Marlar Richard A, Gausman Jana N, Tsuda Hiroko, Rollins-Raval Marian A, Brinkman Herm Jan M
Department of Pathology, TriCore Reference Laboratories, University of New Mexico, Albuquerque, NM, USA.
OU Medicine, Inc, Laboratory, University of Oklahoma Medical Center, Oklahoma City, OK, USA.
J Thromb Haemost. 2021 Jan;19(1):68-74. doi: 10.1111/jth.15109.
Hereditary deficiencies of protein S (PS) increase the risk of venous thrombosis; however, assessing the plasma levels of PS can be difficult because of its complex physiological interactions in plasma, sample-related preanalytical variables, and numerous acquired disease processes. Reliable laboratory assays are essential for accurate evaluation of PS when diagnosing a congenital deficiency based on the plasma phenotype alone. This report presents the current evidence-based recommendations for clinical PS assays as well as when to test for PS abnormalities.
蛋白S(PS)的遗传性缺乏会增加静脉血栓形成的风险;然而,由于其在血浆中的复杂生理相互作用、与样本相关的分析前变量以及众多获得性疾病过程,评估血浆中PS的水平可能会很困难。在仅根据血浆表型诊断先天性缺乏时,可靠的实验室检测对于准确评估PS至关重要。本报告提出了关于临床PS检测以及何时检测PS异常的当前循证建议。