Plasma levels of some blood coagulation parameters in Nigerian homozygous sickle cell patients (HbSS) in steady state
The plasma levels of some blood coagulation parameters; prothrombin time, (PT), partial thromboplastin time with kaolin (PTTK), thrombin clotting time, (TCT), fibrinogen and factor X assay were determined in 50 Nigerian homozygous (HbSS) patients and 50 HbAA healthy individuals for the purpose of as...
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Veröffentlicht in: | Hematology (Luxembourg) 2006-10, Vol.11 (5-6), p.375-379 |
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description | The plasma levels of some blood coagulation parameters; prothrombin time, (PT), partial thromboplastin time with kaolin (PTTK), thrombin clotting time, (TCT), fibrinogen and factor X assay were determined in 50 Nigerian homozygous (HbSS) patients and 50 HbAA healthy individuals for the purpose of assessing their baseline values and susceptibility of patients with sickle cell disease (SCD) to hyper coagulability. Standard procedures were used for all variables. The mean age of the study participants was 21.7 ± 5.0 years. The mean PT of 13.7 ± 1.4s in HbSS patients was found to be significantly longer than the mean PT value of 12.9 ± 1.0 in HbAA control subjects (p < 0.001). The mean PTTK values of 46.0 ± 9.6s in HbSS patients was also found to be significantly higher than the 41.0 ± 3.7s recorded among the control subjects (p < 0.001). The mean TCT of 6.4 ± 0.8s in HbSS patients was however found to be significantly lower than the mean value of 10.6 ± 0.8s obtained in the control group. Fibrinogen level (4.1 ± 2.1 g/l) in HbSS patients and 2.8 ± 0.9 g/l in HbAA controls was also found to be significantly different (p < 0.001). Factor X level in the sickle cell patients, (64.6 ± 14.9%) was equally found to be significantly lower than that of the apparently healthy HbAA control individuals (95.2 ± 7.2%) (p < 0.001). |
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Standard procedures were used for all variables. The mean age of the study participants was 21.7 ± 5.0 years. The mean PT of 13.7 ± 1.4s in HbSS patients was found to be significantly longer than the mean PT value of 12.9 ± 1.0 in HbAA control subjects (p < 0.001). The mean PTTK values of 46.0 ± 9.6s in HbSS patients was also found to be significantly higher than the 41.0 ± 3.7s recorded among the control subjects (p < 0.001). The mean TCT of 6.4 ± 0.8s in HbSS patients was however found to be significantly lower than the mean value of 10.6 ± 0.8s obtained in the control group. Fibrinogen level (4.1 ± 2.1 g/l) in HbSS patients and 2.8 ± 0.9 g/l in HbAA controls was also found to be significantly different (p < 0.001). Factor X level in the sickle cell patients, (64.6 ± 14.9%) was equally found to be significantly lower than that of the apparently healthy HbAA control individuals (95.2 ± 7.2%) (p < 0.001).</description><identifier>ISSN: 1607-8454</identifier><identifier>EISSN: 1607-8454</identifier><identifier>DOI: 10.1080/10245330600841287</identifier><identifier>PMID: 17607590</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>Adolescent ; Adult ; Anemia, Sickle Cell - blood ; Anemia, Sickle Cell - complications ; Blood Coagulation Factors - analysis ; Blood Coagulation Tests ; Case-Control Studies ; FACTOR X ; Factor Xa - analysis ; Factor Xa - metabolism ; Female ; FIBRINOGEN ; Fibrinogen - analysis ; HBSS ; Homozygote ; Humans ; Male ; NIGERIA ; PROTHROMBIN TIME ; THROMBIN CLOTTING TIME ; Thrombophilia - diagnosis</subject><ispartof>Hematology (Luxembourg), 2006-10, Vol.11 (5-6), p.375-379</ispartof><rights>2006 Maney Publishing 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c395t-8a0850d5d8f010a5a4f52c408bd3aa44ef36ea00979a9d7797977f51aee2f2f83</citedby><cites>FETCH-LOGICAL-c395t-8a0850d5d8f010a5a4f52c408bd3aa44ef36ea00979a9d7797977f51aee2f2f83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17607590$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Buseri, Fiekumo I.