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Physiology, Coagulation Pathways
Authors
Raheel Chaudhry1; Syed Muhammad Usama2; Hani M. Babiker3.
Affiliations
1 Ross University School Of Medicine
2 Dow University of Health Sciences
3 University of Arizona Cancer Center
Last Update: August 29, 2022.
Introduction
The coagulation pathway is a cascade of events that leads to hemostasis. The intricate pathway allows for rapid
healing and prevention of spontaneous bleeding. Two paths, intrinsic and extrinsic, originate separately but converge
at a specific point, leading to fibrin activation. The purpose is to ultimately stabilize the platelet plug with a fibrin
mesh.[1][2][3]
Function
The function of the coagulation pathway is to keep hemostasis, which is the blockage of a bleeding or hemorrhage.
Primary hemostasis is an aggregation of platelets forming a plug at the damaged site of exposed endothelial cells.
Secondary hemostasis includes the two main coagulation pathways, intrinsic and extrinsic, that meet up at a point to
form the common pathway. The common pathway ultimately activates fibrinogen into fibrin. These fibrin subunits
have an affinity for each other and combine into fibrin strands that bind the platelets together, stabilizing the platelet
plug.[4][5][6][7]
Mechanism
The mechanism by which coagulation allows for hemostasis is an intricate process that is done through a series of
clotting factors. The intrinsic pathway consists of factors I, II, IX, X, XI, and XII. Respectively, each one is named,
fibrinogen, prothrombin, Christmas factor, Stuart-Prower factor, plasma thromboplastin, and Hageman factor. The
extrinsic pathway consists of factors I, II, VII, and X. Factor VII is called stable factor. The common pathway consists
of factors I, II, V, VIII, X. The factors circulate through the bloodstream as zymogens and are activated into serine
proteases. These serine proteases act as a catalyst to cleave the next zymogen into more serine proteases and ultimately
activate fibrinogen. The following are serine proteases: factors II, VII, IX, X, XI and XII. These are not serine
proteases: factors V, VIII, XIII. The intrinsic pathway is activated through exposed endothelial collagen, and the
extrinsic pathway is activated through tissue factor released by endothelial cells after external damage.
Intrinsic Pathway
This pathway is the longer pathway of secondary hemostasis. It begins with the activation of Factor XII (a zymogen,
inactivated serine protease) which becomes Factor XIIA (activated serine protease) after exposure to endothelial
collagen. Endothelial collagen is only exposed when endothelial damage occurs. Factor XIIA acts as a catalyst to
activate factor XI to Factor XIA. Factor XIA then goes on to activate factor IX to factor IXA. Factor IXA goes on to
serve as a catalyst for turning factor X into factor Xa. This is known as a cascade. When each factor is activated, it
goes on to activate many more factors in the next steps. As you move further down the cascade, the concentration of
that factor increases in the blood. For example, the concentration of factor IX is more than that of factor XI. When
factor II is activated by either intrinsic or extrinsic pathway, it can reinforce the intrinsic pathway by giving positive
feedback to factors V, VII, VIII, XI, XIII. This makes factor XII less critical; patients can actually clot well without
factor XII. The intrinsic pathway is clinically measured as the partial thromboplastin time (PTT).
Extrinsic Pathway
The extrinsic pathway is the shorter pathway of secondary hemostasis. Once the damage to the vessel is done, the
endothelial cells release tissue factor which goes on to activate factor VII to factor VIIa. Factor VIIa goes on to
activate factor X into factor Xa. This is the point where both extrinsic and intrinsic pathways become one. The
extrinsic pathway is clinically measured as the prothrombin time (PT).
Common Pathway
This pathway begins at factor X which is activated to factor Xa. The process of activating factor Xa is a complicated
reaction. Tenase is the complex that cleaves factor X into factor Xa. Tenase has two forms: extrinsic, consisting
of factor VII, factor III (tissue factor) and Ca2+, or intrinsic, made up of cofactor factor VIII, factor IXA, a
phospholipid, and Ca2+. Once activated to factor Xa, it goes on to activate factor II (prothrombin) into factor IIa
(thrombin). Also, factor Xa requires factor V as a cofactor to cleave prothrombin into thrombin. Factor IIa (thrombin)
goes on to activate fibrinogen into fibrin. Thrombin also goes on to activate other factors in the intrinsic pathway
(factor XI) as well as cofactors V and VIII and factor XIII. Fibrin subunits come together to form fibrin strands, and
factor XIII acts on fibrin strands to form a fibrin mesh. This mesh helps to stabilize the platelet plug.
Negative Feedback
To prevent over-coagulation, which causes widespread thrombosis, there are certain processes to keep the coagulation
cascade in check. As thrombin acts as a procoagulant, it also acts as a negative feedback by activating plasminogen to
plasmin and stimulating the production of antithrombin (AT). Plasmin acts directly on the fibrin mesh and breaks it
down. AT decreases the production of thrombin from prothrombin and decreases the amount of activated factor X.
Protein C and S also act to prevent coagulation, mainly by inactivating factors V and VIII.
Organs Involved
One of the organs intimately involved in the coagulation process is the liver. The liver is responsible for the formation
of factors I, II, V, VII, VIII, IX, X, XI, XIII, and protein C and S. Factor VII is created by the vascular endothelium.
Pathology to the liver can cause lack of coagulation factors and lead to hemorrhage. A decrease in coagulation factors
typically means severe liver damage. Factor VII has the shortest half-life, leading to elevated PT first in liver disease.
INR can be greater than 6.5 (normal is close to 1.0). Coagulopathy in liver disease is treated with fresh frozen plasma.
Pathophysiology
Hemophilia A and B are inherited in an x-linked recessive pattern. In hemophilia A there is a deficiency in factor VIII.
In hemophilia B there is a deficiency in factor IX.[2][8][9][10][11]
Hemophilia C is an autosomal recessive mutation, where there is a deficiency in factor XI.
Factor V Leiden is a genetic mutation more prevalent in people European descent. This defect causes a state of
hypercoagulability. The genetic mutation causes a defect in factor V such that protein C cannot inactivate it, allowing
factor V to continuously activate downstream factors.
Deficiencies in protein C and S also can lead to hypercoagulable states due to an inability to appropriately inhibit
factors V and VIII respectively.
Clinical Significance
PT and PTT evaluate the time it takes for the extrinsic and intrinsic pathways to take effect, respectively.
Mixing studies are done to determine whether a PT or PTT is elevated due to a factor deficiency or a factor inhibitor
(antibodies to specific factors). It is done by mixing the patient's plasma with a control plasma. If the mixed plasma PT
and PTT normalize, the PT and PTT prolongation is due to a factor deficiency. If they do not normalize, the
prolongation is due to a factor inhibitor. An example of an inhibitor is lupus anticoagulant.
Vitamin K deficiency can lead to elevated PT and PTT. It can present as hemarthrosis, intramuscular bleeding, or
gastrointestinal bleeding. Vitamin K deficiency is commonly seen in newborns due to the lack of gut colonization by
bacteria. It also can be seen in malabsorption (cystic fibrosis, celiacs disease, Crohn disease).
Heparin is an anticoagulant used in hospital settings for deep venous thrombosis prophylaxis. Heparin binds and
activates AT. AT goes on to inactivate thrombin and factor Xa.
Warfarin is used for long-term therapy in patients with atrial fibrillation to prevent a thrombus from forming in the left
atrium. It acts by inhibiting epoxide reductase. Epoxide reductase is a critical component in coagulation factor
production because it helps recycle Vitamin K. Without vitamin K more coagulation factors cannot be produced by the
liver.
Review Questions
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