Factor VII activation and menopausal status
The incidence of coronary heart disease (CHD) is higher in postmenopausal or oophorectomised women than in premenopausal women of the same age. The difference cannot be explicable in terms of conventional CHD risk factors. Since factor VII may be relevant to the pathogenesis of CHD, we have investig...
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Veröffentlicht in: | Thrombosis research 1990-01, Vol.57 (2), p.227-234 |
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creator | Scarabin, P.Y. Bonithon-Kopp, C. Bara, L. Malmejac, A. Guize, L. Samama, M. |
description | The incidence of coronary heart disease (CHD) is higher in postmenopausal or oophorectomised women than in premenopausal women of the same age. The difference cannot be explicable in terms of conventional CHD risk factors. Since factor VII may be relevant to the pathogenesis of CHD, we have investigated the menopause-related changes in factor VII activation in 228 healthy women aged 45–54 years. A standard factor VII clotting assay (FVIIc) and a factor VII antigen assay (FVIlag) ware carried out on the same plasma samples. Both FVIIc and FVIlag levels were significantly higher in postmenopausal than in premenopausal women. Despite the strong correlation between the two essays (r=0.80), the FVIIc/FVIIag ratio was positively and significantly associated with the menopause, suggesting that activated factor VII form might in part account for the high FVIIc levels in postmenopausal women. With respect to the type of menopause, the highest levels of both FVIIc and FVIIc/FVIlag ratio were found in women having undergone bilateral oophorectomy. These results suggest that raised factor VII coagulant activity may contribute to an increased risk of CHD in postmenopausal women. |
doi_str_mv | 10.1016/0049-3848(90)90322-4 |
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The difference cannot be explicable in terms of conventional CHD risk factors. Since factor VII may be relevant to the pathogenesis of CHD, we have investigated the menopause-related changes in factor VII activation in 228 healthy women aged 45–54 years. A standard factor VII clotting assay (FVIIc) and a factor VII antigen assay (FVIlag) ware carried out on the same plasma samples. Both FVIIc and FVIlag levels were significantly higher in postmenopausal than in premenopausal women. Despite the strong correlation between the two essays (r=0.80), the FVIIc/FVIIag ratio was positively and significantly associated with the menopause, suggesting that activated factor VII form might in part account for the high FVIIc levels in postmenopausal women. With respect to the type of menopause, the highest levels of both FVIIc and FVIIc/FVIlag ratio were found in women having undergone bilateral oophorectomy. These results suggest that raised factor VII coagulant activity may contribute to an increased risk of CHD in postmenopausal women.</description><identifier>ISSN: 0049-3848</identifier><identifier>EISSN: 1879-2472</identifier><identifier>DOI: 10.1016/0049-3848(90)90322-4</identifier><identifier>PMID: 2315887</identifier><identifier>CODEN: THBRAA</identifier><language>eng</language><publisher>New York, NY: Elsevier Ltd</publisher><subject>activated factor VII ; Antigens - metabolism ; Biological and medical sciences ; Cardiology. Vascular system ; Coronary Disease - blood ; Coronary Disease - etiology ; Coronary heart disease ; factor VII ; Factor VII - immunology ; Factor VII - metabolism ; Factor VIIa - metabolism ; Female ; Heart ; Humans ; Medical sciences ; menopause ; Menopause - blood ; Middle Aged ; Risk Factors</subject><ispartof>Thrombosis research, 1990-01, Vol.57 (2), p.227-234</ispartof><rights>1990</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-259b07d754377618c952bec9352c4aa194adf3195a805bc3cf85df70afd1acc13</citedby><cites>FETCH-LOGICAL-c481t-259b07d754377618c952bec9352c4aa194adf3195a805bc3cf85df70afd1acc13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/0049384890903224$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6802498$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2315887$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Scarabin, P.Y.</creatorcontrib><creatorcontrib>Bonithon-Kopp, C.</creatorcontrib><creatorcontrib>Bara, L.</creatorcontrib><creatorcontrib>Malmejac, A.</creatorcontrib><creatorcontrib>Guize, L.</creatorcontrib><creatorcontrib>Samama, M.</creatorcontrib><title>Factor VII activation and menopausal status</title><title>Thrombosis research</title><addtitle>Thromb Res</addtitle><description>The incidence of coronary heart disease (CHD) is higher in postmenopausal or oophorectomised women than in premenopausal women of the same age. The difference cannot be explicable in terms of conventional CHD risk factors. Since factor VII may be relevant to the pathogenesis of CHD, we have investigated the menopause-related changes in factor VII activation in 228 healthy women aged 45–54 years. A standard factor VII clotting assay (FVIIc) and a factor VII antigen assay (FVIlag) ware carried out on the same plasma samples. Both FVIIc and FVIlag levels were significantly higher in postmenopausal than in premenopausal women. Despite the strong correlation between the two essays (r=0.80), the FVIIc/FVIIag ratio was positively and significantly associated with the menopause, suggesting that activated factor VII form might in part account for the high FVIIc levels in postmenopausal women. With respect to the type of menopause, the highest levels of both FVIIc and FVIIc/FVIlag ratio were found in women having undergone bilateral oophorectomy. These results suggest that raised factor VII coagulant activity may contribute to an increased risk of CHD in postmenopausal women.