Proportion of venous thromboembolism attributed to recognized prothrombotic genotypes in men and women

Data on the proportion of venous thromboembolism (VTE) risk attributed to prothrombotic genotypes in men and women are limited. We aimed to estimate the population attributable fraction (PAF) of VTE for recognized, common prothrombotic genotypes in men and women using a population-based case cohort....

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Veröffentlicht in:Research and practice in thrombosis and haemostasis 2024-02, Vol.8 (2), p.102343-102343, Article 102343
Hauptverfasser: Løchen Arnesen, Carl Arne, Evensen, Line H., Hveem, Kristian, Gabrielsen, Maiken E., Hansen, John-Bjarne, Brækkan, Sigrid K.
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container_title Research and practice in thrombosis and haemostasis
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creator Løchen Arnesen, Carl Arne
Evensen, Line H.
Hveem, Kristian
Gabrielsen, Maiken E.
Hansen, John-Bjarne
Brækkan, Sigrid K.
description Data on the proportion of venous thromboembolism (VTE) risk attributed to prothrombotic genotypes in men and women are limited. We aimed to estimate the population attributable fraction (PAF) of VTE for recognized, common prothrombotic genotypes in men and women using a population-based case cohort. Cases with incident VTE (n = 1493) and a randomly sampled subcohort (n = 13,069) were derived from the Tromsø study (1994-2012) and the Trøndelag Health Study (1995-2008) cohorts. DNA samples were genotyped for 17 single-nucleotide polymorphisms (SNPs) previously associated with VTE. PAFs with 95% bias-corrected CIs (based on 10,000 bootstrap samples) were estimated for SNPs significantly associated with VTE, and a 6-SNP cumulative model was constructed for both sexes. In women, the individual PAFs for SNPs included in the cumulative model were 16.9% for ABO (rs8176719), 17.6% for F11 (rs2036914), 15.1% for F11 (rs2289252), 8.7% for FVL (rs6025), 6.0% for FGG (rs2066865), and 0.2% for F2 (rs1799963). The cumulative PAF for this 6-SNP model was 37.8%. In men, the individual PAFs for SNPs included in the cumulative model were 21.3% for ABO, 12.2% for F11 (rs2036914), 10.4% for F11 (rs2289252), 7.5% for FVL, 7.8% for FGG, and 1.1% for F2. This resulted in a cumulative PAF in men of 51.9%. Our findings in a Norwegian population suggest that 52% and 38% of the VTEs can be attributed to known prothrombotic genotypes in men and women, respectively. •Sex-specific data on venous thrombosis risk attributed to prothrombotic genotypes are scarce.•We estimated the cumulative population attributable risk of 6 single-nucleotide polymorphisms in men and women.•For this 6-single-nucleotide polymorphism model, the cumulative population attributable risk was 51.9% in men and 37.8% in women.•Prothrombotic genotypes appeared to explain a higher proportion of venous thromboses in men than in women.
