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Recent Advances on the Molecular Mechanism and Clinical Trials of Venous Thromboembolism
Venous thromboembolism is a condition that includes deep vein thrombosis and pulmonary embolism. It is the third most common cardiovascular disease behind acute coronary heart disease and stroke. Over the past few years, growing research suggests that venous thrombosis is also related to the immune...
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Published in: | Journal of inflammation research 2023-01, Vol.16, p.6167-6178 |
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description | Venous thromboembolism is a condition that includes deep vein thrombosis and pulmonary embolism. It is the third most common cardiovascular disease behind acute coronary heart disease and stroke. Over the past few years, growing research suggests that venous thrombosis is also related to the immune system and inflammatory factors have been confirmed to be involved in venous thrombosis. The role of inflammation and inflammation-related biomarkers in cerebrovascular thrombotic disease is the subject of ongoing debate. P-selectin leads to platelet-monocyte aggregation and stimulates vascular inflammation and thrombosis. The dysregulation of miRNAs has also been reported in venous thrombosis, suggesting the involvement of miRNAs in the progression of venous thrombosis. Plasminogen activator inhibitor-1 (PAI-1) is a crucial component of the plasminogen-plasmin system, and elevated levels of PAI-1 in conjunction with advanced age are significant risk factors for thrombosis. In addition, it has been showed that one of the ways that neutrophils promote venous thrombosis is the formation of neutrophil extracellular traps (NETs). In recent years, the role of extracellular vesicles (EVs) in the occurrence and development of VTE has been continuously revealed. With the advancement of research technology, the complex regulatory role of EVs on the coagulation process has been gradually discovered. However, our understanding of the causes and consequences of these changes in venous thrombosis is still limited. Therefore, we review our current understanding the molecular mechanisms of venous thrombosis and the related clinical trials, which is crucial for the future treatment of venous thrombosis. |
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It is the third most common cardiovascular disease behind acute coronary heart disease and stroke. Over the past few years, growing research suggests that venous thrombosis is also related to the immune system and inflammatory factors have been confirmed to be involved in venous thrombosis. The role of inflammation and inflammation-related biomarkers in cerebrovascular thrombotic disease is the subject of ongoing debate. P-selectin leads to platelet-monocyte aggregation and stimulates vascular inflammation and thrombosis. The dysregulation of miRNAs has also been reported in venous thrombosis, suggesting the involvement of miRNAs in the progression of venous thrombosis. Plasminogen activator inhibitor-1 (PAI-1) is a crucial component of the plasminogen-plasmin system, and elevated levels of PAI-1 in conjunction with advanced age are significant risk factors for thrombosis. In addition, it has been showed that one of the ways that neutrophils promote venous thrombosis is the formation of neutrophil extracellular traps (NETs). In recent years, the role of extracellular vesicles (EVs) in the occurrence and development of VTE has been continuously revealed. With the advancement of research technology, the complex regulatory role of EVs on the coagulation process has been gradually discovered. However, our understanding of the causes and consequences of these changes in venous thrombosis is still limited. Therefore, we review our current understanding the molecular mechanisms of venous thrombosis and the related clinical trials, which is crucial for the future treatment of venous thrombosis.</description><identifier>ISSN: 1178-7031</identifier><identifier>EISSN: 1178-7031</identifier><identifier>DOI: 10.2147/JIR.S439205</identifier><identifier>PMID: 38111686</identifier><language>eng</language><publisher>New Zealand: Dove Medical Press Limited</publisher><subject>B cells ; Clinical trials ; Coronary heart disease ; evs ; Inflammation ; inflammatory factor ; MicroRNA ; mirna ; neutrophil extracellular traps ; plasminogen activator inhibitor-1 ; Pulmonary embolism ; Review ; Risk factors ; Stroke (Disease) ; Thromboembolism ; venous thromboembolism</subject><ispartof>Journal of inflammation research, 2023-01, Vol.16, p.6167-6178</ispartof><rights>2023 Huang et al.