Literature DB >> 21287408

Clinical features of severe acquired ADAMTS13 deficiency in thrombotic thrombocytopenic purpura: the Korean TTP registry experience.

Moon Ju Jang1, So Young Chong1, In-Ho Kim2, Jee-Hyun Kim2, Chul-Won Jung3, Ja Young Kim4, Ji-Chan Park5, Sun Min Lee6, Yeo-Kyeoung Kim7, Ji-Eun Lee8, Sung-Su Jang9, Jin-Seok Kim10, Deog-Yeon Jo11, Dae-Young Zang12, Young-Yiul Lee13, Ho-Young Yhim14, Doyeun Oh15.   

Abstract

The clinical significance of ADAMTS13 activity for response to treatment, mortality rate, recurrence, and prognosis is unclear. Therefore, we investigated the characteristics of severe ADAMTS13 deficiency and evaluated its prognostic features in Thrombotic thrombocytopenic purpura (TTP). The Korean TTP Registry includes 66 patients from 13 teaching hospitals in Korea who received the diagnosis of TTP from January 2005 to December 2008. Blood samples obtained upon admission were sent for ADAMTS13 analysis (multimer analysis by sodium dodecyl sulfate electrophoresis) to a central laboratory along with patient clinical information. Patients with severe ADAMTS13 deficiency had lower serum creatinine levels (P = 0.001) than patients with non-severe ADAMTS13 deficiency. Although severe ADAMTS13 deficiency was associated with better response rate (75 vs. 53%, P = 0.145), remission rate (81 vs. 61%, P = 0.209), and mortality rate (19 vs. 31%, P = 0.508) than non-severe ADAMTS13 deficiency, treatment outcomes did not differ significantly between groups. After adjusting for clinical and laboratory features, multivariate analysis did not reveal any independent risk factors for TTP-associated mortality. Patients with severe ADAMTS13 deficiency had lower serum creatinine levels at presentation, but severe ADAMTS13 activity deficiency at TTP diagnosis does not appear to have prognostic significance.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21287408     DOI: 10.1007/s12185-011-0771-5

Source DB:  PubMed          Journal:  Int J Hematol        ISSN: 0925-5710            Impact factor:   2.490


  26 in total

Review 1.  Thrombotic microangiopathies.

Authors:  Joel L Moake
Journal:  N Engl J Med       Date:  2002-08-22       Impact factor: 91.245

2.  ADAMTS-13 metalloprotease interacts with the endothelial cell-derived ultra-large von Willebrand factor.

Authors:  Jing-fei Dong; Joel L Moake; Aubrey Bernardo; Kazuo Fujikawa; Chalmette Ball; Leticia Nolasco; José A López; Miguel A Cruz
Journal:  J Biol Chem       Date:  2003-05-29       Impact factor: 5.157

3.  A second national questionnaire survey of TMA.

Authors:  Naomi Ito-Habe; Hideo Wada; Masanori Matsumoto; Yoshihiro Fujimura; Mitsuru Murata; Takashi Izuno; Minoru Sugita; Yasuo Ikeda
Journal:  Int J Hematol       Date:  2010-06-05       Impact factor: 2.490

4.  Antibody inhibitors to von Willebrand factor metalloproteinase and increased binding of von Willebrand factor to platelets in ticlopidine-associated thrombotic thrombocytopenic purpura.

Authors:  H M Tsai; L Rice; R Sarode; T W Chow; J L Moake
Journal:  Ann Intern Med       Date:  2000-05-16       Impact factor: 25.391

5.  Specific von Willebrand factor-cleaving protease in thrombotic microangiopathies: a study of 111 cases.

Authors:  A Veyradier; B Obert; A Houllier; D Meyer; J P Girma
Journal:  Blood       Date:  2001-09-15       Impact factor: 22.113

6.  Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura.

Authors:  G G Levy; W C Nichols; E C Lian; T Foroud; J N McClintick; B M McGee; A Y Yang; D R Siemieniak; K R Stark; R Gruppo; R Sarode; S B Shurin; V Chandrasekaran; S P Stabler; H Sabio; E E Bouhassira; J D Upshaw; D Ginsburg; H M Tsai
Journal:  Nature       Date:  2001-10-04       Impact factor: 49.962

7.  Predictive features of severe acquired ADAMTS13 deficiency in idiopathic thrombotic microangiopathies: the French TMA reference center experience.

Authors:  Paul Coppo; Michael Schwarzinger; Marc Buffet; Alain Wynckel; Karine Clabault; Claire Presne; Pascale Poullin; Sandrine Malot; Philippe Vanhille; Elie Azoulay; Lionel Galicier; Virginie Lemiale; Jean-Paul Mira; Christophe Ridel; Eric Rondeau; Jacques Pourrat; Stéphane Girault; Dominique Bordessoule; Samir Saheb; Michel Ramakers; Mohamed Hamidou; Jean-Paul Vernant; Bertrand Guidet; Martine Wolf; Agnès Veyradier
Journal:  PLoS One       Date:  2010-04-23       Impact factor: 3.240

8.  The Japanese experience with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome.

Authors:  Masanori Matsumoto; Hideo Yagi; Hiromichi Ishizashi; Hideo Wada; Yoshihiro Fujimura
Journal:  Semin Hematol       Date:  2004-01       Impact factor: 3.851

9.  Severe ADAMTS13 deficiency in adult idiopathic thrombotic microangiopathies defines a subset of patients characterized by various autoimmune manifestations, lower platelet count, and mild renal involvement.

