Protein C

Overview and Clinical Significance

Protein C is a vitamin K-dependent anticoagulant that plays a crucial role in blood clot regulation, inflammation control, and vascular health. It is synthesized in the liver and works alongside Protein S to prevent excessive clot formation.

Clinical Significance

  • Anticoagulant Function & Clot Prevention: Protein C inactivates clotting factors Va and VIIIa, reducing the risk of thrombosis.
  • Thrombophilia & Clotting Disorders: Deficiency in Protein C increases the risk of deep vein thrombosis (DVT), pulmonary embolism (PE), and stroke.
  • Sepsis & Inflammatory Regulation: Protein C has anti-inflammatory properties, helping mitigate sepsis-induced coagulopathy.
  • Genetic & Acquired Deficiencies: Protein C deficiency can be inherited or acquired, often linked to liver disease, vitamin K deficiency, or certain medications.
  • Diagnostic & Therapeutic Applications: Protein C testing helps assess clotting disorders, sepsis risk, and anticoagulant therapy effectiveness.

Protein C is a key regulator of coagulation and immune response, influencing thrombosis prevention, vascular health, and inflammatory balance.

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High Protein C Levels

  • Rare Genetic Variants – Some individuals may have naturally elevated Protein C levels without clinical significance.
  • Compensatory Response – In certain conditions, the body may increase Protein C production to counteract excessive clotting.

Low Protein C Levels

  • Protein C Deficiency – A genetic or acquired condition that increases the risk of deep vein thrombosis (DVT) and pulmonary embolism.
  • Liver Disease – Since Protein C is synthesized in the liver, conditions like cirrhosis or hepatitis can reduce its levels.
  • Vitamin K DeficiencyProtein C requires vitamin K for activation, so deficiencies (due to malnutrition or warfarin therapy) can lower its levels.
  • Severe Infections or SepsisInflammatory states can lead to excessive consumption of Protein C, contributing to disseminated intravascular coagulation (DIC).

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Life-Phase Considerations for Protein C

  • NewbornsNaturally lower Protein C levels at birth, which gradually increase over time. Severe congenital deficiency can lead to purpura fulminans, a life-threatening clotting disorder.
  • AdultsProtein C deficiency may remain asymptomatic until a triggering event (such as surgery, pregnancy, or prolonged immobility) increases clotting risk.
  • ElderlyAge-related changes in coagulation may alter Protein C activity, increasing susceptibility to thrombotic events.

Coagulation Markers

  • Protein C:
    A natural anticoagulant that helps prevent excessive clotting by inactivating specific clotting factors.

  • Prothrombin Index:
    Reflects the efficiency of the extrinsic coagulation pathway, providing insight into the blood’s capacity to form clots.

  • Serum Fibrinogen:
    A key factor converted into fibrin to stabilize clots; it also rises during inflammatory states.

  • Peripheric Blood Thrombocytes (Platelet Count):
    Platelets are essential for primary hemostasis, aggregating at injury sites to initiate clot formation.

Together, these markers offer a comprehensive view of the coagulation system—from clot formation to its regulation—assisting in the evaluation of bleeding or thrombotic disorders.

All Markers