Iolascon A, Stewart G W, Ajetunmobi J F, Perrotta S, Delaunay J, Carella M, Zelante L, Gasparini P
D Biomed Età Evolutiva, University di Bari, Bari, Italy; the Department of Medicine, University College London, Rayne Institute, London, UK.
Blood. 1999 May 1;93(9):3120-3.
Familial pseudohyperkalemia is a "leaky red blood cell" condition in which the cells show a temperature-dependent loss of potassium (K) from red blood cells when stored at room temperature, manifesting as apparent hyperkalemia. The red blood cells show a reduced lifespan in vivo but there is no frank hemolysis. Studies of cation content and transport show a marginal increase in permeability at 37 degrees C and a degree of cellular dehydration, qualitatively similar to the changes seen in dehydrated hereditary stomatocytosis (hereditary xerocytosis). Physiological studies have shown that the passive leak to K has an abnormal temperature dependence, such that the leak is less sensitive to temperature than that in normal cells. We performed genetic mapping on the original family and found that the condition in this kindred maps to the same locus (16q23-ter) that we have previously identified for an Irish family with dehydrated hereditary stomatocytosis, which does not show the same temperature effects.
家族性假性高钾血症是一种“红细胞渗漏”病症,在这种病症中,细胞在室温下储存时会出现温度依赖性的红细胞钾(K)丢失,表现为明显的高钾血症。红细胞在体内的寿命缩短,但无明显溶血现象。对阳离子含量和转运的研究表明,在37摄氏度时通透性略有增加,且存在一定程度的细胞脱水,在性质上与脱水遗传性口形红细胞增多症(遗传性干燥细胞增多症)中所见的变化相似。生理学研究表明,钾的被动渗漏对温度具有异常依赖性,因此这种渗漏对温度的敏感性低于正常细胞。我们对最初的家族进行了基因定位,发现这个家族的病症定位于我们之前为一个患有脱水遗传性口形红细胞增多症的爱尔兰家族所确定的同一基因座(16q23 - 末端),而该爱尔兰家族并未表现出相同的温度效应。