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We aimed to estimate the population attributable fraction (PAF) of VTE for recognized, common prothrombotic genotypes in men and women using a population-based case cohort. Cases with incident VTE (n = 1493) and a randomly sampled subcohort (n = 13,069) were derived from the Tromsø study (1994-2012) and the Trøndelag Health Study (1995-2008) cohorts. DNA samples were genotyped for 17 single-nucleotide polymorphisms (SNPs) previously associated with VTE. PAFs with 95% bias-corrected CIs (based on 10,000 bootstrap samples) were estimated for SNPs significantly associated with VTE, and a 6-SNP cumulative model was constructed for both sexes. In women, the individual PAFs for SNPs included in the cumulative model were 16.9% for ABO (rs8176719), 17.6% for F11 (rs2036914), 15.1% for F11 (rs2289252), 8.7% for FVL (rs6025), 6.0% for FGG (rs2066865), and 0.2% for F2 (rs1799963). The cumulative PAF for this 6-SNP model was 37.8%. In men, the individual PAFs for SNPs included in the cumulative model were 21.3% for ABO, 12.2% for F11 (rs2036914), 10.4% for F11 (rs2289252), 7.5% for FVL, 7.8% for FGG, and 1.1% for F2. This resulted in a cumulative PAF in men of 51.9%. 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We aimed to estimate the population attributable fraction (PAF) of VTE for recognized, common prothrombotic genotypes in men and women using a population-based case cohort. Cases with incident VTE (n = 1493) and a randomly sampled subcohort (n = 13,069) were derived from the Tromsø study (1994-2012) and the Trøndelag Health Study (1995-2008) cohorts. DNA samples were genotyped for 17 single-nucleotide polymorphisms (SNPs) previously associated with VTE. PAFs with 95% bias-corrected CIs (based on 10,000 bootstrap samples) were estimated for SNPs significantly associated with VTE, and a 6-SNP cumulative model was constructed for both sexes. In women, the individual PAFs for SNPs included in the cumulative model were 16.9% for ABO (rs8176719), 17.6% for F11 (rs2036914), 15.1% for F11 (rs2289252), 8.7% for FVL (rs6025), 6.0% for FGG (rs2066865), and 0.2% for F2 (rs1799963). The cumulative PAF for this 6-SNP model was 37.8%. In men, the individual PAFs for SNPs included in the cumulative model were 21.3% for ABO, 12.2% for F11 (rs2036914), 10.4% for F11 (rs2289252), 7.5% for FVL, 7.8% for FGG, and 1.1% for F2. This resulted in a cumulative PAF in men of 51.9%. Our findings in a Norwegian population suggest that 52% and 38% of the VTEs can be attributed to known prothrombotic genotypes in men and women, respectively. •Sex-specific data on venous thrombosis risk attributed to prothrombotic genotypes are scarce.•We estimated the cumulative population attributable risk of 6 single-nucleotide polymorphisms in men and women.•For this 6-single-nucleotide polymorphism model, the cumulative population attributable risk was 51.9% in men and 37.8% in women.•Prothrombotic genotypes appeared to explain a higher proportion of venous thromboses in men than in women.</description><subject>epidemiology</subject><subject>Original</subject><subject>risk factors</subject><subject>sex differences</subject><subject>single-nucleotide polymorphism</subject><subject>venous thromboembolism</subject><issn>2475-0379</issn><issn>2475-0379</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>3HK</sourceid><recordid>eNp9UV1rHCEUlZLShDR_oA-tj3nZrR8zjkKhhNB8QKB9aJ_F0Tu7LjM6VXdL-uvrspuQvBQUr95zjnoOQh8oWVJCxefNMs1lvWSENfWA8Ya_QWes6doF4Z06eVGfooucN4SQiq2jfYdOuWw60bTqDA0_UpxjKj4GHAe8gxC3GZd1ilMfoc7R5wmbUpLvtwUcLhEnsHEV_N-6m1M8You3eFXZ5XGGjH3AEwRsgsN_Yq3eo7eDGTNcHNdz9Ovm28_ru8XD99v766uHhW04LQvlOtcORvaW0NY6a5UQfJCOsq4jrVTEAe-MHcxACDVgekstZYpK0wgjqeTn6OtBd972EzgLoSQz6jn5yaRHHY3XrzvBr_Uq7jQliglGSVX4dFCwyefigw4xmdquTmredFJVxOXxjhR_byEXPflsYRxNgGqeZqoVQhJBRYWyJ7GYc4Lh-SWU6H2MeqP3Mep9jPoQYyV9fPmHZ8pTaBXw5QCA6uTOQ9LZeggWnK_RFO2i_5_-P6HosMk</recordid><startdate>20240201</startdate><enddate>20240201</enddate><creator>Løchen Arnesen, Carl Arne</creator><creator>Evensen, Line H.</creator><creator>Hveem, Kristian</creator><creator>Gabrielsen, Maiken E.</creator><creator>Hansen, John-Bjarne</creator><creator>Brækkan, Sigrid K.