</creatorcontrib><creatorcontrib>Jeremiah, Zaccheaus A.</creatorcontrib><creatorcontrib>Shokunbi, Wuraola A.</creatorcontrib><title>Plasma levels of some blood coagulation parameters in Nigerian homozygous sickle cell patients (HbSS) in steady state</title><title>Hematology (Luxembourg)</title><addtitle>Hematology</addtitle><description>The plasma levels of some blood coagulation parameters; prothrombin time, (PT), partial thromboplastin time with kaolin (PTTK), thrombin clotting time, (TCT), fibrinogen and factor X assay were determined in 50 Nigerian homozygous (HbSS) patients and 50 HbAA healthy individuals for the purpose of assessing their baseline values and susceptibility of patients with sickle cell disease (SCD) to hyper coagulability. Standard procedures were used for all variables. The mean age of the study participants was 21.7 ± 5.0 years. The mean PT of 13.7 ± 1.4s in HbSS patients was found to be significantly longer than the mean PT value of 12.9 ± 1.0 in HbAA control subjects (p < 0.001). The mean PTTK values of 46.0 ± 9.6s in HbSS patients was also found to be significantly higher than the 41.0 ± 3.7s recorded among the control subjects (p < 0.001). The mean TCT of 6.4 ± 0.8s in HbSS patients was however found to be significantly lower than the mean value of 10.6 ± 0.8s obtained in the control group. Fibrinogen level (4.1 ± 2.1 g/l) in HbSS patients and 2.8 ± 0.9 g/l in HbAA controls was also found to be significantly different (p < 0.001). Factor X level in the sickle cell patients, (64.6 ± 14.9%) was equally found to be significantly lower than that of the apparently healthy HbAA control individuals (95.2 ± 7.2%) (p < 0.001).</description><subject>Adolescent</subject><subject>Adult</subject><subject>Anemia, Sickle Cell - blood</subject><subject>Anemia, Sickle Cell - complications</subject><subject>Blood Coagulation Factors - analysis</subject><subject>Blood Coagulation Tests</subject><subject>Case-Control Studies</subject><subject>FACTOR X</subject><subject>Factor Xa - analysis</subject><subject>Factor Xa - metabolism</subject><subject>Female</subject><subject>FIBRINOGEN</subject><subject>Fibrinogen - analysis</subject><subject>HBSS</subject><subject>Homozygote</subject><subject>Humans</subject><subject>Male</subject><subject>NIGERIA</subject><subject>PROTHROMBIN TIME</subject><subject>THROMBIN CLOTTING TIME</subject><subject>Thrombophilia - diagnosis</subject><issn>1607-8454</issn><issn>1607-8454</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kF9LHDEUxUOx1D_tB-iL5En0YdubmWSSAV9EtBZEC7bPw92ZmzWamaxJpmX76Z1lFxTEp3Ph_s7hcBj7KuCbAAPfBRRSlSVUAEaKwugPbE9UoGdGKrnz6t5l-yk9ABQFaPjEdoWePqqGPTb-8ph65J7-kk88WJ5CT3zuQ-h4G3AxeswuDHyJEXvKFBN3A79xC4oOB34f-vB_tQhj4sm1j554S95PdHY05MSPr-Z3dydrS8qE3WoSzPSZfbToE33Z6gH7c3nx-_xqdn374-f52fWsLWuVZwbBKOhUZywIQIXSqqKVYOZdiSgl2bIiBKh1jXWn9aRaWyWQqLCFNeUBO9rkLmN4GinlpndpXRAHmio3lSmlMFUxgWIDtjGkFMk2y-h6jKtGQLPeunmz9eQ53IaP8566F8d23Ak43QBusCH2-C9E3zUZVz5EG3FoXWrK9_OfATpTjVQ</recordid><startdate>20061001</startdate><enddate>20061001</enddate><creator>Buseri, Fiekumo I.</creator><creator>Jeremiah, Zaccheaus A.</creator><creator>Shokunbi, Wuraola A.