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Published on: May 23, 2025
Anti-prothrombin antibodies are associated with thrombosis in children
Olof Rask1, Andreas Hillarp, Erik Berntorp
1Department of Clinical Sciences, Lund University, Malmö University Hospital, Malmö, Sweden. olof.rask@med.lu.se
Insights
Autoantibodies against prothrombin (anti-PT) were found to be a significant risk factor for thrombosis in children. This study highlights the complex, multifactorial nature of pediatric thrombosis.
Area of Science:
- Pediatric Thrombosis Research
- Autoantibody Analysis
- Risk Factor Identification
Background:
- Pediatric thrombosis is a serious condition with various underlying causes.
- Identifying specific risk factors is crucial for prevention and treatment.
Purpose of the Study:
- To evaluate thrombotic risk factors in children.
- To specifically investigate autoantibodies against prothrombin (anti-PT) and protein S (anti-PS).
Main Methods:
- A cohort of 57 Swedish children with acute thrombotic events was studied.
- Quantitative enzyme-linked immunosorbent assays were used to detect anti-PT and anti-PS autoantibodies.
- Healthy controls (n=47) were included for comparison.
Main Results:
- Anti-PT antibodies were detected in 21% of patients versus 2.1% of controls (OR 12.0, p=0.005).
- Anti-PS antibodies were found in 7% of patients versus 2.1% of controls (OR 3.4, p>0.30).
- Factor V G1691A mutation was present in 25% of patients, and 44% had multiple risk factors.
Conclusions:
- Autoantibodies against prothrombin (anti-PT) appear to be a common risk factor for pediatric thrombosis.
- The study confirms that pediatric thrombosis is often multifactorial, involving various clinical conditions and genetic predispositions.
Introduction:
This investigation aimed to evaluate thrombotic risk factors in children, with special reference to autoantibodies against prothrombin and protein S.
Materials And Methods:
We studied 57 consecutive Swedish children and adolescents referred with a radiologically confirmed acute thrombotic event. Clinical data were collected and a thrombophilia investigation was performed, including analysis of autoantibodies against protein S (anti-PS) and prothrombin (anti-PT). The anti-PS and anti-PT autoantibodies were also investigated in sera from 47 healthy controls. Detection of autoantibodies was performed by quantitative enzyme-linked immunosorbent assays.
Results:
Results for anti-PT antibodies were positive in 21% (12/57) of the patients and 2.1% (1/47) of the controls (OR 12.0, 95% CI 1.7-534; p=0.005). Seven percent (4/57) of the patients and 2.1% (1/47) of the controls were positive for anti-PS antibodies (OR 3.4, 95% CI 0.3-174; p>0.30). The FV G1691A mutation was found in 25% (14/57), and 44% (25/57) had 2 or more prothrombotic risk factors. Sixty percent (34/57) of the thrombosis patients were female. Peaks in frequency of thromboembolic events were found in the neonatal and the adolescent periods. Fifty-three percent (30/57) had thrombosis in the lower venous system. Associated clinical conditions occurred in 91% (52/57): systemic illness in 31% (18/57), infections in 26% (15/57), and oral contraceptive use in 25% (14/57). Four percent (2/57) had no apparent clinical or prothrombotic risk factors.
Conclusions:
This study suggests that anti-PT autoantibodies may be common risk factors for thrombosis in children, and it confirms the multifactorial nature of pediatric thrombosis.
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