Cai Huili, Mullier François, Frotscher Birgit, Briquel Marie-Elisabeth, Toussaint Marie, Massin Frédéric, Lecompte Thomas, Latger-Cannard Véronique
Service d'Hématologie Biologique, CHRU Nancy, Nancy, France.
Laboratory of Hematology, Namur Thrombosis and Hemostasis Center (NTHC), Namur Research Institute for Life Sciences, CHU Dinant Godinne UcL Namur, Yvoir, Belgium.
Semin Thromb Hemost. 2016 Apr;42(3):282-91. doi: 10.1055/s-0035-1564836. Epub 2016 Feb 12.
Dense granule disorder is one of the most common platelet abnormalities, resulting from dense granule deficiency or secretion defect. This study was aimed to evaluate the clinical usefulness of the flow cytometric combination of mepacrine uptake/release assay and CD63 expression detection in the management of patients with suspected dense granule disorder. Over a period of 5 years, patients with abnormal platelet aggregation and/or reduced adenosine triphosphate (ATP) secretion suggestive of dense granule disorder were consecutively enrolled. The flow cytometric assays were systematically performed to further investigate dense granule functionality. Among the 26 included patients, 18 cases showed impaired mepacrine uptake/release and reduced CD63 expression on activated platelets, consistent with δ-storage pool deficiency (SPD). Another seven patients showed decrease in mepacrine release and CD63 expression but mepacrine uptake was normal, indicating secretion defect rather than δ-SPD. Unfortunately, ATP secretion could not be measured in 7 out of the 26 patients due to insufficient sample and/or severe thrombocytopenia. This test combination provides a rapid and effective method to detect the heterogeneous abnormalities of platelet dense granule by distinguishing between storage and release defects. This combination is particularly advantageous for severely thrombocytopenic patients and pediatric patients in which only minimal sample is required.
致密颗粒紊乱是最常见的血小板异常之一,由致密颗粒缺乏或分泌缺陷引起。本研究旨在评估吖啶橙摄取/释放试验与CD63表达检测的流式细胞术联合检测在疑似致密颗粒紊乱患者管理中的临床应用价值。在5年的时间里,连续纳入血小板聚集异常和/或三磷酸腺苷(ATP)分泌减少提示致密颗粒紊乱的患者。系统地进行流式细胞术检测以进一步研究致密颗粒功能。在纳入的26例患者中,18例显示吖啶橙摄取/释放受损,活化血小板上CD63表达降低,符合δ-储存池缺乏(SPD)。另外7例患者吖啶橙释放和CD63表达降低,但吖啶橙摄取正常,提示分泌缺陷而非δ-SPD。遗憾的是,26例患者中有7例由于样本不足和/或严重血小板减少而无法检测ATP分泌。这种检测组合提供了一种快速有效的方法,通过区分储存和释放缺陷来检测血小板致密颗粒的异质性异常。这种组合对于严重血小板减少患者和儿科患者特别有利,因为这些患者只需要极少的样本。