Literature DB >> 18662260

Second international collaborative study evaluating performance characteristics of methods measuring the von Willebrand factor cleaving protease (ADAMTS-13).

A Tripodi1, F Peyvandi, V Chantarangkul, R Palla, A Afrasiabi, M T Canciani, D W Chung, S Ferrari, Y Fujimura, M Karimi, K Kokame, J A Kremer Hovinga, B Lämmle, S F de Meyer, B Plaimauer, K Vanhoorelbeke, K Varadi, P M Mannucci.   

Abstract

BACKGROUND: Over the last 4 years ADAMTS-13 measurement underwent dramatic progress with newer and simpler methods. AIMS: Blind evaluation of newer methods for their performance characteristics.
DESIGN: The literature was searched for new methods and the authors invited to join the evaluation. Participants were provided with a set of 60 coded frozen plasmas that were prepared centrally by dilutions of one ADAMTS-13-deficient plasma (arbitrarily set at 0%) into one normal-pooled plasma (set at 100%). There were six different test plasmas ranging from 100% to 0%. Each plasma was tested 'blind' 10 times by each method and results expressed as percentage vs. the local and the common standard provided by the organizer.
RESULTS: There were eight functional and three antigen assays. Linearity of observed-vs.-expected ADAMTS-13 levels assessed as r2 ranged from 0.931 to 0.998. Between-run reproducibility expressed as the (mean) CV for repeated measurements was below 10% for three methods, 10-15% for five methods and up to 20% for the remaining three. F-values (analysis of variance) calculated to assess the capacity to distinguish between ADAMTS-13 levels (the higher the F-value, the better the capacity) ranged from 3965 to 137. Between-method variability (CV) amounted to 24.8% when calculated vs. the local and to 20.5% when calculated vs. the common standard. Comparative analysis showed that functional assays employing modified von Willebrand factor peptides as substrate for ADAMTS-13 offer the best performance characteristics.
CONCLUSIONS: New assays for ADAMTS-13 have the potential to make the investigation/management of patients with thrombotic microangiopathies much easier than in the past.

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Year:  2008        PMID: 18662260      PMCID: PMC6537877          DOI: 10.1111/j.1538-7836.2008.03099.x

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN: 1538-7836            Impact factor:   5.824


  14 in total

Review 1.  Thrombotic microangiopathies: a general approach to diagnosis and management.

Authors:  Donald M Arnold; Christopher J Patriquin; Ishac Nazy
Journal:  CMAJ       Date:  2016-10-17       Impact factor: 8.262

2.  Validation of PLASMIC score and follow-up data in a cohort of patients with suspected microangiopathies from Southern Italy.

Authors:  Giovanni Luca Tiscia; Angelo Ostuni; Nicola Cascavilla; Filomena Cappucci; Potito Scalzulli; Cosima Battista; Antonio Abrescia; Filippo Aucella; Caterina Buquicchio; Maurizio Brigante; Giovanna D'Andrea; Bruno Di Paolo; Giulio Giordano; Barbara Infante; Silvia Piano; Prudenza Ranieri; Livio Tullo; Elvira Grandone
Journal:  J Thromb Thrombolysis       Date:  2018-08       Impact factor: 2.300

3.  Escherichia coli-derived von Willebrand factor-A2 domain fluorescence/Förster resonance energy transfer proteins that quantify ADAMTS13 activity.

Authors:  Kannayakanahalli M Dayananda; Shobhit Gogia; Sriram Neelamegham
Journal:  Anal Biochem       Date:  2010-12-10       Impact factor: 3.365

4.  Blood group O and black race are independent risk factors for thrombotic thrombocytopenic purpura associated with severe ADAMTS13 deficiency.

Authors:  Deirdra R Terrell; David G Motto; Johanna A Kremer Hovinga; Bernhard Lämmle; James N George; Sara K Vesely
Journal:  Transfusion       Date:  2011-04-06       Impact factor: 3.157

5.  ADAMTS13 test and/or PLASMIC clinical score in management of acquired thrombotic thrombocytopenic purpura: a cost-effective analysis.

Authors:  Chong H Kim; Sierra C Simmons; Lance A Williams; Elizabeth M Staley; X Long Zheng; Huy P Pham
Journal:  Transfusion       Date:  2017-06-23       Impact factor: 3.157

6.  An optimized fluorogenic ADAMTS13 assay with increased sensitivity for the investigation of patients with thrombotic thrombocytopenic purpura.

Authors:  J Muia; W Gao; S L Haberichter; L Dolatshahi; J Zhu; L A Westfield; S C Covill; K D Friedman; J E Sadler
Journal:  J Thromb Haemost       Date:  2013-08       Impact factor: 5.824

7.  Correlation between ADAMTS13 activity and neurological impairment in acute thrombotic microangiopathy patients.

Authors:  Giulia Berti de Marinis; Stefano Novello; Silvia Ferrari; Isabella Barzon; Irene Cortella; Maria Antonietta Businaro; Fabrizio Fabris; Anna Maria Lombardi
Journal:  J Thromb Thrombolysis       Date:  2016-11       Impact factor: 2.300

8.  Residual plasmatic activity of ADAMTS13 is correlated with phenotype severity in congenital thrombotic thrombocytopenic purpura.

Authors:  Luca A Lotta; Haifeng M Wu; Ian J Mackie; Marina Noris; Agnes Veyradier; Marie A Scully; Giuseppe Remuzzi; Paul Coppo; Ri Liesner; Roberta Donadelli; Chantal Loirat; Richard A Gibbs; April Horne; Shangbin Yang; Isabella Garagiola; Khaled M Musallam; Flora Peyvandi
Journal:  Blood       Date:  2012-04-23       Impact factor: 22.113

9.  ADAMTS-13 in the Diagnosis and Management of Thrombotic Microangiopathies.

Authors:  Galit Sarig
Journal:  Rambam Maimonides Med J       Date:  2014-10-29

Review 10.  Thrombotic thrombocytopenic purpura.

Authors:  Paul Knöbl
Journal:  Memo       Date:  2018-08-17
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