Crofton P M
Department of Paediatric Biochemistry, Royal Hospital for Sick Children, Edinburgh, U.K.
Clin Chem. 1992 May;38(5):663-70.
This modified lectin affinity electrophoresis method is suitable for simultaneous measurement of liver, bone, and high-molecular-mass (high-Mr) isoforms of alkaline phosphatase (ALP; EC 3.1.3.1) in children. Age-related isoform reference ranges were derived for 247 children, ages 0-13 years. Liver ALP did not appear in plasma until after six months of age, and remained constant after one year of age. Bone ALP was highest in the youngest age group, and declined to relatively constant activities thereafter. High-MrALP was not detected in normal children. In bone disease, the bone isoform was increased in all age groups. In liver disease, only 5 of 30 infants younger than six months had detectable liver ALP, although half had increased bone ALP. Among children older than six months, 5 patients with biliary atresia and 15 patients with hepatitis A all had increased liver isoform activity. Liver ALP was also a sensitive index of early hepatobiliary complications in 27 nonjaundiced children with cystic fibrosis. Measurement of ALP isoforms therefore yields useful clinical information in children older than six months but is of doubtful value in younger infants.
这种改良的凝集素亲和电泳方法适用于同时检测儿童肝脏、骨骼和高分子量(高Mr)碱性磷酸酶(ALP;EC 3.1.3.1)同工酶。得出了247名0至13岁儿童与年龄相关的同工酶参考范围。肝脏ALP直到6个月龄后才出现在血浆中,1岁后保持稳定。骨骼ALP在最年幼的年龄组中最高,此后下降至相对稳定的活性。正常儿童未检测到高MrALP。在骨骼疾病中,所有年龄组的骨骼同工酶均升高。在肝脏疾病中,30名6个月以下婴儿中只有5名可检测到肝脏ALP,尽管一半婴儿的骨骼ALP升高。在6个月以上儿童中,5例胆道闭锁患者和15例甲型肝炎患者的肝脏同工酶活性均升高。肝脏ALP也是27例非黄疸型囊性纤维化儿童早期肝胆并发症的敏感指标。因此,检测ALP同工酶对6个月以上儿童可提供有用的临床信息,但对较小婴儿的价值存疑。