9uZsd5-Qp9vx42gaze4nd6PhLMpFKrtII8RJkqKSMYeYp6CFwAJywEIuSp4gSJ2IEk1InqhEhJG5KiVPUYd5NYgTcrX1XTr73hvfZU3lc1PX2Brb-0yCYkpLFcDLX-Cb7V0bsmUg4uCaathQsKVyZ713psyWrmrQrTPOss0Gsr8bCKKLnXW_aEzxI9l9eQButoDHF_PT9x_Lb5d1i0U</recordid><startdate>20021001</startdate><enddate>20021001</enddate><creator>Heilmann, Lothar</creator><creator>Tempelhoff, Georg-Friedrich v.</creator><creator>Pollow, Kuhnhart</creator><general>SAGE Publications</general><general>SAGE PUBLICATIONS, INC</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>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20021001</creationdate><title>ProC® Global Assay in the Evaluation of Women with History of Severe Preeclampsia or HELLP Syndrome</title><author>Heilmann, Lothar ; Tempelhoff, Georg-Friedrich v. ; Pollow, Kuhnhart</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c367t-9a24556a874124162933ad2c2ad7bf15a27953fae722585300418f716a9723923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2002</creationdate><topic>Adult</topic><topic>Anticoagulants</topic><topic>Biomarkers - blood</topic><topic>Blood Coagulation Tests - standards</topic><topic>Case-Control Studies</topic><topic>Female</topic><topic>Health risk assessment</topic><topic>HELLP Syndrome - blood</topic><topic>HELLP Syndrome - diagnosis</topic><topic>HELLP Syndrome - etiology</topic><topic>Humans</topic><topic>Lupus</topic><topic>Pre-Eclampsia - blood</topic><topic>Pre-Eclampsia - diagnosis</topic><topic>Pre-Eclampsia - etiology</topic><topic>Preeclampsia</topic><topic>Pregnancy</topic><topic>Protein C - analysis</topic><topic>Protein C - metabolism</topic><topic>Proteins</topic><topic>Reagent Kits, Diagnostic - standards</topic><topic>Sensitivity and Specificity</topic><topic>Thrombophilia - blood</topic><topic>Thrombophilia - diagnosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Heilmann, Lothar</creatorcontrib><creatorcontrib>Tempelhoff, Georg-Friedrich v.</creatorcontrib><creatorcontrib>Pollow, Kuhnhart</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</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>Publicly Available Content (ProQuest)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Clinical and applied thrombosis/hemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Heilmann, Lothar</au><au>Tempelhoff, Georg-Friedrich v.</au><au>Pollow, Kuhnhart</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>ProC® Global Assay in the Evaluation of Women with History of Severe Preeclampsia or HELLP Syndrome</atitle><jtitle>Clinical and applied thrombosis/hemostasis</jtitle><addtitle>Clin Appl Thromb Hemost</addtitle><date>2002-10-01</date><risdate>2002</risdate><volume>8</volume><issue>4</issue><spage>319</spage><epage>324</epage><pages>319-324</pages><issn>1076-0296</issn><eissn>1938-2723</eissn><abstract>Preeclampsia/HELLP syndrome has been associated with a high incidence of defects in the protein C pathway and increased anticardiolipin-antibodies/lupus anticoagulants. It is also apparent that thrombophilia is responsible for other pregnancy complications, such as recurrent spontaneous abortion, fetal growth restriction, intrauterine fetal death, and abruptio placentae. ProC® Global is a new global clotting assay designed to evaluate the abnormalities in the protein C anticoagulant pathway. It is based on the ability of endogenous activated protein C, generated by activation of protein C by Protac®, to prolong an activated partial thromboplastin time. A total of 61 patients with a history of severe preeclampsia or HELLP syndrome and 61 normal pregnant women (controls) were evaluated, 15 of whom had factor V Leiden mutation, 12 had protein C/S deficiency, 30 had a repeated lupus anticoagulants, and 27 increased anticardiolipin antibodies (ACA). All carriers of factor V Leiden mutation (N= 15) as well as all the patients with low activated protein C (APC) resistance ratio (N= 15) had a ProC® Global normalized ratio (NR) less than 0.80 (sensitivity 100%). Twenty-four patients positive for the lupus anticoagulants (LA) and 19 patients positive for ACA (> 5.0 IgG U/mL) had a ProC® Global NR less than 0.8, while six and eight, respectively, had a ProC® Global NR greater than 0.8 (sensitivity, 70%-80%). The detection of a reduced protein C/protein S activity (<70%) was low (sensitivity, 33%-44%). In 25 cases with pathologic ProC® Global results, a thrombophilic defect (protein S/LA/ACA without APC resistance) was diagnosed in 18 women; but in 7 cases, no known thrombophilic defect was present. ProC® Global is a new screening test to identify patients with defects of the protein C system and an activated clotting system in preeclampsia but cannot correctly cover each thrombophilic component.</abstract><cop>Thousand Oaks, CA</cop><pub>SAGE Publications</pub><pmid>12518722</pmid><doi>10.1177/107602960200800403</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | ISSN: 1076-0296 |
ispartof | Clinical and applied thrombosis/hemostasis, 2002-10, Vol.8 (4), p.319-324 |
issn | 1076-0296 1938-2723 |
language | eng |
recordid | cdi_proquest_miscellaneous_72808978 |
source | SAGE Open Access |
subjects | Adult Anticoagulants Biomarkers - blood Blood Coagulation Tests - standards Case-Control Studies Female Health risk assessment HELLP Syndrome - blood HELLP Syndrome - diagnosis HELLP Syndrome - etiology Humans Lupus Pre-Eclampsia - blood Pre-Eclampsia - diagnosis Pre-Eclampsia - etiology Preeclampsia Pregnancy Protein C - analysis Protein C - metabolism Proteins Reagent Kits, Diagnostic - standards Sensitivity and Specificity Thrombophilia - blood Thrombophilia - diagnosis |
title | ProC® Global Assay in the Evaluation of Women with History of Severe Preeclampsia or HELLP Syndrome |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-02T19%3A19%3A36IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_AFRWT&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=ProC%C2%AE%20Global%20Assay%20in%20the%20Evaluation%20of%20Women%20with%20History%20of%20Severe%20Preeclampsia%20or%20HELLP%20Syndrome&rft.jtitle=Clinical%20and%20applied%20thrombosis/hemostasis&rft.au=Heilmann,%20Lothar&rft.date=2002-10-01&rft.volume=8&rft.issue=4&rft.spage=319&rft.epage=324&rft.pages=319-324&rft.issn=1076-0296&rft.eissn=1938-2723&rft_id=info:doi/10.1177/107602960200800403&rft_dat=%3Cproquest_AFRWT%3E2344186928%3C/proquest_AFRWT%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c367t-9a24556a874124162933ad2c2ad7bf15a27953fae722585300418f716a9723923%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2344186928&rft_id=info:pmid/12518722&rft_sage_id=10.1177_107602960200800403&rfr_iscdi=true |