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Autoimmune Diseases Affecting Hemostasis: A Narrative Review.
Emmanuel J Favaloro1,2,3, Leonardo Pasalic1,4, Giuseppe Lippi5
1Haematology, Institute of Clinical Pathology and Medical Research (ICPMR), Sydney Centres for Thrombosis and Haemostasis, NSW Health Pathology, Westmead Hospital, Westmead, Sydney, NSW 2145, Australia.
Autoimmune diseases can disrupt hemostasis, leading to bleeding or thrombosis. Conditions like acquired hemophilia A and antiphospholipid syndrome, and even COVID-19, illustrate this complex interaction.
Area of Science:
- Hematology
- Immunology
- Internal Medicine
Background:
- Hemostasis is a critical balance between pro-coagulant and anti-coagulant forces.
- Imbalances can result in bleeding disorders or thrombosis.
- Autoimmune diseases significantly impact hemostasis, causing diverse clinical outcomes.
Purpose of the Study:
- To review the intricate relationship between autoimmune diseases and hemostasis.
- To highlight how autoimmunity can lead to both bleeding and thrombotic events.
- To discuss contemporary examples like COVID-19 in the context of autoimmune-mediated hemostatic dysregulation.
Main Methods:
- This study is a narrative review.
- It synthesizes existing literature on autoimmunity and hemostasis.
- Key examples of autoimmune conditions affecting blood clotting are discussed.
Main Results:
- Autoantibodies against clotting factors can cause bleeding, exemplified by acquired hemophilia A.
- Antibodies targeting phospholipids promote thrombosis, as seen in antiphospholipid syndrome (APS).
- Emerging conditions like COVID-19 demonstrate autoimmunity's potential to induce thrombotic tendencies, with occasional bleeding risks.
Conclusions:
- Autoimmune processes represent a significant, often underappreciated, cause of hemostatic abnormalities.
- Understanding these interactions is crucial for diagnosing and managing patients with both autoimmune diseases and bleeding/thrombotic disorders.
- Further research into the mechanisms linking autoimmunity and hemostasis is warranted.
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