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APTT reagent with ellagic acid as activator shows adequate lupus anticoagulant sensitivity in comparison to silica‐based reagent

Background:  Lupus anticoagulant (LA) is an antibody that interferes with phospholipid‐dependent coagulation reactions. Activated partial thromboplastin time (APTT) is widely used as a test for LA screening. APTT reagents are composed of activators, such as silica or ellagic acid, and phospholipids,...

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Published in:Journal of thrombosis and haemostasis 2012-11, Vol.10 (11), p.2338-2343
Main Authors: KUMANO, O., IEKO, M., NAITO, S., YOSHIDA, M., TAKAHASHI, N.
Format: Article
Language:English
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Summary:Background:  Lupus anticoagulant (LA) is an antibody that interferes with phospholipid‐dependent coagulation reactions. Activated partial thromboplastin time (APTT) is widely used as a test for LA screening. APTT reagents are composed of activators, such as silica or ellagic acid, and phospholipids, and APTT reagents with silica are recommended for LA screening because of greater sensitivity. However, the effects of activators on LA activity have not been adequately investigated. Objectives:  In this study, we examined whether an ellagic acid‐based reagent was highly sensitive to LA in a low phospholipid condition and useful for LA screening. Methods:  Silica‐based (SL) and ellagic acid‐based (EA) reagents were prepared in‐house with the same composition and concentration of phospholipids, while the commercial APTT reagents APTT‐SLA (SLA), Actin FSL (FSL), APTT‐SP (SP) and PTT‐LA (PTT) were also included in the study. Results:  The normal reference ranges for SL and EA were 30.1–47.0 and 28.0–40.2 s, respectively, while the cut‐off index values for circulating anticoagulant activity (ICA) calculated from the results obtained with SL, EA, SLA, FSL, SP and PTT were 12.9, 11.5, 13.2, 15.6, 14.3 and 14.0, respectively. The sensitivity of those reagents based on those cut‐off values was 91%, 96%, 68%, 46%, 91% and 86%, respectively. Conclusions:  Our results showed that the ellagic acid‐based reagent was more sensitive to LA than silica‐based reagents in a low phospholipid condition and had adequate sensitivity to detect LA. We concluded that the sensitivity of APTT reagents for LA is dependent on phospholipid concentration and not the activator.
ISSN:1538-7933
1538-7836
1538-7836
DOI:10.1111/j.1538-7836.2012.04906.x