</rights><rights>COPYRIGHT 2023 Dove Medical Press Limited</rights><rights>2023 Huang et al. 2023 Huang et al.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c504t-5b3dc03ca18d25c9bdad202665292fff8311edd3700ddc8dafd2cb543920a6e73</cites><orcidid>0009-0003-3642-960X ; 0000-0002-8643-3215</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10726951/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10726951/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,37013,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38111686$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Huang, Shao-Li</creatorcontrib><creatorcontrib>Xin, Hong-Yi</creatorcontrib><creatorcontrib>Wang, Xiao-Yan</creatorcontrib><creatorcontrib>Feng, Guang-Gui</creatorcontrib><creatorcontrib>Wu, Fu-Qing</creatorcontrib><creatorcontrib>Feng, Zhi-Peng</creatorcontrib><creatorcontrib>Xing, Zhou</creatorcontrib><creatorcontrib>Zhang, Xi-He</creatorcontrib><creatorcontrib>Xin, Hong-Wu</creatorcontrib><creatorcontrib>Luo, Wen-Ying</creatorcontrib><title>Recent Advances on the Molecular Mechanism and Clinical Trials of Venous Thromboembolism</title><title>Journal of inflammation research</title><addtitle>J Inflamm Res</addtitle><description>Venous thromboembolism is a condition that includes deep vein thrombosis and pulmonary embolism. It is the third most common cardiovascular disease behind acute coronary heart disease and stroke. Over the past few years, growing research suggests that venous thrombosis is also related to the immune system and inflammatory factors have been confirmed to be involved in venous thrombosis. The role of inflammation and inflammation-related biomarkers in cerebrovascular thrombotic disease is the subject of ongoing debate. P-selectin leads to platelet-monocyte aggregation and stimulates vascular inflammation and thrombosis. The dysregulation of miRNAs has also been reported in venous thrombosis, suggesting the involvement of miRNAs in the progression of venous thrombosis. Plasminogen activator inhibitor-1 (PAI-1) is a crucial component of the plasminogen-plasmin system, and elevated levels of PAI-1 in conjunction with advanced age are significant risk factors for thrombosis. In addition, it has been showed that one of the ways that neutrophils promote venous thrombosis is the formation of neutrophil extracellular traps (NETs). In recent years, the role of extracellular vesicles (EVs) in the occurrence and development of VTE has been continuously revealed. With the advancement of research technology, the complex regulatory role of EVs on the coagulation process has been gradually discovered. However, our understanding of the causes and consequences of these changes in venous thrombosis is still limited. Therefore, we review our current understanding the molecular mechanisms of venous thrombosis and the related clinical trials, which is crucial for the future treatment of venous thrombosis.</description><subject>B cells</subject><subject>Clinical trials</subject><subject>Coronary heart disease</subject><subject>evs</subject><subject>Inflammation</subject><subject>inflammatory factor</subject><subject>MicroRNA</subject><subject>mirna</subject><subject>neutrophil extracellular traps</subject><subject>plasminogen activator inhibitor-1</subject><subject>Pulmonary embolism</subject><subject>Review</subject><subject>Risk factors</subject><subject>Stroke (Disease)</subject><subject>Thromboembolism</subject><subject>venous thromboembolism</subject><issn>1178-7031</issn><issn>1178-7031</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>DOA</sourceid><recordid>eNptkl1rFDEUhgdRbKm98l4Cggiyaz5mJjNXsix-rLQIdRXvQiY52UnJJDWZKfjvzXTXsgsmhIST57ycc3iL4iXBS0pK_v7r5mb5vWQtxdWT4pwQ3iw4ZuTp0fusuEzpFs-L45KWz4sz1hBC6qY-L37dgAI_opW-l15BQsGjsQd0HRyoycmIrkH10ts0IOk1WjvrrZIObaOVLuMG_QQfpoS2fQxDFyAfl-kXxTOTAbg83BfFj08ft-svi6tvnzfr1dVCVbgcF1XHtMJMSdJoWqm201JTTOu6oi01xjSMENCacYy1Vo2WRlPVVQ8dyxo4uyg2e10d5K24i3aQ8Y8I0oqHQIg7IeNolQNR1VjzWuU8Q0ppeNtg1ikJzFAigc9aH_Zad1M3gJ4HE6U7ET398bYXu3AvCOa0biuSFd4eFGL4PUEaxWCTAuekhzwkQVvMmpo0vM3o6z26k7k2603IkmrGxYo3GNPc81zS8j9U3hoGq4IHY3P8JOHNUUIP0o19Cm4abfDpFHy3B1UMKUUwj30SLGZviewtcfBWpl8dj-aR_eck9hceKMgR</recordid><startdate>20230101</startdate><enddate>20230101</enddate><creator>Huang, Shao-Li</creator><creator>Xin, Hong-Yi</creator><creator>Wang, Xiao-Yan</creator><creator>Feng, Guang-Gui</creator><creator>Wu, Fu-Qing</creator><creator>Feng, Zhi-Peng</creator><creator>Xing, Zhou</creator><creator>Zhang, Xi-He</creator><creator>Xin, Hong-Wu</creator><creator>Luo, Wen-Ying</creator><general>Dove Medical Press Limited</general><general>Dove</general><general>Dove Medical