Dolin Hallie H, Maitta Robert W
Department of Pathology, University Hospitals Cleveland Medical Center, Case Western Reserve University, Cleveland, OH 44106, USA.
Biomedicines. 2024 Mar 11;12(3):621. doi: 10.3390/biomedicines12030621.
Thrombotic thrombocytopenic purpura (TTP) is an uncommon, but potentially disabling or even deadly, thrombotic microangiopathy with a well-studied mechanism of ADAMTS13 deficiency or dysfunction. While established treatments are largely effective, the standard ADAMTS13 testing required to definitively diagnose TTP may cause delays in diagnosis and treatment, highlighting the need for rapid and effective diagnostic methods. Additionally, the heterogeneous presentation and varied inciting events of TTP suggest more variation in its mechanism than previously thought, implying three potential pathways rather than the accepted two. The recent discovery of ADAMTS13 conformation as a potential contributor to TTP in addition to the proposal of using the absolute immature platelet count (A-IPC) as a biomarker, present novel areas for monitoring and treatment. A-IPC in particular may serve as a more rapid and accurate diagnostic test to distinguish TTP from non-TTP TMAs and to monitor treatment response and relapse. These considerations highlight the need to further study TTP in order to improve best practices and patient care.
血栓性血小板减少性紫癜(TTP)是一种罕见但可能致残甚至致命的血栓性微血管病,其发病机制为ADAMTS13缺乏或功能障碍,这一机制已得到充分研究。虽然现有治疗方法大多有效,但明确诊断TTP所需的标准ADAMTS13检测可能会导致诊断和治疗延迟,这凸显了快速有效诊断方法的必要性。此外,TTP的临床表现各异,诱发因素多样,这表明其发病机制的变异比之前认为的更多,意味着存在三条潜在途径而非公认的两条。除了提出将绝对未成熟血小板计数(A-IPC)作为生物标志物外,最近发现ADAMTS13构象可能是TTP的一个促成因素,这为监测和治疗提供了新领域。特别是A-IPC可能作为一种更快速、准确的诊断测试,用于区分TTP与非TTP血栓性微血管病,并监测治疗反应和复发情况。这些考量凸显了进一步研究TTP以改善最佳实践和患者护理的必要性。