Scriver C R
Department of Pediatrics, McGill University, Montreal, Canada.
Acta Paediatr Suppl. 1994 Dec;407:11-8. doi: 10.1111/j.1651-2227.1994.tb13441.x.
Science addresses ignorance; medicine uses facts. The scientific approach to phenylketonuria (PKU) led to the discovery of its causes, both ultimate (allelic heterogeneity at the PAH locus) and proximate (dietary phenylalanine), the proximal phenotype (phenylalanine hydroxylase deficiency), the associated metabolic phenotype and the major distal phenotype (impaired cognitive development and neuropsychological function) for which the pathogenesis is still being investigated. By applying knowledge through newborn screening, early diagnosis and treatment, the brain disease of PKU has been greatly ameliorated. The population approach, which converted incidence into cases, revealed genetic heterogeneity in hyperphenylalaninemia involving four other loci, controlling cofactor (BH4) synthesis and recycling, and non-random geographic distribution of mutant PAH alleles of which more than 170 were known in April 1994. Various mechanisms including founder effect, genetic drift, hypermutability and selection (perhaps) explain the polymorphic aggregate frequency (approximately 0.01) and spectrum of PKU mutations in human populations.
科学应对未知;医学运用事实。对苯丙酮尿症(PKU)的科学研究方法促成了其病因的发现,包括最终病因(苯丙氨酸羟化酶基因座的等位基因异质性)和近端病因(膳食苯丙氨酸)、近端表型(苯丙氨酸羟化酶缺乏)、相关代谢表型以及主要远端表型(认知发育和神经心理功能受损),其发病机制仍在研究中。通过新生儿筛查、早期诊断和治疗应用知识,PKU 这种脑部疾病已得到极大改善。将发病率转化为病例数的群体研究方法揭示了高苯丙氨酸血症中的基因异质性,涉及其他四个基因座,控制辅因子(BH4)的合成和循环利用,以及突变型 PAH 等位基因的非随机地理分布,1994 年 4 月已知的此类等位基因超过 170 种。包括奠基者效应、遗传漂变、高突变性和选择(可能)在内的各种机制解释了人群中 PKU 突变的多态性聚集频率(约为 0.01)和谱系。