Stuart-Prower factor

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Stuart-Prower factor, also known as Factor X or FX, is a crucial enzyme in the coagulation system, which helps in the clotting of blood. This factor is named after two patients, Audrey Prower and Rufus Stuart, from whom the factor was first identified. The discovery of Factor X is a significant milestone in the field of hematology, providing insights into the complex process of blood coagulation and the management of bleeding disorders.

Overview[edit | edit source]

Factor X is synthesized in the liver and requires vitamin K for its synthesis. It plays a pivotal role in the coagulation cascade, a series of reactions that ultimately lead to the formation of a blood clot. Specifically, Factor X is involved in the conversion of prothrombin to thrombin, an essential step in the formation of a fibrin clot. This process is critical for stopping bleeding and initiating the healing process after tissue injury.

Genetics and Biochemistry[edit | edit source]

The gene responsible for Factor X production is located on the chromosome 13 (13q34). Mutations in this gene can lead to Factor X deficiency, a rare bleeding disorder characterized by a propensity to bleed. On a biochemical level, Factor X is a serine protease enzyme that is activated to its enzymatic form, Factor Xa, through either the intrinsic or extrinsic pathways of the coagulation cascade.

Clinical Significance[edit | edit source]

Factor X deficiency, also known as Stuart-Prower deficiency, is a rare condition that can lead to various bleeding manifestations, ranging from mild to severe. Diagnosis typically involves coagulation tests that measure the activity of Factor X in the blood. Treatment may include fresh frozen plasma or Factor X concentrate to manage bleeding episodes or as prophylaxis during surgery.

In addition to its role in bleeding disorders, Factor Xa is a target for new anticoagulant drugs, which are used to prevent and treat thrombosis. These Factor Xa inhibitors, such as rivaroxaban and apixaban, offer alternatives to traditional anticoagulants like warfarin, with the advantage of not requiring regular monitoring of blood coagulation levels.

Research and Future Directions[edit | edit source]

Research on Factor X and its activated form, Factor Xa, continues to be a vibrant area of study, with implications for understanding coagulation disorders and developing new therapeutic agents. The exploration of Factor X's structure, function, and genetic variations provides valuable insights into the coagulation process and potential strategies for managing bleeding and thrombotic disorders.


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Contributors: Prab R. Tumpati, MD