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抗磷脂抗体患者血小板计数的血栓风险分层:一项纵向研究。

Thrombotic risk stratification by platelet count in patients with antiphospholipid antibodies: a longitudinal study.

机构信息

Department of Rheumatology, Endocrinology and Nephrology, Graduate School of Medicine and Faculty of Medicine, Hokkaido University, Sapporo, Japan.

出版信息

J Thromb Haemost. 2017 Sep;15(9):1782-1787. doi: 10.1111/jth.13763. Epub 2017 Aug 5.

Abstract

UNLABELLED

Essentials Thrombotic risk stratification is an unmet need in antiphospholipid antibody carriers. Platelet count and antiphospholipid score (aPL-S) were combined to predict thrombotic events. Patients with high aPL-S are at high thrombotic risk regardless of platelet count. If platelet count is low, patients with low aPL-S are also on high thrombotic risk.

SUMMARY

Background Thrombocytopenia is a non-criteria clinical manifestation of antiphospholipid syndrome. However, it remains to be elucidated whether thrombocytopenia increases thrombotic risk in antiphospholipid antibody (aPL) carriers. Objectives To investigate the impact of platelet count in terms of predicting thrombotic events in aPL carriers, and to stratify the thrombotic risk by combining platelet count and antiphospholipid score (aPL-S), which represents a quantification of aPL varieties and titers. Patients/methods A single-center, retrospective, longitudinal study comprising 953 consecutive patients who were suspected of having autoimmune disease between January 2002 and December 2006 was performed. Low platelet count was defined as a count of < 150 × 10 μL at the time of aPL testing. Results A negative correlation was observed between aPL-S and platelet count (r = - 0.2477). Among aPL-positive patients, those with a low platelet count developed thrombosis more frequently than those without (hazard ratio [HR] 2.95, 95% confidence interval [CI] 1.11-7.88). Among aPL-negative patients, no difference was found in the predictive value of thrombosis regardless of platelet count. Patients with aPLs were further divided into two subgroups according to aPL-S. Among low-aPL-S patients, those with low platelet counts developed thrombosis more frequently than those without (HR 3.44, 95% CI 1.05-11.2). In contrast, high-aPL-S patients developed thrombosis frequently regardless of platelet count. Conclusions aPL carriers with low platelet counts are at high risk of developing thrombosis. In particular, 'low-aPL-S carriers' may be stratified by platelet count in terms of predicting future thrombotic events.

摘要

背景

血小板减少症是抗磷脂综合征的一种非标准临床表现。然而,血小板减少症是否会增加抗磷脂抗体(aPL)携带者的血栓形成风险仍有待阐明。

目的

本研究旨在探讨血小板计数对 aPL 携带者发生血栓事件的预测作用,并通过联合血小板计数和抗磷脂评分(aPL-S)来分层血栓形成风险,该评分代表了 aPL 种类和滴度的量化。

患者/方法:进行了一项单中心、回顾性、纵向研究,共纳入 953 例 2002 年 1 月至 2006 年 12 月期间疑似自身免疫性疾病的连续患者。低血小板计数定义为 aPL 检测时计数<150×10μL。

结果

aPL-S 与血小板计数呈负相关(r=-0.2477)。在 aPL 阳性患者中,血小板计数低的患者比血小板计数正常的患者更易发生血栓形成(风险比[HR]2.95,95%置信区间[CI]1.11-7.88)。在 aPL 阴性患者中,无论血小板计数如何,血栓形成的预测价值均无差异。根据 aPL-S,将 aPL 患者进一步分为两组。在低 aPL-S 患者中,血小板计数低的患者比血小板计数正常的患者更易发生血栓形成(HR 3.44,95%CI 1.05-11.2)。相比之下,高 aPL-S 患者无论血小板计数如何均易发生血栓形成。

结论

血小板计数低的 aPL 携带者发生血栓形成的风险较高。特别是,“低 aPL-S 携带者”可能需要根据血小板计数来分层预测未来的血栓形成事件。

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