首页 | 本学科首页   官方微博 | 高级检索  
检索        


Evaluation of a chromogenic commercial assay using VWF-73 peptide for ADAMTS13 activity measurement
Authors:Bérangère Joly  Alain Stepanian  David Hajage  Sandrine Thouzeau  Sophie Capdenat  Paul Coppo  Agnès Veyradier
Institution:1. Service d’Hématologie biologique, Hôpital Antoine Béclère, Assistance Publique-Hôpitaux de Paris, Clamart, Université Paris 11, France;2. Service d’Hématologie biologique, Hôpital Louis Mourier, Assistance Publique-Hôpitaux de Paris, Colombes, Université Paris 7, France;3. Département d’épidémiologie et de recherche clinique, Hôpital Louis Mourier, Assistance Publique-Hôpitaux de Paris, Colombes, Université Paris 7, France;4. French Reference Center for Thrombotic Microangiopathies (CNR-MAT), Hôpital Saint Antoine, Assistance Publique-Hôpitaux de Paris, Paris, Université Paris 6, France;5. Service d’Hématologie, Hôpital Saint Antoine, Assistance Publique-Hôpitaux de Paris, Paris, France
Abstract:

Introduction

Thrombotic thrombocytopenic purpura (TTP) is a thrombotic microangiopathy (TMA), related to a severe functional deficiency of ADAMTS13 activity (< 10% of normal). ADAMTS13 activity is thus crucial to confirm the clinical suspicion of TTP, to distinguish it from other TMAs, and to perform the follow-up of TTP patients.

Material and methods

We compared the performance of the commercial chromogenic assay Technozym® ADAMTS13 Activity ELISA (chromogenic VWF73 substrate, Chr-VWF73, Technoclone, Vienna, Austria), to that of our in-house FRETS-VWF73 used as reference method. A large group of 247 subjects (30 healthy volunteers and 217 patients with miscellaneaous TMAs) was studied.

Results

The lower limit of detection of the Chr-VWF73 was 3%, which is well adapted to the clinically relevant threshold for TTP diagnosis (10%). Our results showed a reasonable agreement between FRETS-VWF73 and Chr-VWF73 assays to distinguish samples with an ADAMTS13 activity < 10% from those with an ADAMTS13 activity > 10%. However, Chr-VWF73 assay provided false negative results in ~ 12% of acute TTP patients. Inversely, the Chr-VWF73 assay globally underestimated ADAMTS13 activity in detectable values ranging from 11 to 100% (with a great variability compared to FRETS-VWF73), which may be a concern for the follow-up of TTP patients in remission.

Conclusion

In-house assays developed and performed by expert laboratories remain the reference methods that should be used without limitation to control values provided by commercial assays when needed. Also, the development of an international reference preparation will be crucial to improve standardization.
Keywords:ADAMTS13  A disintegrin and metalloprotease with thrombospondin type 1 repeats  member 13  CV  Coefficient of variation  FRETS-VWF73  Fluorescence resonance energy transfer-VWF73  HELLP  Hemolysis elevated liver enzymes low platelet count  HUS  Hemolytic uremic syndrome  IH  In-house  LLD  lower limit of detection  NPP  Normal pool plasma  NPV  Negative predictive value  PPV  Positive predictive value  QC  Quality control  SD  Standard deviation  TMA  Thrombotic microangiopathy  TTP  Thrombotic thrombocytopenic purpura  USS  Upshaw-Schulman syndrome  VWF  von Willebrand factor
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号