Ballas Samir K, Files Beatrice, Luchtman-Jones Lori, Benjamin Lennette, Swerdlow Paul, Hilliard Lee, Coates Thomas, Abboud Miguel, Wojtowicz-Praga Slawomir, Kuypers Frans A, Michael Grindel J
Thomas Jefferson University, Philadelphia, PA 19107, USA.
Hemoglobin. 2006;30(2):165-70. doi: 10.1080/03630260600642260.
In a multicenter study (eight centers), we determined secretory phospholipase A(2) (sPLA(2)) levels in patients with sickle cell disease and acute chest syndrome (ACS). The diagnosis of ACS was made according to established criteria. The sPLA2 levels were determined in blood samples collected at baseline (time of diagnosis) and serially thereafter up to day 22-35 follow-up visits. Thirty-four of 43 (80%) patients with ACS had enzyme levels > or =1.00 AU at baseline. The enzyme levels decreased significantly on Days 2 through Days 25-35 after baseline. Nine of 43 (20%) patients had baseline sPLA2 values of <1.00 AU with six of them never exceeding 1.00 AU at any point in time during follow-up. The data indicate that the reliability of sPLA(2( for predicting the development of ACS is not perfect (100%) as was previously reported but occurs in about 80% of the patients.
在一项多中心研究(八个中心)中,我们测定了镰状细胞病和急性胸部综合征(ACS)患者的分泌型磷脂酶A2(sPLA2)水平。ACS的诊断依据既定标准。在基线(诊断时)采集的血样中测定sPLA2水平,并在之后连续进行直至第22 - 35天的随访。43例ACS患者中有34例(80%)在基线时酶水平≥1.00 AU。基线后第2天至第25 - 35天酶水平显著下降。43例患者中有9例(20%)基线sPLA2值<1.00 AU,其中6例在随访期间任何时间点都未超过1.00 AU。数据表明,sPLA2预测ACS发生的可靠性并不像之前报道的那样完美(100%),而是约80%的患者会出现。