</creator><general>Taylor & Francis</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>7X8</scope></search><sort><creationdate>20061001</creationdate><title>Plasma levels of some blood coagulation parameters in Nigerian homozygous sickle cell patients (HbSS) in steady state</title><author>Buseri, Fiekumo I. ; Jeremiah, Zaccheaus A. ; Shokunbi, Wuraola A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c395t-8a0850d5d8f010a5a4f52c408bd3aa44ef36ea00979a9d7797977f51aee2f2f83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Anemia, Sickle Cell - blood</topic><topic>Anemia, Sickle Cell - complications</topic><topic>Blood Coagulation Factors - analysis</topic><topic>Blood Coagulation Tests</topic><topic>Case-Control Studies</topic><topic>FACTOR X</topic><topic>Factor Xa - analysis</topic><topic>Factor Xa - metabolism</topic><topic>Female</topic><topic>FIBRINOGEN</topic><topic>Fibrinogen - analysis</topic><topic>HBSS</topic><topic>Homozygote</topic><topic>Humans</topic><topic>Male</topic><topic>NIGERIA</topic><topic>PROTHROMBIN TIME</topic><topic>THROMBIN CLOTTING TIME</topic><topic>Thrombophilia - diagnosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Buseri, Fiekumo I.</creatorcontrib><creatorcontrib>Jeremiah, Zaccheaus A.</creatorcontrib><creatorcontrib>Shokunbi, Wuraola A.</creatorcontrib><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>Hematology (Luxembourg)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Buseri, Fiekumo I.</au><au>Jeremiah, Zaccheaus A.</au><au>Shokunbi, Wuraola A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma levels of some blood coagulation parameters in Nigerian homozygous sickle cell patients (HbSS) in steady state</atitle><jtitle>Hematology (Luxembourg)</jtitle><addtitle>Hematology</addtitle><date>2006-10-01</date><risdate>2006</risdate><volume>11</volume><issue>5-6</issue><spage>375</spage><epage>379</epage><pages>375-379</pages><issn>1607-8454</issn><eissn>1607-8454</eissn><abstract>The plasma levels of some blood coagulation parameters; prothrombin time, (PT), partial thromboplastin time with kaolin (PTTK), thrombin clotting time, (TCT), fibrinogen and factor X assay were determined in 50 Nigerian homozygous (HbSS) patients and 50 HbAA healthy individuals for the purpose of assessing their baseline values and susceptibility of patients with sickle cell disease (SCD) to hyper coagulability. Standard procedures were used for all variables. The mean age of the study participants was 21.7 ± 5.0 years. The mean PT of 13.7 ± 1.4s in HbSS patients was found to be significantly longer than the mean PT value of 12.9 ± 1.0 in HbAA control subjects (p < 0.001). The mean PTTK values of 46.0 ± 9.6s in HbSS patients was also found to be significantly higher than the 41.0 ± 3.7s recorded among the control subjects (p < 0.001). The mean TCT of 6.4 ± 0.8s in HbSS patients was however found to be significantly lower than the mean value of 10.6 ± 0.8s obtained in the control group. Fibrinogen level (4.1 ± 2.1 g/l) in HbSS patients and 2.8 ± 0.9 g/l in HbAA controls was also found to be significantly different (p < 0.001). Factor X level in the sickle cell patients, (64.6 ± 14.9%) was equally found to be significantly lower than that of the apparently healthy HbAA control individuals (95.2 ± 7.2%) (p < 0.001).</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>17607590</pmid><doi>10.1080/10245330600841287</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Anemia, Sickle Cell - blood Anemia, Sickle Cell - complications Blood Coagulation Factors - analysis Blood Coagulation Tests Case-Control Studies FACTOR X Factor Xa - analysis Factor Xa - metabolism Female FIBRINOGEN Fibrinogen - analysis HBSS Homozygote Humans Male NIGERIA PROTHROMBIN TIME THROMBIN CLOTTING TIME Thrombophilia - diagnosis |
title | Plasma levels of some blood coagulation parameters in Nigerian homozygous sickle cell patients (HbSS) in steady state |
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