Wolf B H, Weening R S, Schutgens R B, van Noorden C J, Vogels I M, Nagelkerke N J
Department of Pediatrics, University of Amsterdam, The Netherlands.
Clin Chim Acta. 1987 Sep 30;168(2):129-36. doi: 10.1016/0009-8981(87)90281-6.
The results of a quantitative spectrophotometric enzyme assay, a fluorescent spot test and a cytochemical assay for glucose-6-phosphate dehydrogenase deficiency were compared systematically. The high sensitivity of the spectrophotometric assay and the fluorescent spot test in the detection of severely deficient individuals was confirmed. For the detection of heterozygote females, however both tests were unreliable; the sensitivities of the fluorescent spot test and the spectrophotometric assay being 32% and 11% respectively. Specificities for both tests were high (99%). Introduction of the ratio of glucose-6-phosphate dehydrogenase and pyruvate kinase (G-6-PD/PK ratio) activities increased the sensitivity of the spectrophotometric assay to nearly 100%. It is concluded that the fluorescent spot test should be used for the diagnosis of G-6-PD deficiency in developing countries; whereas if spectrophotometric enzyme assays are available, the G-6-PD/PK ratio should always be performed. In cases where the ratio is less than 0.70, cytochemical analysis is indicated.
系统比较了定量分光光度酶法、荧光斑点试验和葡萄糖-6-磷酸脱氢酶缺乏症的细胞化学分析结果。分光光度法和荧光斑点试验在检测严重缺乏个体方面的高灵敏度得到了证实。然而,对于杂合子女性的检测,这两种测试都不可靠;荧光斑点试验和分光光度法的灵敏度分别为32%和11%。两种测试的特异性都很高(99%)。引入葡萄糖-6-磷酸脱氢酶和丙酮酸激酶的活性比(G-6-PD/PK比)可将分光光度法的灵敏度提高到近100%。结论是,荧光斑点试验应用于发展中国家葡萄糖-6-磷酸脱氢酶缺乏症的诊断;而如果有分光光度酶法,应始终进行G-6-PD/PK比检测。在该比值小于0.70的情况下,需进行细胞化学分析。