Suppr超能文献

血浆置换对特发性和非特发性血栓性血小板减少性紫癜患者血浆ADAMTS13金属蛋白酶活性、抑制剂水平及临床结局的影响

Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura.

作者信息

Zheng X Long, Kaufman Richard M, Goodnough Lawrence T, Sadler J Evan

机构信息

Department of Pathology and Laboratory Medicine, The Children's Hospital of Philadelphia, The University of Pennsylvania School of Medicine, 34th Street and Civic Center Boulevard, ARC 316, Philadelphia, PA 19104, USA.

出版信息

Blood. 2004 Jun 1;103(11):4043-9. doi: 10.1182/blood-2003-11-4035. Epub 2004 Feb 24.

Abstract

Therapeutic plasma exchange is an effective empiric treatment for thrombotic thrombocytopenic purpura (TTP), but how therapy affects the level of a disintegrin and metalloprotease with thrombospondin type 1 motif 13 (ADAMTS13) or inhibitor has not been reported in many patients. We prospectively analyzed ADAMTS13 activity and inhibitor levels in 37 adults with TTP. ADAMTS13 level at presentation was lower than 5% in 16 of 20 patients with idiopathic TTP and in none of 17 patients with TTP associated with hematopoietic stem cell transplantation, cancer, drugs, or pregnancy (P <.00001). Seven of the 16 patients with ADAMTS13 activity lower than 5% ( approximately 44%) had inhibitors. For 8 patients followed serially with ADAMTS13 activity lower than 5% but no inhibitor at presentation, plasma exchange led to complete clinical remission and a rise in ADAMTS13 level. In contrast, 4 patients with low ADAMTS13 activity but high-titer inhibitor (> 5 units/mL) had neither a rise in ADAMTS13 activity nor a reduction in the inhibitor titer: 3 had recurrent disease and 1 died. Among 17 patients with AD-AMTS13 activity at presentation higher than 25%, 10 died. Mortality rate for idiopathic TTP was 15%, whereas mortality for nonidiopathic TTP was 59% (P <.02). We conclude that assays of ADAMTS13 activity and inhibitors in addition to the clinical categories (idiopathic TTP and nonidiopathic TTP) are predictive of outcome and may be useful to tailor patient treatment.

摘要

治疗性血浆置换是血栓性血小板减少性紫癜(TTP)的一种有效经验性治疗方法,但在许多患者中,该疗法如何影响具有血小板反应蛋白基序的解聚素和金属蛋白酶13(ADAMTS13)或其抑制剂的水平尚未见报道。我们前瞻性分析了37例成人TTP患者的ADAMTS13活性和抑制剂水平。20例特发性TTP患者中有16例就诊时ADAMTS13水平低于5%,而17例与造血干细胞移植、癌症、药物或妊娠相关的TTP患者中无一例如此(P<.00001)。16例ADAMTS13活性低于5%的患者中有7例(约44%)存在抑制剂。对于8例就诊时ADAMTS13活性低于5%但无抑制剂的患者进行连续随访,血浆置换导致临床完全缓解且ADAMTS13水平升高。相比之下,4例ADAMTS13活性低但抑制剂滴度高(>5单位/mL)的患者,其ADAMTS13活性既未升高,抑制剂滴度也未降低:3例复发,1例死亡。17例就诊时ADAMTS13活性高于25%的患者中有10例死亡。特发性TTP的死亡率为15%,而非特发性TTP的死亡率为59%(P<.02)。我们得出结论,除了临床分类(特发性TTP和非特发性TTP)外,检测ADAMTS13活性和抑制剂可预测预后,可能有助于调整患者的治疗方案。

相似文献

3
Recent advances in thrombotic thrombocytopenic purpura.
Hematology Am Soc Hematol Educ Program. 2004:407-23. doi: 10.1182/asheducation-2004.1.407.
4
5
Platelets: thrombotic thrombocytopenic purpura.
Hematology Am Soc Hematol Educ Program. 2002:315-34. doi: 10.1182/asheducation-2002.1.315.
8
Performance of a clinical prediction score for thrombotic thrombocytopenic purpura in an independent cohort.
Vox Sang. 2013 Nov;105(4):313-8. doi: 10.1111/vox.12050. Epub 2013 May 11.

引用本文的文献

1
Bone marrow metastasis of gastric signet ring cell carcinoma complicated by thrombotic microangiopathy: A case report.
World J Gastrointest Oncol. 2025 Aug 15;17(8):109424. doi: 10.4251/wjgo.v17.i8.109424.
2
Thrombotic Thrombocytopenic Purpura and Evans Syndrome: Validating and Exploring 20 Years of Routine Hospital Care.
J Blood Med. 2025 Jun 7;16:279-292. doi: 10.2147/JBM.S513578. eCollection 2025.
3
Thrombotic Thrombocytopenic Purpura in Pediatric Patients.
Biomedicines. 2025 Apr 25;13(5):1038. doi: 10.3390/biomedicines13051038.
4
Fatal interplay between acquired thrombotic thrombocytopenic purpura and posterior reversible encephalopathy syndrome: a case report.
Radiol Case Rep. 2025 Mar 27;20(6):2995-2999. doi: 10.1016/j.radcr.2025.02.094. eCollection 2025 Jun.
6
Animal models for thrombotic thrombocytopenic purpura: a narrative review.
Ann Blood. 2023 Sep 30;8. doi: 10.21037/aob-22-18. Epub 2022 Nov 16.
7
Immune thrombotic thrombocytopenic purpura: pathogenesis and novel therapies: a narrative review.
Ann Blood. 2023 Sep 30;8. doi: 10.21037/aob-22-29. Epub 2023 Jan 6.
8
Novel mechanisms of action of emerging therapies of hereditary thrombotic thrombocytopenic purpura.
Expert Rev Hematol. 2024 Jul;17(7):341-351. doi: 10.1080/17474086.2024.2356763. Epub 2024 May 20.
10
How We Interpret Thrombosis with Thrombocytopenia Syndrome?
Int J Mol Sci. 2024 May 1;25(9):4956. doi: 10.3390/ijms25094956.

本文引用的文献

2
Molecular characterization of ADAMTS13 gene mutations in Japanese patients with Upshaw-Schulman syndrome.
Blood. 2004 Feb 15;103(4):1305-10. doi: 10.1182/blood-2003-06-1796. Epub 2003 Oct 16.
3
Congenital thrombotic thrombocytopenic purpura in association with a mutation in the second CUB domain of ADAMTS13.
Blood. 2004 Jan 15;103(2):627-9. doi: 10.1182/blood-2003-04-1346. Epub 2003 Sep 25.
7
Cleavage of von Willebrand factor requires the spacer domain of the metalloprotease ADAMTS13.
J Biol Chem. 2003 Aug 8;278(32):30136-41. doi: 10.1074/jbc.M305331200. Epub 2003 Jun 5.
8
Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency.
Kidney Int. 2003 Jun;63(6):1995-9. doi: 10.1046/j.1523-1755.63.6s.1.x.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验