Magnesium‐dependent activated partial thromboplastin time assay—Simple method for lupus anticoagulant detection
Introduction Detection of lupus anticoagulant (LA), an antiphospholipid (aPL) antibody, in a clotting time test is an important finding for diagnosis of antiphospholipid syndrome (APS). However, confirmation of LA requires several different testing procedures, some of which can be difficult and requ...
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Published in | International journal of laboratory hematology Vol. 42; no. 1; pp. 46 - 51 |
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Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Wiley Subscription Services, Inc
01.02.2020
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Subjects | |
Online Access | Get full text |
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Summary: | Introduction
Detection of lupus anticoagulant (LA), an antiphospholipid (aPL) antibody, in a clotting time test is an important finding for diagnosis of antiphospholipid syndrome (APS). However, confirmation of LA requires several different testing procedures, some of which can be difficult and require time. We report here a simple and highly specific method for detecting LA.
Materials and Methods
We examined 66 plasma samples obtained from LA‐positive (LA) and 75 from LA‐negative (non‐LA) subjects, which included patients with acquired hemophilia and coagulation disorders, as well as from 43 healthy volunteer samples as normal controls. Activated partial thromboplastin time (APTT) was determined by adding 20 mmol of CaCl2 (Ca‐APTT) or 25 mmol of a mixture of Mg and Ca (Mg‐APTT). The ratio of Mg‐APTT/Ca‐APTT was then calculated and used as the Mg/Ca Index.
Results
The Mg/Ca Index value for the LA group was significantly lower than that for the non‐LA and normal control groups (P < .0001). When the cutoff value of the Mg/Ca Index was less than 1.00, the sensitivity of LA determination using the Mg‐APTT assay was 80.3%, while specificity was 100%.
Conclusion
Our findings indicate that the present Mg‐APTT assay is a simple yet highly specific method for LA detection. |
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Bibliography: | Funding information This study was supported in part by a Shinshu Medical Promotion Association subsidy (2014). ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 ObjectType-Article-2 ObjectType-Feature-1 content type line 23 |
ISSN: | 1751-5521 1751-553X 1751-553X |
DOI: | 10.1111/ijlh.13134 |