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Published on: June 2, 2015
Laboratory evaluation of antiphospholipid antibodies in patients with venous thromboembolism
J Hirmerova1, Z Ulcova-Gallova, J Seidlerova
12nd Department of Internal Medicine, University Hospital, Faculty of Medicine, Charles University, Pilsen, Czech Republic. hirmerova@fnplzen.cz
Insights
This study found that IgM-antiphosphatidylethanolamine antibodies were more prevalent in patients with venous thromboembolism. This suggests their potential role in diagnosing antiphospholipid syndrome when other criteria antibodies are absent.
Area of Science:
- Immunology
- Hematology
- Rheumatology
Background:
- Antiphospholipid syndrome (APS) is characterized by recurrent thrombosis and specific antiphospholipid antibodies.
- Current diagnostic criteria focus on anticardiolipin and anti-beta 2 glycoprotein I antibodies.
- The role of non-criteria antiphospholipid antibodies in venous thromboembolism (VTE) without systemic autoimmune disease requires further investigation.
Purpose of the Study:
- To evaluate the significance of an extended antiphospholipid antibody profile in patients with VTE but no systemic autoimmune disease.
- To identify non-criteria antiphospholipid antibodies that are significantly more prevalent in VTE patients.
- To assess the overlap between criteria and non-criteria antiphospholipid antibodies in this cohort.
Main Methods:
- Enzyme-linked immunosorbent assays (ELISA), both commercial and in-house, were employed.
- The study included 140 patients with VTE and 136 control participants.
- A comprehensive panel of antibodies was tested, including anticardiolipin, anti-beta 2 glycoprotein I (anti-beta2-GPI), and non-criteria antibodies such as antiphosphatidic acid, antiphosphatidylethanolamine, antiphosphatidylglycerol, antiphosphatidylinositol, and antiphosphatidylserine.
Main Results:
- Immunoglobulin (Ig) M-anticardiolipin antibodies (12.9%), IgG-anti-beta2-GPI (16.4%), and IgM-antiphosphatidylethanolamine (14.3%) showed significantly higher prevalence in VTE patients compared to controls.
- Of the non-criteria antibodies tested, only IgM-antiphosphatidylethanolamine demonstrated a statistically significant higher prevalence in the VTE group (P = 0.014).
- These three significantly prevalent antibodies exhibited minimal overlap in their presence among the patients.
Conclusions:
- Antiphosphatidylethanolamine antibodies are significantly more prevalent in patients with VTE, even in the absence of criteria antiphospholipid antibodies.
- These findings suggest that antiphosphatidylethanolamine antibodies may hold clinical utility in suspecting antiphospholipid syndrome.
- The study highlights the potential diagnostic value of investigating non-criteria antiphospholipid antibodies, particularly antiphosphatidylethanolamine, in specific clinical scenarios.
Abstract:
The objective of our study was to evaluate the significance of extended antiphospholipid profile in patients with venous thromboembolism without any systemic autoimmune disease. In 140 patients (age 18-69 years; 47.1% men) with venous thromboembolism and 136 control participants we tested anticardiolipin antibodies, anti-beta 2 glycoprotein I (anti-beta2-GPI) and also non-criteria antiphospholipid antibodies: antiphosphatidic acid, antiphosphatidylethanolamine, antiphosphatidylglycerol, antiphosphatidylinositol, antiphosphatidylserine. Commercial and in-house enzyme-linked immunosorbent assays were used. The antibodies with significantly higher prevalence in patients (compared to controls) were: immunoglobulin (Ig) M-anticardiolipin antibodies (12.9%; P = 0.035), IgG-anti-beta2-GPI (16.4%; P = 0.0032), IgM-antiphosphatidylethanolamine (14.3%; P = 0.014). In most cases, these three antibodies did not overlap. In conclusion, of non-criteria antiphospholipid antibodies, only antiphosphatidylethanolamine were significantly more prevalent in patients with venous thromboembolism, with only minor overlapping with the criteria antiphospholipid antibodies. Our results suggest the possible utility of searching for antiphosphatidylethanolamine in the clinical suspicion of antiphospholipid syndrome and the absence of criteria antiphospholipid antibodies.
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