Takeda T, Nagai B
Tohoku J Exp Med. 1986 Feb;148(2):119-23. doi: 10.1620/tjem.148.119.
A NH4Cl-HCO3(-)-mediated, acetazolamide modulated hemolysis test was carried out in seven patients with hereditary spherocytosis (HS), and the amount of enzyme antigen as well as activities of carbonic anhydrase (CA) were determined. Except for a decrease in CA-B activity (p less than 0.05), the amount of enzyme antigen, total and specific activities of both isozymes of CA and dependent activity of CA-C were within the normal range. Fifty percent and 95% hemolysis times were significantly shorter than the normal range, and they remained abnormal even in the presence of acetazolamide. This hemolysis test, especially H50 valuse, was therefore shown to have diagnostic value in HS.
对7例遗传性球形红细胞增多症(HS)患者进行了氯化铵-碳酸氢根(-)介导的乙酰唑胺调节溶血试验,并测定了酶抗原量以及碳酸酐酶(CA)的活性。除CA-B活性降低(p<0.05)外,酶抗原量、CA两种同工酶的总活性和比活性以及CA-C的依赖活性均在正常范围内。50%和95%溶血时间明显短于正常范围,即使在存在乙酰唑胺的情况下仍异常。因此,该溶血试验,尤其是H50值,在HS中具有诊断价值。