首页> 外文期刊>Blood coagulation & fibrinolysis: an international journal in haemostasis and thrombosis >Low intraindividual variability of activated partial thromboplastin time revealed in a population of 10487 control individuals
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Low intraindividual variability of activated partial thromboplastin time revealed in a population of 10487 control individuals

机译:在10487名对照人群中发现激活的部分凝血活酶时间的低个体差异

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The activated partial thromboplastin time (aPTT) is a routine coagulation test that reflects the activities of multiple coagulation proteins. Given the known genetic elements underlying the different coagulation factor activities, a low intraindividual variability is expected in aPTT values, but has not been demonstrated in a large population. In this regard, we evaluated the intraindividual variability of aPTT by analyzing serial aPTTs from a large population. The study population consisted of control individuals who had three or more consecutive aPTT values at at least 6-month intervals at a single institution. The coefficient of variation of serial aPTT values was determined in each control individual, and the mean value of the coefficient of variations in the control population was calculated. The aPTT values from a total of 10487 individuals [mean age 57 years (range 21-93 years); male-to-female ratio 1:0.9] were included. The mean value of the coefficient of variation of aPTTs in those individuals was 3.75%, which indicates a very low intraindividual variability. This is the first study to demonstrate a low intraindividual variability of aPTT in a large population. The result supports the previous notion that aPTT is a genetically determined parameter and has potential clinical implications.
机译:激活的部分凝血活酶时间(aPTT)是常规凝血测试,反映了多种凝血蛋白的活性。考虑到不同凝血因子活性的潜在遗传因素,aPTT值的个体内变异性较低,但尚未在大量人群中得到证实。在这方面,我们通过分析来自大量人群的一系列aPTT来评估aPTT的个体内变异性。研究人群由在单个机构中至少六个月间隔具有三个或三个以上连续aPTT值的对照个体组成。在每个对照个体中确定一系列aPTT值的变异系数,并计算对照群体中变异系数的平均值。共有10487个人的aPTT值[平均年龄57岁(范围21-93岁);男女比例为1:0.9]。这些人中aPTT的变异系数的平均值为3.75%,这表明其个体差异非常小。这是第一项证明aPTT在大量人群中个体内变异性低的研究。该结果支持以前的观点,即aPTT是遗传确定的参数,具有潜在的临床意义。

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