Zheng X Long, Kaufman Richard M, Goodnough Lawrence T, Sadler J Evan
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.
Blood. 2004 Jun 1;103(11):4043-9. doi: 10.1182/blood-2003-11-4035. Epub 2004 Feb 24.
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.
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。