</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>3HK</scope><scope>5PM</scope></search><sort><creationdate>20240201</creationdate><title>Proportion of venous thromboembolism attributed to recognized prothrombotic genotypes in men and women</title><author>Løchen Arnesen, Carl Arne ; Evensen, Line H. ; Hveem, Kristian ; Gabrielsen, Maiken E. ; Hansen, John-Bjarne ; Brækkan, Sigrid K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-9d7d5fa8bc015cdcc9663f8d127705890de37acfaf001aeabc1c12918a46a8183</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>epidemiology</topic><topic>Original</topic><topic>risk factors</topic><topic>sex differences</topic><topic>single-nucleotide polymorphism</topic><topic>venous thromboembolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Løchen Arnesen, Carl Arne</creatorcontrib><creatorcontrib>Evensen, Line H.</creatorcontrib><creatorcontrib>Hveem, Kristian</creatorcontrib><creatorcontrib>Gabrielsen, Maiken E.</creatorcontrib><creatorcontrib>Hansen, John-Bjarne</creatorcontrib><creatorcontrib>Brækkan, Sigrid K.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>NORA - Norwegian Open Research Archives</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Research and practice in thrombosis and haemostasis</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Løchen Arnesen, Carl Arne</au><au>Evensen, Line H.</au><au>Hveem, Kristian</au><au>Gabrielsen, Maiken E.</au><au>Hansen, John-Bjarne</au><au>Brækkan, Sigrid K.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Proportion of venous thromboembolism attributed to recognized prothrombotic genotypes in men and women</atitle><jtitle>Research and practice in thrombosis and haemostasis</jtitle><addtitle>Res Pract Thromb Haemost</addtitle><date>2024-02-01</date><risdate>2024</risdate><volume>8</volume><issue>2</issue><spage>102343</spage><epage>102343</epage><pages>102343-102343</pages><artnum>102343</artnum><issn>2475-0379</issn><eissn>2475-0379</eissn><abstract>Data on the proportion of venous thromboembolism (VTE) risk attributed to prothrombotic genotypes in men and women are limited. We aimed to estimate the population attributable fraction (PAF) of VTE for recognized, common prothrombotic genotypes in men and women using a population-based case cohort. Cases with incident VTE (n = 1493) and a randomly sampled subcohort (n = 13,069) were derived from the Tromsø study (1994-2012) and the Trøndelag Health Study (1995-2008) cohorts. DNA samples were genotyped for 17 single-nucleotide polymorphisms (SNPs) previously associated with VTE. PAFs with 95% bias-corrected CIs (based on 10,000 bootstrap samples) were estimated for SNPs significantly associated with VTE, and a 6-SNP cumulative model was constructed for both sexes. In women, the individual PAFs for SNPs included in the cumulative model were 16.9% for ABO (rs8176719), 17.6% for F11 (rs2036914), 15.1% for F11 (rs2289252), 8.7% for FVL (rs6025), 6.0% for FGG (rs2066865), and 0.2% for F2 (rs1799963). The cumulative PAF for this 6-SNP model was 37.8%. In men, the individual PAFs for SNPs included in the cumulative model were 21.3% for ABO, 12.2% for F11 (rs2036914), 10.4% for F11 (rs2289252), 7.5% for FVL, 7.8% for FGG, and 1.1% for F2. This resulted in a cumulative PAF in men of 51.9%. Our findings in a Norwegian population suggest that 52% and 38% of the VTEs can be attributed to known prothrombotic genotypes in men and women, respectively. •Sex-specific data on venous thrombosis risk attributed to prothrombotic genotypes are scarce.•We estimated the cumulative population attributable risk of 6 single-nucleotide polymorphisms in men and women.•For this 6-single-nucleotide polymorphism model, the cumulative population attributable risk was 51.9% in men and 37.8% in women.•Prothrombotic genotypes appeared to explain a higher proportion of venous thromboses in men than in women.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>38476459</pmid><doi>10.1016/j.rpth.2024.102343</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects epidemiology
Original
risk factors
sex differences
single-nucleotide polymorphism
venous thromboembolism
title Proportion of venous thromboembolism attributed to recognized prothrombotic genotypes in men and women
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