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Prevalence and coagulation correlation of anticardiolipin antibodies in patients with COVID-19
Hui Zeng1,2, Meihong Cai3, Han Xue2
1Center of Clinical Laboratory, Hangzhou Ninth People's Hospital, Hangzhou, Zhejiang, China.
Insights
Anticardiolipin antibodies (ACLs) were more prevalent in critically ill COVID-19 patients, particularly IgG isotype. However, ACLs showed weak correlation with coagulation variables and did not clearly link to thrombosis in these patients.
Area of Science:
- Immunology
- Hematology
- Infectious Diseases
Background:
- Anticardiolipin antibodies (ACLs) are associated with thrombotic events.
- Coronavirus disease 2019 (COVID-19) is linked to coagulopathies.
- The role of ACLs in COVID-19 pathogenesis requires further investigation.
Purpose of the Study:
- To determine the prevalence and characteristics of ACLs in COVID-19 patients.
- To correlate ACLs with laboratory coagulation variables.
- To assess the association between ACLs and disease severity in COVID-19.
Main Methods:
- Retrospective analysis of 87 COVID-19 patients.
- Measurement of serum anticardiolipin antibodies (IgA, IgG).
- Correlation analysis with coagulation parameters (aPTT, TT).
Main Results:
- ACLs detected in 61.91% of critically ill vs. 31.82% of non-critically ill patients.
- IgG isotype was significantly more prevalent in critically ill patients (OR=2.721).
- ACLs-IgG showed weak correlations with activated partial thromboplastin time and thrombin time.
Conclusions:
- ACLs, particularly IgG, are more common in severe COVID-19.
- ACLs do not appear to strongly correlate with coagulation abnormalities or thrombosis in COVID-19 patients.
- Further research is needed to elucidate the role of ACLs in COVID-19.
Abstract:
We aimed to determine prevalence and characteristics of anticardiolipin antibodies (ACLs) and its correlations with laboratory coagulation variables in patients with coronavirus disease 2019 (COVID-19). We retrospectively analyzed the prevalence of serum ACLs and its correlation with coagulative laboratory variables in 87 patients with COVID-19. ACLs were detected in 13/21 (61.91%) critically ill patients, and 21/66 (31.82%) in non-critically ill patients. For ACLs, IgA, and IgG were the most common types. The prevalence of IgG in critical ill patients was much higher than that in non-critical patients with odd ratio = 2.721. And the levels of all isotypes of ACLs in critically ill patients were much higher than those in non-critically ill patients. Correlation analysis showed that activated partial thromboplastin time and thrombin time had weak correlation with ACLs-IgG (R = 0.308, P = .031; R = 0.337, P = .018, respectively). Only the prevalence of ACLs-IgG shows a significant difference when compared critically ill patients with non-critically ill patients. ACLs do not seem to have a clear correlation with thrombosis occurred in COVID-19 patients.
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