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Published on: April 19, 2024
Clot waveform analysis in Clauss fibrinogen assay contributes to classification of fibrinogen disorders
Atsuo Suzuki1, Nobuaki Suzuki2, Takeshi Kanematsu3
1Department of Medical Technique, Nagoya University Hospital, Japan.
Insights
Clot waveform analysis (CWA) of the Clauss fibrinogen assay (CFA) can differentiate fibrinogen disorders. Maximum coagulation velocity (Min1) serves as a fibrinogen antigen surrogate, enabling easier classification of these conditions.
Area of Science:
- Hematology
- Clinical Chemistry
- Diagnostic Medicine
Background:
- The Clauss fibrinogen assay (CFA) is a standard screening tool for fibrinogen disorders.
- CFA measures functional fibrinogen activity (Ac) but cannot distinguish quantitative from qualitative defects without fibrinogen antigen (Ag) determination.
- Accurate classification of fibrinogen disorders necessitates differentiating between reduced levels and impaired function.
Purpose of the Study:
- To develop a novel method for classifying fibrinogen disorders using CFA.
- To explore the utility of clot waveform analysis (CWA) parameters from CFA.
- To identify a surrogate marker for fibrinogen antigen (Ag) within CFA data.
Main Methods:
- CWA parameters were analyzed from CFA results of normal individuals (n=91) and patients with fibrinogen disorders (n=27).
- Plasma samples were analyzed using a CS-5100 autoanalyzer.
- Correlation between CWA parameters and fibrinogen antigen levels was investigated.
Main Results:
- Maximum coagulation velocity (Min1) strongly correlated with fibrinogen Ag, serving as its surrogate.
- The Ac/Min1 ratio differed significantly between normal individuals and those with hypofibrinogenemia or hypodysfibrinogenemia.
- Estimated fibrinogen antigen (eAg) derived from Min1 allowed distinction between type I and type II deficiencies, with altered Ac/eAg ratios observed in dysfibrinogenemia and hypodysfibrinogenemia.
Conclusions:
- CWA of CFA can effectively distinguish various fibrinogen disorders.
- The combination of Ac/Min1 and Ac/eAg ratios provides a novel approach for qualitative detection of fibrinogen disorders.
- This CWA-based method offers a simpler and potentially more accessible screening test for fibrinogen abnormalities.
Background:
Clauss fibrinogen assay (CFA) is widely used as a screening test to detect fibrinogen disorders. However, CFA alone cannot distinguish quantitative and qualitative defects because it depends on functional fibrinogen activity (Ac), and fibrinogen antigen (Ag) determination is required to classify fibrinogen disorders.
Objectives:
To establish a novel approach to classify fibrinogen disorders, we investigated the potential of clot waveform analysis (CWA) of CFA and searched for a surrogate marker for fibrinogen Ag.
Materials And Methods:
We analyzed CWA parameters obtained from CFA using plasma from normal patients (n = 91) and those with fibrinogen disorders (n = 27, including 15 hypofibrinogenemia, 6 dysfibrinogenemia and 6 hypodysfibrinogenemia) with a CS-5100 autoanalyzer.
Results:
We found that maximum coagulation velocity (Min1) levels were most strongly correlated with fibrinogen Ag in both normal and fibrinogen disorders. Hence, Min1 appeared to function as a surrogate for fibrinogen Ag. Although the Ac/Min1 ratio did not simply reflect the measured Ac/Ag ratio, we found that the Ac/Min1 ratio was significantly higher than normal in hypofibrinogenemia and hypodysfibrinogenemia, but not in dysfibrinogenemia. On the other hand, we could distinguish type II deficiency from type I using estimated fibrinogen Ag (eAg) predicted from Min1. The Ac/eAg ratios of dysfibrinogenemia and hypodysfibrinogenemia were significantly lower than those of normal and hypofibrinogenemia.
Conclusion:
The CWA of CFA could distinguish fibrinogen disorders using a combination of Ac/Min1 and Ac/eAg values. This analysis allows the qualitative detection of fibrinogen disorder easily and represents a novel screening test for fibrinogen disorders.
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