Macfarlane J D, Poorthuis B J, van de Kamp J J, Russell R G, Caswell A M
Department of Rheumatology, University of Leiden, The Netherlands.
Clin Chem. 1988 Sep;34(9):1937-41.
Hypophosphatasia is an inherited disease in which a deficiency of the bone/liver/kidney or tissue nonspecific isoenzyme of alkaline phosphatase (AP; EC 3.1.3.1) occurs. All forms of the disease are characterized clinically by defective mineralization. Several biochemical abnormalities are associated with the deficiency of AP activity, e.g., increased urinary excretion of inorganic pyrophosphate (PPi) and phosphoethanolamine (PEA). Measurement of these analytes in kindreds of patients with hypophosphatasia may be useful in identifying carriers, and in understanding the inheritance of the disease. We studied biochemically 22 members of the kindred of a 24-year-old woman with hypophosphatasia. We measured activity of AP in serum and leukocytes, and the urinary excretion of PPi and PEA. Within this kindred, urinary excretion of PPi appeared to indicate carrier status, and among the clinically normal adults, values for this analyte were inversely correlated with the activity of AP in serum. These results suggest that urinary excretion of PPi is sensitive to subtle changes in the activity of AP.
低磷酸酯酶症是一种遗传性疾病,其中会出现骨/肝/肾或组织非特异性碱性磷酸酶(AP;EC 3.1.3.1)同工酶缺乏的情况。该疾病的所有形式在临床上均以矿化缺陷为特征。几种生化异常与AP活性缺乏有关,例如,无机焦磷酸(PPi)和磷酸乙醇胺(PEA)的尿排泄增加。在低磷酸酯酶症患者的亲属中测量这些分析物可能有助于识别携带者,并有助于了解该疾病的遗传方式。我们对一名患有低磷酸酯酶症的24岁女性的亲属中的22名成员进行了生化研究。我们测量了血清和白细胞中AP的活性,以及PPi和PEA的尿排泄量。在这个家系中,PPi的尿排泄似乎表明了携带者状态,并且在临床正常的成年人中,该分析物的值与血清中AP的活性呈负相关。这些结果表明,PPi的尿排泄对AP活性的细微变化敏感。