Press</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0009-0003-3642-960X</orcidid><orcidid>https://orcid.org/0000-0002-8643-3215</orcidid></search><sort><creationdate>20230101</creationdate><title>Recent Advances on the Molecular Mechanism and Clinical Trials of Venous Thromboembolism</title><author>Huang, Shao-Li ; Xin, Hong-Yi ; Wang, Xiao-Yan ; Feng, Guang-Gui ; Wu, Fu-Qing ; Feng, Zhi-Peng ; Xing, Zhou ; Zhang, Xi-He ; Xin, Hong-Wu ; Luo, Wen-Ying</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c504t-5b3dc03ca18d25c9bdad202665292fff8311edd3700ddc8dafd2cb543920a6e73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>B cells</topic><topic>Clinical trials</topic><topic>Coronary heart disease</topic><topic>evs</topic><topic>Inflammation</topic><topic>inflammatory factor</topic><topic>MicroRNA</topic><topic>mirna</topic><topic>neutrophil extracellular traps</topic><topic>plasminogen activator inhibitor-1</topic><topic>Pulmonary embolism</topic><topic>Review</topic><topic>Risk factors</topic><topic>Stroke (Disease)</topic><topic>Thromboembolism</topic><topic>venous thromboembolism</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Shao-Li</creatorcontrib><creatorcontrib>Xin, Hong-Yi</creatorcontrib><creatorcontrib>Wang, Xiao-Yan</creatorcontrib><creatorcontrib>Feng, Guang-Gui</creatorcontrib><creatorcontrib>Wu, Fu-Qing</creatorcontrib><creatorcontrib>Feng, Zhi-Peng</creatorcontrib><creatorcontrib>Xing, Zhou</creatorcontrib><creatorcontrib>Zhang, Xi-He</creatorcontrib><creatorcontrib>Xin, Hong-Wu</creatorcontrib><creatorcontrib>Luo, Wen-Ying</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Journal of inflammation research</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Shao-Li</au><au>Xin, Hong-Yi</au><au>Wang, Xiao-Yan</au><au>Feng, Guang-Gui</au><au>Wu, Fu-Qing</au><au>Feng, Zhi-Peng</au><au>Xing, Zhou</au><au>Zhang, Xi-He</au><au>Xin, Hong-Wu</au><au>Luo, Wen-Ying</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Recent Advances on the Molecular Mechanism and Clinical Trials of Venous Thromboembolism</atitle><jtitle>Journal of inflammation research</jtitle><addtitle>J Inflamm Res</addtitle><date>2023-01-01</date><risdate>2023</risdate><volume>16</volume><spage>6167</spage><epage>6178</epage><pages>6167-6178</pages><issn>1178-7031</issn><eissn>1178-7031</eissn><abstract>Venous thromboembolism is a condition that includes deep vein thrombosis and pulmonary embolism. It is the third most common cardiovascular disease behind acute coronary heart disease and stroke. Over the past few years, growing research suggests that venous thrombosis is also related to the immune system and inflammatory factors have been confirmed to be involved in venous thrombosis. The role of inflammation and inflammation-related biomarkers in cerebrovascular thrombotic disease is the subject of ongoing debate. P-selectin leads to platelet-monocyte aggregation and stimulates vascular inflammation and thrombosis. The dysregulation of miRNAs has also been reported in venous thrombosis, suggesting the involvement of miRNAs in the progression of venous thrombosis. Plasminogen activator inhibitor-1 (PAI-1) is a crucial component of the plasminogen-plasmin system, and elevated levels of PAI-1 in conjunction with advanced age are significant risk factors for thrombosis. In addition, it has been showed that one of the ways that neutrophils promote venous thrombosis is the formation of neutrophil extracellular traps (NETs). In recent years, the role of extracellular vesicles (EVs) in the occurrence and development of VTE has been continuously revealed. With the advancement of research technology, the complex regulatory role of EVs on the coagulation process has been gradually discovered. However, our understanding of the causes and consequences of these changes in venous thrombosis is still limited. Therefore, we review our current understanding the molecular mechanisms of venous thrombosis and the related clinical trials, which is crucial for the future treatment of venous thrombosis.</abstract><cop>New Zealand</cop><pub>Dove Medical Press Limited</pub><pmid>38111686</pmid><doi>10.2147/JIR.S439205</doi><tpages>12</tpages><orcidid>https://orcid.org/0009-0003-3642-960X</orcidid><orcidid>https://orcid.org/0000-0002-8643-3215</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | B cells Clinical trials Coronary heart disease evs Inflammation inflammatory factor MicroRNA mirna neutrophil extracellular traps plasminogen activator inhibitor-1 Pulmonary embolism Review Risk factors Stroke (Disease) Thromboembolism venous thromboembolism |
title | Recent Advances on the Molecular Mechanism and Clinical Trials of Venous Thromboembolism |
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