</description><subject>activated factor VII</subject><subject>Antigens - metabolism</subject><subject>Biological and medical sciences</subject><subject>Cardiology. Vascular system</subject><subject>Coronary Disease - blood</subject><subject>Coronary Disease - etiology</subject><subject>Coronary heart disease</subject><subject>factor VII</subject><subject>Factor VII - immunology</subject><subject>Factor VII - metabolism</subject><subject>Factor VIIa - metabolism</subject><subject>Female</subject><subject>Heart</subject><subject>Humans</subject><subject>Medical sciences</subject><subject>menopause</subject><subject>Menopause - blood</subject><subject>Middle Aged</subject><subject>Risk Factors</subject><issn>0049-3848</issn><issn>1879-2472</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1990</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMtKAzEUhoMotVbfQGEWIoqM5tokG0GKl0LBjboNZ5IMROZSk5mCb-_UDl26Ogf-7xx-PoTOCb4jmMzvMeY6Z4qra41vNGaU5vwATYmSOqdc0kM03SPH6CSlL4yJJFpM0IQyIpSSU3T7DLZrY_a5XGbDFjbQhbbJoHFZ7Zt2DX2CKksddH06RUclVMmfjXOGPp6f3hev-ertZbl4XOWWK9LlVOgCSycFZ1LOibJa0MJbzQS1HIBoDq5kQw9QWBSW2VIJV0oMpSNgLWEzdLX7u47td-9TZ-qQrK8qaHzbJyP1XCqF8QDyHWhjm1L0pVnHUEP8MQSbrSOzFWC2AozG5s-R4cPZxfi_L2rv9kejlCG_HHNIFqoyQmND2mNzhSnXasAedpgfXGyCjybZ4BvrXYjedsa14f8ev45TgPE</recordid><startdate>19900115</startdate><enddate>19900115</enddate><creator>Scarabin, P.Y.</creator><creator>Bonithon-Kopp, C.</creator><creator>Bara, L.</creator><creator>Malmejac, A.</creator><creator>Guize, L.</creator><creator>Samama, M.</creator><general>Elsevier Ltd</general><general>Elsevier Science</general><scope>IQODW</scope><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>7X8</scope></search><sort><creationdate>19900115</creationdate><title>Factor VII activation and menopausal status</title><author>Scarabin, P.Y. ; Bonithon-Kopp, C. ; Bara, L. ; Malmejac, A. ; Guize, L. ; Samama, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-259b07d754377618c952bec9352c4aa194adf3195a805bc3cf85df70afd1acc13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1990</creationdate><topic>activated factor VII</topic><topic>Antigens - metabolism</topic><topic>Biological and medical sciences</topic><topic>Cardiology. Vascular system</topic><topic>Coronary Disease - blood</topic><topic>Coronary Disease - etiology</topic><topic>Coronary heart disease</topic><topic>factor VII</topic><topic>Factor VII - immunology</topic><topic>Factor VII - metabolism</topic><topic>Factor VIIa - metabolism</topic><topic>Female</topic><topic>Heart</topic><topic>Humans</topic><topic>Medical sciences</topic><topic>menopause</topic><topic>Menopause - blood</topic><topic>Middle Aged</topic><topic>Risk Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Scarabin, P.Y.</creatorcontrib><creatorcontrib>Bonithon-Kopp, C.</creatorcontrib><creatorcontrib>Bara, L.</creatorcontrib><creatorcontrib>Malmejac, A.</creatorcontrib><creatorcontrib>Guize, L.</creatorcontrib><creatorcontrib>Samama, M.</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Thrombosis research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scarabin, P.Y.</au><au>Bonithon-Kopp, C.</au><au>Bara, L.</au><au>Malmejac, A.</au><au>Guize, L.</au><au>Samama, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Factor VII activation and menopausal status</atitle><jtitle>Thrombosis research</jtitle><addtitle>Thromb Res</addtitle><date>1990-01-15</date><risdate>1990</risdate><volume>57</volume><issue>2</issue><spage>227</spage><epage>234</epage><pages>227-234</pages><issn>0049-3848</issn><eissn>1879-2472</eissn><coden>THBRAA</coden><abstract>The incidence of coronary heart disease (CHD) is higher in postmenopausal or oophorectomised women than in premenopausal women of the same age. The difference cannot be explicable in terms of conventional CHD risk factors. Since factor VII may be relevant to the pathogenesis of CHD, we have investigated the menopause-related changes in factor VII activation in 228 healthy women aged 45–54 years. A standard factor VII clotting assay (FVIIc) and a factor VII antigen assay (FVIlag) ware carried out on the same plasma samples. Both FVIIc and FVIlag levels were significantly higher in postmenopausal than in premenopausal women. Despite the strong correlation between the two essays (r=0.80), the FVIIc/FVIIag ratio was positively and significantly associated with the menopause, suggesting that activated factor VII form might in part account for the high FVIIc levels in postmenopausal women. With respect to the type of menopause, the highest levels of both FVIIc and FVIIc/FVIlag ratio were found in women having undergone bilateral oophorectomy. These results suggest that raised factor VII coagulant activity may contribute to an increased risk of CHD in postmenopausal women.</abstract><cop>New York, NY</cop><pub>Elsevier Ltd</pub><pmid>2315887</pmid><doi>10.1016/0049-3848(90)90322-4</doi><tpages>8</tpages></addata></record> |
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subjects | activated factor VII Antigens - metabolism Biological and medical sciences Cardiology. Vascular system Coronary Disease - blood Coronary Disease - etiology Coronary heart disease factor VII Factor VII - immunology Factor VII - metabolism Factor VIIa - metabolism Female Heart Humans Medical sciences menopause Menopause - blood Middle Aged Risk Factors |
title | Factor VII activation and menopausal status |
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