Authors:  Paul Coppo; Djaouida Bengoufa; Agnès Veyradier; Martine Wolf; Annette Bussel; Gaël Armel Millot; Sandrine Malot; Farhad Heshmati; Jean-Paul Mira; Emmanuelle Boulanger; Lionel Galicier; Marie-Agnès Durey-Dragon; Véronique Frémeaux-Bacchi; Michel Ramakers; André Pruna; Dominique Bordessoule; Valérie Gouilleux; Marie-Lorraine Scrobohaci; Jean-Paul Vernant; Delphine Moreau; Elie Azoulay; Benoît Schlemmer; Loïc Guillevin; Kaïss Lassoued
Journal:  Medicine (Baltimore)       Date:  2004-07       Impact factor: 1.889

10.  Involvement of large plasma von Willebrand factor (vWF) multimers and unusually large vWF forms derived from endothelial cells in shear stress-induced platelet aggregation.

Authors:  J L Moake; N A Turner; N A Stathopoulos; L H Nolasco; J D Hellums
Journal:  J Clin Invest       Date:  1986-12       Impact factor: 14.808

View more
  9 in total

1.  Lombardy diagnostic and therapeutic network of thrombotic microangiopathy.

Authors:  I Mancini; P Agosti; M Boscarino; B Ferrari; A Artoni; R Palla; M Spreafico; G Crovetti; E Volpato; S Rossini; C Novelli; S Gattillo; L Barcella; M Salmoiraghi; A Falanga; F Peyvandi
Journal:  Orphanet J Rare Dis       Date:  2022-06-23       Impact factor: 4.303

2.  Acquired idiopathic ADAMTS13 activity deficient thrombotic thrombocytopenic purpura in a population from Japan.

Authors:  Masanori Matsumoto; Charles L Bennett; Ayami Isonishi; Zaina Qureshi; Yuji Hori; Masaki Hayakawa; Yoko Yoshida; Hideo Yagi; Yoshihiro Fujimura
Journal:  PLoS One       Date:  2012-03-12       Impact factor: 3.240

3.  Clinical Practice Guidelines for the Management of Atypical Hemolytic Uremic Syndrome in Korea.

Authors:  Hae Il Cheong; Sang Kyung Jo; Sung Soo Yoon; Heeyeon Cho; Jin Seok Kim; Young Ok Kim; Ja Ryong Koo; Yong Park; Young Seo Park; Jae Il Shin; Kee Hwan Yoo; Doyeun Oh
Journal:  J Korean Med Sci       Date:  2016-10       Impact factor: 2.153

4.  Prognostic utility of ADAMTS13 activity for the atypical hemolytic uremic syndrome (aHUS) and comparison of complement serology between aHUS and thrombotic thrombocytopenic purpura.

Authors:  Jisu Oh; Doyeun Oh; Seon Ju Lee; Jeong Oh Kim; Nam Keun Kim; So Young Chong; Ji Young Huh; Ross I Baker
Journal:  Blood Res       Date:  2019-09-25

5.  Comparison of Clinical Scoring Systems in the Management of Patients with Microangiopathic Hemolytic Anemia and Thrombocytopenia

Authors:  Mehmet Baysal; Elif Ümit; Hakkı Onur Kırkızlar; Ahmet Muzaffer Demir
Journal:  Turk J Haematol       Date:  2020-11-09       Impact factor: 1.831

Review 6.  Recent advances in the management of immune-mediated thrombotic thrombocytopenic purpura.

Authors:  Sung Hwa Bae; Sung-Hyun Kim; Soo-Mee Bang
Journal:  Blood Res       Date:  2022-04-30

Review 7.  The Challenges in Diagnosis and Management of Acquired Thrombotic Thrombocytopenic Purpura: Consensus Report from Three Gulf Countries.

Authors:  Murtadha Al-Khabori; Faisal Alsayegh; Hasan Al Yaseen; Sabir Hussien; Amar Lal; Muna Al Rasheed; Mohammad Al Bader; Salam Al Kindi; Mahmoud Marashi
Journal:  Oman Med J       Date:  2022-07-31

8.  ADAMTS13 Autoantibodies and Burden of Care in Immune Thrombotic Thrombocytopenic purpura: New Evidence and Future Implications.

Authors:  Cristina Dainese; Federica Valeri; Eleonora Pizzo; Alessandra Valpreda; Piera Sivera; Barbara Montaruli; Annamaria Porreca; Massimo Massaia; Benedetto Bruno; Alessandra Borchiellini
Journal:  Clin Appl Thromb Hemost       Date:  2022 Jan-Dec       Impact factor: 3.512

9.  Acquired thrombotic thrombocytopenic purpura with possible association with AstraZeneca-Oxford COVID-19 vaccine.

Authors:  Mona Al-Ahmad; Mona Al-Rasheed; Neveen Abo Bakr Shalaby
Journal:  EJHaem       Date:  2021-05-18
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.