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Coagulation factors XI and XII as possible targets for anticoagulant therapy.
Kluge, Karsten Engseth; Seljeflot, Ingebjørg; Arnesen, Harald; Jensen, Torstein; Halvorsen, Sigrun; Helseth, Ragnhild.
  • Kluge KE; Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital Ullevål, Norway; University of Oslo, Norway. Electronic address: K.e.kluge@studmed.uio.no.
  • Seljeflot I; Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital Ullevål, Norway; University of Oslo, Norway; Department of Cardiology, Oslo University Hospital Ullevål, Norway.
  • Arnesen H; Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital Ullevål, Norway; University of Oslo, Norway.
  • Jensen T; Department of Cardiology, Oslo University Hospital Ullevål, Norway.
  • Halvorsen S; University of Oslo, Norway; Department of Cardiology, Oslo University Hospital Ullevål, Norway.
  • Helseth R; Center for Clinical Heart Research, Department of Cardiology, Oslo University Hospital Ullevål, Norway; University of Oslo, Norway; Department of Cardiology, Oslo University Hospital Ullevål, Norway.
Thromb Res ; 214: 53-62, 2022 06.
Article in English | MEDLINE | ID: covidwho-1852144
ABSTRACT
In this review, we give an overview over observational and experimental studies supporting factors XI and XII as targets for anticoagulant therapy. The majority of observational studies on FXI report low concentrations of FXI to be protective against ischemic stroke and venous thrombosis. There is also extensive evidence from experimental and animal studies supporting FXI inhibition as a target for anticoagulant therapy, alone or in combination with other antithrombotic treatments. Four Phase 2 clinical trials on patients undergoing total knee arthroplasty showed non-inferiority or superiority of FXI inhibition compared to enoxaparin for the primary outcome, which was incidence of venous thromboembolism. One Phase 2 trial reported that FXI inhibition is associated with fewer bleeding events than apixaban. The results from observational studies on FXII are more conflicting. Some show that low FXII concentrations confer protection against thrombosis, while others have found it to be deleterious. Results from experimental studies are inconclusive, but suggest that FXII inhibition might be useful in preventing thrombosis caused by foreign objects like catheters or mechanical heart valves. One Phase 2 study not conducted on thrombosis has reported FXII inhibition as safe. In conclusion, FXI seems to be a promising target for antithrombotic therapy, both alone and in combination with existing therapies, while the potential of targeting FXII is still unclear.
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Thrombosis / Factor XII Type of study: Observational study / Prognostic study / Randomized controlled trials Limits: Animals / Humans Language: English Journal: Thromb Res Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Thrombosis / Factor XII Type of study: Observational study / Prognostic study / Randomized controlled trials Limits: Animals / Humans Language: English Journal: Thromb Res Year: 2022 Document Type: Article