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Updated: May 12, 2026

Thrombus Profiling Assay: A Microfluidics-Based Platform for Comprehensively Characterizing Biomechanical Thrombogenesis
Published on: January 9, 2026
Testosterone, thrombophilia, and thrombosis
Charles J Glueck1, Caitlin Richardson-Royer, Reiker Schultz
11The Jewish Hospital Cholesterol Center, Cincinnati, OH, USA.
Insights
Testosterone therapy can lead to dangerous blood clots like deep venous thrombosis (DVT) and pulmonary embolism (PE), and bone death (osteonecrosis). Patients with undiagnosed clotting disorders (thrombophilia) are at higher risk.
Area of Science:
- Endocrinology
- Hematology
- Vascular Medicine
Background:
- Testosterone therapy is increasingly used for various conditions.
- The potential risks, especially thrombotic events, require careful consideration.
- Undiagnosed thrombophilia-hypofibrinolysis may predispose individuals to adverse events.
Observation:
- A study observed thrombosis, deep venous thrombosis (DVT), pulmonary embolism (PE), and hip-knee osteonecrosis in 14 patients after testosterone therapy.
- These patients were previously healthy and had no prior history of thrombosis.
- Several patients presented with previously undiagnosed thrombophilia-hypofibrinolysis, including Factor V Leiden, high Factor VIII, and PAI-1 4G4G homozygosity.
Findings:
- Testosterone therapy was associated with the development of DVT, PE, and osteonecrosis in patients with underlying thrombophilia.
- Recurrent DVT-PE occurred in some patients even with therapeutic anticoagulation when testosterone was continued.
- High estradiol levels (a metabolite of testosterone) were observed in a significant percentage of men on testosterone therapy, suggesting a potential mechanism for E2-induced thrombophilia.
Implications:
- Thrombophilia should be screened for before initiating testosterone therapy to mitigate risks.
- The aromatization of testosterone to estradiol may play a role in testosterone-induced thrombophilia.
- Clinicians should be vigilant for thrombotic complications in patients undergoing testosterone replacement therapy, particularly those with risk factors.
Abstract:
We describe thrombosis, deep venous thrombosis (DVT) pulmonary embolism (PE; n = 9) and hip-knee osteonecrosis (n = 5) that developed after testosterone therapy (median 11 months) in 14 previously healthy patients (13 men and 1 woman; 13 Caucasian and 1 African American), with no antecedent thrombosis and previously undiagnosed thrombophilia-hypofibrinolysis. Of the 14 patients, 3 were found to be factor V Leiden heterozygotes, 3 had high factor VIII, 3 had plasminogen activator inhibitor 1 4G4G homozygosity, 2 had high factor XI, 2 had high homocysteine, 1 had low antithrombin III, 1 had the lupus anticoagulant, 1 had high anticardiolipin antibody Immunoglobulin G, and 1 had no clotting abnormalities. In 4 men with thrombophilia, DVT-PE recurred when testosterone was continued despite therapeutic international normalized ratio on warfarin. In 60 men on testosterone, 20 (33%) had high estradiol (E2 >42.6 pg/mL). When exogenous testosterone is aromatized to E2, and E2-induced thrombophilia is superimposed on thrombophilia-hypofibrinolysis, thrombosis occurs. The DVT-PE and osteonecrosis after starting testosterone are associated with previously undiagnosed thrombophilia-hypofibrinolysis. Thrombophilia should be ruled out before administration of exogenous testosterone.
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